Catherine Dodé
Assistance Publique – Hôpitaux de Paris(FR)Maternité Port Royal(FR)
Publications by Year
Research Areas
Hypothalamic control of reproductive hormones, Inflammasome and immune disorders, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Ovarian function and disorders, Genetic Neurodegenerative Diseases
Most-Cited Works
- → European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment(2015)847 cited
- → Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome(2003)827 cited
- → Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene(1997)636 cited
- Phenotypic Characterization of Individuals with 30–40 CAG Repeats in the Huntington Disease (HD) Gene Reveals HD Cases with 36 Repeats and Apparently Normal Elderly Individuals with 36–39 Repeats(1996)
- → Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2(2006)451 cited
- → Infevers: An evolving mutation database for auto-inflammatory syndromes(2004)317 cited
- → New Mutations of CIAS1 That Are Responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A Novel Mutation Underlies Both Syndromes