Professor Bertram Muller-Myhsok
Health Data Science
- Work email Bertram.Muller-Myhsok@liverpool.ac.uk
Publications
Filter the publication list
Filter list by type
- Show all
- Journal article
- Conference paper
- Chapter
- Other
2023
Genetic and modifiable risk factors combine multiplicatively in common disease (Journal article)
Pang, S., Yengo, L., Nelson, C. P., Bourier, F., Zeng, L., Li, L., . . . Schunkert, H. (2022). Genetic and modifiable risk factors combine multiplicatively in common disease. CLINICAL RESEARCH IN CARDIOLOGY. doi:10.1007/s00392-022-02081-4Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder (Journal article)
Hahn, T., Winter, N. R., Ernsting, J., Gruber, M., Mauritz, M. J., Fisch, L., . . . Repple, J. (2023). Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder. MOLECULAR PSYCHIATRY. doi:10.1038/s41380-022-01936-62022
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities (Journal article)
Price, K. M., Wigg, K. G., Eising, E., Feng, Y., Blokland, K., Wilkinson, M., . . . Barr, C. L. (2022). Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. TRANSLATIONAL PSYCHIATRY, 12(1). doi:10.1038/s41398-022-02250-zGenome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. (Journal article)
Eising, E., Mirza-Schreiber, N., de Zeeuw, E. L., Wang, C. A., Truong, D. T., Allegrini, A. G., . . . Fisher, S. E. (2022). Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.. Proceedings of the National Academy of Sciences of the United States of America, 119(35), e2202764119. doi:10.1073/pnas.2202764119Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning (Journal article)
Rost, N., Bruckl, T. M., Koutsouleris, N., Binder, E. B., & Mueller-Myhsok, B. (2022). Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning. BMC MEDICAL INFORMATICS AND DECISION MAKING, 22(1). doi:10.1186/s12911-022-01926-2ExomeChip-based rare variant association study in restless legs syndrome (Journal article)
Tilch, E., Schormair, B., Zhao, C., Hoegl, B., Stefani, A., Berger, K., . . . Winkelmann, J. (2022). ExomeChip-based rare variant association study in restless legs syndrome. SLEEP MEDICINE, 94, 26-30. doi:10.1016/j.sleep.2022.04.001Cis-epistasis at the LPA locus and risk of cardiovascular diseases (Journal article)
Zeng, L., Moser, S., Mirza-Schreiber, N., Lamina, C., Coassin, S., Nelson, C. P., . . . Schunkert, H. (2022). Cis-epistasis at the LPA locus and risk of cardiovascular diseases. CARDIOVASCULAR RESEARCH, 118(4), 1088-1102. doi:10.1093/cvr/cvab136GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating alpha-Klotho levels (Journal article)
Gergei, I., Zheng, J., Andlauer, T. F. M., Brandenburg, V., Mirza-Schreiber, N., Mueller-Myhsok, B., . . . Tobias, J. H. (2022). GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating alpha-Klotho levels. HUMAN MOLECULAR GENETICS, 31(5), 792-802. doi:10.1093/hmg/ddab263DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder (Journal article)
Moser, S., Martins, J., Czamara, D., Lange, J., Mueller-Myhsok, B., & Erhardt, A. (2022). DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder. TRANSLATIONAL PSYCHIATRY, 12(1). doi:10.1038/s41398-022-01802-7Genome and transcriptome profiling of spontaneous preterm birth phenotypes (Journal article)
Gupta, J. K., Care, A., Goodfellow, L., Alfirevic, Z., Muller-Myhsok, B., & Alfirevic, A. (2022). Genome and transcriptome profiling of spontaneous preterm birth phenotypes. SCIENTIFIC REPORTS, 12(1). doi:10.1038/s41598-022-04881-0Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders (Journal article)
Blokland, G. A. M., Grove, J., Chen, C. -Y., Cotsapas, C., Tobet, S., Handa, R., . . . Goldstein, J. M. (2022). Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. BIOLOGICAL PSYCHIATRY, 91(1), 102-117. doi:10.1016/j.biopsych.2021.02.9722021
Sex differences in the genetic regulation of the blood transcriptome response to glucocorticoid receptor activation (Journal article)
Moore, S. R., Halldorsdottir, T., Martins, J., Lucae, S., Mueller-Myhsok, B., Mueller, N. S., . . . Arloth, J. (2021). Sex differences in the genetic regulation of the blood transcriptome response to glucocorticoid receptor activation. TRANSLATIONAL PSYCHIATRY, 11(1). doi:10.1038/s41398-021-01756-2Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study (Journal article)
Goodfellow, L., Verwijs, M. C., Care, A., Sharp, A., Ivandic, J., Poljak, B., . . . van de Wijgert, J. H. H. M. (2021). Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study. BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 128(13), 2061-2072. doi:10.1111/1471-0528.16816A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts. (Journal article)
Ni, G., Zeng, J., Revez, J. A., Wang, Y., Zheng, Z., Ge, T., . . . Wray, N. R. (2021). A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.. Biological psychiatry, 90(9), 611-620. doi:10.1016/j.biopsych.2021.04.018Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping (Journal article)
Miranda, L., Paul, R., Puetz, B., Koutsouleris, N., & Mueller-Myhsok, B. (2021). Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping. FRONTIERS IN PSYCHIATRY, 12. doi:10.3389/fpsyt.2021.665536Association and genetic overlap between clinical chemistry tests and migraine. (Journal article)
Tanha, H. M., Martin, N. G., Whitfield, J. B., Nyholt, D. R., & International Headache Genetics Consortium (IHGC). (2021). Association and genetic overlap between clinical chemistry tests and migraine.. Cephalalgia : an international journal of headache, 41(11-12), 1208-1221. doi:10.1177/03331024211018131Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning (Journal article)
Pelin, H., Ising, M., Stein, F., Meinert, S., Meller, T., Brosch, K., . . . Andlauer, T. F. M. (2021). Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning. NEUROPSYCHOPHARMACOLOGY, 46(11), 1895-1905. doi:10.1038/s41386-021-01051-0Metabolic profiling of maternal serum of women a high-risk of spontaneous preterm birth using NMR and MGWAS approach (Journal article)
Gupta, J. K., Care, A., Goodfellow, L., Alfirevic, Z., Lian, L. -Y., Mueller-Myhsok, B., . . . Phelan, M. M. (2021). Metabolic profiling of maternal serum of women a high-risk of spontaneous preterm birth using NMR and MGWAS approach. BIOSCIENCE REPORTS, 41(9). doi:10.1042/BSR20210759Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. (Journal article)
Coleman, J. R. I., Peyrot, W. J., Purves, K. L., Davis, K. A. S., Rayner, C., Choi, S. W., . . . Breen, G. (2021). Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.. Molecular psychiatry, 26(9), 5465. doi:10.1038/s41380-020-0779-4Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: a nested case control study (Journal article)
Care, A. G., Gupta, J. K., Goodfellow, L., Zhang, G., Monangi, N., Belling, E., . . . Alfirevic, Z. (2021). Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: a nested case control study. European Journal of Obstetrics & Gynecology and Reproductive Biology. doi:10.1016/j.ejogrb.2021.08.015Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression (Journal article)
Forstner, A. J., Awasthi, S., Wolf, C., Maron, E., Erhardt, A., Czamara, D., . . . Schumacher, J. (2021). Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. MOLECULAR PSYCHIATRY, 26(8), 4179-4190. doi:10.1038/s41380-019-0590-2Plasma long-chain omega-3 fatty acid status and risk of recurrent early spontaneous preterm birth: a prospective observational study (Journal article)
Goodfellow, L., Care, A., Harrold, J., Sharp, A., Ivandic, J., Poljak, B., . . . Alfirevic, Z. (2021). Plasma long-chain omega-3 fatty acid status and risk of recurrent early spontaneous preterm birth: a prospective observational study. ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 100(8), 1401-1411. doi:10.1111/aogs.14147Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia (Journal article)
Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., . . . Schulte-Koerne, G. (2021). Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26(7), 3004-3017. doi:10.1038/s41380-020-00898-xNovel EDGE encoding method enhances ability to identify genetic interactions (Journal article)
Hall, M. A., Wallace, J., Lucas, A. M., Bradford, Y., Verma, S. S., Mueller-Myhsok, B., . . . Ritchie, M. D. (2021). Novel EDGE encoding method enhances ability to identify genetic interactions. PLOS GENETICS, 17(6). doi:10.1371/journal.pgen.1009534Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. (Journal article)
Amare, A. T., Schubert, K. O., Hou, L., Clark, S. R., Papiol, S., Cearns, M., . . . Baune, B. T. (2021). Association of polygenic score for major depression with response to lithium in patients with bipolar disorder.. Molecular psychiatry, 26(6), 2457-2470. doi:10.1038/s41380-020-0689-5Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology (Journal article)
Mullins, N., Forstner, A. J., O'Connell, K. S., Coombes, B., Coleman, J. R. I., Qiao, Z., . . . Andreassen, O. A. (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. NATURE GENETICS, 53(6), 817-+. doi:10.1038/s41588-021-00857-4The association between genetically determined ABO blood types and major depressive disorder (Journal article)
Garvert, L., Baune, B. T., Berger, K., Boomsma, D. I., Breen, G., Greinacher, A., . . . Van der Auwera, S. (2021). The association between genetically determined ABO blood types and major depressive disorder. PSYCHIATRY RESEARCH, 299. doi:10.1016/j.psychres.2021.113837Interaction of developmental factors and ordinary stressful life events on brain structure in adults (Journal article)
Ringwald, K. G., Meller, T., Schmitt, S., Andlauer, T. F. M., Stein, F., Brosch, K., . . . Kircher, T. (2021). Interaction of developmental factors and ordinary stressful life events on brain structure in adults. NEUROIMAGE-CLINICAL, 30. doi:10.1016/j.nicl.2021.102683Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity (Journal article)
Schmitt, S., Meller, T., Stein, F., Brosch, K., Ringwald, K., Pfarr, J. -K., . . . Nenadic, I. (2021). Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity. PSYCHOLOGICAL MEDICINE. doi:10.1017/S0033291721001082Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders (Journal article)
Andlauer, T. F. M., Guzman-Parra, J., Streit, F., Strohmaier, J., Gonzalez, M. J., Gil Flores, S., . . . Rietschel, M. (2021). Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. MOLECULAR PSYCHIATRY, 26(4), 1286-1298. doi:10.1038/s41380-019-0558-2Genetic factors influencing a neurobiological substrate for psychiatric disorders (Journal article)
Andlauer, T. F. M., Muehleisen, T. W., Hoffstaedter, F., Teumer, A., Wittfeld, K., Teuber, A., . . . Cichon, S. (2021). Genetic factors influencing a neurobiological substrate for psychiatric disorders. TRANSLATIONAL PSYCHIATRY, 11(1). doi:10.1038/s41398-021-01317-7"The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment (Journal article)
Heilbronner, U., Papiol, S., Budde, M., Andlauer, T. F. M., Strohmaier, J., Streit, F., . . . Schulze, T. G. (2021). "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 186(2), 77-89. doi:10.1002/ajmg.b.32837A polygenic resilience score moderates the genetic risk for schizophrenia. (Journal article)
Hess, J. L., Tylee, D. S., Mattheisen, M., Schizophrenia Working Group of the Psychiatric Genomics Consortium., Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH)., Børglum, A. D., . . . Glatt, S. J. (2021). A polygenic resilience score moderates the genetic risk for schizophrenia.. Molecular psychiatry, 26(3), 800-815. doi:10.1038/s41380-019-0463-8Congenital heart disease risk loci identified by genome-wide association study in European patients (Journal article)
Lahm, H., Jia, M., Dressen, M., Wirth, F., Puluca, N., Gilsbach, R., . . . Krane, M. (2021). Congenital heart disease risk loci identified by genome-wide association study in European patients. JOURNAL OF CLINICAL INVESTIGATION, 131(2). doi:10.1172/JCI141837Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study (Journal article)
Goodfellow, L., Verwijs, M., Care, A., Sharp, A., Ivandic, J., Poljak, B., . . . van de Wijgert, J. H. H. M. (2021). Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study. doi:10.1101/2021.01.14.21249680Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT) (Journal article)
Kappelmann, N., Mueller-Myhsok, B., & Kopf-Beck, J. (2021). Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT). TRIALS, 22(1). doi:10.1186/s13063-020-04965-0Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity (Journal article)
Ostkamp, P., Salmen, A., Pignolet, B., Goerlich, D., Andlauer, T. F. M., Schulte-Mecklenbeck, A., . . . Schwab, N. (2021). Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 118(1). doi:10.1073/pnas.2018457118A Network Control Theory Approach to Longitudinal Symptom Dynamics in Major Depressive Disorder. (Journal article)
Hahn, T., Jamalabadi, H., Emden, D., Goltermann, J., Ernsting, J., Winter, N. R., . . . Opel, N. (2021). A Network Control Theory Approach to Longitudinal Symptom Dynamics in Major Depressive Disorder.. CoRR, abs/2107.10178.Identification of early pregnancy metabolomic biomarkers of women at high-risk of preterm birth using NMR and mGWAS (Conference Paper)
Gupta, J., Care, A., Goodfellow, L., Alfirevic, Z., Lian, L. -Y., Muller-Myhsok, B., . . . Phelan, M. (2021). Identification of early pregnancy metabolomic biomarkers of women at high-risk of preterm birth using NMR and mGWAS. In BRITISH JOURNAL OF PHARMACOLOGY Vol. 178 (pp. 432-433). Retrieved from https://www.webofscience.com/Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies (Journal article)
Munn-Chernoff, M. A., Johnson, E. C., Chou, Y. -L., Coleman, J. R. I., Thornton, L. M., Walters, R. K., . . . Agrawal, A. (2021). Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. ADDICTION BIOLOGY, 26(1). doi:10.1111/adb.128802020
Cerebral small vessel disease genomics and its implications across the lifespan. (Journal article)
Sargurupremraj, M., Suzuki, H., Jian, X., Sarnowski, C., Evans, T. E., Bis, J. C., . . . Debette, S. (2020). Cerebral small vessel disease genomics and its implications across the lifespan.. Nature communications, 11(1), 6285. doi:10.1038/s41467-020-19111-2A large-scale genome-wide association study meta-analysis of cannabis use disorder. (Journal article)
Johnson, E. C., Demontis, D., Thorgeirsson, T. E., Walters, R. K., Polimanti, R., Hatoum, A. S., . . . Agrawal, A. (2020). A large-scale genome-wide association study meta-analysis of cannabis use disorder.. The lancet. Psychiatry, 7(12), 1032-1045. doi:10.1016/s2215-0366(20)30339-4Habitual sleep disturbances and migraine: a Mendelian randomization study. (Journal article)
Daghlas, I., Vgontzas, A., Guo, Y., Chasman, D. I., International Headache Genetics Consortium., & Saxena, R. (2020). Habitual sleep disturbances and migraine: a Mendelian randomization study.. Annals of clinical and translational neurology, 7(12), 2370-2380. doi:10.1002/acn3.51228Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease (Conference Paper)
Gola, D., Erdmann, J., Lall, K., Magi, R., Muller-Myhsok, B., Schunkert, H., & Konig, I. R. (2020). Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease. In CIRCULATION-GENOMIC AND PRECISION MEDICINE Vol. 13 (pp. 569-575). doi:10.1161/CIRCGEN.120.002932Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS (Journal article)
Andlauer, T. F. M., Link, J., Martin, D., Ryner, M., Hermanrud, C., Grummel, V., . . . Hemmer, B. (2020). Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. BMC MEDICINE, 18(1). doi:10.1186/s12916-020-01769-6A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q (Journal article)
Grimm, T., Garshasbi, M., Puettmann, L., Chen, W., Ullmann, R., Muller-Myhsok, B., . . . Kuss, A. W. (2020). A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE, 48(6), 478-489. doi:10.1024/1422-4917/a000758Sex differences in the genetic regulation of the blood transcriptome response to glucocorticoid receptor activation (Preprint)
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. (Journal article)
Hofer, E., Roshchupkin, G. V., Adams, H. H. H., Knol, M. J., Lin, H., Li, S., . . . Seshadri, S. (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.. Nature communications, 11(1), 4796. doi:10.1038/s41467-020-18367-yGene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes (Journal article)
Faber, H., Kurtoic, D., Krishnamoorthy, G., Weber, P., Puetz, B., Mueller-Myhsok, B., . . . Andlauer, T. F. M. (2020). Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes. FRONTIERS IN IMMUNOLOGY, 11. doi:10.3389/fimmu.2020.02165Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study (Journal article)
Zhou, J., Passero, K., Palmiero, N. E., Mueller-Myhsok, B., Kleber, M. E., Maerz, W., & Hall, M. A. (2020). Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. PLOS ONE, 15(9). doi:10.1371/journal.pone.0238304Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression (Journal article)
Hagenaars, S. P., Coleman, J. R. I., Choi, S. W., Gaspar, H., Adams, M. J., Howard, D. M., . . . Lewis, C. M. (2020). Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183(6), 309-330. doi:10.1002/ajmg.b.32807The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. (Journal article)
Coleman, J. R. I., Gaspar, H. A., Bryois, J., Bipolar Disorder Working Group of the Psychiatric Genomics Consortium., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium., & Breen, G. (2019). The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.. Biological psychiatry. doi:10.1016/j.biopsych.2019.10.015A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. (Journal article)
Guo, Y., Rist, P. M., Daghlas, I., Giulianini, F., International Headache Genetics Consortium., 23andMe Research Team., . . . Chasman, D. I. (2020). A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.. Nature communications, 11(1). doi:10.1038/s41467-020-17002-0Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (Journal article)
Coleman, J. R. I., Peyrot, W. J., Purves, K. L., Davis, K. A. S., Rayner, C., Choi, S. W., . . . Sullivan, P. F. (2020). Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY, 25(7), 1430-1446. doi:10.1038/s41380-019-0546-6Complement genes contribute sex-biased vulnerability in diverse disorders. (Journal article)
Kamitaki, N., Sekar, A., Handsaker, R. E., de Rivera, H., Tooley, K., Morris, D. L., . . . McCarroll, S. A. (2020). Complement genes contribute sex-biased vulnerability in diverse disorders.. Nature, 582(7813), 577-581. doi:10.1038/s41586-020-2277-xSalivary cortisol response to psychosocial stress in the late evening depends on CRHR1 genotype (Journal article)
Weeger, J., Ising, M., Mueller-Myhsok, B., Uhr, M., Schmidt, U., & Steiger, A. (2020). Salivary cortisol response to psychosocial stress in the late evening depends on CRHR1 genotype. PSYCHONEUROENDOCRINOLOGY, 116. doi:10.1016/j.psyneuen.2020.104685A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. (Journal article)
