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BMC Medical Genetics|July 12, 2008
Design considerations in a sib-pair study of linkage for susceptibility loci in cancerRichard A Kerber, Christopher I Amos, Beow Y Yeap, et al.
Cancer Research|March 18, 2004
An evolutionary perspective on single-nucleotide polymorphism screening in molecular cancer epidemiologyYong Zhu, Margaret R Spitz, Christopher I Amos, et al.
British Journal of Haematology|August 13, 2024
Prognostic stratification in DLBCL patients with aberrant MYC geneJian-Rong Li, Vikram R Shaw, Abi Parthasarathy, et al.
Annals of the Rheumatic Diseases|July 31, 2025
HLA loci heterozygosity modulates genetic risk in idiopathic inflammatory myopathiesGang Chen, Catherine Zhu, Hector Chinoy, et al.
American Journal of Human Genetics|January 9, 2008
Shifting paradigm of association studies: value of rare single-nucleotide polymorphismsIvan P Gorlov, Olga Y Gorlova, Shamil R Sunyaev, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 15, 2007
Influence of methylenetetrahydrofolate reductase gene polymorphisms C677T and A1298C on age-associated risk for colorectal cancer in a caucasian lynch syndrome populationMala Pande, Jinyun Chen, Christopher I Amos, et al.
Human Heredity|September 3, 2005
Empirical bayes method for incorporating data from multiple genome scansT Mark Beasley, Howard Wiener, Kui Zhang, et al.
British Journal of Cancer|November 30, 2019
Clinical relevance of TP53 hotspot mutations in high-grade serous ovarian cancersMusaffe Tuna, Zhenlin Ju, Kosuke Yoshihara, et al.
Human Genetics|June 21, 2011
Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriersShenying Fang, Ralf Krahe, Linda L Bachinski, et al.
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