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Genetic Epidemiology|November 30, 2007
Multistage designs in the genomic era: providing balance in complex disease studiesMarie-Pierre Dubé, Silke Schmidt, Elizabeth Hauser, et al.
American Journal of Human Genetics|June 25, 2013
Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma riskJia Nee Foo, Karin E Smedby, Nicholas K Akers, et al.
American Journal of Human Genetics|June 4, 2016
A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 BindingJodie N Painter, Susanne Kaufmann, Tracy A O'Mara, et al.
Breast Cancer Research : BCR|November 11, 2010
A genome-wide association scan on estrogen receptor-negative breast cancerJingmei Li, Keith Humphreys, Hatef Darabi, et al.
Cancer Causes & Control : CCC|November 20, 2012
Smoking, variation in N-acetyltransferase 1 (NAT1) and 2 (NAT2), and risk of non-Hodgkin lymphoma: a pooled analysis within the InterLymph consortiumTodd M Gibson, Karin E Smedby, Christine F Skibola, et al.
Breast Cancer Research : BCR|October 8, 2016
Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association ConsortiumTaru A Muranen, Carl Blomqvist, Thilo Dörk, et al.
Endocrine-Related Cancer|October 2, 2013
Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction studyAnja Rudolph, Rebecca Hein, Sara Lindström, et al.
Oncotarget|August 29, 2015
SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survivalMaral Jamshidi, Rainer Fagerholm, Sofia Khan, et al.
Nature Genetics|July 20, 2010
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32Lucia Conde, Eran Halperin, Nicholas K Akers, et al.
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