Shen, X., Howard, D. M., Adams, M. J., Hill, W. D., Clarke, T. -K., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium., . . . McIntosh, A. M. (2020). A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank.. Nature communications, 11(1), 2301. doi:10.1038/s41467-020-16022-0Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (Journal article)
Bryois, J., Skene, N. G., Hansen, T. F., Kogelman, L. J. A., Watson, H. J., Liu, Z., . . . Sullivan, P. F. (2020). Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease.. Nature genetics, 52(5), 482-493. doi:10.1038/s41588-020-0610-9Minimal phenotyping yields genome-wide association signals of low specificity for major depression (Journal article)
Cai, N., Revez, J. A., Adams, M. J., Andlauer, T. F. M., Breen, G., Byrne, E. M., . . . Flint, J. (2020). Minimal phenotyping yields genome-wide association signals of low specificity for major depression. NATURE GENETICS, 52(4), 437-+. doi:10.1038/s41588-020-0594-5The genetic architecture of the human cerebral cortex (Journal article)
Grasby, K. L., Jahanshad, N., Painter, J. N., Colodro-Conde, L., Bralten, J., Hibar, D. P., . . . Medland, S. E. (2020). The genetic architecture of the human cerebral cortex. SCIENCE, 367(6484), 1340-+. doi:10.1126/science.aay6690Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (Journal article)
Glanville, K. P., Coleman, J. R. I., Hanscombe, K. B., Euesden, J., Choi, S. W., Purves, K. L., . . . Borglum, A. D. (2020). Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY, 87(5), 419-430. doi:10.1016/j.biopsych.2019.06.031Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status (Journal article)
Gola, D., Erdmann, J., Mueller-Myhsok, B., Schunkert, H., & Koenig, I. R. (2020). Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status. GENETIC EPIDEMIOLOGY, 44(2), 125-138. doi:10.1002/gepi.22279DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. (Journal article)
Arloth, J., Eraslan, G., Andlauer, T. F. M., Martins, J., Iurato, S., Kühnel, B., . . . Mueller, N. S. (2020). DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning.. PLoS computational biology, 16(2), e1007616. doi:10.1371/journal.pcbi.1007616Identification of Restless Legs Syndrome Genes by Mutational Load Analysis (Journal article)
Tilch, E., Schormair, B., Zhao, C., Salminen, A. V., Nikolic, A. A., Holzknecht, E., . . . Oexle, K. (2020). Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. ANNALS OF NEUROLOGY, 87(2), 184-193. doi:10.1002/ana.25658A different view on fine-scale population structure in Western African populations (Journal article)
Chaichoompu, K., Abegaz, F., Cavadas, B., Fernandes, V., Mueller-Myhsok, B., Pereira, L., & Van Steen, K. (2020). A different view on fine-scale population structure in Western African populations. HUMAN GENETICS, 139(1), 45-59. doi:10.1007/s00439-019-02069-7Deep targeted-NGS identifies RLS genes by differential burden with low-frequency variants and differential target sequencing depth (Conference Paper)
Tilch, E., Schormair, B., Zhao, C., Salminen, A., Nikolic, A. A., Holzknecht, E., . . . Oexle, K. (2020). Deep targeted-NGS identifies RLS genes by differential burden with low-frequency variants and differential target sequencing depth. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 28 (pp. 415). Retrieved from https://www.webofscience.com/IMPACT OF POLYGENIC AND POLY-ENVIRONMENTAL RISK FACTORS ON A PSYCHOSIS RISK PHENOTYPE EXPLAINED THROUGH BRAIN STRUCTURE (Conference Paper)
Meller, T., Schmitt, S., Stein, F., Brosch, K., Grotegerd, D., Dohm, K., . . . Nenadic, I. (2020). IMPACT OF POLYGENIC AND POLY-ENVIRONMENTAL RISK FACTORS ON A PSYCHOSIS RISK PHENOTYPE EXPLAINED THROUGH BRAIN STRUCTURE. In SCHIZOPHRENIA BULLETIN Vol. 46 (pp. S35-S36). Retrieved from https://www.webofscience.com/Influence of CRHR1 genotype on sleep and cortisol of healthy volunteers after Trier Social Stress Test in the late evening (Conference Paper)
Weeger, J., Ising, M., Mueller-Myhsok, B., Uhr, M., Schmidt, U., Yassouridis, A., & Steiger, A. (2020). Influence of CRHR1 genotype on sleep and cortisol of healthy volunteers after Trier Social Stress Test in the late evening. In JOURNAL OF SLEEP RESEARCH Vol. 29 (pp. 117-118). Retrieved from https://www.webofscience.com/Phenome-wide association studies on cardiovascular health and fatty acids considering phenotype quality control practices for epidemiological data (Journal article)
Passero, K., He, X., Zhou, J., Mueller-Myhsok, B., Kleber, M. E., Maerz, W., & Hall, M. A. (2020). Phenome-wide association studies on cardiovascular health and fatty acids considering phenotype quality control practices for epidemiological data. PACIFIC SYMPOSIUM ON BIOCOMPUTING 2020, 659-670. Retrieved from https://www.webofscience.com/Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects. (Journal article)
Nenadić, I., Meller, T., Schmitt, S., Stein, F., Brosch, K., Mosebach, J., . . . Kircher, T. (n.d.). Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.. Psychological medicine. doi:10.1017/s00332917200028222019
Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways (Journal article)
Foo, J. C., Trautmann, N., Sticht, C., Treutlein, J., Frank, J., Streit, F., . . . Rietschel, M. (2019). Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways. TRANSLATIONAL PSYCHIATRY, 9(1). doi:10.1038/s41398-019-0671-7SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection (Journal article)
Gassen, N. C., Niemeyer, D., Muth, D., Corman, V. M., Martinelli, S., Gassen, A., . . . Rein, T. (2019). SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection. NATURE COMMUNICATIONS, 10. doi:10.1038/s41467-019-13659-4Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (Journal article)
Lee, P. H., Anttila, V., Won, H., Feng, Y. -C. A., Rosenthal, J., Zhu, Z., . . . Smoller, J. W. (2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. CELL, 179(7), 1469-+. doi:10.1016/j.cell.2019.11.020Migraine polygenic risk score associates with efficacy of migraine-specific drugs (Journal article)
Kogelman, L. J. A., Esserlind, A. -L., Christensen, A. F., Awasthi, S., Ripke, S., Ingason, A., . . . Consortium, I. H. G. (2019). Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Neurology Genetics, 5(6). doi:10.1212/NXG.0000000000000364Genetic architecture of subcortical brain structures in 38,851 individuals (Journal article)
Satizabal, C. L., Adams, H. H. H., Hibar, D. P., White, C. C., Knol, M. J., Stein, J. L., . . . Ikram, M. A. (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS, 51(11), 1624-+. doi:10.1038/s41588-019-0511-yINVESTIGATING THE COMMON GENETIC BASIS OF ANTIDEPRESSANT RESPONSE (Conference Paper)
Pain, O., Hodgson, K., Trubetskoy, V., Baune, B., Biernacka, J., Fabbri, C., . . . Lewis, C. (2019). INVESTIGATING THE COMMON GENETIC BASIS OF ANTIDEPRESSANT RESPONSE. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S91-S92). doi:10.1016/j.euroneuro.2019.07.198LONGITUDINAL TRANSCRIPTOME-WIDE GENE EXPRESSION ANALYSIS OF SLEEP DEPRIVATION TREATMENT INDICATES INVOLVEMENT OF CIRCADIAN GENES AND IMMUNE PATHWAYS (Conference Paper)
Foo, J., Trautmann, N., Sticht, C., Treutlein, J., Frank, J., Streit, F., . . . Rietschel, M. (2019). LONGITUDINAL TRANSCRIPTOME-WIDE GENE EXPRESSION ANALYSIS OF SLEEP DEPRIVATION TREATMENT INDICATES INVOLVEMENT OF CIRCADIAN GENES AND IMMUNE PATHWAYS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S136). doi:10.1016/j.euroneuro.2019.08.045Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton (Journal article)
Gampawar, P., Saba, Y., Werner, U., Schmidt, R., Mueller-Myhsok, B., & Schmidt, H. (2019). Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton. FRONTIERS IN GENETICS, 10. doi:10.3389/fgene.2019.00856Treatment response classes in major depressive disorder identified by model-based clustering and validated by clinical prediction models (Journal article)
Paul, R., Andlauer, T. F. M., Czamara, D., Hoehn, D., Lucae, S., Puetz, B., . . . Saemann, P. G. (2019). Treatment response classes in major depressive disorder identified by model-based clustering and validated by clinical prediction models. TRANSLATIONAL PSYCHIATRY, 9. doi:10.1038/s41398-019-0524-4GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores (Journal article)
Mullins, N., Bigdeli, T. B., Borglum, A. D., Coleman, J. R. I., Demontis, D., Mehta, D., . . . Consortium, P. G. (2019). GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. American Journal of Psychiatry, 176(8), 651-660. doi:10.1176/appi.ajp.2019.18080957Association of Intrathecal Immunoglobulin G Synthesis With Disability Worsening in Multiple Sclerosis. (Journal article)
Gasperi, C., Salmen, A., Antony, G., Bayas, A., Heesen, C., Kümpfel, T., . . . German Competence Network of Multiple Sclerosis. (2019). Association of Intrathecal Immunoglobulin G Synthesis With Disability Worsening in Multiple Sclerosis.. JAMA neurology, 76(7), 841-849. doi:10.1001/jamaneurol.2019.0905CSF parameters associated with early MRI activity in patients with MS (Journal article)
Klein, A., Selter, R. C., Hapfelmeier, A., Berthele, A., Mueller-Myhsok, B., Pongratz, V., . . . Hemmer, B. (2019). CSF parameters associated with early MRI activity in patients with MS. NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION, 6(4). doi:10.1212/NXI.0000000000000573Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa (Journal article)
Walton, E., Hibar, D., Yilmaz, Z., Jahanshad, N., Cheung, J., Batury, V. -L., . . . Bulik, C. M. (2019). Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56(7), 5146-5156. doi:10.1007/s12035-018-1439-4Iron Metabolism, Hepcidin, and Mortality (the Ludwigshafen Risk and Cardiovascular Health Study) (Journal article)
Grammer, T. B., Scharnagl, H., Dressel, A., Kleber, M. E., Silbernagel, G., Pilz, S., . . . Strnad, P. (2019). Iron Metabolism, Hepcidin, and Mortality (the Ludwigshafen Risk and Cardiovascular Health Study). CLINICAL CHEMISTRY, 65(7), 849-861. doi:10.1373/clinchem.2018.297242Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (Journal article)
Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hamalainen, E., . . . Sullivan, P. F. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10. doi:10.1038/s41467-019-10461-0Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-kappa B-driven inflammation and cardiovascular risk (Journal article)
Zannas, A. S., Jia, M., Hafner, K., Baumert, J., Wiechmann, T., Pape, J. C., . . . Binder, E. B. (2019). Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-kappa B-driven inflammation and cardiovascular risk. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 116(23), 11370-11379. doi:10.1073/pnas.1816847116Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects (Journal article)
Meller, T., Schmitt, S., Stein, F., Brosch, K., Mosebach, J., Yueksel, D., . . . Nenadic, I. (2019). Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects. SCHIZOPHRENIA RESEARCH, 208, 67-75. doi:10.1016/j.schres.2019.04.018Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. (Journal article)
Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardiñas, A. F., . . . Stahl, E. A. (2019). Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.. Nature genetics, 51(6), 1068. doi:10.1038/s41588-019-0435-6Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population (Journal article)
Musliner, K. L., Mortensen, P. B., McGrath, J. J., Suppli, N. P., Hougaard, D. M., Bybjerg-Grauholm, J., . . . Consortium, P. G. (2019). Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population. JAMA PSYCHIATRY, 76(5), 516-525. doi:10.1001/jamapsychiatry.2018.4166Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium (Journal article)
Polimanti, R., Peterson, R. E., Ong, J. -S., MacGregor, S., Edwards, A. C., Clarke, T. -K., . . . Neale, B. M. (2019). Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49(7), 1218-1226. doi:10.1017/S0033291719000667Genome-wide association study identifies 30 loci associated with bipolar disorder (Journal article)
Stahl, E. A., Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V., . . . Sklar, P. (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. NATURE GENETICS, 51(5), 793-+. doi:10.1038/s41588-019-0397-8Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 and Intimate Partner Violence on Emotional and Cognitive Development in Childhood. (Journal article)
Halldorsdottir, T., Kurtoic, D., Müller-Myhsok, B., Binder, E. B., & Blair, C. (2019). Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 and Intimate Partner Violence on Emotional and Cognitive Development in Childhood.. The American journal of psychiatry, appiajp201918091018. doi:10.1176/appi.ajp.2019.18091018Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults A 2-Sample Mendelian Randomization Study (Journal article)
Choi, K. W., Chen, C. -Y., Stein, M. B., Klimentidis, Y. C., Wang, M. -J., Koenen, K. C., . . . Sullivan, P. F. (2019). Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults A 2-Sample Mendelian Randomization Study. JAMA PSYCHIATRY, 76(4), 399-408. doi:10.1001/jamapsychiatry.2018.4175Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity A Meta-analysis (Journal article)
Marini, S., Crawford, K., Morotti, A., Lee, M. J., Pezzini, A., Moomaw, C. J., . . . Sheth, K. (2019). Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity A Meta-analysis. JAMA NEUROLOGY, 76(4), 480-491. doi:10.1001/jamaneurol.2018.4519Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials (Journal article)
Buck, D., Andlauer, T. F. M., Igl, W., Wicklein, E. -M., Muehlau, M., Weber, F., . . . Hemmer, B. (2019). Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. MULTIPLE SCLEROSIS JOURNAL, 25(4), 565-573. doi:10.1177/1352458518763089Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Journal article)
Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardinas, A. F., . . . Working, I. -G. S. (2019). Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. NATURE GENETICS, 51(4), 659-+. doi:10.1038/s41588-019-0364-4Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia (Journal article)
Harold, D., Connolly, S., Riley, B. P., Kendler, K. S., McCarthy, S. E., McCombie, W. R., . . . Morris, D. W. (2019). Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180(3), 223-231. doi:10.1002/ajmg.b.32716Should phenotype of previous preterm birth influence management of women with short cervix in subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary (Journal article)
Care, A., Muller-Myhsok, B., Olearo, E., Todros, T., Caradeux, J., Goya, M., . . . Alfirevic, Z. (2019). Should phenotype of previous preterm birth influence management of women with short cervix in subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 53(4), 529-534. doi:10.1002/uog.19118Identification of common genetic risk variants for autism spectrum disorder (Journal article)
Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H., . . . Wilson, C. H. (2019). Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51(3), 431-+. doi:10.1038/s41588-019-0344-8Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia (Journal article)
Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., . . . Schulte-Koerne, G. (2019). Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9. doi:10.1038/s41398-019-0402-0Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland (Journal article)
Arnau-Soler, A., Macdonald-Dunlop, E., Adams, M. J., Clarke, T. -K., MacIntyre, D. J., Milburn, K., . . . Sullivan, P. F. (2019). Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9. doi:10.1038/s41398-018-0360-yAssociation of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank (Journal article)
Barbu, M. C., Zeng, Y., Shen, X., Cox, S. R., Clarke, T. K., Gibson, J., . . . Nivard, M. G. (2019). Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4(01), 91-100. doi:10.1016/j.bpsc.2018.07.006BLOOD-BASED AUTISM SPECTRUM DISORDER SIGNATURES FROM THE ITALIAN AUTISM NETWORK COLLECTION (Conference Paper)
Filosi, M., Mueller-Myhsok, B., Muglia, P., & Domenici, E. (2019). BLOOD-BASED AUTISM SPECTRUM DISORDER SIGNATURES FROM THE ITALIAN AUTISM NETWORK COLLECTION. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S912). doi:10.1016/j.euroneuro.2017.08.234COMMON GENETIC VARIANTS ASSOCIATED WITH PERSONALITY DIMENSIONS IN THE HEIDELBERG COHORT STUDY OF THE ELDERLY (HeiDE): AN UPDATE (Conference Paper)
Heilbronner, U., Andlauer, T., Papiol, S., Budde, M., Strohmaier, J., Streit, F., . . . Schulze, T. G. (2019). COMMON GENETIC VARIANTS ASSOCIATED WITH PERSONALITY DIMENSIONS IN THE HEIDELBERG COHORT STUDY OF THE ELDERLY (HeiDE): AN UPDATE. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S928). doi:10.1016/j.euroneuro.2017.08.263Establishing high sensitivity and specificity for exome sequencing on Ion Proton (Conference Paper)
Gampawar, P., Saba, Y., Werner, U., Schmidt, R., Mueller-Myhsok, B., & Schmidt, H. (2019). Establishing high sensitivity and specificity for exome sequencing on Ion Proton. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 1636). Retrieved from https://www.webofscience.com/Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy (Journal article)
Foo, J. C., Streit, F., Frank, J., Witt, S. H., Treutlein, J., Baune, B. T., . . . Worki, M. D. D. (2019). Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180(1), 35-45. doi:10.1002/ajmg.b.32700Explaining RLS families using risk SNPs from GWAS (Conference Paper)
Tilch, E., Zhao, C., Salminen, A., Antic, A., Schormair, B., Oexle, K., . . . Winkelmann, J. (2019). Explaining RLS families using risk SNPs from GWAS. In EUROPEAN JOURNAL OF HUMAN GENETICS Vol. 27 (pp. 658-659). Retrieved from https://www.webofscience.com/GENETIC FACTORS INFLUENCING THE COMMON NEUROBIOLOGICAL SUBSTRATE FOR MENTAL DISORDERS (Conference Paper)
Andlauer, T., Muhleisen, T., Hoffstaedter, F., Teumer, A., Teuber, A., Reinbold, C., . . . Cichon, S. (2019). GENETIC FACTORS INFLUENCING THE COMMON NEUROBIOLOGICAL SUBSTRATE FOR MENTAL DISORDERS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 29 (pp. S798). doi:10.1016/j.euroneuro.2017.08.032Identification of functionally relevant genetic variants associated with multiple sclerosis using deep learning (Conference Paper)
Arloth, J., Eraslan, G., Andlauer, T., Gieger, C., Gold, R., Heilmann-Heimbach, S., . . . Mueller, N. (2019). Identification of functionally relevant genetic variants associated with multiple sclerosis using deep learning. In MULTIPLE SCLEROSIS JOURNAL Vol. 25 (pp. 906-907). Retrieved from https://www.webofscience.com/Influence of ultraviolet radiation and diminished-function melanocortin 1 receptor variants on multiple sclerosis disease severity in two large multicenter cohort studies (Conference Paper)
Ostkamp, P., Goerlich, D., Andlauer, T. F. M., Salmen, A., Schulte-Mecklenbeck, A., Pignolet, B., . . . Schwab, N. (2019). Influence of ultraviolet radiation and diminished-function melanocortin 1 receptor variants on multiple sclerosis disease severity in two large multicenter cohort studies. In MULTIPLE SCLEROSIS JOURNAL Vol. 25 (pp. 59-60). Retrieved from https://www.webofscience.com/Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 Intimate Partner Violence on Emotional and Cognitive Development in Childhood (Conference Paper)
