Research outputs
2025
Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation
Alhashmi, M., Gremida, A. M. E., Maharana, S. K., Antonaci, M., Kerr, A., Fu, S., . . . Yamamoto, K. (2025). Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation. BONE RESEARCH, 13(1). doi:10.1038/s41413-024-00393-x
N2B27 media formulations influence gastruloid development
Balayo, T., Lunn, S., Pascual-Mas, P., Fiuza, U. -M., Vasudevan, A., Frenster, J. D., . . . Turner, D. A. (2025). N2B27 media formulations influence gastruloid development. Development, 152(22). doi:10.1242/dev.204774
Dynamic WT1 expression during gastrulation specifies peritoneal smooth muscle fate independently of mesothelial fate
Alsukari, S. H., Ng, H. T., Lang, L., Lunn, S., Beglinger, S., Carr, L., . . . Wilm, B. (2025). Dynamic WT1 expression during gastrulation specifies peritoneal smooth muscle fate independently of mesothelial fate. DEVELOPMENT, 152(13). doi:10.1242/dev.204332
2024
2022
Somatic mutation rates scale with lifespan across mammals
Cagan, A., Baez-Ortega, A., Brzozowska, N., Abascal, F., Coorens, T. H. H., Sanders, M. A., . . . Martincorena, I. (2022). Somatic mutation rates scale with lifespan across mammals. NATURE, 604(7906), 517-+. doi:10.1038/s41586-022-04618-z
Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome
Chapman, G., Alsaqati, M., Lunn, S., Singh, T., Linden, S. C., Linden, D. E. J., . . . Syed, Y. A. (2022). Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome. MOLECULAR PSYCHIATRY, 27(2), 819-830. doi:10.1038/s41380-021-01182-2