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Human Mutation
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February 16, 2018
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Timothy R Rebbeck, Tara M Friebel, Eitan Friedman, et al.
Journal of the National Cancer Institute
|
November 21, 2015
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Huong D Meeks, Honglin Song, Kyriaki Michailidou, et al.
Plos Genetics
|
April 2, 2013
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
Fergus J Couch, Xianshu Wang, Lesley McGuffog, et al.
JAMA
|
April 8, 2015
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
Timothy R Rebbeck, Nandita Mitra, Fei Wan, et al.
Genetic Epidemiology
|
March 3, 2020
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Helian Feng, Alexander Gusev, Bogdan Pasaniuc, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2022
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Eileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, et al.
American Journal of Human Genetics
|
December 18, 2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Nasim Mavaddat, Kyriaki Michailidou, Joe Dennis, et al.
Nature Communications
|
September 8, 2016
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Kate Lawrenson, Siddhartha Kar, Karen McCue, et al.
Nature Genetics
|
May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Haoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.
NPJ Breast Cancer
|
November 9, 2019
The <i>FANCM</i>:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Gisella Figlioli, Massimo Bogliolo, Irene Catucci, et al.
Page
of 43
Search research articles
Search
Showing results (411-420 of 429) with videos related to
Sort By:
Page
of 43
Human Mutation
|
February 16, 2018
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Timothy R Rebbeck, Tara M Friebel, Eitan Friedman, et al.
Journal of the National Cancer Institute
|
November 21, 2015
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Huong D Meeks, Honglin Song, Kyriaki Michailidou, et al.
Plos Genetics
|
April 2, 2013
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
Fergus J Couch, Xianshu Wang, Lesley McGuffog, et al.
JAMA
|
April 8, 2015
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
Timothy R Rebbeck, Nandita Mitra, Fei Wan, et al.
Genetic Epidemiology
|
March 3, 2020
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Helian Feng, Alexander Gusev, Bogdan Pasaniuc, et al.
European Journal of Human Genetics : EJHG
|
January 14, 2022
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Eileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, et al.
American Journal of Human Genetics
|
December 18, 2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Nasim Mavaddat, Kyriaki Michailidou, Joe Dennis, et al.
Nature Communications
|
September 8, 2016
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Kate Lawrenson, Siddhartha Kar, Karen McCue, et al.
Nature Genetics
|
May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Haoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.
NPJ Breast Cancer
|
November 9, 2019
The <i>FANCM</i>:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Gisella Figlioli, Massimo Bogliolo, Irene Catucci, et al.
Page
of 43