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Raha Pazoki

Showing results (41-50 of 56) with videos related to

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Plos Genetics|July 9, 2011
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individualsDan E Arking, M Juhani Junttila, Philippe Goyette, et al.
Nature Genetics|November 4, 2018
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
Nature Genetics|September 27, 2016
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Nature Human Behaviour|July 31, 2019
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disordersEvangelos Evangelou, He Gao, Congying Chu, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
American Journal of Human Genetics|June 28, 2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell TraitsNathalie Chami, Ming-Huei Chen, Andrew J Slater, et al.
American Journal of Human Genetics|June 28, 2016
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 IndividualsJohn D Eicher, Nathalie Chami, Tim Kacprowski, et al.
The Lancet. Diabetes & Endocrinology|December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyAmand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
BMC Cardiovascular Disorders|October 31, 2019
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9Amand F Schmidt, Michael V Holmes, David Preiss, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Plos Genetics|July 9, 2011
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individualsDan E Arking, M Juhani Junttila, Philippe Goyette, et al.
Nature Genetics|November 4, 2018
Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
Nature Genetics|September 27, 2016
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation mapsValentina Iotchkova, Jie Huang, John A Morris, et al.
European Heart Journal|September 1, 2018
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestForam N Ashar, Rebecca N Mitchell, Christine M Albert, et al.
Nature Human Behaviour|July 31, 2019
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disordersEvangelos Evangelou, He Gao, Congying Chu, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
American Journal of Human Genetics|June 28, 2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell TraitsNathalie Chami, Ming-Huei Chen, Andrew J Slater, et al.
American Journal of Human Genetics|June 28, 2016
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 IndividualsJohn D Eicher, Nathalie Chami, Tim Kacprowski, et al.
The Lancet. Diabetes & Endocrinology|December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyAmand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
BMC Cardiovascular Disorders|October 31, 2019
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9Amand F Schmidt, Michael V Holmes, David Preiss, et al.
Pageof 6