Halldorsdottir, T., Kurtoic, D., Mueller-Myhsok, B., Binder, E., & Blair, C. (2019). Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 Intimate Partner Violence on Emotional and Cognitive Development in Childhood. In JOURNAL OF NEURAL TRANSMISSION Vol. 126 (pp. 1569-1570). Retrieved from https://www.webofscience.com/2018
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (Journal article)
de Jong, S., Abdalla Diniz, M. J., Saloma, A., Gadelha, A., Santoro, M. L., Ota, V. K., . . . Shi, J. (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1. doi:10.1038/s42003-018-0155-yAtrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (Journal article)
Pulit, S. L., Weng, L. -C., McArdle, P. F., Trinquart, L., Choi, S. H., Mitchell, B. D., . . . Sheth, K. (2018). Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4(6). doi:10.1212/NXG.0000000000000293Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. (Journal article)
Arnau-Soler, A., Adams, M. J., Generation Scotland., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium., Hayward, C., & Thomson, P. A. (2018). Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder.. PloS one, 13(12), e0209160. doi:10.1371/journal.pone.0209160Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders (Journal article)
Walters, R. K., Polimanti, R., Johnson, E. C., McClintick, J. N., Adams, M. J., Adkins, A. E., . . . Team, A. R. (2018). Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21(12), 1656-1669. doi:10.1038/s41593-018-0275-1Neurobiology of the major psychoses: a translational perspective on brain structure and function-the FOR2107 consortium. (Journal article)
Kircher, T., Wöhr, M., Nenadic, I., Schwarting, R., Schratt, G., Alferink, J., . . . Dannlowski, U. (2018). Neurobiology of the major psychoses: a translational perspective on brain structure and function-the FOR2107 consortium.. European archives of psychiatry and clinical neuroscience. doi:10.1007/s00406-018-0943-xMolecular genetic overlap between migraine and major depressive disorder. (Journal article)
Yang, Y., Zhao, H., Boomsma, D. I., Ligthart, L., Belin, A. C., Smith, G. D., . . . Nyholt, D. R. (2018). Molecular genetic overlap between migraine and major depressive disorder.. European journal of human genetics : EJHG, 26(8), 1202-1216. doi:10.1038/s41431-018-0150-2Shared genetic etiology between alcohol dependence and major depressive disorder (Journal article)
Foo, J. C., Streit, F., Treutlein, J., Ripke, S., Witt, S. H., Strohmaier, J., . . . Frank, J. (2018). Shared genetic etiology between alcohol dependence and major depressive disorder. PSYCHIATRIC GENETICS, 28(4), 66-70. doi:10.1097/YPG.0000000000000201Sleep disturbance by pramipexole is modified by Meis1 in mice. (Journal article)
Salminen, A. V., Schormair, B., Flachskamm, C., Torres, M., Mueller-Myhsok, B., Kimura, M., & Winkelmann, J. (2018). Sleep disturbance by pramipexole is modified by Meis1 in mice. JOURNAL OF SLEEP RESEARCH, 27(4). doi:10.1111/jsr.12557Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. (Journal article)
Peyrot, W. J., Van der Auwera, S., Milaneschi, Y., Dolan, C. V., Madden, P. A. F., Sullivan, P. F., . . . Penninx, B. W. J. H. (2018). Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium.. Biological psychiatry, 84(2), 138-147. doi:10.1016/j.biopsych.2017.09.009Age at first birth in women is genetically associated with increased risk of schizophrenia. (Journal article)
Ni, G., Gratten, J., Wray, N. R., Lee, S. H., & Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia.. Scientific reports, 8(1), 10168. doi:10.1038/s41598-018-28160-zA correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. (Journal article)
LeBlanc, M., Zuber, V., Thompson, W. K., Andreassen, O. A., Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium., Frigessi, A., & Andreassen, B. K. (2018). A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework.. BMC genomics, 19(1), 494. doi:10.1186/s12864-018-4859-7Analysis of shared heritability in common disorders of the brain (Journal article)
Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., . . . Neale, B. M. (2018). Analysis of shared heritability in common disorders of the brain. SCIENCE, 360(6395), 1313-+. doi:10.1126/science.aap8757Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (Journal article)
Ruderfer, D. M., Ripke, S., McQuillin, A., Boocock, J., Stahl, E. A., Pavlides, J. M. W., . . . Case-Control, W. T. (2018). Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. CELL, 173(7), 1705-1715. doi:10.1016/j.cell.2018.05.046From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health (Journal article)
Renzi, C., Provencal, N., Bassil, K. C., Evers, K., Kihlbom, U., Radford, E. J., . . . Rutten, B. P. F. (2018). From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health. NEUROEPIGENETICS AND MENTAL ILLNESS, 158, 299-323. doi:10.1016/bs.pmbts.2018.04.011Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood. (Journal article)
Ni, G., Moser, G., Schizophrenia Working Group of the Psychiatric Genomics Consortium., Wray, N. R., & Lee, S. H. (2018). Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.. American journal of human genetics, 102(6), 1185-1194. doi:10.1016/j.ajhg.2018.03.021Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Journal article)
Gormley, P., Kurki, M. I., Hiekkala, M. E., Veerapen, K., Häppölä, P., Mitchell, A. A., . . . Zwart, J. -A. (2018). Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98(4), 743-753.e4. doi:10.1016/j.neuron.2018.04.014Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (Journal article)
Wray, N. R., Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., . . . Working, M. D. D. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. NATURE GENETICS, 50(05), 668-681. doi:10.1038/s41588-018-0090-3The P2RX7 polymorphism rs2230912 is associated with depression: A meta-analysis (Journal article)
Czamara, D., Mueller-Myhsok, B., & Lucae, S. (2018). The P2RX7 polymorphism rs2230912 is associated with depression: A meta-analysis. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 82, 272-277. doi:10.1016/j.pnpbp.2017.11.003Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder (Journal article)
Muehleisen, T. W., Reinbold, C. S., Forstner, A. J., Abramova, L. I., Alda, M., Babadjanova, G., . . . Cichon, S. (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. JOURNAL OF AFFECTIVE DISORDERS, 228, 20-25. doi:10.1016/j.jad.2017.11.068The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. (Journal article)
Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., . . . Li, M. (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. MOLECULAR PSYCHIATRY, 23(2), 400-412. doi:10.1038/mp.2016.231Genetic factors influencing the development of binding and neutralizing antibodies against interferon beta treatment in multiple sclerosis patients (Conference Paper)
Andlauer, T. F. M., Link, J., Buck, D., Ryner, M., Grummel, V., Auer, M., . . . Hemmer, B. (2018). Genetic factors influencing the development of binding and neutralizing antibodies against interferon beta treatment in multiple sclerosis patients. In MULTIPLE SCLEROSIS JOURNAL Vol. 24 (pp. 507-508). Retrieved from https://www.webofscience.com/How well can we classify coronary artery disease using all genetic data and choosing the best classification algorithm? (Conference Paper)
Gola, D., Andlauer, T., Mirza-Schreiber, N., Zeng, L., Mueller-Myhsok, B., & Koenig, I. R. (2018). How well can we classify coronary artery disease using all genetic data and choosing the best classification algorithm?. In GENETIC EPIDEMIOLOGY Vol. 42 (pp. 701-702). Retrieved from https://www.webofscience.com/2017
DNA Methylation signatures in panic disorder (Journal article)
Iurato, S., Carrillo-Roa, T., Arloth, J., Czamara, D., Diener-Hoelzl, L., Lange, J., . . . Erhardt, A. (2017). DNA Methylation signatures in panic disorder. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/s41398-017-0026-1Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders (Journal article)
Xiao, X., Wang, L., Wang, C., Yuan, T. -F., Zhou, D., Zheng, F., . . . Li, M. (2017). Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/s41398-017-0019-0Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations. (Journal article)
Milaneschi, Y., Lamers, F., Peyrot, W. J., Baune, B. T., Breen, G., Dehghan, A., . . . CHARGE Inflammation Working Group and the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. (2017). Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations.. JAMA psychiatry, 74(12), 1214-1225. doi:10.1001/jamapsychiatry.2017.3016Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus (Journal article)
Schulz, H., Ruppert, A. -K., Herms, S., Wolf, C., Mirza-Schreiber, N., Stegle, O., . . . Cichon, S. (2017). Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS, 8. doi:10.1038/s41467-017-01818-4Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. (Journal article)
Rietschel, L., Streit, F., Zhu, G., McAloney, K., Frank, J., Couvy-Duchesne, B., . . . Rietschel, M. (2017). Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes.. Scientific reports, 7(1), 15351. doi:10.1038/s41598-017-11852-3Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis (Journal article)
Schormair, B., Zhao, C., Bell, S., Tilch, E., Salminen, A. V., Putz, B., . . . Wilson, C. H. (2017). Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Lancet Neurol, 16(11), 898-907. doi:10.1016/S1474-4422(17)30327-7An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. (Journal article)
Direk, N., Williams, S., Smith, J. A., Ripke, S., Air, T., Amare, A. T., . . . Sullivan, P. F. (2017). An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. BIOLOGICAL PSYCHIATRY, 82(5), 322-329. doi:10.1016/j.biopsych.2016.11.013Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017) (Journal article)
White, L. O., Ising, M., von Klitzing, K., Sierau, S., Michel, A., Klein, A. M., . . . Stalder, T. (2017). Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017). JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 58(9), 1011-1013. doi:10.1111/jcpp.12770Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. (Journal article)
Zeng, Y., Navarro, P., Shirali, M., Howard, D. M., Adams, M. J., Hall, L. S., . . . McIntosh, A. M. (2017). Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. BIOLOGICAL PSYCHIATRY, 82(5), 312-321. doi:10.1016/j.biopsych.2016.12.012Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 (Journal article)
Chang, H., Li, L., Peng, T., Grigoroiu-Serbanescu, M., Bergen, S. E., Landen, M., . . . Li, M. (2017). Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1. MOLECULAR NEUROBIOLOGY, 54(7), 5166-5176. doi:10.1007/s12035-016-0041-xReduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence. (Journal article)
White, L. O., Ising, M., von Klitzing, K., Sierau, S., Michel, A., Klein, A. M., . . . Stalder, T. (2017). Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 58(9), 998-1007. doi:10.1111/jcpp.12700Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. (Journal article)
Winsvold, B. S., Bettella, F., Witoelar, A., Anttila, V., Gormley, P., Kurth, T., . . . International Headache Genetics Consortium. (2017). Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.. PloS one, 12(9), e0185663. doi:10.1371/journal.pone.0185663Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations (Journal article)
Kim-Hellmuth, S., Bechheim, M., Puetz, B., Mohammadi, P., Nedelec, Y., Giangreco, N., . . . Hornung, V. (2017). Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. NATURE COMMUNICATIONS, 8. doi:10.1038/s41467-017-00366-1Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. (Journal article)
Rivera, M., Locke, A. E., Corre, T., Czamara, D., Wolf, C., Ching-Lopez, A., . . . McGuffin, P. (2017). Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individualst. BRITISH JOURNAL OF PSYCHIATRY, 211(2), 70-76. doi:10.1192/bjp.bp.116.183475Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. (Journal article)
Treutlein, J., Frank, J., Streit, F., Reinbold, C. S., Juraeva, D., Degenhardt, F., . . . Rietschel, M. (2017). Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. GENES, 8(7). doi:10.3390/genes8070183Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (Journal article)
Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., . . . Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/tp.2017.115Genetic effects influencing risk for major depressive disorder in China and Europe (Journal article)
Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S. -A., Abdellaoui, A., . . . Kendler, K. S. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/tp.2016.292Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (Journal article)
McLaughlin, R. L., Schijven, D., van Rheenen, W., van Eijk, K. R., O'Brien, M., Kahn, R. S., . . . Veldink, J. H. (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. NATURE COMMUNICATIONS, 8. doi:10.1038/ncomms14774Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (Journal article)
Power, R. A., Tansey, K. E., Buttenschon, H. N., Cohen-Woods, S., Bigdeli, T., Hall, L. S., . . . Lewis, C. M. (2017). Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. BIOLOGICAL PSYCHIATRY, 81(4), 325-335. doi:10.1016/j.biopsych.2016.05.010Identification of shared risk loci and pathways for bipolar disorder and schizophrenia (Journal article)
Forstner, A. J., Hecker, J., Hofmann, A., Maaser, A., Reinbold, C. S., Muehleisen, T. W., . . . Noethen, M. M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLOS ONE, 12(2). doi:10.1371/journal.pone.0171595Novel genetic loci associated with hippocampal volume (Journal article)
Hibar, D. P., Adams, H. H. H., Jahanshad, N., Chauhan, G., Stein, J. L., Hofer, E., . . . Ikram, M. A. (2017). Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8. doi:10.1038/ncomms13624Aging- and Stress-Related Epigenetic Disinhibition of FKBP5 Contributes to NF-KB-Driven Inflammation and Cardiovascular Risk (Conference Paper)
Zannas, A., Jia, M., Baumert, J., Hafner, K., Koedel, M., Haehle, A., . . . Binder, E. (2017). Aging- and Stress-Related Epigenetic Disinhibition of FKBP5 Contributes to NF-KB-Driven Inflammation and Cardiovascular Risk. In NEUROPSYCHOPHARMACOLOGY Vol. 42 (pp. S310-S311). Retrieved from https://www.webofscience.com/COMMON GENETIC VARIANTS ASSOCIATED WITH PERSONALITY DIMENSIONS IN THE HEIDELBERG COHORT STUDY OF THE ELDERLY (HEIDE) (Conference Paper)
Heilbronner, U., Andlauer, T. F. M., Papiol, S., Budde, M., Strohmaier, J., Streit, F., . . . Schulze, T. G. (2017). COMMON GENETIC VARIANTS ASSOCIATED WITH PERSONALITY DIMENSIONS IN THE HEIDELBERG COHORT STUDY OF THE ELDERLY (HEIDE). In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S381-S382). doi:10.1016/j.euroneuro.2016.09.413Classification of CAD Status Using Machine Learning Approaches (Conference Paper)
Gola, D., Andlauer, T., Mirza-Schreiber, N., Zeng, L., Delgado, G., Kleber, M., . . . Koneig, I. R. (2017). Classification of CAD Status Using Machine Learning Approaches. In HUMAN HEREDITY Vol. 83 (pp. 9). Retrieved from https://www.webofscience.com/Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (Journal article)
Marshall, C. R., Marshall, C. R., Howrigan, D. P., Merico, D., Thiruvahindrapuram, B., Wu, W., . . . Endophenotypes, P. (2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. NATURE GENETICS, 49(1), 27-35. doi:10.1038/ng.3725IDENTIFICATION OF GENETIC INTERACTIONS INVOLVED IN DYSLEXIA PATHOGENESIS (Conference Paper)
Karbalai, N., Czamara, D., Moll, K., Ramus, F., Malik, R., Scerri, T. S., . . . Muller-Myhsok, B. (2017). IDENTIFICATION OF GENETIC INTERACTIONS INVOLVED IN DYSLEXIA PATHOGENESIS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S183-S184). Retrieved from https://www.webofscience.com/POLYGENIC RISK FOR BIP, MDD, AND SCZ IN ANDALUSIAN MULTIPLEX FAMILIES (Conference Paper)
Andlauer, T., Parra, J. G., Strohmaier, J., Streit, F., Frank, J., Forstner, A. J., . . . Rietschel, M. (2017). POLYGENIC RISK FOR BIP, MDD, AND SCZ IN ANDALUSIAN MULTIPLEX FAMILIES. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S385-S386). doi:10.1016/j.euroneuro.2016.09.419POLYGENIC SCORES DERIVED FROM NEUROIMAGING ENDOPHENOTYPES PREDICT OUTCOMES TO PSYCHOTHERAPY AND MEDICATION TREATMENTS FOR MAJOR DEPRESSIVE DISORDER (Conference Paper)
Carrillo-Roa, T., Boadie, D., McGrath, C., Mueller-Myhsok, B., Craighed, E., Mayberg, H., & Binder, E. (2017). POLYGENIC SCORES DERIVED FROM NEUROIMAGING ENDOPHENOTYPES PREDICT OUTCOMES TO PSYCHOTHERAPY AND MEDICATION TREATMENTS FOR MAJOR DEPRESSIVE DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S486). doi:10.1016/j.euroneuro.2016.09.576SEX-SPECIFIC DNA METHYLATION SIGNATURES IN PANIC DISORDER (Conference Paper)
Iurato, S., Carrillo-Roa, T., Arloth, J., Czamara, D., Ising, M., Lucae, S., . . . Erhardt, A. (2017). SEX-SPECIFIC DNA METHYLATION SIGNATURES IN PANIC DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S446-S447). doi:10.1016/j.euroneuro.2016.09.512USING POLYGENIC SCORES BASED ON SCHNEIDERIAN FIRST RANK SYMPTOMS TO CHARACTERIZE DISEASE TRAJECTORIES IN SEVERE MENTAL ILLNESSES (Conference Paper)
Anderson-Schmidt, H., Papiol, S., Andlauer, T. F. M., Heilbronner, U., Budde, M., Kalman, J., . . . Schulze, T. G. (2017). USING POLYGENIC SCORES BASED ON SCHNEIDERIAN FIRST RANK SYMPTOMS TO CHARACTERIZE DISEASE TRAJECTORIES IN SEVERE MENTAL ILLNESSES. In EUROPEAN NEUROPSYCHOPHARMACOLOGY Vol. 27 (pp. S395-S396). doi:10.1016/j.euroneuro.2016.09.4332016
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis (Journal article)
Li, M., Huang, L., Grigoroiu-Serbanescu, M., Bergen, S. E., Landen, M., Hultman, C. M., . . . Rietschel, M. (2016). Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. MOLECULAR NEUROBIOLOGY, 53(10), 6608-6619. doi:10.1007/s12035-015-9559-6Novel genetic loci underlying human intracranial volume identified through genome-wide association (Journal article)
Adams, H. H. H., Hibar, D. P., Chouraki, V., Stein, J. L., Nyquist, P. A., Renteria, M. E., . . . SYS. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19(12), 1569-1582. doi:10.1038/nn.4398Genetic variants in RBFOX3 are associated with sleep latency (Journal article)
Amin, N., Allebrandt, K. V., van der Spek, A., Mueller-Myhsok, B., Hek, K., Teder-Laving, M., . . . van Duijn, C. M. (2016). Genetic variants in RBFOX3 are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24(10), 1488-1495. doi:10.1038/ejhg.2016.31No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study (Journal article)
Johnson, E. C., Bjelland, D. W., Howrigan, D. P., Abdellaoui, A., Breen, G., Borglum, A., . . . Keller, M. C. (2016). No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLOS GENETICS, 12(10). doi:10.1371/journal.pgen.1006343Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. (Journal article)
Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., . . . Palotie, A. (2016). Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.. Nature genetics, 48(10), 1296. doi:10.1038/ng1016-1296cAssociation between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses. (Journal article)
Khankari, N. K., Shu, X. -O., Wen, W., Kraft, P., Lindström, S., Peters, U., . . . Transdisciplinary Research in Cancer of the Lung (TRICL). (2016). Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses.. PLoS medicine, 13(9), e1002118. doi:10.1371/journal.pmed.1002118Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations (Journal article)
Fehringer, G., Kraft, P., Pharoah, P. D., Eeles, R. A., Chatterjee, N., Schumacher, F. R., . . . Hung, R. J. (2016). Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. CANCER RESEARCH, 76(17), 5103-5114. doi:10.1158/0008-5472.CAN-15-2980Hair cortisol in maltreated children and adolescents: Importance of developmental period and maltreatment characteristics (Journal article)
Stalder, T., Ising, M., von Klitzing, K., Sierau, S., Michel, A., Klein, A., . . . White, L. O. (2016). Hair cortisol in maltreated children and adolescents: Importance of developmental period and maltreatment characteristics. PSYCHONEUROENDOCRINOLOGY, 71, 73. doi:10.1016/j.psyneuen.2016.07.190Influence of 25(OH)D levels and genetic variants on disease severity in MS. (Conference Paper)
Andlauer, T. F. M., Koechert, K., Muehlau, M., Munger, K. L., Fitzgerald, K. C., Arnason, B. G. W., . . . Mueller-Myhsok, B. (2016). Influence of 25(OH)D levels and genetic variants on disease severity in MS.. In MULTIPLE SCLEROSIS JOURNAL Vol. 22 (pp. 842-843). Retrieved from https://www.webofscience.com/Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (Journal article)
Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., . . . Milani, L. (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48(8), 856-866. doi:10.1038/ng.3598Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. (Journal article)
Andlauer, T. F. M., Buck, D., Antony, G., Bayas, A., Bechmann, L., Berthele, A., . . . Müller-Myhsok, B. (2016). Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.. Science advances, 2(6), 0. doi:10.1126/sciadv.1501678Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. (Journal article)
Zhao, H., Eising, E., de Vries, B., Vijfhuizen, L. S., Anttila, V., Winsvold, B. S., . . . Nyholt, D. R. (2016). Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. CEPHALALGIA, 36(7), 648-657. doi:10.1177/0333102415591497Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer. (Journal article)
Gao, C., Patel, C. J., Michailidou, K., Peters, U., Gong, J., Schildkraut, J., . . . the Colorectal Transdisciplinary Study (CORECT); Discovery, Biology and Risk of Inherited Variants in Breast Cancer (DRIVE); Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE); Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI); and Transdisciplinary Research in Cancer of the Lung (TRICL). (2016). Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer.. International journal of epidemiology, 45(3), 896-908. doi:10.1093/ije/dyw129Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts (Journal article)
Schwantes-An, T. -H., Zhang, J., Chen, L. -S., Hartz, S. M., Culverhouse, R. C., Chen, X., . . . Saccone, N. L. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. BEHAVIOR GENETICS, 46(2), 151-169. doi:10.1007/s10519-015-9737-3Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept (Journal article)
Franke, B., Stein, J. L., Ripke, S., Anttila, V., Hibar, D. P., van Hulzen, K. J. E., . . . Sullivan, P. F. (2016). Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience, 19(3), 420-431. doi:10.1038/nn.4228Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness (Journal article)
Bigdeli, T. B., Ripke, S., Bacanu, S. -A., Lee, S. H., Wray, N. R., Gejman, P. V., . . . Fanous, A. H. (2016). Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 171(2), 276-289. doi:10.1002/ajmg.b.32402Schizophrenia risk from complex variation of complement component 4 (Journal article)
Sekar, A., Bialas, A. R., de Rivera, H., Davis, A., Hammond, T. R., Kamitaki, N., . . . McCarroll, S. A. (2016). Schizophrenia risk from complex variation of complement component 4. Nature, 530(7589), 177-183. doi:10.1038/nature16549Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (vol 48, pg 856, 2016) (Journal article)
Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., . . . Palotie, A. (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (vol 48, pg 856, 2016). NATURE GENETICS, 48(10), 1296. doi:10.1038/ng1016-1296cPolygenic Scores Derived from Neuroimaging Endophenotypes Predict Outcomes to Psychotherapy and Medication Treatments for Major Depressive Disorder (Conference Paper)
Carrillo-Roa, T., Dunlop, B. W., McGrath, C. L., Czamara, D., Zannas, A. S., Kelley, M. E., . . . Binder, E. B. (2016). Polygenic Scores Derived from Neuroimaging Endophenotypes Predict Outcomes to Psychotherapy and Medication Treatments for Major Depressive Disorder. In BIOLOGICAL PSYCHIATRY Vol. 79 (pp. 155S-156S). Retrieved from https://www.webofscience.com/2015
Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array (Journal article)
Dankowski, T., Buck, D., Andlauer, T. F. M., Antony, G., Bayas, A., Bechmann, L., . . . Ziegler, A. (2015). Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array. GENETIC EPIDEMIOLOGY, 39(8), 601-608. doi:10.1002/gepi.21933Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder (Journal article)
Forstner, A. J., Hofmann, A., Maaser, A., Sumer, S., Khudayberdiev, S., Muehleisen, T. W., . . . Noethen, M. M. (2015). Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. TRANSLATIONAL PSYCHIATRY, 5. doi:10.1038/tp.2015.159Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma (Journal article)
Becker, J., May, A., Gerges, C., Anders, M., Veits, L., Weise, K., . . . Schumacher, J. (2015). Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma. CANCER MEDICINE, 4(11), 1700-1704. doi:10.1002/cam4.500Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. (Journal article)
Vilhjálmsson, B. J., Yang, J., Finucane, H. K., Gusev, A., Lindström, S., Ripke, S., . . . Price, A. L. (2015). Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.. American journal of human genetics, 97(4), 576-592. doi:10.1016/j.ajhg.2015.09.001Familiality and SNP heritability of age at onset and episodicity in major depressive disorder (Journal article)
Ferentinos, P., Koukounari, A., Power, R., Rivera, M., Uher, R., Craddock, N., . . . Lewis, C. M. (2015). Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. PSYCHOLOGICAL MEDICINE, 45(10), 2215-2225. doi:10.1017/S0033291715000215The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects. (Journal article)
Peyrot, W. J., Lee, S. H., Milaneschi, Y., Abdellaoui, A., Byrne, E. M., Esko, T., . . . Social Science Genetic Association Consortium Corporate Collaborator. (2015). The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects.. Molecular psychiatry, 20(6), 735-743. doi:10.1038/mp.2015.50Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol (Journal article)
White, L. O., Klein, A. M., Kirschbaum, C., Kurz-Adam, M., Uhr, M., Mueller-Myhsok, B., . . . von Klitzing, K. (2015). Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol. BMC PSYCHIATRY, 15. doi:10.1186/s12888-015-0512-zGenetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders (Journal article)
Arloth, J., Bogdan, R., Weber, P., Frishman, G., Menke, A., Wagner, K. V., . . . PGC, P. G. C. (2015). Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. NEURON, 86(05), 1189-1202. doi:10.1016/j.neuron.2015.05.034ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis (Journal article)
Breitenstein, B., Brueckl, T. M., Ising, M., Mueller-Myhsok, B., Holsboer, F., & Czamara, D. (2015). ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 168(4), 274-283. doi:10.1002/ajmg.b.32309Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice (Journal article)
Brenndoerfer, J., Altmann, A., Widner-Andrae, R., Puetz, B., Czamara, D., Tilch, E., . . . Czibere, L. (2015). Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice. PLOS ONE, 10(5). doi:10.1371/journal.pone.0128465Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies (Journal article)
Nyholt, D. R., Anttila, V., Winsvold, B. S., Kurth, T., Stefansson, H., Kallela, M., . . . Palotie, A. (2015). Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. CEPHALALGIA, 35(6), 489-499. doi:10.1177/0333102414547784Identification and characterization of HPA-axis reactivity endophenotypes in a cohort of female PTSD patients (Journal article)
Zaba, M., Kirmeier, T., Ionescu, I. A., Wollweber, B., Buell, D. R., Gall-Kleebach, D. J., . . . Schmidt, U. (2015). Identification and characterization of HPA-axis reactivity endophenotypes in a cohort of female PTSD patients. PSYCHONEUROENDOCRINOLOGY, 55, 102-115. doi:10.1016/j.psyneuen.2015.02.005A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder (Journal article)
Hung, C. -F., Breen, G., Czamara, D., Corre, T., Wolf, C., Kloiber, S., . . . Rivera, M. (2015). A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. BMC MEDICINE, 13. doi:10.1186/s12916-015-0334-3Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (Journal article)
Debette, S., Verbaas, C. A. I., Bressler, J., Schuur, M., Smith, A., Bis, J. C., . . . Mosley, T. H. J. (2015). Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. BIOLOGICAL PSYCHIATRY, 77(8), 749-763. doi:10.1016/j.biopsych.2014.08.027Common genetic variants influence human subcortical brain structures (Journal article)
Hibar, D. P., Stein, J. L., Renteria, M. E., Arias-Vasquez, A., Desrivieres, S., Jahanshad, N., . . . SYS. (2015). Common genetic variants influence human subcortical brain structures. NATURE, 520(7546), 224-229. doi:10.1038/nature14101Association of a Brain Methylation Site With Clinical Outcomes in Depression Does Not Replicate Across Populations (Journal article)
Uher, R., Ripke, S., Mueller-Myhsok, B., Lewis, C. M., & Perlis, R. H. (2015). Association of a Brain Methylation Site With Clinical Outcomes in Depression Does Not Replicate Across Populations. AMERICAN JOURNAL OF PSYCHIATRY, 172(4), 395-396. doi:10.1176/appi.ajp.2015.14101348Genetic Relationship Between Depression and Body Mass Index (Conference Paper)
Rivera, M., Locke, A. E., Corre, T., Czamara, D., Wolf, C., Ching-Lopez, A., . . . McGuffin, P. (2015). Genetic Relationship Between Depression and Body Mass Index. In EUROPEAN PSYCHIATRY Vol. 30. doi:10.1016/S0924-9338(15)30560-5LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. (Journal article)
Bulik-Sullivan, B. K., Loh, P. -R., Finucane, H. K., Ripke, S., Yang, J., Schizophrenia Working Group of the Psychiatric Genomics Consortium., . . . Neale, B. M. (2015). LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.. Nature genetics, 47(3), 291-295. doi:10.1038/ng.3211Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (Journal article)
O'Dushlaine, C., Rossin, L., Lee, P. H., Duncan, L., Parikshak, N. N., Newhouse, S., . . . Breen, G. (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. NATURE NEUROSCIENCE, 18(2), 199-209. doi:10.1038/nn.3922MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene (Journal article)
Nischwitz, S., Wolf, C., Andlauer, T. F. M., Czamara, D., Zettl, U. K., Rieckmann, P., . . . Weber, F. (2015). MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. JOURNAL OF NEUROIMMUNOLOGY, 279, 46-49. doi:10.1016/j.jneuroim.2015.01.008Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. (Journal article)
Maier, R., Moser, G., Chen, G. -B., Ripke, S., Cross-Disorder Working Group of the Psychiatric Genomics Consortium., Coryell, W., . . . Lee, S. H. (2015). Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.. American journal of human genetics, 96(2), 283-294. doi:10.1016/j.ajhg.2014.12.006Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis (Conference Paper)
Dankowski, T., Buck, D., Andlauer, T. F., Antony, G., Bayas, A., Bechmann, L., . . . Ziegler, A. (2015). Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis. In HUMAN HEREDITY Vol. 79 (pp. 32-33). Retrieved from https://www.webofscience.com/Exome array GWAS in 10,000 Germans identifies association between MUC22 and multiple sclerosis (Conference Paper)
Buck, D., Dankowski, T., Bayas, A., Gold, R., Heesen, C., Hohlfeld, R., . . . Hemmer, B. (2015). Exome array GWAS in 10,000 Germans identifies association between MUC22 and multiple sclerosis. In EUROPEAN JOURNAL OF NEUROLOGY Vol. 22 (pp. 29). Retrieved from https://www.webofscience.com/Genome-wide association analysis in a German multiple sclerosis cohort (Conference Paper)
Andlauer, T. F. M., Buck, D., Hemmer, B., & Mueller-Myhsok, B. (2015). Genome-wide association analysis in a German multiple sclerosis cohort. In MULTIPLE SCLEROSIS JOURNAL Vol. 21 (pp. 144). Retrieved from https://www.webofscience.com/Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk (Journal article)
Lin, W. -Y., Camp, N. J., Ghoussaini, M., Beesley, J., Michailidou, K., Hopper, J. L., . . . Cox, A. (2015). Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. HUMAN MOLECULAR GENETICS, 24(1), 285-298. doi:10.1093/hmg/ddu431Polygenic Predictors of Antidepressant Treatment-Specific Response (Conference Paper)
Carrillo-Roa, T., McGrath, C. L., Zannas, A. S., Muller-Myhsok, B., Kelley, M. E., Craighead, W. E., . . . Binder, E. B. (2015). Polygenic Predictors of Antidepressant Treatment-Specific Response. In BIOLOGICAL PSYCHIATRY Vol. 77. Retrieved from https://www.webofscience.com/XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans (Journal article)
Juraeva, D., Treutlein, J., Scholz, H., Frank, J., Degenhardt, F., Cichon, S., . . . Rietschel, M. (2015). XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans. NEUROPSYCHOPHARMACOLOGY, 40(2), 361-371. doi:10.1038/npp.2014.1782014
MicroRNA Related Polymorphisms and Breast Cancer Risk (Journal article)
Khan, S., Greco, D., Michailidou, K., Milne, R. L., Muranen, T. A., Heikkinen, T., . . . Nevanlinna, H. (2014). MicroRNA Related Polymorphisms and Breast Cancer Risk. PLOS ONE, 9(11). doi:10.1371/journal.pone.0109973Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (Journal article)
Gusev, A., Lee, S. H., Trynka, G., Finucane, H., Vilhjálmsson, B. J., Xu, H., . . . SWE-SCZ Consortium. (2014). Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.. American journal of human genetics, 95(5), 535-552. doi:10.1016/j.ajhg.2014.10.004Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes (Journal article)
Kim, S., Becker, J., Bechheim, M., Kaiser, V., Noursadeghi, M., Fricker, N., . . . Schumacher, J. (n.d.). Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes. Nature Communications, 5. doi:10.1038/ncomms6236The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels (Journal article)
van Leeuwen, E. M., Smouter, F. A. S., Kam-Thong, T., Karbalai, N., Smith, A. V., Harris, T. B., . . . van Duijn, C. M. (2014). The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels. PLOS ONE, 9(10). doi:10.1371/journal.pone.0109290Biological insights from 108 schizophrenia-associated genetic loci (Journal article)
Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. -H., Holmans, P. A., . . . Consor, W. T. C. -C. (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature, 511(7510), 421-427. doi:10.1038/nature13595Targeted Resequencing and Systematic In Vivo Functional Testing Identifies Rare Variants in MEIS1 as Significant Contributors to Restless Legs Syndrome (Journal article)
Schulte, E. C., Kousi, M., Tan, P. L., Tilch, E., Knauf, F., Lichtner, P., . . . Winkelmann, J. (2014). Targeted Resequencing and Systematic In Vivo Functional Testing Identifies Rare Variants in MEIS1 as Significant Contributors to Restless Legs Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS, 95(1), 85-95. doi:10.1016/j.ajhg.2014.06.005Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome (Journal article)
Schulte, E. C., Schramm, K., Schurmann, C., Lichtner, P., Herder, C., Roden, M., . . . Winkelmann, J. (2014). Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome. PLOS ONE, 9(5). doi:10.1371/journal.pone.0098092Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS (Journal article)
Ruf, C. G., Schmelz, H. -U., Port, M., Wagner, W., Matthies, C., Mueller-Myhsok, B., . . . Abend, M. (2014). Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS. BRITISH JOURNAL OF CANCER, 110(11), 2738-2746. doi:10.1038/bjc.2014.134Genetic risk prediction and neurobiological understanding of alcoholism (Journal article)
Levey, D. F., Le-Niculescu, H., Frank, J., Ayalew, M., Jain, N., Kirlin, B., . . . Niculescu, A. B. (2014). Genetic risk prediction and neurobiological understanding of alcoholism. TRANSLATIONAL PSYCHIATRY, 4. doi:10.1038/tp.2014.29Clinically Apparent and Occult Metastasized Seminoma: Almost Indistinguishable on the Transcriptional Level (Journal article)
Ruf, C. G., Port, M., Schmelz, H. -U., Wagner, W., Mueller, F., Senf, S., . . . Abend, M. (2014). Clinically Apparent and Occult Metastasized Seminoma: Almost Indistinguishable on the Transcriptional Level. PLOS ONE, 9(5). doi:10.1371/journal.pone.0095009A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age (Journal article)
Ahsan, H., Halpern, J., Kibriya, M. G., Pierce, B. L., Tong, L., Gamazon, E., . . . Whittemore, A. S. (2014). A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 23(4), 658-669. doi:10.1158/1055-9965.EPI-13-0340Genome-wide association study reveals two new risk loci for bipolar disorder (Journal article)
Muehleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., . . . Cichon, S. (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. NATURE COMMUNICATIONS, 5. doi:10.1038/ncomms4339Small RNAs in the peripheral blood discriminate metastasized from non-metastasized seminoma (Journal article)
Ruf, C. G., Dinger, D., Port, M., Schmelz, H. -U., Wagner, W., Matthies, C., . . . Abend, M. (2014). Small RNAs in the peripheral blood discriminate metastasized from non-metastasized seminoma. MOLECULAR CANCER, 13. doi:10.1186/1476-4598-13-47Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk (Journal article)
Bonifaci, N., Colas, E., Serra-Musach, J., Karbalai, N., Brunet, J., Gomez, A., . . . Angel Pujana, M. (2014). Integrating gene expression and epidemiological data for the discovery of genetic interactions associated with cancer risk. CARCINOGENESIS, 35(3), 578-585. doi:10.1093/carcin/bgt403Cognitive mechanisms underlying reading and spelling development in five European orthographies (Journal article)
Moll, K., Ramus, F., Bartling, J., Bruder, J., Kunze, S., Neuhoff, N., . . . Landerl, K. (2014). Cognitive mechanisms underlying reading and spelling development in five European orthographies. LEARNING AND INSTRUCTION, 29, 65-77. doi:10.1016/j.learninstruc.2013.09.003Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution (Journal article)
