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

Nathan O Stitziel

Showing results (31-40 of 92) with videos related to

Pageof 10
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2016
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humansVivian S Lee, Carmen M Halabi, Erin P Hoffman, et al.
Cell Reports. Medicine|May 30, 2025
Effect of complete, lifelong ANGPTL3 deficiency on triglyceride-rich lipoprotein kineticsAlan Fappi, Bruce W Patterson, Kendal H Burks, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
NERINE reveals rare variant associations in gene networks across multiple phenotypes and implicates an <i>SNCA-PRL-LRRK2</i> subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn Morrow, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
Pangenome-based human genome analysis improves trait association and genomic predictionShuangjia Lu, Wen-Wei Liao, Marianne K DeGorter, et al.
Circulation|February 23, 2017
Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention SettingPradeep Natarajan, Robin Young, Nathan O Stitziel, et al.
Circulation. Cardiovascular Genetics|March 26, 2016
Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic TraitsJessica R Golbus, Nathan O Stitziel, Wei Zhao, et al.
Iscience|July 11, 2024
Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery diseasePaul C Lee, In-Hyuk Jung, Shreeya Thussu, et al.
American Journal of Human Genetics|September 13, 2024
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studiesDerek Shyr, Rounak Dey, Xihao Li, et al.
Cell Genomics|June 22, 2026
NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn R Morrow, et al.
Journal of Lipid Research|January 14, 2024
ANGPTL3 deficiency impairs lipoprotein production and produces adaptive changes in hepatic lipid metabolismKendall H Burks, Yan Xie, Michael Gildea, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2016
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humansVivian S Lee, Carmen M Halabi, Erin P Hoffman, et al.
Cell Reports. Medicine|May 30, 2025
Effect of complete, lifelong ANGPTL3 deficiency on triglyceride-rich lipoprotein kineticsAlan Fappi, Bruce W Patterson, Kendal H Burks, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
NERINE reveals rare variant associations in gene networks across multiple phenotypes and implicates an <i>SNCA-PRL-LRRK2</i> subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn Morrow, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
Pangenome-based human genome analysis improves trait association and genomic predictionShuangjia Lu, Wen-Wei Liao, Marianne K DeGorter, et al.
Circulation|February 23, 2017
Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention SettingPradeep Natarajan, Robin Young, Nathan O Stitziel, et al.
Circulation. Cardiovascular Genetics|March 26, 2016
Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic TraitsJessica R Golbus, Nathan O Stitziel, Wei Zhao, et al.
Iscience|July 11, 2024
Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery diseasePaul C Lee, In-Hyuk Jung, Shreeya Thussu, et al.
American Journal of Human Genetics|September 13, 2024
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studiesDerek Shyr, Rounak Dey, Xihao Li, et al.
Cell Genomics|June 22, 2026
NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn R Morrow, et al.
Journal of Lipid Research|January 14, 2024
ANGPTL3 deficiency impairs lipoprotein production and produces adaptive changes in hepatic lipid metabolismKendall H Burks, Yan Xie, Michael Gildea, et al.
Pageof 10