Béatrice Laudier

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

Jeanne Amiel, Béatrice Laudier, Tania Attié‐Bitach et al. · Nature Genetics · 2003 · 850 citations · Full text

Genetic Disorder, Genetics, Inherited Metabolic Disease +8

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot et al. · The American Journal of Human Genetics · 2004 · 756 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Mendelian Disorder +15

PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome

Delphine Trochet, Louise M. O’Brien, David Gozal et al. · The American Journal of Human Genetics · 2005 · 243 citations · Full text

Phox2b Genotype Allows, Genetic Disorder, Genetics +11

Rescue of fragile X syndrome phenotypes in Fmr1KO mice by a BKCa channel opener molecule

Betty Hébert, Susanna Pietropaolo, Sandra Même et al. · Orphanet Journal of Rare Diseases · 2014 · 96 citations · Full text

<i>PMX2B</i>, a new candidate gene for Hirschsprung's disease

HK Benailly, J.M. Lapierre, Béatrice Laudier et al. · Clinical Genetics · 2003 · 62 citations