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Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).
- Published in:
- Scientific Reports, 2016, p. 32512, doi. 10.1038/srep32512
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- Publication type:
- Article
Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.
- Published in:
- NPJ Breast Cancer, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41523-021-00255-3
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- Publication type:
- Article
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer.
- Published in:
- NPJ Breast Cancer, 2020, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41523-020-00185-6
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- Publication type:
- Article
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.
- Published in:
- Cancers, 2022, v. 14, n. 14, p. N.PAG, doi. 10.3390/cancers14143363
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- Publication type:
- Article
CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival.
- Published in:
- Cancers, 2022, v. 14, n. 2, p. 353, doi. 10.3390/cancers14020353
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- Publication type:
- Article
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
- Published in:
- Breast Cancer Research & Treatment, 2017, v. 161, n. 1, p. 117, doi. 10.1007/s10549-016-4018-2
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- Publication type:
- Article
DSNetwork: An Integrative Approach to Visualize Predictions of Variants' Deleteriousness.
- Published in:
- Frontiers in Genetics, 2020, v. 10, p. 1, doi. 10.3389/fgene.2019.01349
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- Publication type:
- Article
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13058-015-0567-2
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- Publication type:
- Article
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
- Published in:
- 2015
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- Publication type:
- journal article
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.
- Published in:
- 2013
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- Publication type:
- Letter
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
- Published in:
- 2012
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- Publication type:
- journal article
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 23, p. 4732
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- Publication type:
- Article
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3304
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- Publication type:
- Article
ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156820
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- Publication type:
- Article
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
- Published in:
- British Journal of Cancer, 2023, v. 128, n. 12, p. 2283, doi. 10.1038/s41416-023-02263-5
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- Publication type:
- Article
Human Phenol Sulfotransferase Gene Contains Two Alternative Promoters: Structure and Expression of the Gene.
- Published in:
- DNA & Cell Biology, 1996, v. 15, n. 5, p. 367, doi. 10.1089/dna.1996.15.367
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- Publication type:
- Article
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 4, p. 1, doi. 10.1371/journal.pgen.1004256
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- Publication type:
- Article
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003212
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- Publication type:
- Article
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003173
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- Publication type:
- Article
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Mutation, 2012, v. 33, n. 4, p. 690, doi. 10.1002/humu.22025
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- Publication type:
- Article
Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control.
- Published in:
- Genes, 2019, v. 10, n. 3, p. 186, doi. 10.3390/genes10030186
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- Publication type:
- Article
VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis.
- Published in:
- Bioinformatics, 2017, v. 33, n. 9, p. 1389, doi. 10.1093/bioinformatics/btw826
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- Publication type:
- Article
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- 2017
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- Publication type:
- journal article
Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.
- Published in:
- BMC Cancer, 2006, v. 6, p. 230, doi. 10.1186/1471-2407-6-230
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- Publication type:
- Article