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- 2022
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Mark
Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes : Pooled Analysis of Population-Based Studies
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- Contribution to journal › Article
- 2021
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Lifetime alcohol intake, drinking patterns over time and risk of stomach cancer : A pooled analysis of data from two prospective cohort studies
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- Contribution to journal › Article
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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers : an international cohort study
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- Contribution to journal › Article
- 2020
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Alcohol consumption, cigarette smoking, and risk of breast cancer for BRCA1 and BRCA2 mutation carriers : Results from the BRCA1 and BRCA2 cohort consortium
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- Contribution to journal › Article
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Mark
Cancer risks associated with germline PALB2 pathogenic variants : An international study of 524 families
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- Contribution to journal › Article
- 2018
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Genetic and environmental factors affecting birth size variation : A pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts
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- Contribution to journal › Article
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Associations between birth size and later height from infancy through adulthood : An individual based pooled analysis of 28 twin cohorts participating in the CODATwins project
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- Contribution to journal › Article
- 2017
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Mark
Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
- 2016
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
2016) In Nature Genetics(
- Contribution to journal › Article
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Mark
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
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- Contribution to journal › Article
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BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
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- Contribution to journal › Article
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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
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- Contribution to journal › Article
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Mark
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
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- Contribution to journal › Article
- 2015
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Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
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- Contribution to journal › Article
- 2014
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Mark
Alcohol Consumption and Survival after a Breast Cancer Diagnosis: A Literature-Based Meta-analysis and Collaborative Analysis of Data for 29,239 Cases
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- Contribution to journal › Article
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Mark
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
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- Contribution to journal › Article
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Mark
Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
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- Contribution to journal › Article
- 2013
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Mark
Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
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- Contribution to journal › Article
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Mark
A variant in FTO shows association with melanoma risk not due to BMI
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- Contribution to journal › Article
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Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
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- Contribution to journal › Article
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
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- Contribution to journal › Article
- 2012
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Mark
Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
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- Contribution to journal › Article
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Mark
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
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- Contribution to journal › Article
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Mark
Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
2012) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 21(4). p.645-657(
- Contribution to journal › Article
- 2011
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Mark
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
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- Contribution to journal › Article
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Mark
Genome-wide association study identifies three new melanoma susceptibility loci
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- Contribution to journal › Article
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Mark
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.
(
- Contribution to journal › Article
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Mark
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
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Mark
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
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- Contribution to journal › Article
- 2010
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Mark
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
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- Contribution to journal › Article
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Mark
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
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- Contribution to journal › Article
- 2009
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Mark
Genome-wide association study identifies three loci associated with melanoma risk
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- Contribution to journal › Article
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Mark
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
- 2008
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Mark
Common sequence variants on 20q11.22 confer melanoma susceptibility
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- Contribution to journal › Article