Séverine Marcos

Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

Véronique Pingault, Virginie Bodereau, Viviane Baral et al. · The American Journal of Human Genetics · 2013 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

SFRPs act as negative modulators of ADAM10 to regulate retinal neurogenesis

Pilar Esteve, África Sandonís, Marcos J. Cardozo et al. · Nature Neuroscience · 2011 · 100 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +12

The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

Séverine Marcos, Julie Sarfati, Chrystel Leroy et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Tubulin Tyrosination Is Required for the Proper Organization and Pathfinding of the Growth Cone

Séverine Marcos, Julie Moreau, Stéphanie Backer et al. · PLoS ONE · 2009 · 77 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice

Séverine Marcos, Carine Monnier, Xavier Rovira et al. · Human Molecular Genetics · 2017 · 48 citations

Medicine, Genetics, Molecular Genetics +17