Christelle Arrondel

<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

COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome

Ilaria Longo, Paola Porcedda, Francesca Mari et al. · Kidney International · 2002 · 232 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Expression of the Nonmuscle Myosin Heavy Chain IIA in the Human Kidney and Screening for MYH9 Mutations in Epstein and Fechtner Syndromes

Christelle Arrondel, Nicolas Vodovar, Bertrand Knebelmann et al. · Journal of the American Society of Nephrology · 2002 · 218 citations

Medicine, Genetics, Molecular Genetics +16

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

Svjetlana Lovric, Sara Gonçalves, Heon Yung Gee et al. · Journal of Clinical Investigation · 2017 · 208 citations · Full text

Medicine, Genetics, Molecular Genetics +17

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