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Breast Cancer Research : BCR
|
July 28, 2016
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Chenjie Zeng, Xingyi Guo, Jirong Long, et al.
Nature Communications
|
May 15, 2021
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Nature Communications
|
April 28, 2016
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Fergus J Couch, Karoline B Kuchenbaecker, Kyriaki Michailidou, et al.
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.
Nature Genetics
|
September 29, 2015
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Felix R Day, Katherine S Ruth, Deborah J Thompson, 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.
Nature Genetics
|
March 2, 2016
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Alison M Dunning, Kyriaki Michailidou, Karoline B Kuchenbaecker, et al.
Page
of 40
Search research articles
Search
Showing results (371-380 of 395) with videos related to
Sort By:
Page
of 40
Breast Cancer Research : BCR
|
July 28, 2016
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Chenjie Zeng, Xingyi Guo, Jirong Long, et al.
Nature Communications
|
May 15, 2021
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, Michael Lush, Jonathan Beesley, et al.
Nature Communications
|
April 28, 2016
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Fergus J Couch, Karoline B Kuchenbaecker, Kyriaki Michailidou, et al.
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.
Nature Genetics
|
September 29, 2015
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Felix R Day, Katherine S Ruth, Deborah J Thompson, 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.
Nature Genetics
|
March 2, 2016
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Alison M Dunning, Kyriaki Michailidou, Karoline B Kuchenbaecker, et al.
Page
of 40