Kristiina Aittomäki

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Kristiina Aittomäki, JoséLuis Dieguez Lucena, Pirjo Pakarinen et al. · Cell · 1995 · 979 citations · Full text

Infertility, Mendelian Disorder, Genetic Disorder +10

Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

Juha S. Tapanainen, Kristiina Aittomäki, Min Jiang et al. · Nature Genetics · 1997 · 574 citations

Spermatogenesis, Infertility, Andrology +11

A CHEK2 Genetic Variant Contributing to a Substantial Fraction of Familial Breast Cancer

Pia Vahteristo, Jiřina Bártková, Hannaleena Eerola et al. · The American Journal of Human Genetics · 2002 · 475 citations · Full text

Breast Oncology, Medicine, Pathology +8

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 · 288 citations

Intrahepatic cholestasis of pregnancy as an indicator of liver and biliary diseases

Anne Ropponen, Reijo Sund, Seija Riikonen et al. · Hepatology · 2006 · 224 citations · Full text