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

Kenneth M Rice

Showing results (71-80 of 112) with videos related to

Pageof 12
Sort By:
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.
Plos One|March 8, 2016
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE ConsortiumAbbas Dehghan, Joshua C Bis, Charles C White, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Journal of Medical Genetics|January 1, 2017
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortiumRaymond Noordam, Colleen M Sitlani, Christy L Avery, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Stroke|July 14, 2018
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance ImagingXueqiu Jian, Claudia L Satizabal, Albert V Smith, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
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.
Plos One|March 8, 2016
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE ConsortiumAbbas Dehghan, Joshua C Bis, Charles C White, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Journal of Medical Genetics|January 1, 2017
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortiumRaymond Noordam, Colleen M Sitlani, Christy L Avery, et al.
Nature Methods|October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studiesZilin Li, Xihao Li, Hufeng Zhou, et al.
BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.
Stroke|July 14, 2018
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance ImagingXueqiu Jian, Claudia L Satizabal, Albert V Smith, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
Pageof 12