Lionel Forestier

Determination of the Genomic Structure of the COL4A4 Gene and of Novel Mutations Causing Autosomal Recessive Alport Syndrome

Eileen Boye, Géraldine Mollet, Lionel Forestier et al. · The American Journal of Human Genetics · 1998 · 140 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Molecular Characterization of CTNS Deletions in Nephropathic Cystinosis: Development of a PCR-Based Detection Assay

Lionel Forestier, G Jean, Marlene Attard et al. · The American Journal of Human Genetics · 1999 · 96 citations · Full text

Urology, Nephropathic Cystinosis, Ctns Deletions +6

Mutations in the Vasopressin V2 Receptor and Aquaporin-2 Genes in Twelve Families with Congenital Nephrogenic Diabetes Insipidus

Rosa Vargas-Poussou, Lionel Forestier, M D Dautzenberg et al. · Advances in experimental medicine and biology · 1998 · 74 citations

Osmoregulation, Genetics, Physiology +6

Mutations in the vasopressin V2 receptor and aquaporin-2 genes in 12 families with congenital nephrogenic diabetes insipidus.

Rosa Vargas-Poussou, Lionel Forestier, M D Dautzenberg et al. · Journal of the American Society of Nephrology · 1997 · 66 citations

Genetics, Molecular Genetics, Disease Gene Identification +16