Tania Attié‐Bitach
Hôpital Necker-Enfants Malades(FR)Université de Pau et des Pays de l'Adour(FR)Inserm(FR)Inserm(FR)Université Paris Cité(FR)Sorbonne Université(FR)Sorbonne Paris Cité(FR)Assistance Publique – Hôpitaux de Paris(FR)Assistance Publique – Hôpitaux de Paris(FR)Technologie Médicale (France)(FR)Hôpital des Enfants(FR)Institut des Maladies Génétiques Imagine(FR)
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, Hedgehog Signaling Pathway Studies, Fetal and Pediatric Neurological Disorders, Renal and related cancers, Prenatal Screening and Diagnostics
Most-Cited Works
- → Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome(2003)854 cited
- → The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome(2007)489 cited
- → Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)(1996)457 cited
- → Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome(2008)395 cited
- → TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum(2011)376 cited
- → Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis(2010)350 cited