Ferentinos, P., Rivera, M., Ising, M., Spain, S. L., Cohen-Woods, S., Butler, A. W., . . . Lewis, C. M. (2014). Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution. JOURNAL OF AFFECTIVE DISORDERS, 155, 81-89. doi:10.1016/j.jad.2013.10.027ABCB1 Genetics and Function Determine Penetrance of Antidepressants Into the Brain: Treatment Implications and Open Research Questions (Conference Paper)
Holsboer, F., Mueller-Myhsok, B., & Uhr, M. (2014). ABCB1 Genetics and Function Determine Penetrance of Antidepressants Into the Brain: Treatment Implications and Open Research Questions. In BIOLOGICAL PSYCHIATRY Vol. 75 (pp. 23S). Retrieved from https://www.webofscience.com/Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (Journal article)
Li, M., Luo, X. -J., Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., . . . Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. MOLECULAR PSYCHIATRY, 19(4), 452-461. doi:10.1038/mp.2013.37Genetic Relationships Between Suicide Attempts, Suicidal Ideation and Major Psychiatric Disorders: A Genome-Wide Association and Polygenic Scoring Study (Journal article)
Mullins, N., Perroud, N., Uher, R., Butler, A. W., Cohen-Woods, S., Rivera, M., . . . Lewis, C. M. (2014). Genetic Relationships Between Suicide Attempts, Suicidal Ideation and Major Psychiatric Disorders: A Genome-Wide Association and Polygenic Scoring Study. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 165(5), 428-437. doi:10.1002/ajmg.b.32247Genetic Risk Prediction and Neurobiological Understanding of Alcoholism (Conference Paper)
Levey, D. F., Le-Niculescu, H., Frank, J., Ayalew, M., Jain, N., Kirlin, B., . . . Niculescu, A. B. (2014). Genetic Risk Prediction and Neurobiological Understanding of Alcoholism. In BIOLOGICAL PSYCHIATRY Vol. 75 (pp. 352S). Retrieved from https://www.webofscience.com/Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort (Journal article)
Becker, J., Czamara, D., Scerri, T. S., Ramus, F., Csepe, V., Talcott, J. B., . . . Schumacher, J. (2014). Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS, 22(5), 675-680. doi:10.1038/ejhg.2013.199Genetic modification of 25(OH)D levels in MS (Conference Paper)
Munger, K., Kochert, K., Fitzgerald, K., Arnason, B., Barkhof, F., Comi, G., . . . Pohl, C. (2014). Genetic modification of 25(OH)D levels in MS. In MULTIPLE SCLEROSIS JOURNAL Vol. 20 (pp. 249). Retrieved from https://www.webofscience.com/Genetic risk prediction and neurobiological understanding of alcoholism (vol 4, pg e456, 2014) (Journal article)
Levey, D. F., Le-Niculescu, H., Frank, J., Ayalew, M., Jain, N., Kirlin, B., . . . Niculescu, A. B. (2014). Genetic risk prediction and neurobiological understanding of alcoholism (vol 4, pg e456, 2014). TRANSLATIONAL PSYCHIATRY, 4. doi:10.1038/tp.2014.74Genome-Wide Genotyping Demonstrates a Polygenic Risk Score Associated With White Matter Hyperintensity Volume in CADASIL (Journal article)
Opherk, C., Gonik, M., Duering, M., Malik, R., Jouvent, E., Herve, D., . . . Dichgans, M. (2014). Genome-Wide Genotyping Demonstrates a Polygenic Risk Score Associated With White Matter Hyperintensity Volume in CADASIL. STROKE, 45(4), 968-972. doi:10.1161/STROKEAHA.113.004461P2RX7-a susceptibility gene for mood disorders? (Conference Paper)
Aprile-Garcia, F., Metzger, M. W., Dedic, N., Walser, S. M., Jakubcakova, V., Czamara, D., . . . Deussing, J. M. (2014). P2RX7-a susceptibility gene for mood disorders?. In PURINERGIC SIGNALLING Vol. 10 (pp. 718). Retrieved from https://www.webofscience.com/Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon (Journal article)
Spieler, D., Kaffe, M., Knauf, F., Bessa, J., Tena, J. J., Giesert, F., . . . Winkelmann, J. (2014). Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon. GENOME RESEARCH, 24(4), 592-603. doi:10.1101/gr.166751.113The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (Journal article)
Thompson, P. M., Stein, J. L., Medland, S. E., Hibar, D. P., Vasquez, A. A., Renteria, M. E., . . . Drevets, W. (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. BRAIN IMAGING AND BEHAVIOR, 8(2), 153-182. doi:10.1007/s11682-013-9269-52013
Rare variants in PLXNA4 and Parkinson's disease. (Journal article)
Schulte, E. C., Stahl, I., Czamara, D., Ellwanger, D. C., Eck, S., Graf, E., . . . Winkelmann, J. (2013). Rare variants in PLXNA4 and Parkinson's disease.. PloS one, 8(11), e79145. doi:10.1371/journal.pone.0079145Estimating the heritability of reporting stressful life events captured by common genetic variants. (Journal article)
Power, R. A., Wingenbach, T., Cohen-Woods, S., Uher, R., Ng, M. Y., Butler, A. W., . . . McGuffin, P. (2013). Estimating the heritability of reporting stressful life events captured by common genetic variants.. Psychological medicine, 43(9), 1965-1971. doi:10.1017/s0033291712002589Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. (Journal article)
Cross-Disorder Group of the Psychiatric Genomics Consortium., Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., . . . International Inflammatory Bowel Disease Genetics Consortium (IIBDGC). (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.. Nature genetics, 45(9), 984-994. doi:10.1038/ng.2711Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. (Journal article)
Kloiber, S., Ripke, S., Kohli, M. A., Reppermund, S., Salyakina, D., Uher, R., . . . Lucae, S. (2013). Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels.. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 23(7), 653-662. doi:10.1016/j.euroneuro.2012.08.010Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach. (Journal article)
Hennings, J. M., Kohli, M. A., Czamara, D., Giese, M., Eckert, A., Wolf, C., . . . Lucae, S. (2013). Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach.. PloS one, 8(6), e64947. doi:10.1371/journal.pone.0064947Predictors of developmental dyslexia in European orthographies with varying complexity. (Journal article)
Landerl, K., Ramus, F., Moll, K., Lyytinen, H., Leppänen, P. H. T., Lohvansuu, K., . . . Schulte-Körne, G. (2013). Predictors of developmental dyslexia in European orthographies with varying complexity.. Journal of child psychology and psychiatry, and allied disciplines, 54(6), 686-694. doi:10.1111/jcpp.12029Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders. (Journal article)
Wegerer, M., Adena, S., Pfennig, A., Czamara, D., Sailer, U., Bettecken, T., . . . Ising, M. (2013). Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders.. Psychological medicine, 43(6), 1207-1217. doi:10.1017/s0033291711002923Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies. (Journal article)
Czamara, D., Tiesler, C. M. T., Kohlböck, G., Berdel, D., Hoffmann, B., Bauer, C. -P., . . . Heinrich, J. (2013). Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies.. PloS one, 8(5), e63859. doi:10.1371/journal.pone.0063859Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder. (Journal article)
Mehta, D., Mehta, D., Klengel, T., Conneely, K. N., Smith, A. K., Altmann, A., . . . Binder, E. B. (2013). Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder.. Proceedings of the National Academy of Sciences of the United States of America, 110(20), 8302-8307. doi:10.1073/pnas.1217750110Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility (Journal article)
Li, M., Luo, X. -J., Rietschel, M., Lewis, C. M., Mattheisen, M., Müller-Myhsok, B., . . . Wright, M. J. (2014). Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19(4), 527. doi:10.1038/mp.2013.73A mega-analysis of genome-wide association studies for major depressive disorder (Journal article)
Ripke, S., Wray, N. R., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., . . . Sullivan, P. F. (2013). A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18(4), 497-511. doi:10.1038/mp.2012.21Dilution of candidates: the case of iron-related genes in restless legs syndrome. (Journal article)
Oexle, K., Schormair, B., Ried, J. S., Czamara, D., Heim, K., Frauscher, B., . . . Winkelmann, J. (2013). Dilution of candidates: the case of iron-related genes in restless legs syndrome.. European journal of human genetics : EJHG, 21(4), 410-414. doi:10.1038/ejhg.2012.193Genome-wide association studies identify four ER negative-specific breast cancer risk loci. (Journal article)
Garcia-Closas, M., Couch, F. J., Lindstrom, S., Michailidou, K., Schmidt, M. K., Brook, M. N., . . . Kraft, P. (2013). Genome-wide association studies identify four ER negative-specific breast cancer risk loci. . Nature genetics, 45(4), 392-398e2. doi:10.1038/ng.2561Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. (Journal article)
Arélin, M., Schulze, B., Müller-Myhsok, B., Horn, D., Diers, A., Uhlenberg, B., . . . Hoffmann, K. (2013). Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects.. European journal of human genetics : EJHG, 21(4), 367-372. doi:10.1038/ejhg.2012.198Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (Journal article)
Michailidou, K., Hall, P., Gonzalez-Neira, A., Ghoussaini, M., Dennis, J., Milne, R. L., . . . Easton, D. F. (2013). Large-scale genotyping identifies 41 new loci associated with breast cancer risk. . Nature genetics, 45(4), 353-361e2. doi:10.1038/ng.2563Using affected sib-pairs to uncover rare disease variants. (Journal article)
Perdry, H., Müller-Myhsok, B., & Clerget-Darpoux, F. (2012). Using affected sib-pairs to uncover rare disease variants.. Human heredity, 74(3-4), 129-141. doi:10.1159/000346788Cost-effective GPU-grid for genome-wide epistasis calculations. (Journal article)
Pütz, B., Kam-Thong, T., Karbalai, N., Altmann, A., & Müller-Myhsok, B. (2013). Cost-effective GPU-grid for genome-wide epistasis calculations.. Methods of information in medicine, 52(1), 91-95. doi:10.3414/me11-02-0049A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. (Journal article)
Ludwig, K. U., Sämann, P., Alexander, M., Becker, J., Bruder, J., Moll, K., . . . Czamara, D. (2013). A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.. Translational psychiatry, 3, e229. doi:10.1038/tp.2012.148Common Genetic Variation and Antidepressant Efficacy in Major Depressive Disorder: A Meta-Analysis of Three Genome-Wide Pharmacogenetic Studies (Journal article)
Uher, R., Tansey, K. E., Henigsberg, N., Wolfgang, M., Mors, O., Hauser, J., . . . Perlis, R. H. (2013). Common Genetic Variation and Antidepressant Efficacy in Major Depressive Disorder: A Meta-Analysis of Three Genome-Wide Pharmacogenetic Studies. American Journal of Psychiatry, 170(2), 207-217. doi:10.1176/appi.ajp.2012.12020237A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila. (Journal article)
Allebrandt, K. V., Amin, N., Müller-Myhsok, B., Esko, T., Teder-Laving, M., Azevedo, R. V. D. M., . . . Roenneberg, T. (2013). A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.. Molecular psychiatry, 18(1), 122-132. doi:10.1038/mp.2011.1422012
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites. (Journal article)
Glas, J., Seiderer, J., Czamara, D., Pasciuto, G., Diegelmann, J., Wetzke, M., . . . Brand, S. (2012). PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.. PloS one, 7(12), e52873. doi:10.1371/journal.pone.0052873A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. (Journal article)
Siddiq, A., Couch, F. J., Chen, G. K., Lindström, S., Eccles, D., Millikan, R. C., . . . Vachon, C. M. (2012). A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.. Human molecular genetics, 21(24), 5373-5384. doi:10.1093/hmg/dds381Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. (Journal article)
Li, M., Wang, Y., Zheng, X. -B., Ikeda, M., Iwata, N., Luo, X. -J., . . . MooDS Consortium. (2012). Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility.. Schizophrenia research, 142(1-3), 200-205. doi:10.1016/j.schres.2012.10.008Rare variants in TMEM132D in a case-control sample for panic disorder. (Journal article)
Quast, C., Altmann, A., Weber, P., Arloth, J., Bader, D., Heck, A., . . . Binder, E. B. (2012). Rare variants in TMEM132D in a case-control sample for panic disorder.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 159B(8), 896-907. doi:10.1002/ajmg.b.32096The endocrine stress response is linked to one specific locus on chromosome 3 in a mouse model based on extremes in trait anxiety. (Journal article)
Gonik, M., Frank, E., Keßler, M. S., Czamara, D., Bunck, M., Yen, Y. -C., . . . Czibere, L. (2012). The endocrine stress response is linked to one specific locus on chromosome 3 in a mouse model based on extremes in trait anxiety.. BMC genomics, 13, 579. doi:10.1186/1471-2164-13-579A beginners guide to SNP calling from high-throughput DNA-sequencing data. (Journal article)
Altmann, A., Weber, P., Bader, D., Preuss, M., Binder, E. B., & Müller-Myhsok, B. (2012). A beginners guide to SNP calling from high-throughput DNA-sequencing data.. Human genetics, 131(10), 1541-1554. doi:10.1007/s00439-012-1213-zDissecting the genetic heterogeneity of depression through age at onset. (Journal article)
Power, R. A., Keers, R., Ng, M. Y., Butler, A. W., Uher, R., Cohen-Woods, S., . . . Lewis, C. M. (2012). Dissecting the genetic heterogeneity of depression through age at onset.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 159B(7), 859-868. doi:10.1002/ajmg.b.32093Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. (Journal article)
Meier, S., Mattheisen, M., Vassos, E., Strohmaier, J., Treutlein, J., Josef, F., . . . Szelinger, S. (2012). Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.. Translational psychiatry, 2, e165. doi:10.1038/tp.2012.81Replication and meta-analysis of TMEM132D gene variants in panic disorder. (Journal article)
Erhardt, A., Akula, N., Schumacher, J., Czamara, D., Karbalai, N., Müller-Myhsok, B., . . . Binder, E. B. (2012). Replication and meta-analysis of TMEM132D gene variants in panic disorder.. Translational psychiatry, 2, e156. doi:10.1038/tp.2012.85Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study. (Journal article)
Vávrová, J., Kemlink, D., Sonka, K., Havrdová, E., Horáková, D., Pardini, B., . . . Winkelmann, J. (2012). Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study.. Sleep medicine, 13(7), 848-851. doi:10.1016/j.sleep.2012.03.012Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling. (Journal article)
Becker, J., Czamara, D., Hoffmann, P., Landerl, K., Blomert, L., Brandeis, D., . . . Schumacher, J. (2012). Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling.. Translational psychiatry, 2, e136. doi:10.1038/tp.2012.62The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. (Journal article)
Anthoni, H., Sucheston, L. E., Lewis, B. A., Tapia-Páez, I., Fan, X., Zucchelli, M., . . . Kere, J. (2012). The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.. Behavior genetics, 42(4), 509-527. doi:10.1007/s10519-012-9532-3Genome-wide association analysis identifies susceptibility loci for migraine without aura. (Journal article)
Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, M., Terwindt, G. M., . . . International Headache Genetics Consortium. (2012). Genome-wide association analysis identifies susceptibility loci for migraine without aura.. Nature genetics, 44(7), 777-782. doi:10.1038/ng.2307Erratum: Imaging genetics of FOXP2 in dyslexia (Journal article)
Wilcke, A., Jana Burkhardt, C. L., Alexander, M., Wolf, C., Quente, E., Ahnert, P., . . . Kirsten, H. (2012). Erratum: Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics, 20(6), 714. doi:10.1038/ejhg.2012.31Evidence for the late MMN as a neurophysiological endophenotype for dyslexia. (Journal article)
Neuhoff, N., Bruder, J., Bartling, J., Warnke, A., Remschmidt, H., Müller-Myhsok, B., & Schulte-Körne, G. (2012). Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.. PloS one, 7(5), e34909. doi:10.1371/journal.pone.0034909Identification of common variants associated with human hippocampal and intracranial volumes. (Journal article)
Stein, J. L., Medland, S. E., Vasquez, A. A., Hibar, D. P., Senstad, R. E., Winkler, A. M., . . . Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium. (2012). Identification of common variants associated with human hippocampal and intracranial volumes.. Nature genetics, 44(5), 552-561. doi:10.1038/ng.2250Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. (Journal article)
Degenhardt, F., Priebe, L., Herms, S., Mattheisen, M., Mühleisen, T. W., Meier, S., . . . Cichon, S. (2012). Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 159B(3), 263-273. doi:10.1002/ajmg.b.32034Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. (Journal article)
Menke, A., Sämann, P., Kloiber, S., Czamara, D., Lucae, S., Hennings, J., . . . Binder, E. B. (2012). Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes.. Psychoneuroendocrinology, 37(4), 565-575. doi:10.1016/j.psyneuen.2011.09.003Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis. (Journal article)
Babron, M. -C., Perdry, H., Handel, A. E., Ramagopalan, S. V., Damotte, V., Fontaine, B., . . . Clerget-Darpoux, F. (2012). Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.. European journal of human genetics : EJHG, 20(3), 321-325. doi:10.1038/ejhg.2011.197Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. (Journal article)
International Stroke Genetics Consortium (ISGC)., Wellcome Trust Case Control Consortium 2 (WTCCC2)., Bellenguez, C., Bevan, S., Gschwendtner, A., Spencer, C. C. A., . . . Markus, H. S. (2012). Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.. Nature genetics, 44(3), 328-333. doi:10.1038/ng.1081Genome-wide association study of antidepressant treatment-emergent suicidal ideation. (Journal article)
Menke, A., Domschke, K., Czamara, D., Klengel, T., Hennings, J., Lucae, S., . . . Binder, E. B. (2012). Genome-wide association study of antidepressant treatment-emergent suicidal ideation.. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 37(3), 797-807. doi:10.1038/npp.2011.257Genome-wide association analysis identifies three new breast cancer susceptibility loci. (Journal article)
Ghoussaini, M., Fletcher, O., Michailidou, K., Turnbull, C., Schmidt, M. K., Dicks, E., . . . Easton, D. F. (2012). Genome-wide association analysis identifies three new breast cancer susceptibility loci. . Nature genetics, 44(3), 312-318. doi:10.1038/ng.1049ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples. (Journal article)
Kloiber, S., Czamara, D., Karbalai, N., Müller-Myhsok, B., Hennings, J., Holsboer, F., & Lucae, S. (2012). ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples.. Journal of psychiatric research, 46(8), 973-979. doi:10.1016/j.jpsychires.2012.04.017Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients. (Journal article)
Menke, A., Arloth, J., Pütz, B., Weber, P., Klengel, T., Mehta, D., . . . Binder, E. B. (2012). Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients.. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 37(6), 1455-1464. doi:10.1038/npp.2011.331Don't give up on GWAS. (Journal article)
