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Meredith Yeager

Showing results (211-220 of 398) with videos related to

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Human Genetics|July 4, 2014
Characterization of T gene sequence variants and germline duplications in familial and sporadic chordomaMichael J Kelley, Jianxin Shi, Bari Ballew, et al.
Journal of the National Cancer Institute|April 22, 2015
Germline TP53 variants and susceptibility to osteosarcomaLisa Mirabello, Meredith Yeager, Phuong L Mai, et al.
Viruses|October 26, 2021
Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral GenomesMaisa Pinheiro, Ariana Harari, Mark Schiffman, et al.
Oncotarget|December 1, 2016
Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genesDanielle M Karyadi, Milan S Geybels, Eric Karlins, et al.
The Prostate|January 16, 2008
TNF polymorphisms and prostate cancer riskKim N Danforth, Carmen Rodriguez, Richard B Hayes, et al.
Lancet (London, England)|August 23, 2005
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analysesMontserrat García-Closas, Núria Malats, Debra Silverman, et al.
Nature Communications|June 2, 2026
HPV16 genetic variation provides evidence of positive natural selection driven by HLA class IChase W Nelson, Sambit K Mishra, Michael Dean, et al.
Human Mutation|July 24, 2010
A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiencyHong-Ying Wang, Vivek Gopalan, Ivona Aksentijevich, et al.
Nature Genetics|January 24, 2009
Variation in KLK genes, prostate-specific antigen and risk of prostate cancerJiyoung Ahn, Sonja I Berndt, Sholom Wacholder, et al.
Cancer Causes & Control : CCC|August 2, 2013
Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma riskMahboobeh Safaeian, Preetha Rajaraman, Patricia Hartge, et al.
Pageof 40

Showing results (211-220 of 398) with videos related to

Sort By:
Pageof 40
Human Genetics|July 4, 2014
Characterization of T gene sequence variants and germline duplications in familial and sporadic chordomaMichael J Kelley, Jianxin Shi, Bari Ballew, et al.
Journal of the National Cancer Institute|April 22, 2015
Germline TP53 variants and susceptibility to osteosarcomaLisa Mirabello, Meredith Yeager, Phuong L Mai, et al.
Viruses|October 26, 2021
Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral GenomesMaisa Pinheiro, Ariana Harari, Mark Schiffman, et al.
Oncotarget|December 1, 2016
Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genesDanielle M Karyadi, Milan S Geybels, Eric Karlins, et al.
The Prostate|January 16, 2008
TNF polymorphisms and prostate cancer riskKim N Danforth, Carmen Rodriguez, Richard B Hayes, et al.
Lancet (London, England)|August 23, 2005
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analysesMontserrat García-Closas, Núria Malats, Debra Silverman, et al.
Nature Communications|June 2, 2026
HPV16 genetic variation provides evidence of positive natural selection driven by HLA class IChase W Nelson, Sambit K Mishra, Michael Dean, et al.
Human Mutation|July 24, 2010
A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiencyHong-Ying Wang, Vivek Gopalan, Ivona Aksentijevich, et al.
Nature Genetics|January 24, 2009
Variation in KLK genes, prostate-specific antigen and risk of prostate cancerJiyoung Ahn, Sonja I Berndt, Sholom Wacholder, et al.
Cancer Causes & Control : CCC|August 2, 2013
Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma riskMahboobeh Safaeian, Preetha Rajaraman, Patricia Hartge, et al.
Pageof 40