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David R Crosslin

Showing results (51-60 of 116) with videos related to

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Cardiology in the Young|September 21, 2017
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHDConstantine D Mavroudis, Daniel Seung Kim, Nancy Burnham, et al.
American Journal of Obstetrics and Gynecology|April 15, 2020
A genome-wide association study of polycystic ovary syndrome identified from electronic health recordsYanfei Zhang, Kevin Ho, Jacob M Keaton, et al.
Human Genetics|September 13, 2013
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effectsKhader Shameer, Joshua C Denny, Keyue Ding, et al.
Science (New York, N.Y.)|February 26, 2016
The phenotypic legacy of admixture between modern humans and NeandertalsCorinne N Simonti, Benjamin Vernot, Lisa Bastarache, et al.
Cell Host & Microbe|August 10, 2018
An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human DiseaseLiuyang Wang, Kelly J Pittman, Jeffrey R Barker, et al.
Genome Medicine|July 30, 2015
Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE NetworkDavid R Crosslin, Peggy D Robertson, David S Carrell, et al.
Circulation. Cardiovascular Genetics|October 27, 2016
Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical DataJonathan D Mosley, Sara L van Driest, Quinn S Wells, et al.
Plos Genetics|January 3, 2009
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosisSvati H Shah, Neil J Freedman, Lisheng Zhang, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Cardiology in the Young|September 21, 2017
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHDConstantine D Mavroudis, Daniel Seung Kim, Nancy Burnham, et al.
American Journal of Obstetrics and Gynecology|April 15, 2020
A genome-wide association study of polycystic ovary syndrome identified from electronic health recordsYanfei Zhang, Kevin Ho, Jacob M Keaton, et al.
Human Genetics|September 13, 2013
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effectsKhader Shameer, Joshua C Denny, Keyue Ding, et al.
Science (New York, N.Y.)|February 26, 2016
The phenotypic legacy of admixture between modern humans and NeandertalsCorinne N Simonti, Benjamin Vernot, Lisa Bastarache, et al.
Cell Host & Microbe|August 10, 2018
An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human DiseaseLiuyang Wang, Kelly J Pittman, Jeffrey R Barker, et al.
Genome Medicine|July 30, 2015
Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE NetworkDavid R Crosslin, Peggy D Robertson, David S Carrell, et al.
Circulation. Cardiovascular Genetics|October 27, 2016
Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical DataJonathan D Mosley, Sara L van Driest, Quinn S Wells, et al.
Plos Genetics|January 3, 2009
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosisSvati H Shah, Neil J Freedman, Lisheng Zhang, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
Pageof 12