Sullivan, P., & 96 Psychiatric Genetics Investigators. (2012). Don't give up on GWAS.. Molecular psychiatry, 17(1), 2-3. doi:10.1038/mp.2011.94Erratum: Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients (Journal article)
Menke, A., Arloth, J., Pütz, B., Weber, P., Klengel, T., Mehta, D., . . . Binder, E. B. (2012). Erratum: Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients. Neuropsychopharmacology, 37(8), 1972. doi:10.1038/npp.2012.21Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. (Journal article)
Frank, J., Cichon, S., Treutlein, J., Ridinger, M., Mattheisen, M., Hoffmann, P., . . . Rietschel, M. (2012). Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.. Addiction biology, 17(1), 171-180. doi:10.1111/j.1369-1600.2011.00395.xImaging genetics of FOXP2 in dyslexia. (Journal article)
Wilcke, A., Ligges, C., Burkhardt, J., Alexander, M., Wolf, C., Quente, E., . . . Kirsten, H. (2012). Imaging genetics of FOXP2 in dyslexia.. European journal of human genetics : EJHG, 20(2), 224-229. doi:10.1038/ejhg.2011.160Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients (Journal article)
Weber, F., Cepok, S., Wolf, C., Berthele, A., Uhr, M., Bettecken, T., . . . Hemmer, B. (2012). Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. The Pharmacogenomics Journal, 12(3), 238-245. doi:10.1038/tpj.2011.142011
Risk conferring genes in multiple sclerosis. (Journal article)
Nischwitz, S., Müller-Myhsok, B., & Weber, F. (2011). Risk conferring genes in multiple sclerosis.. FEBS letters, 585(23), 3789-3797. doi:10.1016/j.febslet.2011.03.037Evidence for associations between MDGA2 polymorphisms and harm avoidance: replication and extension of a genome-wide association finding. (Journal article)
Heck, A., Pfister, H., Czamara, D., Müller-Myhsok, B., Pütz, B., Lucae, S., . . . Ising, M. (2011). Evidence for associations between MDGA2 polymorphisms and harm avoidance: replication and extension of a genome-wide association finding.. Psychiatric genetics, 21(5), 257-260. doi:10.1097/ypg.0b013e3283457bfbSomatization in major depression--clinical features and genetic associations. (Journal article)
Klengel, T., Heck, A., Pfister, H., Brückl, T., Hennings, J. M., Menke, A., . . . Ising, M. (2011). Somatization in major depression--clinical features and genetic associations.. Acta psychiatrica Scandinavica, 124(4), 317-328. doi:10.1111/j.1600-0447.2011.01743.xPregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease. (Journal article)
Glas, J., Seiderer, J., Fischer, D., Tengler, B., Pfennig, S., Wetzke, M., . . . Brand, S. (2011). Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease.. Inflammatory bowel diseases, 17(9), 1917-1924. doi:10.1002/ibd.21562Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies. (Journal article)
Mehta, D., Mehta, D., Gonik, M., Klengel, T., Rex-Haffner, M., Menke, A., . . . Binder, E. B. (2011). Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies.. Archives of general psychiatry, 68(9), 901-910. doi:10.1001/archgenpsychiatry.2011.50Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs. (Journal article)
Kam-Thong, T., Pütz, B., Karbalai, N., Müller-Myhsok, B., & Borgwardt, K. (2011). Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs.. Bioinformatics (Oxford, England), 27(13), i214-i221. doi:10.1093/bioinformatics/btr218Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. (Journal article)
Winkelmann, J., Czamara, D., Schormair, B., Knauf, F., Schulte, E. C., Trenkwalder, C., . . . Meitinger, T. (2011). Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.. PLoS genetics, 7(7), e1002171. doi:10.1371/journal.pgen.1002171MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. (Journal article)
Schormair, B., Plag, J., Kaffe, M., Gross, N., Czamara, D., Samtleben, W., . . . Winkelmann, J. (2011). MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.. Journal of medical genetics, 48(7), 462-466. doi:10.1136/jmg.2010.087858vipR: variant identification in pooled DNA using R. (Journal article)
Altmann, A., Weber, P., Quast, C., Rex-Haffner, M., Binder, E. B., & Müller-Myhsok, B. (2011). vipR: variant identification in pooled DNA using R.. Bioinformatics (Oxford, England), 27(13), i77-i84. doi:10.1093/bioinformatics/btr205More CLEC16A gene variants associated with multiple sclerosis. (Journal article)
Nischwitz, S., Cepok, S., Kroner, A., Wolf, C., Knop, M., Müller-Sarnowski, F., . . . Weber, F. (2011). More CLEC16A gene variants associated with multiple sclerosis.. Acta neurologica Scandinavica, 123(6), 400-406. doi:10.1111/j.1600-0404.2010.01421.xTMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. (Journal article)
Erhardt, A., Czibere, L., Roeske, D., Lucae, S., Unschuld, P. G., Ripke, S., . . . Binder, E. B. (2011). TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.. Molecular psychiatry, 16(6), 647-663. doi:10.1038/mp.2010.41CEACAM6 gene variants in inflammatory bowel disease. (Journal article)
Glas, J., Seiderer, J., Fries, C., Tillack, C., Pfennig, S., Weidinger, M., . . . Brand, S. (2011). CEACAM6 gene variants in inflammatory bowel disease.. PloS one, 6(4), e19319. doi:10.1371/journal.pone.0019319The neuronal transporter gene SLC6A15 confers risk to major depression. (Journal article)
Kohli, M. A., Lucae, S., Saemann, P. G., Schmidt, M. V., Demirkan, A., Hek, K., . . . Binder, E. B. (2011). The neuronal transporter gene SLC6A15 confers risk to major depression.. Neuron, 70(2), 252-265. doi:10.1016/j.neuron.2011.04.005EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units. (Journal article)
Kam-Thong, T., Czamara, D., Tsuda, K., Borgwardt, K., Lewis, C. M., Erhardt-Lehmann, A., . . . Müller-Myhsok, B. (2011). EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units.. European journal of human genetics : EJHG, 19(4), 465-471. doi:10.1038/ejhg.2010.196Role of PPARG gene variants in inflammatory bowel disease. (Journal article)
Glas, J., Seiderer, J., Markus, C., Pfennig, S., Wetzke, M., Paschos, E., . . . Brand, S. (2011). Role of PPARG gene variants in inflammatory bowel disease.. Inflammatory bowel diseases, 17(4), 1057-1058. doi:10.1002/ibd.21425Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (Journal article)
Cichon, S., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Miró, X., Strohmaier, J., . . . Nöthen, M. M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder. The American Journal of Human Genetics, 88(3), 396. doi:10.1016/j.ajhg.2011.03.001Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (Journal article)
Cichon, S., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Miró, X., Strohmaier, J., . . . Nöthen, M. M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.. American journal of human genetics, 88(3), 372-381. doi:10.1016/j.ajhg.2011.01.017Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. (Journal article)
Oexle, K., Ried, J. S., Hicks, A. A., Tanaka, T., Hayward, C., Bruegel, M., . . . Meitinger, T. (2011). Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.. Human molecular genetics, 20(5), 1042-1047. doi:10.1093/hmg/ddq538Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility. (Journal article)
Couturier, N., Bucciarelli, F., Nurtdinov, R. N., Debouverie, M., Lebrun-Frenay, C., Defer, G., . . . Brassat, D. (2011). Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility.. Brain : a journal of neurology, 134(Pt 3), 693-703. doi:10.1093/brain/awr010Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. (Journal article)
Czamara, D., Bruder, J., Becker, J., Bartling, J., Hoffmann, P., Ludwig, K. U., . . . Schulte-Körne, G. (2011). Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia.. Behavior genetics, 41(1), 110-119. doi:10.1007/s10519-010-9413-6First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. (Journal article)
Roeske, D., Ludwig, K. U., Neuhoff, N., Becker, J., Bartling, J., Bruder, J., . . . Schulte-Körne, G. (2011). First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.. Molecular psychiatry, 16(1), 97-107. doi:10.1038/mp.2009.102Genetic Markers for PTSD Risk and Resilience Among Survivors of the World Trade Center Attacks (Journal article)
Sarapas, C., Cai, G., Bierer, L. M., Golier, J. A., Galea, S., Ising, M., . . . Yehuda, R. (2011). Genetic Markers for PTSD Risk and Resilience Among Survivors of the World Trade Center Attacks. Disease Markers, 30(2-3), 101-110. doi:10.1155/2011/328054Genomewide association scan of suicidal thoughts and behaviour in major depression. (Journal article)
Schosser, A., Butler, A. W., Ising, M., Perroud, N., Uher, R., Ng, M. Y., . . . Lewis, C. M. (2011). Genomewide association scan of suicidal thoughts and behaviour in major depression.. PloS one, 6(7), e20690. doi:10.1371/journal.pone.0020690Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. (Journal article)
König, I. R., Schumacher, J., Hoffmann, P., Kleensang, A., Ludwig, K. U., Grimm, T., . . . Schulte-Körne, G. (2011). Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 156B(1), 36-43. doi:10.1002/ajmg.b.311352010
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. (Journal article)
Glas, J., Seiderer, J., Tillack, C., Pfennig, S., Beigel, F., Jürgens, M., . . . Brand, S. (2010). The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.. PloS one, 5(12), e14466. doi:10.1371/journal.pone.0014466Erratum: Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression (Journal article)
Kloiber, S., Kohli, M. A., Brueckl, T., Ripke, S., Ising, M., Uhr, M., . . . Lucae, S. (2010). Erratum: Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression. Molecular Psychiatry, 15(11), 1123. doi:10.1038/mp.2009.8Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. (Journal article)
Nischwitz, S., Cepok, S., Kroner, A., Wolf, C., Knop, M., Müller-Sarnowski, F., . . . Weber, F. (2010). Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.. Journal of neuroimmunology, 227(1-2), 162-166. doi:10.1016/j.jneuroim.2010.06.003Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. (Journal article)
Anttila, V., Stefansson, H., Kallela, M., Todt, U., Terwindt, G. M., Calafato, M. S., . . . International Headache Genetics Consortium. (2010). Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.. Nature genetics, 42(10), 869-873. doi:10.1038/ng.652Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. (Journal article)
Rietschel, M., Mattheisen, M., Frank, J., Treutlein, J., Degenhardt, F., Breuer, R., . . . Cichon, S. (2010). Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.. Biological psychiatry, 68(6), 578-585. doi:10.1016/j.biopsych.2010.05.038Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways. (Journal article)
Ditzen, C., Varadarajulu, J., Czibere, L., Gonik, M., Targosz, B. S., Hambsch, B., . . . Turck, C. W. (2010). Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways.. Molecular psychiatry, 15(7), 702-711. doi:10.1038/mp.2008.146Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression. (Journal article)
Kloiber, S., Kohli, M. A., Brueckl, T., Ripke, S., Ising, M., Uhr, M., . . . Lucae, S. (2010). Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression.. Molecular psychiatry, 15(7), 736-747. doi:10.1038/mp.2008.142Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients. (Journal article)
Hemminki, K., Müller-Myhsok, B., Lichtner, P., Engel, C., Chen, B., Burwinkel, B., . . . Meindl, A. (2010). Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients.. International journal of cancer, 126(12), 2858-2862. doi:10.1002/ijc.24986CLOCK gene variants associate with sleep duration in two independent populations. (Journal article)
Allebrandt, K. V., Teder-Laving, M., Akyol, M., Pichler, I., Müller-Myhsok, B., Pramstaller, P., . . . Roenneberg, T. (2010). CLOCK gene variants associate with sleep duration in two independent populations.. Biological psychiatry, 67(11), 1040-1047. doi:10.1016/j.biopsych.2009.12.026Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response. (Journal article)
Unschuld, P. G., Ising, M., Roeske, D., Erhardt, A., Specht, M., Kloiber, S., . . . Binder, E. B. (2010). Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response.. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 35(7), 1583-1592. doi:10.1038/npp.2010.30Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. (Journal article)
Muglia, P., Tozzi, F., Galwey, N. W., Francks, C., Upmanyu, R., Kong, X. Q., . . . Roses, A. D. (2010). Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.. Molecular psychiatry, 15(6), 589-601. doi:10.1038/mp.2008.131Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. (Journal article)
Meindl, A., Hellebrand, H., Wiek, C., Erven, V., Wappenschmidt, B., Niederacher, D., . . . Hanenberg, H. (2010). Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.. Nature genetics, 42(5), 410-414. doi:10.1038/ng.569Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients. (Journal article)
Kohli, M. A., Salyakina, D., Pfennig, A., Lucae, S., Horstmann, S., Menke, A., . . . Binder, E. B. (2010). Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients.. Archives of general psychiatry, 67(4), 348-359. doi:10.1001/archgenpsychiatry.2009.201Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. (Journal article)
Ludwig, K. U., Roeske, D., Herms, S., Schumacher, J., Warnke, A., Plume, E., . . . Hoffmann, P. (2010). Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 153B(2), 503-511. doi:10.1002/ajmg.b.31007An extensive comparison of quantitative trait Loci mapping methods. (Journal article)
Kleensang, A., Franke, D., Alcaïs, A., Abel, L., Müller-Myhsok, B., & Ziegler, A. (2010). An extensive comparison of quantitative trait Loci mapping methods.. Human heredity, 69(3), 202-211. doi:10.1159/000289596Genome-wide association study of PR interval. (Journal article)
Pfeufer, A., van Noord, C., Marciante, K. D., Arking, D. E., Larson, M. G., Smith, A. V., . . . Heckbert, S. R. (2010). Genome-wide association study of PR interval.. Nature genetics, 42(2), 153-159. doi:10.1038/ng.517Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma. (Journal article)
Wolf, C., Gramer, E., Müller-Myhsok, B., Pasutto, F., Gramer, G., Wissinger, B., & Weisschuh, N. (2010). Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma.. Journal of glaucoma, 19(2), 136-141. doi:10.1097/ijg.0b013e31819f9330Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment. (Journal article)
Horstmann, S., Lucae, S., Menke, A., Hennings, J. M., Ising, M., Roeske, D., . . . Binder, E. B. (2010). Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment.. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 35(3), 727-740. doi:10.1038/npp.2009.180Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population. (Journal article)
Wolf, C., Gramer, E., Müller-Myhsok, B., Pasutto, F., Wissinger, B., & Weisschuh, N. (2010). Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population.. BMC genetics, 11, 8. doi:10.1186/1471-2156-11-8HTR2A gene variation is involved in antidepressant treatment response. (Journal article)
Lucae, S., Ising, M., Horstmann, S., Baune, B. T., Arolt, V., Müller-Myhsok, B., . . . Domschke, K. (2010). HTR2A gene variation is involved in antidepressant treatment response.. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 20(1), 65-68. doi:10.1016/j.euroneuro.2009.08.0062009
Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders. (Journal article)
Unschuld, P. G., Ising, M., Specht, M., Erhardt, A., Ripke, S., Heck, A., . . . Binder, E. B. (2009). Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 150B(8), 1100-1109. doi:10.1002/ajmg.b.30938Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks. (Journal article)
Yehuda, R., Cai, G., Golier, J. A., Sarapas, C., Galea, S., Ising, M., . . . Buxbaum, J. D. (2009). Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks.. Biological psychiatry, 66(7), 708-711. doi:10.1016/j.biopsych.2009.02.034Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. (Journal article)
Wolf, C., Gramer, E., Müller-Myhsok, B., Pasutto, F., Reinthal, E., Wissinger, B., & Weisschuh, N. (2009). Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study.. BMC medical genetics, 10, 91. doi:10.1186/1471-2350-10-91A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression. (Journal article)
Ising, M., Lucae, S., Binder, E. B., Bettecken, T., Uhr, M., Ripke, S., . . . Müller-Myhsok, B. (2009). A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression.. Archives of general psychiatry, 66(9), 966-975. doi:10.1001/archgenpsychiatry.2009.95Supporting evidence for LRRTM1 imprinting effects in schizophrenia. (Journal article)
Ludwig, K. U., Mattheisen, M., Mühleisen, T. W., Roeske, D., Schmäl, C., Breuer, R., . . . Cichon, S. (2009). Supporting evidence for LRRTM1 imprinting effects in schizophrenia.. Molecular psychiatry, 14(8), 743-745. doi:10.1038/mp.2009.28Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease. (Journal article)
Török, H. P., Glas, J., Endres, I., Tonenchi, L., Teshome, M. Y., Wetzke, M., . . . Brand, S. (2009). Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.. The American journal of gastroenterology, 104(7), 1723-1733. doi:10.1038/ajg.2009.184Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease. (Journal article)
Glas, J., Stallhofer, J., Ripke, S., Wetzke, M., Pfennig, S., Klein, W., . . . Brand, S. (2009). Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.. The American journal of gastroenterology, 104(7), 1737-1744. doi:10.1038/ajg.2009.163Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. (Journal article)
Heck, A., Lieb, R., Ellgas, A., Pfister, H., Lucae, S., Roeske, D., . . . Ising, M. (2009). Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking.. Genes, brain, and behavior, 8(4), 464-472. doi:10.1111/j.1601-183x.2009.00494.xThe GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders. (Journal article)
Thoeringer, C. K., Ripke, S., Unschuld, P. G., Lucae, S., Ising, M., Bettecken, T., . . . Erhardt, A. (2009). The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders.. Journal of neural transmission (Vienna, Austria : 1996), 116(6), 649-657. doi:10.1007/s00702-008-0075-yA hypomorphic vasopressin allele prevents anxiety-related behavior. (Journal article)
Bunck, M., Czibere, L., Horvath, C., Graf, C., Frank, E., Kessler, M. S., . . . Landgraf, R. (2009). A hypomorphic vasopressin allele prevents anxiety-related behavior.. PloS one, 4(4), e5129. doi:10.1371/journal.pone.0005129Common variants at ten loci modulate the QT interval duration in the QTSCD Study. (Journal article)
Pfeufer, A., Sanna, S., Arking, D. E., Müller, M., Gateva, V., Fuchsberger, C., . . . Chakravarti, A. (2009). Common variants at ten loci modulate the QT interval duration in the QTSCD Study.. Nature genetics, 41(4), 407-414. doi:10.1038/ng.362Further evidence for DYX1C1 as a susceptibility factor for dyslexia. (Journal article)
