Prof Bertram Muller-Myhsok

Molecular and Clinical Pharmacology

Publications

2019

Association 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., . . . Consortium, I. G. (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.2018.4519

DOI: 10.1001/jamaneurol.2018.4519

Association 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.2019.0905

DOI: 10.1001/jamaneurol.2019.0905

Association 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.2018.4166

DOI: 10.1001/jamapsychiatry.2018.4166

Associations 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.2019.04.018

DOI: 10.1016/j.schres.2019.04.018

BLOOD-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.2017.08.234

DOI: 10.1016/j.euroneuro.2017.08.234

COMMON 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.2017.08.263

DOI: 10.1016/j.euroneuro.2017.08.263

Epigenetic 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.1816847116

DOI: 10.1073/pnas.1816847116

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.32700

DOI: 10.1002/ajmg.b.32700

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.2017.08.032

DOI: 10.1016/j.euroneuro.2017.08.032

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. (Journal article)

Mullins, N., Bigdeli, T. B., Børglum, A. D., Coleman, J. R. I., Demontis, D., Mehta, D., . . . Lewis, C. M. (2019). GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.. The American journal of psychiatry, 176(8), 651-660. doi:10.1176/appi.ajp.2019.18080957

DOI: 10.1176/appi.ajp.2019.18080957

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., 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/s41588-019-0364-4

DOI: 10.1038/s41588-019-0364-4

Genome-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/s41398-019-0402-0

DOI: 10.1038/s41398-019-0402-0

Genome-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., . . . Psych, B. D. W. G. (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. NATURE GENETICS, 51(5), 793-+. doi:10.1038/s41588-019-0397-8

DOI: 10.1038/s41588-019-0397-8

Genome-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., . . . Consortium, P. G. (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-y

DOI: 10.1038/s41398-018-0360-y

Identification 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., . . . Team, A. R. (2019). Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51(3), 431-+. doi:10.1038/s41588-019-0344-8

DOI: 10.1038/s41588-019-0344-8

Integrated 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., . . . Consortium, P. G. (2019). Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10. doi:10.1038/s41467-019-10461-0

DOI: 10.1038/s41467-019-10461-0

Neurobiology 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.2019.18091018

DOI: 10.1176/appi.ajp.2019.18091018

Population-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., . . . Psychiat, S. W. G. (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.32716

DOI: 10.1002/ajmg.b.32716

Publisher 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/s41588-019-0435-6

DOI: 10.1038/s41588-019-0435-6

Should 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.19118

DOI: 10.1002/uog.19118

Treatment 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/s41398-019-0524-4

DOI: 10.1038/s41398-019-0524-4

2018

A 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/s12864-018-4859-7

DOI: 10.1186/s12864-018-4859-7

Age 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-z

DOI: 10.1038/s41598-018-28160-z

Analysis 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., . . . Consortium, B. (2018). Analysis of shared heritability in common disorders of the brain. SCIENCE, 360(6395), 1313-+. doi:10.1126/science.aap8757

DOI: 10.1126/science.aap8757

Association 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., . . . Owen, M. J. (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(1), 91-100. doi:10.1016/j.bpsc.2018.07.006

DOI: 10.1016/j.bpsc.2018.07.006

Common 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.2018.04.014

DOI: 10.1016/j.neuron.2018.04.014

Does 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.2017.09.009

DOI: 10.1016/j.biopsych.2017.09.009

Effect 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., . . . Grp, B. E. N. E. F. I. T. S. (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:10.1177/1352458518763089

DOI: 10.1177/1352458518763089

Estimation 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.2018.03.021

DOI: 10.1016/j.ajhg.2018.03.021

From 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.2018.04.011

DOI: 10.1016/bs.pmbts.2018.04.011

Gene 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.2017.11.068

DOI: 10.1016/j.jad.2017.11.068

Genetic 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 http://gateway.webofknowledge.com/

Genome-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(5), 668-+. doi:10.1038/s41588-018-0090-3

DOI: 10.1038/s41588-018-0090-3

Genome-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.0209160

DOI: 10.1371/journal.pone.0209160

Genomic 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-+. doi:10.1016/j.cell.2018.05.046

DOI: 10.1016/j.cell.2018.05.046

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 http://gateway.webofknowledge.com/

Molecular 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/s41431-018-0150-2

DOI: 10.1038/s41431-018-0150-2

Neurobiology 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-x

DOI: 10.1007/s00406-018-0943-x

Shared 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., . . . Consortium, P. G. (2018). Shared genetic etiology between alcohol dependence and major depressive disorder. PSYCHIATRIC GENETICS, 28(4), 66-70. doi:10.1097/YPG.0000000000000201

