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Fergus J Couch

Showing results (371-380 of 544) with videos related to

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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.
Scientific Reports|April 14, 2022
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 womenXiaoliang Wang, Pooja Middha Kapoor, Paul L Auer, et al.
American Journal of Human Genetics|March 22, 2008
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Amanda B Spurdle, Olga M Sinilnikova, 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.
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.
Human Molecular Genetics|July 2, 2015
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factorPaolo Peterlongo, Irene Catucci, Mara Colombo, 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.
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.
Pageof 55

Showing results (371-380 of 544) with videos related to

Sort By:
Pageof 55
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.
Scientific Reports|April 14, 2022
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 womenXiaoliang Wang, Pooja Middha Kapoor, Paul L Auer, et al.
American Journal of Human Genetics|March 22, 2008
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Amanda B Spurdle, Olga M Sinilnikova, 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.
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.
Human Molecular Genetics|July 2, 2015
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factorPaolo Peterlongo, Irene Catucci, Mara Colombo, 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.
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.
Pageof 55