Dahdouh, F., Anthoni, H., Tapia-Páez, I., Peyrard-Janvid, M., Schulte-Körne, G., Warnke, A., . . . Zucchelli, M. (2009). Further evidence for DYX1C1 as a susceptibility factor for dyslexia.. Psychiatric genetics, 19(2), 59-63. doi:10.1097/ypg.0b013e32832080e1Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations. (Journal article)
Freilinger, T., Bevan, S., Ripke, S., Gschwendtner, A., Lichtner, P., Müller-Myhsok, B., . . . Dichgans, M. (2009). Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations.. Stroke, 40(3), 970-972. doi:10.1161/strokeaha.107.510800rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population. (Journal article)
Glas, J., Seiderer, J., Pasciuto, G., Tillack, C., Diegelmann, J., Pfennig, S., . . . Brand, S. (2009). rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.. The American journal of gastroenterology, 104(3), 665-672. doi:10.1038/ajg.2008.65Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. (Journal article)
Heck, A., Lieb, R., Ellgas, A., Pfister, H., Lucae, S., Erhardt, A., . . . Ising, M. (2009). Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 150B(1), 104-114. doi:10.1002/ajmg.b.30784A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. (Journal article)
Hoffmann, K., Planitz, C., Rüschendorf, F., Müller-Myhsok, B., Stassen, H. H., Lucke, B., . . . Lindner, T. H. (2009). A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany.. Journal of hypertension, 27(5), 983-990. doi:10.1097/hjh.0b013e328328123dMouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12. (Journal article)
Gusareva, E. S., Havelková, H., Blazková, H., Kosarová, M., Kucera, P., Král, V., . . . Lipoldová, M. (2009). Mouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12.. Immunogenetics, 61(1), 15-25. doi:10.1007/s00251-008-0343-xSequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. (Journal article)
Gschwendtner, A., Bevan, S., Cole, J. W., Plourde, A., Matarin, M., Ross-Adams, H., . . . International Stroke Genetics Consortium. (2009). Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.. Annals of neurology, 65(5), 531-539. doi:10.1002/ana.215902008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. (Journal article)
Ludwig, K. U., Schumacher, J., Schulte-Körne, G., König, I. R., Warnke, A., Plume, E., . . . Hoffmann, P. (2008). Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.. Psychiatric genetics, 18(6), 310-312. doi:10.1097/ypg.0b013e3283063a78Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. (Journal article)
Ludwig, K. U., Roeske, D., Schumacher, J., Schulte-Körne, G., König, I. R., Warnke, A., . . . Hoffmann, P. (2008). Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.. Journal of neural transmission (Vienna, Austria : 1996), 115(11), 1587-1589. doi:10.1007/s00702-008-0124-6Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder. (Journal article)
Keck, M. E., Kern, N., Erhardt, A., Unschuld, P. G., Ising, M., Salyakina, D., . . . Binder, E. B. (2008). Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 147B(7), 1196-1204. doi:10.1002/ajmg.b.30750Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism. (Journal article)
Heck, A., Lieb, R., Unschuld, P. G., Ellgas, A., Pfister, H., Lucae, S., . . . Ising, M. (2008). Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism.. Molecular psychiatry, 13(9), 831-832. doi:10.1038/mp.2008.2Genetic markers within glutamate receptors associated with antidepressant treatment-emergent suicidal ideation. (Journal article)
Menke, A., Lucae, S., Kloiber, S., Horstmann, S., Bettecken, T., Uhr, M., . . . Binder, E. B. (2008). Genetic markers within glutamate receptors associated with antidepressant treatment-emergent suicidal ideation.. The American journal of psychiatry, 165(7), 917-918. doi:10.1176/appi.ajp.2008.08020274Increased plasma concentration of surfactant protein D in chronic periodontitis independent of SFTPD genotype: potential role as a biomarker. (Journal article)
Glas, J., Beynon, V., Bachstein, B., Steckenbiller, J., Manolis, V., Euba, A., . . . Folwaczny, M. (2008). Increased plasma concentration of surfactant protein D in chronic periodontitis independent of SFTPD genotype: potential role as a biomarker.. Tissue antigens, 72(1), 21-28. doi:10.1111/j.1399-0039.2008.01056.xPolymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls. (Journal article)
Ising, M., Depping, A. -M., Siebertz, A., Lucae, S., Unschuld, P. G., Kloiber, S., . . . Holsboer, F. (2008). Polymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls.. The European journal of neuroscience, 28(2), 389-398. doi:10.1111/j.1460-9568.2008.06332.xRefining genetic associations in multiple sclerosis. (Journal article)
International Multiple Sclerosis Genetics Consortium (IMSGC). (2008). Refining genetic associations in multiple sclerosis.. The Lancet. Neurology, 7(7), 567-569. doi:10.1016/s1474-4422(08)70122-4Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21. (Journal article)
Schumacher, J., König, I. R., Schröder, T., Duell, M., Plume, E., Propping, P., . . . Nöthen, M. M. (2008). Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.. Psychiatric genetics, 18(3), 137-142. doi:10.1097/ypg.0b013e3282fb7fc6Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. (Journal article)
Gschwendtner, A., Ripke, S., Freilinger, T., Lichtner, P., Müller-Myhsok, B., Wichmann, H. -E., . . . Dichgans, M. (2008). Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans.. Stroke, 39(5), 1593-1596. doi:10.1161/strokeaha.107.502179Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. (Journal article)
Freilinger, T., Bohe, M., Wegener, B., Müller-Myhsok, B., Dichgans, M., & Knoblauch, H. (2008). Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.. Cephalalgia : an international journal of headache, 28(4), 403-407. doi:10.1111/j.1468-2982.2008.01540.xGenotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease. (Journal article)
Seiderer, J., Dambacher, J., Leistner, D., Tillack, C., Glas, J., Niess, J. -H., . . . Brand, S. (2008). Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease.. Clinical immunology (Orlando, Fla.), 127(1), 49-55. doi:10.1016/j.clim.2007.11.016Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD. (Journal article)
Seiderer, J., Elben, I., Diegelmann, J., Glas, J., Stallhofer, J., Tillack, C., . . . Brand, S. (2008). Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.. Inflammatory bowel diseases, 14(4), 437-445. doi:10.1002/ibd.20339Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks. (Journal article)
Erhardt, A., Lucae, S., Kern, N., Unschuld, P. G., Ising, M., Lieb, R., . . . Holsboer, F. (2008). Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks.. Molecular psychiatry, 13(3), 242-243. doi:10.1038/sj.mp.4002094The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population. (Journal article)
Glas, J., Konrad, A., Schmechel, S., Dambacher, J., Seiderer, J., Schroff, F., . . . Brand, S. (2008). The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.. The American journal of gastroenterology, 103(3), 682-691. doi:10.1111/j.1572-0241.2007.01694.xGenetics of restless legs syndrome: a burning urge to move. (Journal article)
Winkelmann, J., & Müller-Myhsok, B. (2008). Genetics of restless legs syndrome: a burning urge to move.. Neurology, 70(9), 664-665. doi:10.1212/01.wnl.0000302178.53759.92Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. (Journal article)
Winkelmann, J., Lichtner, P., Schormair, B., Uhr, M., Hauk, S., Stiasny-Kolster, K., . . . Müller-Myhsok, B. (2008). Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.. Movement disorders : official journal of the Movement Disorder Society, 23(3), 350-358. doi:10.1002/mds.21647Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression. (Journal article)
Uhr, M., Tontsch, A., Namendorf, C., Ripke, S., Lucae, S., Ising, M., . . . Holsboer, F. (2008). Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression.. Neuron, 57(2), 203-209. doi:10.1016/j.neuron.2007.11.017Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts. (Journal article)
Browning, B. L., Annese, V., Barclay, M. L., Bingham, S. A., Brand, S., Büning, C., . . . Witt, H. (2008). Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.. Journal of medical genetics, 45(1), 36-42. doi:10.1136/jmg.2007.050773IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. (Journal article)
Weber, F., Fontaine, B., Cournu-Rebeix, I., Kroner, A., Knop, M., Lutz, S., . . . Müller-Myhsok, B. (2008). IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.. Genes and immunity, 9(3), 259-263. doi:10.1038/gene.2008.14PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. (Journal article)
Schormair, B., Kemlink, D., Roeske, D., Eckstein, G., Xiong, L., Lichtner, P., . . . Winkelmann, J. (2008). PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.. Nature genetics, 40(8), 946-948. doi:10.1038/ng.190Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. (Journal article)
Unschuld, P. G., Ising, M., Erhardt, A., Lucae, S., Kohli, M., Kloiber, S., . . . Keck, M. E. (2008). Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder.. Journal of affective disorders, 105(1-3), 177-184. doi:10.1016/j.jad.2007.05.0062007
Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks. (Journal article)
Thoeringer, C. K., Binder, E. B., Salyakina, D., Erhardt, A., Ising, M., Unschuld, P. G., . . . Keck, M. E. (2007). Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks.. Journal of psychiatric research, 41(7), 579-584. doi:10.1016/j.jpsychires.2006.06.001rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants. (Journal article)
Glas, J., Seiderer, J., Wetzke, M., Konrad, A., Török, H. -P., Schmechel, S., . . . Brand, S. (2007). rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.. PloS one, 2(9), e819. doi:10.1371/journal.pone.0000819Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders. (Journal article)
Erhardt, A., Lucae, S., Unschuld, P. G., Ising, M., Kern, N., Salyakina, D., . . . Holsboer, F. (2007). Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders.. Journal of affective disorders, 101(1-3), 159-168. doi:10.1016/j.jad.2006.11.016Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease. (Journal article)
Rosenberger, A., Sharma, M., Müller-Myhsok, B., Gasser, T., & Bickeböller, H. (2007). Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.. BMC genetics, 8, 44. doi:10.1186/1471-2156-8-44Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. (Journal article)
Unschuld, P. G., Ising, M., Erhardt, A., Lucae, S., Kloiber, S., Kohli, M., . . . Keck, M. E. (2007). Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 144B(4), 424-429. doi:10.1002/ajmg.b.30412A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. (Journal article)
Anthoni, H., Zucchelli, M., Matsson, H., Müller-Myhsok, B., Fransson, I., Schumacher, J., . . . Peyrard-Janvid, M. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.. Human molecular genetics, 16(6), 667-677. doi:10.1093/hmg/ddm009Assoziation zwischen Herzerkrankungen und Depressionen (Journal article)
Baghai, T. C., Binder, E., Schüle, C., Lucae, S., Eser, D., Müller-Myhsok, B., . . . Bondy, B. (2007). Assoziation zwischen Herzerkrankungen und Depressionen. Biologie in unserer Zeit, 37(5), 284-286. doi:10.1002/biuz.200790076Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. (Journal article)
Winkelmann, J., Schormair, B., Lichtner, P., Ripke, S., Xiong, L., Jalilzadeh, S., . . . Meitinger, T. (2007). Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.. Nature genetics, 39(8), 1000-1006. doi:10.1038/ng20992006
Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunity. (Journal article)
Graefe, S. E. B., Streichert, T., Budde, B. S., Nürnberg, P., Steeg, C., Müller-Myhsok, B., & Fleischer, B. (2006). Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunity.. PloS one, 1, e57. doi:10.1371/journal.pone.0000057Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers. (Journal article)
Opherk, C., Peters, N., Holtmannspötter, M., Gschwendtner, A., Müller-Myhsok, B., & Dichgans, M. (2006). Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers.. Stroke, 37(11), 2684-2689. doi:10.1161/01.str.0000245084.35575.66Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism. (Journal article)
Baghai, T. C., Binder, E. B., Schule, C., Salyakina, D., Eser, D., Lucae, S., . . . Bondy, B. (2006). Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism.. Molecular psychiatry, 11(11), 1003-1015. doi:10.1038/sj.mp.4001884P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder. (Journal article)
Lucae, S., Salyakina, D., Barden, N., Harvey, M., Gagné, B., Labbé, M., . . . Müller-Myhsok, B. (2006). P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder.. Human molecular genetics, 15(16), 2438-2445. doi:10.1093/hmg/ddl166Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder. (Journal article)
Barden, N., Harvey, M., Gagné, B., Shink, E., Tremblay, M., Raymond, C., . . . Müller-Myhsok, B. (2006). Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 141B(4), 374-382. doi:10.1002/ajmg.b.30303Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. (Journal article)
Winkelmann, J., Lichtner, P., Pütz, B., Trenkwalder, C., Hauk, S., Meitinger, T., . . . Muller-Myhsok, B. (2006). Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.. Movement disorders : official journal of the Movement Disorder Society, 21(1), 28-33. doi:10.1002/mds.20627Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes. (Journal article)
Glas, J., Török, H. -P., Tonenchi, L., Müller-Myhsok, B., Mussack, T., Wetzke, M., . . . Folwaczny, C. (2006). Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes.. Inflammatory bowel diseases, 12(7), 606-611. doi:10.1097/01.ibd.0000225346.23765.6b2005
Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype. (Journal article)
Glas, J., Török, H. -P., Tonenchi, L., Kapser, J., Schiemann, U., Müller-Myhsok, B., . . . Folwaczny, C. (2005). Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype.. Inflammatory bowel diseases, 11(12), 1031-1037. doi:10.1097/01.mib.0000187574.41290.b1SimPed: a simulation program to generate haplotype and genotype data for pedigree structures. (Journal article)
Leal, S. M., Yan, K., & Müller-Myhsok, B. (2005). SimPed: a simulation program to generate haplotype and genotype data for pedigree structures.. Human heredity, 60(2), 119-122. doi:10.1159/000088914Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. (Journal article)
Török, H. -P., Glas, J., Tonenchi, L., Lohse, P., Müller-Myhsok, B., Limbersky, O., . . . Folwaczny, C. (2005). Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.. Gut, 54(10), 1421-1427. doi:10.1136/gut.2005.066340Evaluation of Nyholt's procedure for multiple testing correction. (Journal article)
Salyakina, D., Seaman, S. R., Browning, B. L., Dudbridge, F., & Muller-Myhsok, B. (2005). Evaluation of Nyholt's procedure for multiple testing correction.. Human heredity, 60(1), 19-25. doi:10.1159/000087540Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. (Journal article)
Martinez, M., Brice, A., Vaughan, J. R., Zimprich, A., Breteler, M. M. B., Meco, G., . . . Dürr, A. (2005). Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 136B(1), 72-74. doi:10.1002/ajmg.b.30196Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design. (Journal article)
Ziegler, A., König, I. R., Deimel, W., Plume, E., Nöthen, M. M., Propping, P., . . . Schulte-Körne, G. (2005). Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.. Human heredity, 59(3), 136-143. doi:10.1159/000085572Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease. (Journal article)
Klopstock, T., Elstner, M., Lücking, C. B., Müller-Myhsok, B., Gasser, T., Botz, E., . . . Hörtnagel, K. (2005). Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease.. Neuroscience letters, 379(3), 195-198. doi:10.1016/j.neulet.2004.12.061Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome. (Journal article)
Asmus, F., Schoenian, S., Lichtner, P., Munz, M., Mayer, P., Muller-Myhsok, B., . . . Gasser, T. (2005). Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome.. Neurogenetics, 6(1), 55-56. doi:10.1007/s10048-004-0206-zOn rapid stimulation of P values in association studies. (Journal article)
Lin, D. Y. (2005). On rapid stimulation of P values in association studies.. American journal of human genetics, 77(3), 513-514. doi:10.1086/432817PARK11 is not linked with Parkinson's disease in European families. (Journal article)
Prestel, J., Sharma, M., Leitner, P., Zimprich, A., Vaughan, J. R., Dürr, A., . . . European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). (2005). PARK11 is not linked with Parkinson's disease in European families.. European journal of human genetics : EJHG, 13(2), 193-197. doi:10.1038/sj.ejhg.5201317Rapid simulation of P values for product methods and multiple-testing adjustment in association studies. (Journal article)
Seaman, S. R., & Müller-Myhsok, B. (2005). Rapid simulation of P values for product methods and multiple-testing adjustment in association studies.. American journal of human genetics, 76(3), 399-408. doi:10.1086/4281402004
Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function. (Journal article)
Brattig, N. W., Timmann, C., Abraha, R. S., Lepping, B., Müller-Myhsok, B., & Horstmann, R. D. (2005). Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function.. Clinical and experimental immunology, 139(1), 127-131. doi:10.1111/j.1365-2249.2005.02667.xPolymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. (Journal article)
Binder, E. B., Salyakina, D., Lichtner, P., Wochnik, G. M., Ising, M., Pütz, B., . . . Muller-Myhsok, B. (2004). Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment.. Nature genetics, 36(12), 1319-1325. doi:10.1038/ng1479Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. (Journal article)
Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., . . . Gasser, T. (2004). Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.. Neuron, 44(4), 601-607. doi:10.1016/j.neuron.2004.11.005Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen. (Journal article)
Timmann, C., Fuchs, S., Thoma, C., Lepping, B., Brattig, N. W., Sievertsen, J., . . . Horstmann, R. D. (2004). Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen.. Genes and immunity, 5(4), 256-260. doi:10.1038/sj.gene.6364094Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. (Journal article)
Wszolek, Z. K., Pfeiffer, R. F., Tsuboi, Y., Uitti, R. J., McComb, R. D., Stoessl, A. J., . . . Dickson, D. W. (2004). Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.. Neurology, 62(9), 1619-1622. doi:10.1212/01.wnl.0000125015.06989.dbA gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33. (Journal article)
Giehl, K. A., Eckstein, G. N., Benet-Pagès, A., Tosti, A., de Berker, D. A. R., Meitinger, T., . . . Strom, T. M. (2004). A gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33.. The Journal of investigative dermatology, 123(6), 1073-1077. doi:10.1111/j.0022-202x.2004.23423.xAssociation of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis. (Journal article)