DOI: 10.1097/YPG.0000000000000201

Transancestral 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-+. doi:10.1038/s41593-018-0275-1

DOI: 10.1038/s41593-018-0275-1

2017

Aging- 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 http://gateway.webofknowledge.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.2016.09.413

DOI: 10.1016/j.euroneuro.2016.09.413

Classification 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 http://gateway.webofknowledge.com/

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 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.12770

DOI: 10.1111/jcpp.12770

Common 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., . . . Consortium, M. B. (2017). Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/s41398-017-0019-0

DOI: 10.1038/s41398-017-0019-0

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.3725

DOI: 10.1038/ng.3725

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/s41398-017-0026-1

DOI: 10.1038/s41398-017-0026-1

Genetic 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.2017.3016

DOI: 10.1001/jamapsychiatry.2017.3016

Genetic 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/genes8070183

DOI: 10.3390/genes8070183

Genetic 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., . . . Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.. Nature communications, 8, 14774. doi:10.1038/ncomms14774

DOI: 10.1038/ncomms14774

Genetic 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., . . . Consortium, C. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. TRANSLATIONAL PSYCHIATRY, 7. doi:10.1038/tp.2016.292

DOI: 10.1038/tp.2016.292

Genetic 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/s41467-017-00366-1

DOI: 10.1038/s41467-017-00366-1

Genome-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., . . . Consortium, P. G. (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.2017.115

DOI: 10.1038/tp.2017.115

Genome-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/s41467-017-01818-4

DOI: 10.1038/s41467-017-01818-4

Hair 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/s41598-017-11852-3

DOI: 10.1038/s41598-017-11852-3

IDENTIFICATION 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 http://gateway.webofknowledge.com/

Identification 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., Puetz, B., . . . Grp, D. E. S. I. R. S. (2017). Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. LANCET NEUROLOGY, 16(11), 898-907. doi:10.1016/S1474-4422(17)30327-7

DOI: 10.1016/S1474-4422(17)30327-7

Identification 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.0171595

DOI: 10.1371/journal.pone.0171595

Interaction 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.116.183475

DOI: 10.1192/bjp.bp.116.183475

Novel 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/ncomms13624

DOI: 10.1038/ncomms13624

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., . . . Workin, M. D. D. (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.2016.09.419

DOI: 10.1016/j.euroneuro.2016.09.419

POLYGENIC 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.2016.09.576

DOI: 10.1016/j.euroneuro.2016.09.576

Reduced 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.12700

DOI: 10.1111/jcpp.12700

SEX-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.2016.09.512

DOI: 10.1016/j.euroneuro.2016.09.512

Sleep 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.12557

DOI: 10.1111/jsr.12557

The 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.2017.11.003

DOI: 10.1016/j.pnpbp.2017.11.003

The 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., . . . Consortium, M. B. (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.2016.231

DOI: 10.1038/mp.2016.231

USING 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.2016.09.433

DOI: 10.1016/j.euroneuro.2016.09.433

2016

An 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.2016.11.013

DOI: 10.1016/j.biopsych.2016.11.013

Association 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.1002118

DOI: 10.1371/journal.pmed.1002118

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 (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/s10519-015-9737-3

DOI: 10.1007/s10519-015-9737-3

Corrigendum: 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/ng1016-1296c

DOI: 10.1038/ng1016-1296c

Cross-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., . . . Canc, A. A. P. (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-15-2980

DOI: 10.1158/0008-5472.CAN-15-2980

Gene-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., . . . Consortium, I. H. G. (2016). Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. CEPHALALGIA, 36(7), 648-657. doi:10.1177/0333102415591497

DOI: 10.1177/0333102415591497

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. (Journal article)

Franke, B., Franke, B., Stein, J. L., Ripke, S., Anttila, V., Hibar, D. P., . . . 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.4228

DOI: 10.1038/nn.4228

Genetic 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.2016.31

DOI: 10.1038/ejhg.2016.31

Genome-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., . . . Consortium, G. (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.2016.05.010

DOI: 10.1016/j.biopsych.2016.05.010

Genome-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., . . . Consortium, P. G. (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.2016.12.012

DOI: 10.1016/j.biopsych.2016.12.012

Genome-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.32402

DOI: 10.1002/ajmg.b.32402

Hair 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.2016.07.190

DOI: 10.1016/j.psyneuen.2016.07.190

Identification 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., . . . Consortium, 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-x

