Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Rich

Showing results (1051-1060 of 1,201) with videos related to

Pageof 121
Sort By:
Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
BMJ (Clinical Research Ed.)|January 18, 2023
Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohortsKwok Leung Ong, Matti Marklund, Liping Huang, et al.
Circulation. Genomic and Precision Medicine|July 16, 2021
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride ConcentrationsDanielle E Haslam, Gina M Peloso, Melanie Guirette, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 121

Showing results (1051-1060 of 1,201) with videos related to

Sort By:
Pageof 121
Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
BMJ (Clinical Research Ed.)|January 18, 2023
Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohortsKwok Leung Ong, Matti Marklund, Liping Huang, et al.
Circulation. Genomic and Precision Medicine|July 16, 2021
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride ConcentrationsDanielle E Haslam, Gina M Peloso, Melanie Guirette, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 121