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Plos Biology
|
November 24, 2011
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
Christopher A Maxwell, Javier Benítez, Laia Gómez-Baldó, et al.
Human Molecular Genetics
|
August 7, 2009
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antonis C Antoniou, Olga M Sinilnikova, Lesley McGuffog, et al.
American Journal of Human Genetics
|
October 6, 2020
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Iris Kramer, Maartje J Hooning, Nasim Mavaddat, et al.
Journal of the National Cancer Institute
|
April 20, 2015
Identification of novel genetic markers of breast cancer survival
Qi Guo, Marjanka K Schmidt, Peter Kraft, et al.
Plos One
|
July 28, 2016
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Elena Vigorito, Karoline B Kuchenbaecker, Jonathan Beesley, et al.
Plos Genetics
|
April 19, 2014
Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Elinor Sawyer, Rebecca Roylance, Christos Petridis, et al.
Breast Cancer Research : BCR
|
February 10, 2016
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Valentina Silvestri, Daniel Barrowdale, Anna Marie Mulligan, et al.
Breast Cancer Research : BCR
|
January 5, 2022
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Thomas U Ahearn, Haoyu Zhang, Kyriaki Michailidou, et al.
British Journal of Sports Medicine
|
November 3, 2022
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
Suzanne C Dixon-Suen, Sarah J Lewis, Richard M Martin, et al.
Hereditary Cancer in Clinical Practice
|
October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Pål Møller, Toni Seppälä, James G Dowty, et al.
Page
of 25
Search research articles
Search
Showing results (191-200 of 247) with videos related to
Sort By:
Page
of 25
Plos Biology
|
November 24, 2011
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
Christopher A Maxwell, Javier Benítez, Laia Gómez-Baldó, et al.
Human Molecular Genetics
|
August 7, 2009
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antonis C Antoniou, Olga M Sinilnikova, Lesley McGuffog, et al.
American Journal of Human Genetics
|
October 6, 2020
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Iris Kramer, Maartje J Hooning, Nasim Mavaddat, et al.
Journal of the National Cancer Institute
|
April 20, 2015
Identification of novel genetic markers of breast cancer survival
Qi Guo, Marjanka K Schmidt, Peter Kraft, et al.
Plos One
|
July 28, 2016
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Elena Vigorito, Karoline B Kuchenbaecker, Jonathan Beesley, et al.
Plos Genetics
|
April 19, 2014
Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Elinor Sawyer, Rebecca Roylance, Christos Petridis, et al.
Breast Cancer Research : BCR
|
February 10, 2016
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Valentina Silvestri, Daniel Barrowdale, Anna Marie Mulligan, et al.
Breast Cancer Research : BCR
|
January 5, 2022
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Thomas U Ahearn, Haoyu Zhang, Kyriaki Michailidou, et al.
British Journal of Sports Medicine
|
November 3, 2022
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
Suzanne C Dixon-Suen, Sarah J Lewis, Richard M Martin, et al.
Hereditary Cancer in Clinical Practice
|
October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Pål Møller, Toni Seppälä, James G Dowty, et al.
Page
of 25