DOI: 10.1007/s12035-016-0041-x

Influence 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., . . . Grp, B. E. Y. O. N. D. S. (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 http://gateway.webofknowledge.com/

Mendelian 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/dyw129

DOI: 10.1093/ije/dyw129

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., . . . Consortium, I. H. G. (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. NATURE GENETICS, 48(8), 856-+. doi:10.1038/ng.3598

DOI: 10.1038/ng.3598

Meta-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., . . . Consortium, I. H. G. (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/ng1016-1296c

DOI: 10.1038/ng1016-1296c

No 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., . . . Consortium, P. G. (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.1006343

DOI: 10.1371/journal.pgen.1006343

Novel 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.4398

DOI: 10.1038/nn.4398

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation (Journal article)

Andlauer, T. F. M., Buck, D., Antony, G., Bayas, A., Bechmann, L., Berthele, A., . . . Mueller-Myhsok, B. (2016). Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. SCIENCE ADVANCES, 2(6). doi:10.1126/sciadv.1501678

DOI: 10.1126/sciadv.1501678

Polygenic 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 http://gateway.webofknowledge.com/

Schizophrenia 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/nature16549

DOI: 10.1038/nature16549

2015

A 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/s12916-015-0334-3

DOI: 10.1186/s12916-015-0334-3

ABCB1 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.32309

DOI: 10.1002/ajmg.b.32309

Analyzing 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-z

DOI: 10.1186/s12888-015-0512-z

Association 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.2015.14101348

DOI: 10.1176/appi.ajp.2015.14101348

Common 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-U216. doi:10.1038/nature14101

DOI: 10.1038/nature14101

Concordance 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., . . . Consortium, I. H. G. (2015). Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. CEPHALALGIA, 35(6), 489-499. doi:10.1177/0333102414547784

DOI: 10.1177/0333102414547784

Connecting 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.0128465

DOI: 10.1371/journal.pone.0128465

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., . . . Grp, S. B. S. (2016). Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. MOLECULAR NEUROBIOLOGY, 53(10), 6608-6619. doi:10.1007/s12035-015-9559-6

DOI: 10.1007/s12035-015-9559-6

Exome 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., . . . Multiple, G. C. N. (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 http://gateway.webofknowledge.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 http://gateway.webofknowledge.com/

Familiality 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/S0033291715000215

DOI: 10.1017/S0033291715000215

Genetic 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(5), 1189-1202. doi:10.1016/j.neuron.2015.05.034

DOI: 10.1016/j.neuron.2015.05.034

Genetic 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)30560-5

DOI: 10.1016/S0924-9338(15)30560-5

Genome-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., . . . Genom, C. H. A. R. I. (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.2014.08.027

DOI: 10.1016/j.biopsych.2014.08.027

Genome-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.2015.159

DOI: 10.1038/tp.2015.159

Genome-wide association analysis in a German multiple sclerosis cohort (Conference Paper)

Andlauer, T. F. M., Buck, D., Hemmer, B., Mueller-Myhsok, B., KKNMS., Base-II., . . . SHIP. (2015). Genome-wide association analysis in a German multiple sclerosis cohort. In MULTIPLE SCLEROSIS JOURNAL Vol. 21 (pp. 144). Retrieved from http://gateway.webofknowledge.com/

Identification 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.2015.02.005

DOI: 10.1016/j.psyneuen.2015.02.005

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., . . . Susceptibility, B. O. C. (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/ddu431

DOI: 10.1093/hmg/ddu431

Joint 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.2014.12.006

DOI: 10.1016/j.ajhg.2014.12.006

LD 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.3211

DOI: 10.1038/ng.3211

MS 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.2015.01.008

DOI: 10.1016/j.jneuroim.2015.01.008

Modeling 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.2015.09.001

DOI: 10.1016/j.ajhg.2015.09.001

Polygenic 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 http://gateway.webofknowledge.com/

Psychiatric 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., . . . Psyc, N. P. A. S. (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. NATURE NEUROSCIENCE, 18(2), 199-209. doi:10.1038/nn.3922

DOI: 10.1038/nn.3922

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., . . . Network, G. C. (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.21933

DOI: 10.1002/gepi.21933

Supportive 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/cam4.500

DOI: 10.1002/cam4.500

The 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.2015.50

DOI: 10.1038/mp.2015.50

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.2014.178

DOI: 10.1038/npp.2014.178

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 (Journal article)

Ahsan, H., Halpern, J., Kibriya, M. G., Pierce, B. L., Tong, L., Gamazon, E., . . . Study, F. B. C. (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-13-0340

