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- 2022
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Mark
Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer
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- Contribution to journal › Article
- 2021
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Mark
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families
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- Contribution to journal › Article
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Mark
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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Mark
Breast cancer survival in Nordic BRCA2 mutation carriers—unconventional association with oestrogen receptor status
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- Contribution to journal › Article
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Mark
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
- 2019
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Mark
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
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- Contribution to journal › Article
- 2018
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Mark
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant : Breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
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- Contribution to journal › Article
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Mark
Oral Contraceptive Use and Breast Cancer Risk : Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study
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- Contribution to journal › Article
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Mark
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
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- Contribution to journal › Article
- 2017
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Mark
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families
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- Contribution to journal › Article
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Mark
Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
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Mark
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
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- Contribution to journal › Article
- 2016
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Mark
Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4.
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- Contribution to journal › Article
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Mark
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.
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- 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