Elizabeth Berry‐Kravis

Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey et al. · The American Journal of Human Genetics · 2003 · 765 citations · Full text

Medicine, Neurology, Neuroscience +13

Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

Sébastien Jacquemont, Aurore Curie, Vincent des Portes et al. · Science Translational Medicine · 2011 · 611 citations

Life Sciences, Molecular Biology, Neuroscience +17

An Official ATS Clinical Policy Statement: Congenital Central Hypoventilation Syndrome: Genetic Basis, Diagnosis, and Management

Debra E. Weese‐Mayer, Elizabeth Berry‐Kravis, Isabella Ceccherini et al. · American Journal of Respiratory and Critical Care Medicine · 2010 · 505 citations

Medicine, Internal Medicine, Pediatrics +3

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

Xueya Zhou, Pamela Feliciano, Chang Shu et al. · Nature Genetics · 2022 · 461 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome

Elizabeth Berry‐Kravis, David Hessl, Sarah M. Coffey et al. · Journal of Medical Genetics · 2009 · 410 citations · Full text

Medicine, Pharmacokinetics, Pharmacology +13