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Showing results (381-390 of 536) with videos related to

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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.
Human Molecular Genetics|December 21, 2013
DNA mismatch repair gene MSH6 implicated in determining age at natural menopauseJohn R B Perry, Yi-Hsiang Hsu, Daniel I Chasman, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 29, 2012
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer riskCeline M Vachon, Christopher G Scott, Peter A Fasching, et al.
Nature Genetics|February 13, 2007
A common coding variant in CASP8 is associated with breast cancer riskAngela Cox, Alison M Dunning, Montserrat Garcia-Closas, et al.
Endocrine-Related Cancer|November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancerDeborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
Oncotarget|October 30, 2016
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21Yosr Hamdi, Penny Soucy, Véronique Adoue, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 10, 2010
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controlsOlivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, et al.
Journal of Medical Genetics|September 21, 2011
7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association ConsortiumRoger L Milne, Justo Lorenzo-Bermejo, Barbara Burwinkel, et al.
Nature Genetics|May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysisTimothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
Pageof 54

Showing results (381-390 of 536) with videos related to

Sort By:
Pageof 54
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.
Human Molecular Genetics|December 21, 2013
DNA mismatch repair gene MSH6 implicated in determining age at natural menopauseJohn R B Perry, Yi-Hsiang Hsu, Daniel I Chasman, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 29, 2012
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer riskCeline M Vachon, Christopher G Scott, Peter A Fasching, et al.
Nature Genetics|February 13, 2007
A common coding variant in CASP8 is associated with breast cancer riskAngela Cox, Alison M Dunning, Montserrat Garcia-Closas, et al.
Endocrine-Related Cancer|November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancerDeborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
Oncotarget|October 30, 2016
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21Yosr Hamdi, Penny Soucy, Véronique Adoue, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 10, 2010
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controlsOlivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, et al.
Journal of Medical Genetics|September 21, 2011
7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association ConsortiumRoger L Milne, Justo Lorenzo-Bermejo, Barbara Burwinkel, et al.
Nature Genetics|May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysisTimothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
Pageof 54