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Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Genome Medicine
|
March 22, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Plos One
|
November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
John W Cole, Huichun Xu, Kathleen Ryan, et al.
Nature Genetics
|
December 23, 2020
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.
Nature Genetics
|
February 4, 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, et al.
Journal of the American College of Cardiology
|
August 27, 2016
Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study
Sander W van der Laan, Tove Fall, Aicha Soumaré, et al.
Nature Genetics
|
November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.
The Lancet. Neurology
|
October 9, 2012
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Matthew Traylor, Martin Farrall, Elizabeth G Holliday, et al.
Nature Genetics
|
February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
, , Céline Bellenguez, et al.
Stroke
|
June 11, 2020
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Nicola J Armstrong, Karen A Mather, Muralidharan Sargurupremraj, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 176) with videos related to
Sort By:
Page
of 18
Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Genome Medicine
|
March 22, 2025
Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Plos One
|
November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
John W Cole, Huichun Xu, Kathleen Ryan, et al.
Nature Genetics
|
December 23, 2020
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.
Nature Genetics
|
February 4, 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, et al.
Journal of the American College of Cardiology
|
August 27, 2016
Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study
Sander W van der Laan, Tove Fall, Aicha Soumaré, et al.
Nature Genetics
|
November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.
The Lancet. Neurology
|
October 9, 2012
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Matthew Traylor, Martin Farrall, Elizabeth G Holliday, et al.
Nature Genetics
|
February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
, , Céline Bellenguez, et al.
Stroke
|
June 11, 2020
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Nicola J Armstrong, Karen A Mather, Muralidharan Sargurupremraj, et al.
Page
of 18