Tania Attié‐Bitach

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

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

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

Vincent Cantagrel, Jennifer L. Silhavy, Stephanie Bielas et al. · The American Journal of Human Genetics · 2008 · 395 citations · Full text

Developmental Biology, Mendelian Disorder, Joubert Syndrome +10

Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis

Su Kyoung Kim, Asako Shindo, Tae Joo Park et al. · Science · 2010 · 349 citations · Full text

Developmental Biology, Xenopus Embryos, Cell Division +15

Podocin Localizes in the Kidney to the Slit Diaphragm Area

Séverine Roselli, Olivier Gribouval, Nicolas Boute et al. · American Journal Of Pathology · 2002 · 336 citations · Full text

Mechanobiology, Urology, Medicine +10