Alinoë Lavillaureix

Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients

Elouan Chérot, Boris Keren, Christèle Dubourg et al. · Clinical Genetics · 2017 · 110 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Pleiotropic Mechanisms Indicated for Sex Differences in Autism

Ileena Mitra, Kathryn Tsang, Christine Ladd‐Acosta et al. · PLoS Genetics · 2016 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin et al. · The American Journal of Human Genetics · 2021 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders

Ileena Mitra, Alinoë Lavillaureix, Erika Yeh et al. · PLoS Genetics · 2017 · 46 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D

Arnaud Molin, Sandrine Lemoine, Martin Kaufmann et al. · Frontiers in Endocrinology · 2021 · 32 citations · Full text

Medicine, Endocrinology, Genetics +17