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C Morrison

Showing results (1531-1540 of 1,712) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeupYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Nature Genetics|December 17, 2009
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary functionDana B Hancock, Mark Eijgelsheim, Jemma B Wilk, et al.
Plos Neglected Tropical Diseases|September 1, 2023
Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousnessLouis Lambrechts, Robert C Reiner, M Veronica Briesemeister, et al.
Blood|December 31, 2009
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediatorsRenate B Schnabel, Jens Baumert, Maja Barbalic, et al.
Journal of Thrombosis and Haemostasis : JTH|December 16, 2023
A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatmentCristina Gallego-Fabrega, Gerard Temprano-Sagrera, Jara Cárcel-Márquez, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Scientific Reports|May 30, 2024
Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scoresYana Hrytsenko, Benjamin Shea, Michael Elgart, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortiumAlanna C Morrison, Janine F Felix, L Adrienne Cupples, et al.
Pageof 172

Showing results (1531-1540 of 1,712) with videos related to

Sort By:
Pageof 172
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeupYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Nature Genetics|December 17, 2009
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary functionDana B Hancock, Mark Eijgelsheim, Jemma B Wilk, et al.
Plos Neglected Tropical Diseases|September 1, 2023
Direct mosquito feedings on dengue-2 virus-infected people reveal dynamics of human infectiousnessLouis Lambrechts, Robert C Reiner, M Veronica Briesemeister, et al.
Blood|December 31, 2009
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediatorsRenate B Schnabel, Jens Baumert, Maja Barbalic, et al.
Journal of Thrombosis and Haemostasis : JTH|December 16, 2023
A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatmentCristina Gallego-Fabrega, Gerard Temprano-Sagrera, Jara Cárcel-Márquez, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Scientific Reports|May 30, 2024
Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scoresYana Hrytsenko, Benjamin Shea, Michael Elgart, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortiumAlanna C Morrison, Janine F Felix, L Adrienne Cupples, et al.
Pageof 172