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Neil Risch

Showing results (101-110 of 146) with videos related to

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American Journal of Public Health|November 1, 2005
Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological researchEsteban González Burchard, Luisa N Borrell, Shweta Choudhry, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 29, 2025
Sociodemographic modifiers of effects of statin initiation on dementia incidence: An emulated trial design in a large health care member population with 10+ years of follow-upMinhyuk Choi, Scott C Zimmerman, Chen Jiang, et al.
American Journal of Human Genetics|July 1, 2026
Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in AfricansHasan Alkhairo, Satoshi Koyama, Kruthika Iyer, et al.
Human Molecular Genetics|April 30, 2008
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE studyThemistocles L Assimes, Joshua W Knowles, Analabha Basu, et al.
Plos Genetics|January 29, 2015
Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortThomas J Hoffmann, Lori C Sakoda, Ling Shen, et al.
Nature Communications|June 13, 2018
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk lociHélène Choquet, Seyyedhassan Paylakhi, Stephen C Kneeland, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 2003
Natural variation in human membrane transporter genes reveals evolutionary and functional constraintsMaya K Leabman, Conrad C Huang, Joseph DeYoung, et al.
Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.
American Journal of Human Genetics|October 29, 2002
A highly significant association between a COMT haplotype and schizophreniaSagiv Shifman, Michal Bronstein, Meira Sternfeld, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Public Health|November 1, 2005
Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological researchEsteban González Burchard, Luisa N Borrell, Shweta Choudhry, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 29, 2025
Sociodemographic modifiers of effects of statin initiation on dementia incidence: An emulated trial design in a large health care member population with 10+ years of follow-upMinhyuk Choi, Scott C Zimmerman, Chen Jiang, et al.
American Journal of Human Genetics|July 1, 2026
Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in AfricansHasan Alkhairo, Satoshi Koyama, Kruthika Iyer, et al.
Human Molecular Genetics|April 30, 2008
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE studyThemistocles L Assimes, Joshua W Knowles, Analabha Basu, et al.
Plos Genetics|January 29, 2015
Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortThomas J Hoffmann, Lori C Sakoda, Ling Shen, et al.
Nature Communications|June 13, 2018
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk lociHélène Choquet, Seyyedhassan Paylakhi, Stephen C Kneeland, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 2003
Natural variation in human membrane transporter genes reveals evolutionary and functional constraintsMaya K Leabman, Conrad C Huang, Joseph DeYoung, et al.
Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.
American Journal of Human Genetics|October 29, 2002
A highly significant association between a COMT haplotype and schizophreniaSagiv Shifman, Michal Bronstein, Meira Sternfeld, et al.
Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.
Pageof 15