Marion Delous

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Marion Delous, Lekbir Baala, Rémi Salomon et al. · Nature Genetics · 2007 · 489 citations

Cerebello-oculo-renal Syndrome, Ciliary Gene Rpgrip1l, Developmental Biology +9

Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes

Géraldine Mollet, Flora Silbermann, Marion Delous et al. · Human Molecular Genetics · 2005 · 159 citations · Full text

Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome

S. Gerber, Kamil J. Alzayady, Lydie Bürglen et al. · The American Journal of Human Genetics · 2016 · 144 citations · Full text

Allelic Variant, Mendelian Disorder, Genetic Disorder +7

sox9b Is a Key Regulator of Pancreaticobiliary Ductal System Development

Marion Delous, Chunyue Yin, Donghun Shin et al. · PLoS Genetics · 2012 · 122 citations · Full text

Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6

Marion Delous, Nathan E. Hellman, Helori-Maël Gaudé et al. · Human Molecular Genetics · 2009 · 108 citations · Full text