Géraldine Mollet

<i>INF2</i>Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

Olivia Boyer, Fabien Névo, Emmanuelle Plaisier et al. · New England Journal of Medicine · 2011 · 284 citations · Full text

Medicine, Molecular Genetics, Neurology +15

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Daniela A. Braun, Jia Rao, Géraldine Mollet et al. · Nature Genetics · 2017 · 221 citations · Full text

Medicine, Genetics, Molecular Genetics +15

The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

Géraldine Mollet, Rémi Salomon, Olivier Gribouval et al. · Nature Genetics · 2002 · 216 citations

Medicine, Genetics, Molecular Genetics +6

Structure of the Human Type IV Collagen Gene COL4A3 and Mutations in Autosomal Alport Syndrome

Laurence Heidet, Christelle Arrondel, Lionel Forestier et al. · Journal of the American Society of Nephrology · 2001 · 191 citations

Medicine, Genetics, Molecular Genetics +16

Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis

Olivia Boyer, Geneviève Benoît, Olivier Gribouval et al. · Journal of the American Society of Nephrology · 2011 · 168 citations · Full text

Medicine, Genetics, Molecular Genetics +17