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Breast cancer (9)
BRCA1 (6)
BRCA2 (5)
Epithelial ovarian cancer (EOC) (4)
Genome-wide association studies (GWAS) (4)
Ovarian cancer (4)
Risk (4)
Single nucleotide polymorphism (SNP) (4)
Cancer (3)
Variants (3)
Deoxyribonucleic acid (DNA) (2)
Polygenic risk scores (PRS) (2)
Prostate cancer (2)
185delAG mutation (1)
AURKA-RHAMM-TPX2-TUBG1 (1)
Base excision repair (BER) (1)
Body mass index (BMI) (1)
BRAC1 mutation carriers (1)
BRCA1 mutation (1)
BRCA1 mutation carriers (1)
BRCA2 mutation (1)
BRCA2 mutation carriers (1)
BRCA2 mutations (1)
BRCA2-Specific Modifier Locus at 6p24 (1)
Breast and ovarian cancer (1)
Breast cancer (BC) (1)
Breast cancer risk (1)
Breast cancer subtype (1)
Breast carcinogenesis (1)
Cancer epidemiology (1)
Cancer genetics (1)
Cancer risk in carriers (1)
Candidate genetic modifiers (1)
Carriers (1)
Causal gene (1)
CCDC91 (1)
Coiled-coil domain containing 170 (CCDC170) (1)
Corticotropin-releasing hormone (1)
Disease susceptibility (1)
Epidemiology (1)
ER-negative breast cancer (1)
Estrogen Receptor 1 (ESR1) (1)
Ethnicity (1)
Expression (1)
Fine-scale mapping (1)
Founder mutations (1)
Genes (1)
Genetic factors (1)
Genetic risk factor (1)
Genetics (1)
Geography (1)
Germline mutations (1)
Haplotype studies (1)
Height (1)
Hereditary breast and ovarian cancer (1)
Hereditary breast cancer (1)
Hispanics (1)
HOXB2 (1)
Identification (1)
In vitro fertilization (IVF) (1)
Invasive (1)
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Locus (1)
Mendelian randomisation (1)
Mitochondria (1)
Multiple (1)
Mutation (1)
Mutation carriers (1)
Ovarian cancer (OC) (1)
Ovarian Cancer Association Consortium (OCAC) (1)
Pathogenic mutations (1)
Prediction (1)
Prevention (1)
PTHLH (1)
Required for meiotic nuclear division 1 (RMND1) (1)
Risk factors (1)
SDG-03: Good health and well-being (1)
Transcriptome-wide association studies (TWAS) (1)
Transheterozygosity (1)
Transheterozygotes (TH) (1)
Women (1)
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