Viviane Baral

Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4

Nadège Bondurand, Florence Dastot‐Le Moal, Laure Stanchina et al. · The American Journal of Human Genetics · 2007 · 256 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

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 · 195 citations · Full text

Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development

Laure Stanchina, Viviane Baral, Fabienne Robert et al. · Developmental Biology · 2006 · 136 citations

Developmental Biology, Cell Signaling, Neuroscience +7

Identification and functional analysis of<i>SOX10</i>missense mutations in different subtypes of waardenburg syndrome

Asma Chaoui, Yuli Watanabe, Renaud Touraine et al. · Human Mutation · 2011 · 83 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +15

Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4

Nadège Bondurand, Virginie Fouquet, Viviane Baral et al. · European Journal of Human Genetics · 2012 · 39 citations · Full text

Transcriptional Regulation, Alu-mediated Deletion, Sox10 Regulatory Elements +10