Claudine Heinrichs

11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

Irène Netchine, Sylvie Rossignol, Marie‐Noëlle Dufourg et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 312 citations · Full text

Sexual precocity after immigration from developing countries to Belgium: evidence of previous exposure to organochlorine pesticides

Marina Krstevska-Konstantinova, Corinne Charlier, Margarita Craen et al. · Human Reproduction · 2001 · 275 citations · Full text

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.

Marc Abramowicz, L Duprez, Jasmine Parma et al. · Journal of Clinical Investigation · 1997 · 257 citations · Full text

Thyrotropin Receptor, Developmental Biology, Genetic Disorder +15

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

Salah Azzi, Sylvie Rossignol, Virginie Steunou et al. · Human Molecular Genetics · 2009 · 249 citations · Full text

Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients

Laurent Maı̈moun, Pascal Philibert, B. Cammas et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 210 citations