DOI: 10.1158/1055-9965.EPI-13-0340

ABCB1 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 http://gateway.webofknowledge.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., . . . Consortium, C. H. A. R. G. E. (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.2013.37

DOI: 10.1038/mp.2013.37

Biological 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-+. doi:10.1038/nature13595

DOI: 10.1038/nature13595

Blood 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.0098092

DOI: 10.1371/journal.pone.0098092

Characterizing 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. (2014). Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes. NATURE COMMUNICATIONS, 5. doi:10.1038/ncomms6236

DOI: 10.1038/ncomms6236

Clinically 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.0095009

DOI: 10.1371/journal.pone.0095009

Cognitive 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.2013.09.003

DOI: 10.1016/j.learninstruc.2013.09.003

Discriminating 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.2014.134

DOI: 10.1038/bjc.2014.134

Genetic 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.32247

DOI: 10.1002/ajmg.b.32247

Genetic Risk Prediction and Neurobiological Understanding of Alcoholism (Conference Paper)

Levey, D. F., Le-Niculescu, H., Frank, J., Ayalew, M., Jain, N., Kirlin, B., . . . Consortium, G. E. S. G. A. (2014). Genetic Risk Prediction and Neurobiological Understanding of Alcoholism. In BIOLOGICAL PSYCHIATRY Vol. 75 (pp. 352S). Retrieved from http://gateway.webofknowledge.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.2013.199

DOI: 10.1038/ejhg.2013.199

Genetic modification of 25(OH)D levels in MS (Conference Paper)

Munger, K., Kochert, K., Fitzgerald, K., Arnason, B., Barkhof, F., Comi, G., . . . Grp, B. E. Y. O. N. D. S. (2014). Genetic modification of 25(OH)D levels in MS. In MULTIPLE SCLEROSIS JOURNAL Vol. 20 (pp. 249). Retrieved from http://gateway.webofknowledge.com/

Genetic risk prediction and neurobiological understanding of alcoholism (Journal article)

Levey, D. F., Le-Niculescu, H., Frank, J., Ayalew, M., Jain, N., Kirlin, B., . . . Consortium, G. E. S. G. A. (2014). Genetic risk prediction and neurobiological understanding of alcoholism. TRANSLATIONAL PSYCHIATRY, 4. doi:10.1038/tp.2014.29

DOI: 10.1038/tp.2014.29

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., . . . Consortium, G. E. S. G. A. (2014). Genetic risk prediction and neurobiological understanding of alcoholism (vol 4, pg e456, 2014). TRANSLATIONAL PSYCHIATRY, 4. doi:10.1038/tp.2014.74

DOI: 10.1038/tp.2014.74

Genome-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.113.004461

DOI: 10.1161/STROKEAHA.113.004461

Genome-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/ncomms4339

DOI: 10.1038/ncomms4339

Integrating 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/bgt403

DOI: 10.1093/carcin/bgt403

Investigating 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.2013.10.027

DOI: 10.1016/j.jad.2013.10.027

MicroRNA Related Polymorphisms and Breast Cancer Risk (Journal article)

Khan, S., Greco, D., Michailidou, K., Milne, R. L., Muranen, T. A., Heikkinen, T., . . . Network, G. E. N. I. C. A. (2014). MicroRNA Related Polymorphisms and Breast Cancer Risk. PLOS ONE, 9(11). doi:10.1371/journal.pone.0109973

DOI: 10.1371/journal.pone.0109973

P2RX7-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 http://gateway.webofknowledge.com/

Partitioning 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.2014.10.004

DOI: 10.1016/j.ajhg.2014.10.004

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.166751.113

DOI: 10.1101/gr.166751.113

Small 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:10.1186/1476-4598-13-47

DOI: 10.1186/1476-4598-13-47

Targeted 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.2014.06.005

DOI: 10.1016/j.ajhg.2014.06.005

The 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.0109290

DOI: 10.1371/journal.pone.0109290

The 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., . . . Grp, S. Y. S. S. Y. S. (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. BRAIN IMAGING AND BEHAVIOR, 8(2), 153-182. doi:10.1007/s11682-013-9269-5

DOI: 10.1007/s11682-013-9269-5

2013

A 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.2011.142

DOI: 10.1038/mp.2011.142

A 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.2012.148

DOI: 10.1038/tp.2012.148

A mega-analysis of genome-wide association studies for major depressive disorder (Journal article)

A mega-analysis of genome-wide association studies for major depressive disorder (2013). Molecular Psychiatry, 18(4), 497-511. doi:10.1038/mp.2012.21

