Valeria Pensotti

Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

Nasim Mavaddat, Paul D.P. Pharoah, Kyriaki Michailidou et al. · JNCI Journal of the National Cancer Institute · 2015 · 561 citations · Full text

Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer

Timothy R. Rebbeck, Nandita Mitra, Fei Wan et al. · JAMA · 2015 · 484 citations · Full text

Atypical Epithelial Proliferation in Fallopian Tubes in Prophylactic Salpingo-oophorectomy Specimens from BRCA1 and BRCA2 Germline Mutation Carriers

Maria Luisa Carcangiu, Paolo Radice, Siranoush Manoukian et al. · International Journal of Gynecological Pathology · 2003 · 136 citations

Surgical Oncology, Tumoral Pathology, Gynecological Surgery +12

<i>FANCM</i>c.5791C&gt;T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

Paolo Peterlongo, Irene Catucci, Mara Colombo et al. · Human Molecular Genetics · 2015 · 93 citations · Full text

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antonis C. Antoniou, Christiana Kartsonaki, Olga M. Sinilnikova et al. · Human Molecular Genetics · 2011 · 77 citations · Full text

Genetics, Genetic Epidemiology, Common Alleles +16