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An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Ovarian and breast cancer risks associated with pathogenic variants in RAD51C and RAD51D
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes
Cancer Risks for PMS2-Associated Lynch Syndrome
Lifestyle intervention in BRCA1/2 mutation carriers: study protocol for a prospective, randomized, controlled clinical feasibility trial (LIBRE-1 study).