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

Charles Kooperberg

Showing results (401-410 of 530) with videos related to

Pageof 53
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.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
The American Journal of Clinical Nutrition|July 14, 2021
Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: a pathway analysis of genome-wide association studiesSachelly Julián-Serrano, Fangcheng Yuan, William Wheeler, et al.
Cancer Research|February 12, 2021
Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3Evelina Mocci, Prosenjit Kundu, William Wheeler, 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|June 4, 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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 24, 2020
Mendelian Randomization Analysis of n-6 Polyunsaturated Fatty Acid Levels and Pancreatic Cancer RiskDalia H Ghoneim, Jingjing Zhu, Wei Zheng, 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.
Journal of the National Cancer Institute|January 10, 2020
A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic CancerJun Zhong, Ashley Jermusyk, Lang Wu, et al.
Pageof 53

Showing results (401-410 of 530) with videos related to

Sort By:
Pageof 53
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.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
The American Journal of Clinical Nutrition|July 14, 2021
Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: a pathway analysis of genome-wide association studiesSachelly Julián-Serrano, Fangcheng Yuan, William Wheeler, et al.
Cancer Research|February 12, 2021
Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3Evelina Mocci, Prosenjit Kundu, William Wheeler, 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|June 4, 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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 24, 2020
Mendelian Randomization Analysis of n-6 Polyunsaturated Fatty Acid Levels and Pancreatic Cancer RiskDalia H Ghoneim, Jingjing Zhu, Wei Zheng, 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.
Journal of the National Cancer Institute|January 10, 2020
A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic CancerJun Zhong, Ashley Jermusyk, Lang Wu, et al.
Pageof 53