Hubert Nivet

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

Edgar A. Otto, Bernhard Schermer, Tomoko Obara et al. · Nature Genetics · 2003 · 641 citations · Full text

Pathogenesis, Immunology, Iga Glomerulonephritis +6

Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

Marie‐Agnès Dragon‐Durey, Chantal Loirat, Sylvie Cloarec et al. · Journal of the American Society of Nephrology · 2004 · 496 citations

Histocompatibility, Immunology, Pathology +17

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

Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey et al. · Journal of the American Society of Nephrology · 2007 · 427 citations

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Véronique Frémeaux‐Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski et al. · Blood · 2008 · 371 citations · Full text