Dörr, S., Lechtenböhmer, N., Rau, R., Herborn, G., Wagner, U., Müller-Myhsok, B., . . . Keyszer, G. (2004). Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis.. Arthritis research & therapy, 6(3), R199-R207. doi:10.1186/ar1164The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval (Journal article)
Zimprich, A., Müller-Myhsok, B., Farrer, M., Leitner, P., Sharma, M., Hulihan, M., . . . Gasser, T. (2004). The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval. The American Journal of Human Genetics, 74(1), 11-19. doi:10.1086/3806472003
Murine susceptibility to Chagas' disease maps to chromosomes 5 and 17. (Journal article)
Graefe, S. E., Meyer, B. S., Müller-Myhsok, B., Rüschendorf, F., Drosten, C., Laue, T., . . . Fleischer, B. (2003). Murine susceptibility to Chagas' disease maps to chromosomes 5 and 17.. Genes and immunity, 4(5), 321-325. doi:10.1038/sj.gene.6363972Parkin mutations are frequent in patients with isolated early-onset parkinsonism. (Journal article)
Periquet, M., Latouche, M., Lohmann, E., Rawal, N., De Michele, G., Ricard, S., . . . European Consortium on Genetic Susceptibility in Parkinson's Disease. (2003). Parkin mutations are frequent in patients with isolated early-onset parkinsonism.. Brain : a journal of neurology, 126(Pt 6), 1271-1278. doi:10.1093/brain/awg136Is there relatedness between maternal lines of Type 1 diabetic patients? (Journal article)
Klöting, I., Poetsch, M., Müller-Myhsok, B., Rjasanowski, I., Kerner, W., & Klöting, N. (2003). Is there relatedness between maternal lines of Type 1 diabetic patients?. Diabetologia, 46(3), 441-442. doi:10.1007/s00125-003-1048-1Apolipoprotein B-100 gene mutations and cholesterol control in German patients. (Journal article)
Loggen, U., Boden, A., Baron, H., Schuster, H., Tolle, R., Netwich, U., . . . Luft, F. C. (2003). Apolipoprotein B-100 gene mutations and cholesterol control in German patients.. Atherosclerosis, 166(2), 411-412. doi:10.1016/s0021-9150(02)00377-5Genomewide linkage analysis identifies polymorphism in the human interferon-gamma receptor affecting Helicobacter pylori infection. (Journal article)
Thye, T., Burchard, G. D., Nilius, M., Müller-Myhsok, B., & Horstmann, R. D. (2003). Genomewide linkage analysis identifies polymorphism in the human interferon-gamma receptor affecting Helicobacter pylori infection.. American journal of human genetics, 72(2), 448-453. doi:10.1086/367714Association of human leucocyte DR and DQ antigens in Crohn's disease in Asian Indians: a family study. (Journal article)
Thakur, S., Ranjan, P., Ghoshal, U. C., Muller-Myhsok, B., Khan, F., Talwar, S., & Agarwal, S. (2003). Association of human leucocyte DR and DQ antigens in Crohn's disease in Asian Indians: a family study.. Tropical gastroenterology : official journal of the Digestive Diseases Foundation, 24(4), 185-188.2002
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families. (Journal article)
Winkelmann, J., Muller-Myhsok, B., Wittchen, H. -U., Hock, B., Prager, M., Pfister, H., . . . Trenkwalder, C. (2002). Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families.. Annals of neurology, 52(3), 297-302. doi:10.1002/ana.10282Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam. (Journal article)
Blessmann, J., Van Linh, P., Nu, P. A. T., Thi, H. D., Muller-Myhsok, B., Buss, H., & Tannich, E. (2002). Epidemiology of amebiasis in a region of high incidence of amebic liver abscess in central Vietnam.. The American journal of tropical medicine and hygiene, 66(5), 578-583. doi:10.4269/ajtmh.2002.66.578The variant Arg110Gln of human IL-13 is associated with an immunologically hyper-reactive form of onchocerciasis (sowda). (Journal article)
Hoerauf, A., Kruse, S., Brattig, N. W., Heinzmann, A., Mueller-Myhsok, B., & Deichmann, K. A. (2002). The variant Arg110Gln of human IL-13 is associated with an immunologically hyper-reactive form of onchocerciasis (sowda).. Microbes and infection, 4(1), 37-42. doi:10.1016/s1286-4579(01)01507-6Association and Linkage of Human Leukocyte Antigens with Psoriasis – Revisited (Journal article)
Eiermann, T. H., Vejbaesya, S., Prestel, H., Roepke, A., Müller-Myhsok, B., & Schmitt-Egenolf, M. (2002). Association and Linkage of Human Leukocyte Antigens with Psoriasis – Revisited. Transfusion Medicine and Hemotherapy, 29(6), 326-330. doi:10.1159/000068267Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene. (Journal article)
Giess, R., Holtmann, B., Braga, M., Grimm, T., Müller-Myhsok, B., Toyka, K. V., & Sendtner, M. (2002). Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.. American journal of human genetics, 70(5), 1277-1286. doi:10.1086/3404272001
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes. (Journal article)
West, A. B., Zimprich, A., Lockhart, P. J., Farrer, M., Singleton, A., Holtom, B., . . . Gasser, T. (2001). Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.. European journal of human genetics : EJHG, 9(9), 659-666. doi:10.1038/sj.ejhg.5200698Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. (Journal article)
Zimprich, A., Grabowski, M., Asmus, F., Naumann, M., Berg, D., Bertram, M., . . . Gasser, T. (2001). Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.. Nature genetics, 29(1), 66-69. doi:10.1038/ng709Results from a genome-wide search for predisposing genes in sarcoidosis. (Journal article)
Schürmann, M., Reichel, P., Müller-Myhsok, B., Schlaak, M., Müller-Quernheim, J., & Schwinger, E. (2001). Results from a genome-wide search for predisposing genes in sarcoidosis.. American journal of respiratory and critical care medicine, 164(5), 840-846. doi:10.1164/ajrccm.164.5.2007056Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families. (Journal article)
Asmus, F., Zimprich, A., Naumann, M., Berg, D., Bertram, M., Ceballos-Baumann, A., . . . Gasser, T. (2001). Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.. Annals of neurology, 49(1), 121-124. doi:3.0.co;2-8">10.1002/1531-8249(200101)49:1<121::aid-ana20>3.0.co;2-8DOI: 10.1002/1531-8249(200101)49:1<121::aid-ana20>3.0.co;2-8
Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis. (Journal article)
Schürmann, M., Reichel, P., Müller-Myhsok, B., Dieringer, T., Wurm, K., Schlaak, M., . . . Schwinger, E. (2001). Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis.. Journal of internal medicine, 249(1), 77-83. doi:10.1046/j.1365-2796.2001.00776.xOrigin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects. (Journal article)
Periquet, M., Lücking, C., Vaughan, J., Bonifati, V., Dürr, A., De Michele, G., . . . French Parkinson's Disease Genetics Study Group. The European Consortium on Genetic Susceptibility in Parkinson's Disease. (2001). Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.. American journal of human genetics, 68(3), 617-626. doi:10.1086/3187912000
A region on chromosome 3 is linked to dizygotic twinning. (Journal article)
Busjahn, A., Knoblauch, H., Faulhaber, H. D., Aydin, A., Uhlmann, R., Tuomilehto, J., . . . Müller-Myhsok, B. (2000). A region on chromosome 3 is linked to dizygotic twinning.. Nature genetics, 26(4), 398-399. doi:10.1038/82515Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2). (Journal article)
Kress, W., Mueller-Myhsok, B., Ricker, K., Schneider, C., Koch, M. C., Toyka, K. V., . . . Grimm, T. (2000). Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).. Neuromuscular disorders : NMD, 10(7), 478-480. doi:10.1016/s0960-8966(00)00129-2Familial sarcoidosis is linked to the major histocompatibility complex region. (Journal article)
Schürmann, M., Lympany, P. A., Reichel, P., Müller-Myhsok, B., Wurm, K., Schlaak, M., . . . Schwinger, E. (2000). Familial sarcoidosis is linked to the major histocompatibility complex region.. American journal of respiratory and critical care medicine, 162(3 Pt 1), 861-864. doi:10.1164/ajrccm.162.3.9901099Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families. (Journal article)
Pei, W., Baron, H., Müller-Myhsok, B., Knoblauch, H., Al-Yahyaee, S. A., Hui, R., . . . Schuster, H. (2000). Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.. Clinical genetics, 57(1), 29-34. doi:10.1034/j.1399-0004.2000.570105.xA cholesterol-lowering gene maps to chromosome 13q. (Journal article)
Knoblauch, H., Müller-Myhsok, B., Busjahn, A., Ben Avi, L., Bähring, S., Baron, H., . . . Leitersdorf, E. (2000). A cholesterol-lowering gene maps to chromosome 13q.. American journal of human genetics, 66(1), 157-166. doi:10.1086/302704Association of human leucocyte‐DR and DQ antigens in coeliac disease: A family study (Journal article)
Agrawal, S., Gupta, A., Yachha, S., Müller‐Myhsok, B., Mehrotra, P., & Agarwal, S. (2000). Association of human leucocyte‐DR and DQ antigens in coeliac disease: A family study. Journal of Gastroenterology and Hepatology, 15(7), 771-774. doi:10.1046/j.1440-1746.2000.02227.xCD4 alphabeta T lymphocytes express high levels of the T lymphocyte antigen CTLA-4 (CD152) in acute malaria. (Journal article)
Schlotmann, T., Waase, I., Jülch, C., Klauenberg, U., Müller-Myhsok, B., Dietrich, M., . . . Bröker, B. M. (2000). CD4 alphabeta T lymphocytes express high levels of the T lymphocyte antigen CTLA-4 (CD152) in acute malaria.. The Journal of infectious diseases, 182(1), 367-370. doi:10.1086/315690[Linkage of familial combined hyperlipidemia to chromosome 1q21-23 in Chinese and German families]. (Journal article)
Pei, W., Baron, H., & Müller-Myhsok, B. (2000). [Linkage of familial combined hyperlipidemia to chromosome 1q21-23 in Chinese and German families].. Zhonghua yi xue za zhi, 80(1), 25-27.1999
Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. (Journal article)
Arolt, V., Lencer, R., Purmann, S., Schürmann, M., Müller-Myhsok, B., Krecker, K., & Schwinger, E. (1999). Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia.. American journal of medical genetics, 88(6), 603-606. doi:3.0.co;2-x">10.1002/(sici)1096-8628(19991215)88:6<603::aid-ajmg5>3.0.co;2-xDOI: 10.1002/(sici)1096-8628(19991215)88:6<603::aid-ajmg5>3.0.co;2-x
Quantitative trait loci for blood pressure exist near the IGF-1, the Liddle syndrome, the angiotensin II-receptor gene and the renin loci in man. (Journal article)
Nagy, Z., Busjahn, A., Bähring, S., Faulhaber, H. D., Gohlke, H. R., Knoblauch, H., . . . Luft, F. C. (1999). Quantitative trait loci for blood pressure exist near the IGF-1, the Liddle syndrome, the angiotensin II-receptor gene and the renin loci in man.. Journal of the American Society of Nephrology : JASN, 10(8), 1709-1716. doi:10.1681/asn.v1081709A new mutation in the elastin gene causing supravalvular aortic stenosis. (Journal article)
Boeckel, T., Dierks, A., Vergopoulos, A., Bähring, S., Knoblauch, H., Müller-Myhsok, B., . . . Schuster, H. (1999). A new mutation in the elastin gene causing supravalvular aortic stenosis.. The American journal of cardiology, 83(7), 1141-10. doi:10.1016/s0002-9149(99)00032-6Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15. (Journal article)
Nöthen, M. M., Schulte-Körne, G., Grimm, T., Cichon, S., Vogt, I. R., Müller-Myhsok, B., . . . Remschmidt, H. (1999). Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.. European child & adolescent psychiatry, 8 Suppl 3, 56-59. doi:10.1007/pl00010696Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analyses. (Journal article)
Müller-Myhsok, B., & Grimm, T. (1999). Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analyses.. European child & adolescent psychiatry, 8 Suppl 3, 40-42. doi:10.1007/pl00010692Linkage disequilibrium and haplotype analysis in German Friedreich ataxia families. (Journal article)
Zühlke, C., Gehlken, U., Purmann, S., Kunisch, M., Müller-Myhsok, B., Kreuz, F., & Laccone, F. (1999). Linkage disequilibrium and haplotype analysis in German Friedreich ataxia families.. Human heredity, 49(2), 90-96. doi:10.1159/000022851Linkage of proximal myotonic myopathy to chromosome 3q. (Journal article)
Ricker, K., Grimm, T., Koch, M. C., Schneider, C., Kress, W., Reimers, C. D., . . . Mueller, C. R. (1999). Linkage of proximal myotonic myopathy to chromosome 3q.. Neurology, 52(1), 170-171. doi:10.1212/wnl.52.1.170Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects. (Journal article)
Knoblauch, H., Busjahn, A., Müller-Myhsok, B., Faulhaber, H. D., Schuster, H., Uhlmann, R., & Luft, F. C. (1999). Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects.. Arteriosclerosis, thrombosis, and vascular biology, 19(12), 2940-2944. doi:10.1161/01.atv.19.12.2940Significant evidence for linkage of a simulated trait to D1G024--a conclusion reached using multiallelic transmission/disequilibrium tests. (Conference Paper)
Ziegler, A., Hebebrand, J., Kastner, C., & Müller-Myhsok, B. (1999). Significant evidence for linkage of a simulated trait to D1G024--a conclusion reached using multiallelic transmission/disequilibrium tests.. In Genetic epidemiology Vol. 17 Suppl 1 (pp. S785-S789). doi:10.1002/gepi.13701707129hSKCa3: a candidate gene for schizophrenia? (Journal article)
Meissner, B., Purmann, S., Schürmann, M., Zühlke, C., Lencer, R., Arolt, V., . . . Schwinger, E. (1999). hSKCa3: a candidate gene for schizophrenia?. Psychiatric genetics, 9(2), 91-96.1998
Intra-abdominal Candida infection during acute necrotizing pancreatitis has a high prevalence and is associated with increased mortality. (Journal article)
Hoerauf, A., Hammer, S., Müller-Myhsok, B., & Rupprecht, H. (1998). Intra-abdominal Candida infection during acute necrotizing pancreatitis has a high prevalence and is associated with increased mortality.. Critical care medicine, 26(12), 2010-2015. doi:10.1097/00003246-199812000-00031A linkage study of spelling disorder on chromosomes 1, 6, and 15 (Journal article)
Schulte-Körne, G., Nöthen, M. M., Cichon, S., Grimm, T., Müller-Myhsok, B., Propping, P., & Remschmidt, H. (1998). A linkage study of spelling disorder on chromosomes 1, 6, and 15. American Journal of Medical Genetics - Neuropsychiatric Genetics, 81(6), 459.A susceptibility locus for Parkinson's disease maps to chromosome 2p13. (Journal article)
Gasser, T., Müller-Myhsok, B., Wszolek, Z. K., Oehlmann, R., Calne, D. B., Bonifati, V., . . . Horstmann, R. D. (1998). A susceptibility locus for Parkinson's disease maps to chromosome 2p13.. Nature genetics, 18(3), 262-265. doi:10.1038/ng0398-262Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa. (Journal article)
Brobby, G. W., Müller-Myhsok, B., & Horstmann, R. D. (1998). Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa.. The New England journal of medicine, 338(8), 548-550. doi:10.1056/nejm199802193380813Approaches to the genetics of cardiovascular disease through genetic field work. (Conference Paper)
Schuster, H., Lamprecht, A., Junghans, C., Dietz, B., Baron, H., Nothnagel, M., . . . Luft, F. C. (1998). Approaches to the genetics of cardiovascular disease through genetic field work.. In Kidney international Vol. 53 (pp. 1449-1454). doi:10.1046/j.1523-1755.1998.00928.xEvidence for linkage of spelling disability to chromosome 15. (Journal article)
Schulte-Körne, G., Grimm, T., Nöthen, M. M., Müller-Myhsok, B., Cichon, S., Vogt, I. R., . . . Remschmidt, H. (1998). Evidence for linkage of spelling disability to chromosome 15.. American journal of human genetics, 63(1), 279-282. doi:10.1086/301919Genetics of Parkinson's disease (Conference Paper)
Gasser, T., & Muller-Myhsok, B. (1998). Genetics of Parkinson's disease. In Medizinische Genetik Vol. 10 (pp. 387-390).Maximum-likelihood expression of the transmission/disequilibrium test and power considerations. (Journal article)
Abel, L., & Müller-Myhsok, B. (1998). Maximum-likelihood expression of the transmission/disequilibrium test and power considerations.. American journal of human genetics, 63(2), 664-667. doi:10.1086/301975Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship data. (Journal article)
Abel, L., & Müller-Myhsok, B. (1998). Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship data.. American journal of human genetics, 63(2), 638-647. doi:10.1086/3019581997
European Mathematical Genetics Meeting. Munich, Germany, 5-7 April 1997. Abstracts. (Conference Paper)
European Mathematical Genetics Meeting. Munich, Germany, 5-7 April 1997. Abstracts. (1997). In Annals of human genetics Vol. 61 (pp. 531-550). doi:10.1046/j.1469-1809.1997.6160531.xGenetic complexity and Parkinson's disease. (Journal article)
Gasser, T., Müller-Myhsok, B., Wszolek, Z. K., Dürr, A., Vaughan, J. R., Bonifati, V., . . . Wood, N. (1997). Genetic complexity and Parkinson's disease.. Science (New York, N.Y.), 277(5324), 388-389.Genetic analysis of complex diseases. (Journal article)
Müller-Myhsok, B., & Abel, L. (1997). Genetic analysis of complex diseases.. Science (New York, N.Y.), 275(5304), 1328-1329.Genetic analysis of complex diseases. (Journal article)
Scott, W. K., Pericak-Vance, M. A., & Haines, J. L. (1997). Genetic analysis of complex diseases.. Science (New York, N.Y.), 275(5304), 1327. doi:10.1126/science.275.5304.1327A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia. (Journal article)
Vergopoulos, A., Bajari, T., Jouma, M., Knoblauch, H., Aydin, A., Bähring, S., . . . Schuster, H. (1997). A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia.. European journal of human genetics : EJHG, 5(5), 315-323.De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling. (Journal article)
Wirth, B., Schmidt, T., Hahnen, E., Rudnik-Schöneborn, S., Krawczak, M., Müller-Myhsok, B., . . . Zerres, K. (1997). De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling.. American journal of human genetics, 61(5), 1102-1111. doi:10.1086/301608Further evidence suggesting the presence of a locus, on human chromosome 5q31-q33, influencing the intensity of infection with Schistosoma mansoni. (Journal article)
Müller-Myhsok, B., Stelma, F. F., Guissé-Sow, F., Muntau, B., Thye, T., Burchard, G. D., . . . Horstmann, R. D. (1997). Further evidence suggesting the presence of a locus, on human chromosome 5q31-q33, influencing the intensity of infection with Schistosoma mansoni.. American journal of human genetics, 61(2), 452-454. doi:10.1016/s0002-9297(07)64073-7Mapping Undetected Mutations within a Gene &ndash; Evidence for Two Preferential Regions in the DMD Gene (Journal article)
Müller-Myhsok, B., Heiland, H. -J., Müller, C. R., Meng, G., Grimm, T., & Ott, J. U. R. (1997). Mapping Undetected Mutations within a Gene &ndash; Evidence for Two Preferential Regions in the DMD Gene. Human Heredity, 47(2), 61-65. doi:10.1159/0001543931996
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease. (Journal article)
Arolt, V., Lencer, R., Nolte, A., Müller-Myhsok, B., Purmann, S., Schürmann, M., . . . Schwinger, E. (1996). Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.. American journal of medical genetics, 67(6), 564-579. doi:3.0.co;2-r">10.1002/(sici)1096-8628(19961122)67:6<564::aid-ajmg10>3.0.co;2-rDOI: 10.1002/(sici)1096-8628(19961122)67:6<564::aid-ajmg10>3.0.co;2-r