Rémi Salomon

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

Antibiotic Prophylaxis for the Prevention of Recurrent Urinary Tract Infection in Children With Low Grade Vesicoureteral Reflux: Results From a Prospective Randomized Study

G. Roussey-Kesler, Vincent Gadjos, Nadia Idres et al. · The Journal of Urology · 2007 · 368 citations

Medicine, Pediatrics, Urology +17

Prevalence of Mutations in Renal Developmental Genes in Children with Renal Hypodysplasia

Stefanie Weber, Vincent Morinière, Tanja Knüppel et al. · Journal of the American Society of Nephrology · 2006 · 353 citations

Life Sciences, Genetics, Molecular Genetics +17

FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and Man

Hila Barak, Sung‐Ho Huh, Shuang Chen et al. · Developmental Cell · 2012 · 318 citations · Full text

Life Sciences, Developmental Biology, Nephrology +14

Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases

Laurence Heidet, Stéphane Decramer, Audrey Pawtowski et al. · Clinical Journal of the American Society of Nephrology · 2010 · 298 citations · Full text

Medicine, Genetics, Molecular Genetics +15