Lionel Forestier

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

Margaret Town, G Jean, Stéphanie Cherqui et al. · Nature Genetics · 1998 · 642 citations

Medicine, Genetics, Molecular Genetics +4

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 the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

Lothar Károlyi, Martin Konrad, Arnold Köckerling et al. · Human Molecular Genetics · 1997 · 190 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Bertrand Knebelmann, Christelle Breillat, Lionel Forestier et al. · PubMed · 1996 · 156 citations

Life Sciences, Genetics, Molecular Genetics +11

Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin

Marlene Attard, G Jean, Lionel Forestier et al. · Human Molecular Genetics · 1999 · 151 citations · Full text

Medicine, Genetics, Molecular Genetics +15