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Human Molecular Genetics|March 29, 2013
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expressionZsofia Kote-Jarai, Edward J Saunders, Daniel A Leongamornlert, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Polygenic risk scores for prediction of breast cancer risk in Asian populationsWeang-Kee Ho, Mei-Chee Tai, Joe Dennis, 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.
Human Molecular Genetics|July 6, 2016
Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer riskJennifer B Permuth, Ailith Pirie, Y Ann Chen, et al.
American Journal of Human Genetics|February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survivalAnna Morra, Nasim Mavaddat, Taru A Muranen, 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.
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.
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.
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