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Journal of the American College of Cardiology
|
January 30, 2016
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study
Tanya Keenan, Wei Zhao, Asif Rasheed, et al.
Circulation
|
August 16, 2014
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation
Moritz F Sinner, Nathan R Tucker, Kathryn L Lunetta, et al.
Neurology
|
February 6, 2015
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease
Kristiina Rannikmäe, Gail Davies, Pippa A Thomson, et al.
Neurology
|
May 3, 2015
Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants
Rainer Malik, Tobias Freilinger, Bendik S Winsvold, et al.
Stroke
|
January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2
Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Nature Genetics
|
September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
Elizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol
Guido J Falcone, Stacey Q Wolfe, Marialuisa Zedde, et al.
Neurology. Genetics
|
April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Bendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Annals of Neurology
|
December 21, 2016
Genetic variation at 16q24.2 is associated with small vessel stroke
Matthew Traylor, Rainer Malik, Mike A Nalls, et al.
American Journal of Human Genetics
|
March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage
Daniel Woo, Guido J Falcone, William J Devan, et al.
Page
of 18
Search research articles
Search
Showing results (141-150 of 176) with videos related to
Sort By:
Page
of 18
Journal of the American College of Cardiology
|
January 30, 2016
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study
Tanya Keenan, Wei Zhao, Asif Rasheed, et al.
Circulation
|
August 16, 2014
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation
Moritz F Sinner, Nathan R Tucker, Kathryn L Lunetta, et al.
Neurology
|
February 6, 2015
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease
Kristiina Rannikmäe, Gail Davies, Pippa A Thomson, et al.
Neurology
|
May 3, 2015
Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants
Rainer Malik, Tobias Freilinger, Bendik S Winsvold, et al.
Stroke
|
January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2
Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Nature Genetics
|
September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
Elizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol
Guido J Falcone, Stacey Q Wolfe, Marialuisa Zedde, et al.
Neurology. Genetics
|
April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Bendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Annals of Neurology
|
December 21, 2016
Genetic variation at 16q24.2 is associated with small vessel stroke
Matthew Traylor, Rainer Malik, Mike A Nalls, et al.
American Journal of Human Genetics
|
March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage
Daniel Woo, Guido J Falcone, William J Devan, et al.
Page
of 18