Publications
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), 17. doi:10.1038/s41413-024-00393-x
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), 517-524. 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