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M Dunning

Showing results (371-380 of 536) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Polygenic risk scores for prediction of breast cancer risk in Asian populationsWeang-Kee Ho, Mei-Chee Tai, Joe Dennis, et al.
Cancers|July 27, 2022
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 AncestryMartine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
Nature Communications|December 18, 2015
Corrigendum: Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 9, 2016
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC CarriersMarjanka K Schmidt, Frans Hogervorst, Richard van Hien, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
American Journal of Human Genetics|February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survivalAnna Morra, Nasim Mavaddat, Taru A Muranen, et al.
Breast Cancer Research : BCR|January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control studyRoger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
Human Genetics|December 2, 2015
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Pageof 54

Showing results (371-380 of 536) with videos related to

Sort By:
Pageof 54
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Polygenic risk scores for prediction of breast cancer risk in Asian populationsWeang-Kee Ho, Mei-Chee Tai, Joe Dennis, et al.
Cancers|July 27, 2022
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 AncestryMartine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
Nature Communications|December 18, 2015
Corrigendum: Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 9, 2016
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC CarriersMarjanka K Schmidt, Frans Hogervorst, Richard van Hien, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
American Journal of Human Genetics|February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survivalAnna Morra, Nasim Mavaddat, Taru A Muranen, et al.
Breast Cancer Research : BCR|January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control studyRoger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
Human Genetics|December 2, 2015
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Pageof 54