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Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation.
Not available
S-EPMC6057749
|
biostudies-literature
Cite
Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer.
Not available
S-EPMC1242149
|
biostudies-literature
Cite
Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility.
Not available
S-EPMC6732317
|
biostudies-literature
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Feasibility of structured endurance training and Mediterranean diet in BRCA1 and BRCA2 mutation carriers - an interventional randomized controlled multicenter trial (LIBRE-1).
Not available
S-EPMC5681801
|
biostudies-literature
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A breast cancer risk haplotype in the caspase-8 gene.
Not available
S-EPMC2730164
|
biostudies-literature
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Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers.
Not available
S-EPMC8246885
|
biostudies-literature
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Nuclear receptor coregulator SNP discovery and impact on breast cancer risk.
Not available
S-EPMC2804710
|
biostudies-literature
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Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in <i>BRCA1/2</i>: results of the observational AGO-TR1 study (NCT02222883).
Not available
S-EPMC8867275
|
biostudies-literature
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Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction.
Not available
S-EPMC10749276
|
biostudies-literature
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Investigating the genetic relationship between Alzheimer's disease and cancer using GWAS summary statistics.
Not available
S-EPMC5693762
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biostudies-literature
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