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

C Morrison

Showing results (1621-1630 of 1,712) with videos related to

Pageof 172
Sort By:
American Journal of Epidemiology|April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) ProgramAdrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Plos One|July 2, 2014
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung functionWenbo Tang, Matthew Kowgier, Daan W Loth, 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.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing StudyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Plos One|January 21, 2017
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association StudyPaul S de Vries, Maria Sabater-Lleal, Daniel I Chasman, et al.
Genome Biology|September 9, 2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Pageof 172

Showing results (1621-1630 of 1,712) with videos related to

Sort By:
Pageof 172
American Journal of Epidemiology|April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) ProgramAdrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionJemma B Wilk, Nick R G Shrine, Laura R Loehr, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Plos One|July 2, 2014
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung functionWenbo Tang, Matthew Kowgier, Daan W Loth, 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.
Plos Genetics|December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populationsMadeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing StudyYuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Plos One|January 21, 2017
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association StudyPaul S de Vries, Maria Sabater-Lleal, Daniel I Chasman, et al.
Genome Biology|September 9, 2025
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Pageof 172