Élodie M. Richard

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

Mariella Simon, Élodie M. Richard, Xinjian Wang et al. · PLoS Genetics · 2015 · 113 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Mitochondrial Biogenesis +13

Ventral Tegmental Area Cannabinoid Type-1 Receptors Control Voluntary Exercise Performance

Sarah Dubreucq, Audrey Durand, Isabel Matias et al. · Biological Psychiatry · 2012 · 96 citations

Cannabis Use, Psychoactive Drug, Health Sciences +14

Plasma Transcortin Influences Endocrine and Behavioral Stress Responses in Mice

Élodie M. Richard, Jean‐Christophe Helbling, Claudine Tridon et al. · Endocrinology · 2009 · 92 citations · Full text

Glucocorticoid, Social Sciences, Stress +18

Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly

Élodie M. Richard, D.L. Polla, Muhammad Zaman Khan Assir et al. · The American Journal of Human Genetics · 2019 · 92 citations · Full text

Allelic Variant, Developmental Biology, Genetic Disorder +5

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss

Élodie M. Richard, Regie Lyn P. Santos‐Cortez, Rabia Faridi et al. · Human Mutation · 2018 · 84 citations

Genetics, Genetic Epidemiology, Consanguineous Pakistani Families +20