Concepedia
Statistics
Publications
2
Citations
654
H-Index
Active since
2007
Affiliations
Hôpital Robert-Debré(Current)
Centre Hospitalier Universitaire de Tours
Inserm
Université Paris Cité
Tiphanie Lacoste is an author at Hôpital Robert-Debré specializing in mendelian disorders, pediatric genetics, and genetics.
Publications per year
2007–2007
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 · 493 citations
Life Sciences, Genetics, Molecular Genetics +10
High NPHP1 and NPHP6 Mutation Rate in Patients with Joubert Syndrome and Nephronophthisis
Tiphanie Lacoste, Lydie Bürglen, Nathalie Boddaert et al. · Journal of the American Society of Nephrology · 2007 · 161 citations
Life Sciences, Genetics, Molecular Genetics +14
1–2 of 2