Lehman, Anna

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

Hamdan, F. F., Myers, C. T., Cossette, P., Lemay, P., Spiegelman, D., Laporte, A. D., Nassif, C., Diallo, O., Monlong, J., Cadieux-Dion, M., et al. (2017) · The American Journal of Human Genetics

Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders

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Genetic testing in monogenic early-onset atrial fibrillation

Chalazan, B., Freeth, E., Mohajeri, A., Ramanathan, K., Bennett, M., Walia, J., Halperin, L., Roston, T., Lazarte, J., Hegele, R. A., et al. (2023) · European Journal of Human Genetics

Atrial Fibrillation Management and OutcomesCardiac electrophysiology and arrhythmias

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Further delineation of BCAP31‐linked intellectual disability: description of 17 new families with LoF and missense variants

Whalen, S., Shaw, M., Mignot, C., Héron, D., Bastaraud, S. C., Walti, C. C., Liebelt, J., Elmslie, F., Yap, P., Hurst, J., et al. (2021) · European Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

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