DOI: 10.1038/mp.2012.21

Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder. (Journal article)

Mehta, D., Klengel, T., Conneely, K. N., Smith, A. K., Altmann, A., Pace, T. W., . . . 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.1217750110

DOI: 10.1073/pnas.1217750110

Children 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.0063859

DOI: 10.1371/journal.pone.0063859

Common 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.2012.12020237

DOI: 10.1176/appi.ajp.2012.12020237

Cost-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/me11-02-0049

DOI: 10.3414/me11-02-0049

Dilution 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.2012.193

DOI: 10.1038/ejhg.2012.193

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 (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.2013.73

DOI: 10.1038/mp.2013.73

Estimating 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/s0033291712002589

DOI: 10.1017/s0033291712002589

Genetic 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.2711

DOI: 10.1038/ng.2711

Genome-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.2561

DOI: 10.1038/ng.2561

Genome-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.2012.198

DOI: 10.1038/ejhg.2012.198

Large-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.2563

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Possible 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.0064947

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Predictors 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.12029

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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.0079145

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Resistance 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.2012.08.010

DOI: 10.1016/j.euroneuro.2012.08.010

Using 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:10.1159/000346788

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Variants 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/s0033291711002923

DOI: 10.1017/s0033291711002923

2012

A 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-z

DOI: 10.1007/s00439-012-1213-z

A 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/dds381

DOI: 10.1093/hmg/dds381

ANK3 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.2012.04.017

DOI: 10.1016/j.jpsychires.2012.04.017

Association 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.32034

DOI: 10.1002/ajmg.b.32034

Determination 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.2011.197

DOI: 10.1038/ejhg.2011.197

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). 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.2011.331

DOI: 10.1038/npp.2011.331

Dissecting 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.32093

DOI: 10.1002/ajmg.b.32093

Don'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.2011.94

DOI: 10.1038/mp.2011.94

Erratum: 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.2012.21

DOI: 10.1038/npp.2012.21

Evidence 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.2012.62

DOI: 10.1038/tp.2012.62

Evidence 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.0034909

DOI: 10.1371/journal.pone.0034909

Genome-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.2307

DOI: 10.1038/ng.2307

Genome-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.1049

DOI: 10.1038/ng.1049

Genome-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.1081

DOI: 10.1038/ng.1081

Genome-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.2011.257

DOI: 10.1038/npp.2011.257

Genome-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.2012.81

DOI: 10.1038/tp.2012.81

Genome-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.x

DOI: 10.1111/j.1369-1600.2011.00395.x

Identification 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.2250

DOI: 10.1038/ng.2250

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). Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics, 20(6), 714. doi:10.1038/ejhg.2012.31

DOI: 10.1038/ejhg.2012.31

Imaging 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.2011.160

DOI: 10.1038/ejhg.2011.160

Meta-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.2012.10.008

DOI: 10.1016/j.schres.2012.10.008

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.0052873

DOI: 10.1371/journal.pone.0052873

Polymorphisms 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.2011.09.003

DOI: 10.1016/j.psyneuen.2011.09.003

Rare 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.32096

DOI: 10.1002/ajmg.b.32096

Replication 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.2012.85

DOI: 10.1038/tp.2012.85

Restless 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.2012.03.012

DOI: 10.1016/j.sleep.2012.03.012

Single-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.2011.14

DOI: 10.1038/tpj.2011.14

The 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/s10519-012-9532-3

DOI: 10.1007/s10519-012-9532-3

The 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:10.1186/1471-2164-13-579

DOI: 10.1186/1471-2164-13-579

2011

Association 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/s10519-010-9413-6

DOI: 10.1007/s10519-010-9413-6

CEACAM6 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.0019319

DOI: 10.1371/journal.pone.0019319

EPIBLASTER-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.2010.196

DOI: 10.1038/ejhg.2010.196

Epistasis 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/btr218

DOI: 10.1093/bioinformatics/btr218

Evidence 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.0b013e3283457bfb

DOI: 10.1097/ypg.0b013e3283457bfb

First 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.2009.102

DOI: 10.1038/mp.2009.102

Genetic 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:10.1155/2011/328054

DOI: 10.1155/2011/328054

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (Journal article)

Cichon, S., Mühleisen, T., Degenhardt, F., Mattheisen, M., Miró, X., Strohmaier, J., . . . Nöthen, 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.2011.03.001

