Frédérique Kuttenn

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Sandrine Barbaux, Patrick Niaudet, Marie-Claire Gübler et al. · Nature Genetics · 1997 · 748 citations

Life Sciences, Genetics, Molecular Genetics +6

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

Paul Laissue, Sophie Christin‐Maître, Philippe Touraine et al. · European Journal of Endocrinology · 2006 · 289 citations

Medicine, Genetics, Molecular Genetics +17

Late-Onset Adrenal Hyperplasia in Hirsutism

Frédérique Kuttenn, P. Couillin, François Girard et al. · New England Journal of Medicine · 1985 · 218 citations

Life Sciences, Endocrinology, Immunology +15

Clinical and Molecular Characterization of a Cohort of 161 Unrelated Women with Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and 330 Family Members

Maud Bidet, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 214 citations · Full text

Life Sciences, Endocrinology, Genetics +17

ANDROGEN PRODUCTION AND SKIN METABOLISM IN HIRSUTISM

Frédérique Kuttenn, I Mowszowicz, G Schaison et al. · Journal of Endocrinology · 1977 · 196 citations

Life Sciences, Biochemistry, Endocrinology +17