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

I Rotter

Showing results (921-930 of 1,250) with videos related to

Pageof 125
Sort By:
Nature Communications|May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseasesAdriana I Iglesias, Aniket Mishra, Veronique Vitart, 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.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Plos Genetics|June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE ConsortiumNancy L Heard-Costa, M Carola Zillikens, Keri L Monda, 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.
The Pharmacogenomics Journal|December 14, 2016
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working GroupJ S Floyd, C M Sitlani, C L Avery, 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.
Circulation. Genomic and Precision Medicine|August 22, 2020
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial FibrillationLu-Chen Weng, Amelia Weber Hall, Seung Hoan Choi, et al.
Cell|January 19, 2024
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucomaShefali S Verma, Harini V Gudiseva, Venkata R M Chavali, et al.
Pageof 125

Showing results (921-930 of 1,250) with videos related to

Sort By:
Pageof 125
Nature Communications|May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseasesAdriana I Iglesias, Aniket Mishra, Veronique Vitart, 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.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Plos Genetics|June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE ConsortiumNancy L Heard-Costa, M Carola Zillikens, Keri L Monda, 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.
The Pharmacogenomics Journal|December 14, 2016
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working GroupJ S Floyd, C M Sitlani, C L Avery, 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.
Circulation. Genomic and Precision Medicine|August 22, 2020
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial FibrillationLu-Chen Weng, Amelia Weber Hall, Seung Hoan Choi, et al.
Cell|January 19, 2024
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucomaShefali S Verma, Harini V Gudiseva, Venkata R M Chavali, et al.
Pageof 125