DOI: 10.1016/j.ajhg.2011.03.001

Genome-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.2011.01.017

DOI: 10.1016/j.ajhg.2011.01.017

Genome-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.1002171

DOI: 10.1371/journal.pgen.1002171

Genomewide 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.0020690

DOI: 10.1371/journal.pone.0020690

MEIS1 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.2010.087858

DOI: 10.1136/jmg.2010.087858

Mapping 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.31135

DOI: 10.1002/ajmg.b.31135

More 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.x

DOI: 10.1111/j.1600-0404.2010.01421.x

Novel 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/ddq538

DOI: 10.1093/hmg/ddq538

Pregnane 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.21562

DOI: 10.1002/ibd.21562

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.2011.03.037

DOI: 10.1016/j.febslet.2011.03.037

Role 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.21425

DOI: 10.1002/ibd.21425

Somatization 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.x

DOI: 10.1111/j.1600-0447.2011.01743.x

TMEM132D, 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.2010.41

DOI: 10.1038/mp.2010.41

The 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.2011.04.005

DOI: 10.1016/j.neuron.2011.04.005

Tyrosine 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/awr010

DOI: 10.1093/brain/awr010

Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies. (Journal article)

Mehta, D., Gonik, M., Klengel, T., Rex-Haffner, M., Menke, A., Rubel, J., . . . 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.2011.50

DOI: 10.1001/archgenpsychiatry.2011.50

vipR: 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/btr205

DOI: 10.1093/bioinformatics/btr205

2010

An 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:10.1159/000289596

DOI: 10.1159/000289596

Association 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.2009.201

DOI: 10.1001/archgenpsychiatry.2009.201

CLOCK 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.2009.12.026

DOI: 10.1016/j.biopsych.2009.12.026

Erratum: 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., 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.2009.8

DOI: 10.1038/mp.2009.8

Evidence 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.2010.06.003

DOI: 10.1016/j.jneuroim.2010.06.003

Gender-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.2010.30

DOI: 10.1038/npp.2010.30

Genome-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.517

DOI: 10.1038/ng.517

Genome-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.652

DOI: 10.1038/ng.652

Genome-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.2008.131

DOI: 10.1038/mp.2008.131

Genome-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.2010.05.038

DOI: 10.1016/j.biopsych.2010.05.038

Germline 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.569

DOI: 10.1038/ng.569

HTR2A 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.2009.08.006

DOI: 10.1016/j.euroneuro.2009.08.006

Low-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.24986

DOI: 10.1002/ijc.24986

Lysyl 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.0b013e31819f9330

DOI: 10.1097/ijg.0b013e31819f9330

Mitochondrial 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:10.1186/1471-2156-11-8

DOI: 10.1186/1471-2156-11-8

Polymorphisms 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.2009.180

DOI: 10.1038/npp.2009.180

Proteomic-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.2008.146

DOI: 10.1038/mp.2008.146

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.0014466

DOI: 10.1371/journal.pone.0014466

Variation 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.31007

DOI: 10.1002/ajmg.b.31007

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). 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.2008.142

DOI: 10.1038/mp.2008.142

2009

A 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.2009.95

DOI: 10.1001/archgenpsychiatry.2009.95

A 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.0005129

DOI: 10.1371/journal.pone.0005129

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 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.0b013e328328123d

DOI: 10.1097/hjh.0b013e328328123d

Common 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.362

DOI: 10.1038/ng.362

Epistasis 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.2009.184

DOI: 10.1038/ajg.2009.184

Evaluation 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:10.1186/1471-2350-10-91

DOI: 10.1186/1471-2350-10-91

Further 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.0b013e32832080e1

DOI: 10.1097/ypg.0b013e32832080e1

Gene 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.2009.02.034

DOI: 10.1016/j.biopsych.2009.02.034

Genetic 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.107.510800

DOI: 10.1161/strokeaha.107.510800

Investigation 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.x

DOI: 10.1111/j.1601-183x.2009.00494.x

Mouse 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-x

DOI: 10.1007/s00251-008-0343-x

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. (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.2009.163

DOI: 10.1038/ajg.2009.163

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.30938

DOI: 10.1002/ajmg.b.30938

Polymorphisms 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.30784

DOI: 10.1002/ajmg.b.30784

Sequence 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.21590

DOI: 10.1002/ana.21590

Supporting 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.2009.28

DOI: 10.1038/mp.2009.28

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. (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.2008.65

