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Showing results (761-770 of 773) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
Circulation. Cardiovascular Genetics|November 10, 2011
Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen ConsortiumGary F Mitchell, Germaine C Verwoert, Kirill V Tarasov, et al.
Nature Genetics|September 13, 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaqueJoshua C Bis, Maryam Kavousi, Nora Franceschini, et al.
American Journal of Epidemiology|March 13, 2022
Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study DesignElizabeth C Oelsner, Akshaya Krishnaswamy, Pallavi P Balte, et al.
Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Cardiovascular Research|May 31, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcificationPaul S de Vries, Matthew P Conomos, Kuldeep Singh, et al.
Nature Communications|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
Pageof 78

Showing results (761-770 of 773) with videos related to

Sort By:
Pageof 78
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, et al.
Circulation. Cardiovascular Genetics|November 10, 2011
Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen ConsortiumGary F Mitchell, Germaine C Verwoert, Kirill V Tarasov, et al.
Nature Genetics|September 13, 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaqueJoshua C Bis, Maryam Kavousi, Nora Franceschini, et al.
American Journal of Epidemiology|March 13, 2022
Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study DesignElizabeth C Oelsner, Akshaya Krishnaswamy, Pallavi P Balte, et al.
Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Cardiovascular Research|May 31, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcificationPaul S de Vries, Matthew P Conomos, Kuldeep Singh, et al.
Nature Communications|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
Pageof 78