Yvan Herenger

AnnotSV: an integrated tool for structural variations annotation

Véronique Geoffroy, Yvan Herenger, Arnaud Kress et al. · Bioinformatics · 2018 · 475 citations · Full text

Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

Claire Redin, Bénédicte Gérard, Julia Lauer et al. · Journal of Medical Genetics · 2014 · 270 citations · Full text

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

Amélie Piton, Hélène Poquet, Claire Redin et al. · European Journal of Human Genetics · 2013 · 83 citations · Full text

Psychiatry, Genetic Disorder, Genetics +8

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis

Charlotte Gehin, Museer A. Lone, Winston Lee et al. · Journal of Clinical Investigation · 2023 · 39 citations · Full text

Neurodegenerative Diseases, Molecular Physiology, Developmental Biology +14

Long term follow up of two independent patients with Schinzel–Giedion carrying SETBP1 mutations

Yvan Herenger, Corinne Stoetzel, Élise Schaefer et al. · European Journal of Medical Genetics · 2015 · 32 citations

Setbp1 Mutations, Mendelian Disorder, Independent Patients +5