DOI: 10.1038/ajg.2008.65

2008

Association 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.4002094

DOI: 10.1038/sj.mp.4002094

Combined 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.30750

DOI: 10.1002/ajmg.b.30750

Evidence 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.2008.2

DOI: 10.1038/mp.2008.2

Expansion 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.x

DOI: 10.1111/j.1468-2982.2008.01540.x

Further 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.0b013e3282fb7fc6

DOI: 10.1097/ypg.0b013e3282fb7fc6

Gender-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.2007.050773

DOI: 10.1136/jmg.2007.050773

Genetic 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.2008.08020274

DOI: 10.1176/appi.ajp.2008.08020274

Genetic 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.107.502179

DOI: 10.1161/strokeaha.107.502179

Genetics 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.0000302178.53759.92

DOI: 10.1212/01.wnl.0000302178.53759.92

Genotype-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.2007.11.016

DOI: 10.1016/j.clim.2007.11.016

IL2RA 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.2008.14

DOI: 10.1038/gene.2008.14

Increased 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.x

DOI: 10.1111/j.1399-0039.2008.01056.x

Investigation 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/s00702-008-0124-6

DOI: 10.1007/s00702-008-0124-6

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.0b013e3283063a78

DOI: 10.1097/ypg.0b013e3283063a78

PTPRD (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.190

DOI: 10.1038/ng.190

Polymorphisms 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.x

DOI: 10.1111/j.1460-9568.2008.06332.x

Polymorphisms 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.2007.11.017

DOI: 10.1016/j.neuron.2007.11.017

Polymorphisms 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.2007.05.006

DOI: 10.1016/j.jad.2007.05.006

Refining 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)70122-4

DOI: 10.1016/S1474-4422(08)70122-4

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. (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.20339

DOI: 10.1002/ibd.20339

The 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.x

DOI: 10.1111/j.1572-0241.2007.01694.x

Variants 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.21647

DOI: 10.1002/mds.21647

2007

A 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/ddm009

DOI: 10.1093/hmg/ddm009

Association 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.2006.11.016

DOI: 10.1016/j.jad.2006.11.016

Assoziation 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.200790076

DOI: 10.1002/biuz.200790076

Genome-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/ng2099

DOI: 10.1038/ng2099

Meta 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:10.1186/1471-2156-8-44

DOI: 10.1186/1471-2156-8-44

Polymorphisms 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.30412

DOI: 10.1002/ajmg.b.30412

rs1004819 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.0000819

DOI: 10.1371/journal.pone.0000819

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. (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.30303

DOI: 10.1002/ajmg.b.30303

Evidence 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.20627

DOI: 10.1002/mds.20627

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.0000057

DOI: 10.1371/journal.pone.0000057

Heritability 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.0000245084.35575.66

DOI: 10.1161/01.str.0000245084.35575.66

P2RX7, 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/ddl166

DOI: 10.1093/hmg/ddl166

Polymorphisms 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.4001884

DOI: 10.1038/sj.mp.4001884

Role 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.0000225346.23765.6b

DOI: 10.1097/01.ibd.0000225346.23765.6b

2005

Apolipoprotein 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.30196

DOI: 10.1002/ajmg.b.30196

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.b1

DOI: 10.1097/01.mib.0000187574.41290.b1

Developmental 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:10.1159/000085572

DOI: 10.1159/000085572

Epsilon-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-z

DOI: 10.1007/s10048-004-0206-z

Evaluation 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:10.1159/000087540

DOI: 10.1159/000087540

Mutations 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.2004.12.061

DOI: 10.1016/j.neulet.2004.12.061

On 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:10.1086/432817

DOI: 10.1086/432817

PARK11 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.5201317

DOI: 10.1038/sj.ejhg.5201317

Polymorphisms 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.2005.066340

DOI: 10.1136/gut.2005.066340

Rapid 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:10.1086/428140

DOI: 10.1086/428140

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.x

DOI: 10.1111/j.1365-2249.2005.02667.x

SimPed: 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:10.1159/000088914

DOI: 10.1159/000088914

2004

A 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.x

DOI: 10.1111/j.0022-202x.2004.23423.x

Association 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/ar1164

DOI: 10.1186/ar1164

Autosomal 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.db

DOI: 10.1212/01.wnl.0000125015.06989.db

Mutations 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.2004.11.005

DOI: 10.1016/j.neuron.2004.11.005

Polymorphisms 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/ng1479

DOI: 10.1038/ng1479

Promoter 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.6364094

DOI: 10.1038/sj.gene.6364094

The 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:10.1086/380647

DOI: 10.1086/380647

2003

Apolipoprotein 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)00377-5

DOI: 10.1016/s0021-9150(02)00377-5

Association 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.

