Found: 53
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Xenobiotic-Metabolizing gene polymorphisms and ovarian cancer risk.
- Published in:
- Molecular Carcinogenesis, 2011, v. 50, n. 5, p. 397, doi. 10.1002/mc.20714
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- Publication type:
- Article
Candidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4.
- Published in:
- Cancers, 2020, v. 12, n. 1, p. 170, doi. 10.3390/cancers12010170
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- Publication type:
- Article
On the Equivalence of Causal Propagators of the Dirac Equation in Vacuum-Destabilising External Fields.
- Published in:
- Foundations of Physics, 2022, v. 52, n. 1, p. 1, doi. 10.1007/s10701-022-00538-0
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- Publication type:
- Article
Paclitaxel sensitivity in relation to ABCB1 expression, efflux and single nucleotide polymorphisms in ovarian cancer.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep04669
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- Publication type:
- Article
Redefining normal breast cell populations using long noncoding RNAs.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. 12, p. 6389, doi. 10.1093/nar/gkad339
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- Publication type:
- Article
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14100-6
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- Publication type:
- Article
Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancer.
- Published in:
- NPJ Breast Cancer, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41523-022-00425-x
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- Publication type:
- Article
ABCA Transporter Gene Expression and Poor Outcome in Epithelial Ovarian Cancer.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2014, v. 106, n. 7, p. 1, doi. 10.1093/jnci/dju149
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- Publication type:
- Article
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 2, p. 105, doi. 10.1093/jnci/djq494
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- Publication type:
- Article
Association of a Common AKAP9 Variant With Breast Cancer Risk: A Collaborative Analysis.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 6, p. 437, doi. 10.1093/jnci/djn037
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- Publication type:
- Article
Genome-Wide Association Study for Ovarian Cancer Susceptibility Using Pooled DNA.
- Published in:
- Twin Research & Human Genetics, 2012, v. 15, n. 5, p. 615, doi. 10.1017/thg.2012.38
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- Publication type:
- Article
Chromatin interactome mapping at 139 independent breast cancer risk signals.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-019-1877-y
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- Publication type:
- Article
Non-coding RNAs underlie genetic predisposition to breast cancer.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-019-1876-z
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- Publication type:
- Article
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
Genome-wide association study of germline variants and breast cancer-specific mortality.
- Published in:
- 2019
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- Publication type:
- journal article
A Common Cancer Risk-Associated Allele in the hTERT Locus Encodes a Dominant Negative Inhibitor of Telomerase.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005286
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- Publication type:
- Article
No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian women.
- Published in:
- 2011
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- Publication type:
- Report
No evidence that GATA3 rs570613 SNP modifies breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2009, v. 117, n. 2, p. 371, doi. 10.1007/s10549-008-0257-1
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- Publication type:
- Article
No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2009, v. 115, n. 2, p. 307, doi. 10.1007/s10549-008-0083-5
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- Publication type:
- Article
The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case–control and family analysis.
- Published in:
- Breast Cancer Research & Treatment, 2009, v. 115, n. 1, p. 145, doi. 10.1007/s10549-008-0045-y
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- Publication type:
- Article
The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 112, n. 1, p. 35
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- Publication type:
- Article
Progesterone receptor polymorphisms and risk of breast cancer: results from two Australian breast cancer studies.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 109, n. 1, p. 91
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- Publication type:
- Article
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
- Published in:
- 2021
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- Publication type:
- Correction Notice
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20496-3
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- Publication type:
- Article
Mixed ductal‐lobular carcinomas: evidence for progression from ductal to lobular morphology.
- Published in:
- Journal of Pathology, 2018, v. 244, n. 4, p. 460, doi. 10.1002/path.5040
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- Publication type:
- Article
Polymorphisms in the FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium.
- Published in:
- 2009
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- Publication type:
- journal article
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 1, p. 285, doi. 10.1093/hmg/ddu431
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- Publication type:
- Article
DNA mismatch repair gene MSH6 implicated in determining age at natural menopause.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 9, p. 2490
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- Publication type:
- Article
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4442, doi. 10.1093/hmg/ddp372
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- Publication type:
- Article
Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2297
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- Publication type:
- Article
Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/ncomms16193
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- Publication type:
- Article
Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
- Published in:
- Nature Communications, 2018, v. 9, p. 16193, doi. 10.1038/ncomms16193
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- Publication type:
- Article
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12675, doi. 10.1038/ncomms12675
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- Publication type:
- Article
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
- Published in:
- Nature Communications, 2014, v. 5, n. 9, p. 4999, doi. 10.1038/ncomms5999
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- Publication type:
- Article
Functional Polymorphisms in the TERT Promoter Are Associated with Risk of Serous Epithelial Ovarian and Breast Cancers.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024987
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- Publication type:
- Article
Polymorphisms in Stromal Genes and Susceptibility to Serous Epithelial Ovarian Cancer: A Report from the Ovarian Cancer Association Consortium.
- Published in:
- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0019642
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- Publication type:
- Article
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
- Published in:
- Nature Genetics, 2009, v. 41, n. 9, p. 996, doi. 10.1038/ng.424
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- Publication type:
- Article
Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility "Hot- Spot''.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 7, p. 1, doi. 10.1371/journal.pgen.1001016
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- Publication type:
- Article
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99409-3
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- Publication type:
- Article
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.
- Published in:
- Molecular Carcinogenesis, 2015, v. 54, n. 7, p. 513, doi. 10.1002/mc.22116
- By:
- 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
Identification of Novel Genetic Markers of Breast Cancer Survival.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2015, v. 107, n. 5, p. 1, doi. 10.1093/jnci/djv081
- By:
- Publication type:
- Article
Identification of novel genetic markers of breast cancer survival.
- Published in:
- 2015
- By:
- Publication type:
- journal article
SNPs in lncRNA Regions and Breast Cancer Risk.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00550
- By:
- Publication type:
- Article
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The importance of using public data to validate reported associations.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 6, p. 1, doi. 10.1371/journal.pgen.1007416
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- Publication type:
- Article
RNF168 regulates R-loop resolution and genomic stability in BRCA1/2-deficient tumors.
- Published in:
- 2021
- By:
- Publication type:
- journal article
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
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.
- Published in:
- International Journal of Cancer, 2016, v. 139, n. 6, p. 1303, doi. 10.1002/ijc.30150
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- Publication type:
- Article
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08078-w
- By:
- Publication type:
- Article