M. Peuchmaur

Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database

Érick Denamur, Isabelle Henry, M.-O. Cabanis et al. · The American Journal of Human Genetics · 1998 · 232 citations · Full text

Scleroderma, Genetic Disorder, Medicine +15

Investigation of osteocalcin, osteonectin, and dentin sialophosphoprotein in developing human teeth

Pétros Papagerakis, Ariane Berdal, M. Mesbah et al. · Bone · 2002 · 200 citations

Odontology, Developmental Biology, Dentin Sialophosphoprotein +10

WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis

Erick Denamur, N. Bocquet, Véronique Baudouin et al. · Kidney International · 2000 · 93 citations · Full text

Glomerulonephritis, Urology, Genetic Disorder +9

Laparoscopic Adrenal Surgery for Neuroblastomas in Children

Pascal de Lagausie, D. Berrebi, Jean Michon et al. · The Journal of Urology · 2003 · 83 citations

Conditional glucocorticoid receptor expression in the heart induces atrio‐ventricular block

Yannis Sainte–Marie, Aurelie Nguyen Dinh Cat, Romain Perrier et al. · The FASEB Journal · 2007 · 68 citations

Cardiac Muscle, Hypertension, Heart Failure +15