Genomewide 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:10.1086/367714

DOI: 10.1086/367714

Is 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/s00125-003-1048-1

DOI: 10.1007/s00125-003-1048-1

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.6363972

DOI: 10.1038/sj.gene.6363972

Parkin 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/awg136

DOI: 10.1093/brain/awg136

2002

Association 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. Infusionstherapie und Transfusionsmedizin, 29(6), 326-330.

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.10282

DOI: 10.1002/ana.10282

Early 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:10.1086/340427

DOI: 10.1086/340427

Epidemiology 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.2002.66.578

DOI: 10.4269/ajtmh.2002.66.578

2001

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.x

DOI: 10.1046/j.1365-2796.2001.00776.x

Inherited 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;2-8

DOI: 10.1002/1531-8249(200101)49:1<121::aid-ana20>3.0.co;2-8

Mutations 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/ng709

DOI: 10.1038/ng709

Origin 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:10.1086/318791

DOI: 10.1086/318791

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.5200698

DOI: 10.1038/sj.ejhg.5200698

Results 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.164.5.2007056

DOI: 10.1164/ajrccm.164.5.2007056

2000

A 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:10.1086/302704

DOI: 10.1086/302704

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:10.1038/82515

DOI: 10.1038/82515

Association of human leucocyte-DR and DQ antigens in coeliac disease: A family study (Journal article)

Agrawal, S., Gupta, A., Yachha, S., Muller-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.x

DOI: 10.1046/j.1440-1746.2000.02227.x

CD4 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

DOI: 10.1086/315690

Familial 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.162.3.9901099

DOI: 10.1164/ajrccm.162.3.9901099

Support 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.x

DOI: 10.1034/j.1399-0004.2000.570105.x

[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

A 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)00032-6

DOI: 10.1016/s0002-9149(99)00032-6

Genetic 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/pl00010696

DOI: 10.1007/pl00010696

Linkage 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/pl00010692

DOI: 10.1007/pl00010692

Linkage 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:10.1159/000022851

DOI: 10.1159/000022851

Peroxisome 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.19.12.2940

DOI: 10.1161/01.atv.19.12.2940

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.

Significant 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).

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-x

DOI: 10.1002/(sici)1096-8628(19991215)88:6<603::aid-ajmg5>3.0.co;2-x

hSKCa3: 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

A 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/ng0398-262

DOI: 10.1038/ng0398-262

Approaches 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.x

DOI: 10.1046/j.1523-1755.1998.00928.x

Connexin 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/nejm199802193380813

DOI: 10.1056/nejm199802193380813

Evidence 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:10.1086/301919

DOI: 10.1086/301919

Genetics 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).

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:10.1097/00003246-199812000-00031

DOI: 10.1097/00003246-199812000-00031

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:10.1086/301975

DOI: 10.1086/301975

Robustness 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:10.1086/301958

DOI: 10.1086/301958

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. (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:10.1086/301608

DOI: 10.1086/301608

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.x

DOI: 10.1046/j.1469-1809.1997.6160531.x

Further 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)64073-7

DOI: 10.1016/s0002-9297(07)64073-7

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.275.5304.1327

DOI: 10.1126/science.275.5304.1327

Genetic 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.

Mapping Undetected Mutations within a Gene – 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. (1997). Mapping Undetected Mutations within a Gene – Evidence for Two Preferential Regions in the DMD Gene. Human Heredity, 47(2), 61-65. doi:10.1159/000154393

DOI: 10.1159/000154393

1996

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. (Journal article)

Veske, A., Oehlmann, R., Younus, F., Mohyuddin, A., Müller-Myhsok, B., Mehdi, S. Q., & Gal, A. (1996). Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.. Human molecular genetics, 5(1), 165-168. doi:10.1093/hmg/5.1.165

DOI: 10.1093/hmg/5.1.165

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:10.1002/(sici)1096-8628(19961122)67:6<564::aid-ajmg10>3.0.co;2-r

DOI: 10.1002/(sici)1096-8628(19961122)67:6<564::aid-ajmg10>3.0.co;2-r

Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine. (Journal article)

Dichgans, M., Mayer, M., Müller-Myhsok, B., Straube, A., & Gasser, T. (1996). Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.. Genomics, 32(1), 151-154. doi:10.1006/geno.1996.0094

DOI: 10.1006/geno.1996.0094

The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. (Journal article)

Gasser, T., Müller-Myhsok, B., Supala, A., Zimmer, E., Wieditz, G., Wszolek, Z. K., . . . Oertel, W. H. (1996). The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.. Journal of neurology, neurosurgery, and psychiatry, 61(5), 518-520. doi:10.1136/jnnp.61.5.518

DOI: 10.1136/jnnp.61.5.518