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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Shared heritability and functional enrichment across six solid cancers
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
A rareRETgene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening
Greek BRCA1 and BRCA2 mutation spectrum: two BRCA1 mutations account for half the carriers found among high-risk breast/ovarian cancer patients
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype
