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Muredach P Reilly

Showing results (241-250 of 298) with videos related to

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International Journal of Molecular Epidemiology and Genetics|September 15, 2011
Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery diseaseSally L Ricketts, Katrijn L Rensing, Jeff M Holly, et al.
Circulation. Cardiovascular Genetics|February 10, 2012
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complexRobert W Davies, George A Wells, Alexandre F R Stewart, et al.
Lancet (London, England)|January 18, 2011
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesMuredach P Reilly, Mingyao Li, Jing He, et al.
Stroke|November 23, 2013
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variantsMartin Dichgans, Rainer Malik, Inke R König, et al.
Circulation. Cardiovascular Genetics|October 7, 2010
Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controlsMichael Preuss, Inke R König, John R Thompson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 28, 2013
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemiaNathan O Stitziel, Sigrid W Fouchier, Barbara Sjouke, et al.
Journal of the American College of Cardiology|June 4, 2013
Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort)Jane F Ferguson, Gregory J Matthews, Raymond R Townsend, et al.
Nature Medicine|June 8, 2021
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infectionSeyedeh M Zekavat, Shu-Hong Lin, Alexander G Bick, et al.
Nature Genetics|April 27, 2007
A variant in CDKAL1 influences insulin response and risk of type 2 diabetesValgerdur Steinthorsdottir, Gudmar Thorleifsson, Inga Reynisdottir, et al.
Plos Genetics|September 21, 2011
Genetic association for renal traits among participants of African ancestry reveals new loci for renal functionChing-Ti Liu, Maija K Garnaas, Adrienne Tin, et al.
Pageof 30

Showing results (241-250 of 298) with videos related to

Sort By:
Pageof 30
International Journal of Molecular Epidemiology and Genetics|September 15, 2011
Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery diseaseSally L Ricketts, Katrijn L Rensing, Jeff M Holly, et al.
Circulation. Cardiovascular Genetics|February 10, 2012
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complexRobert W Davies, George A Wells, Alexandre F R Stewart, et al.
Lancet (London, England)|January 18, 2011
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesMuredach P Reilly, Mingyao Li, Jing He, et al.
Stroke|November 23, 2013
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variantsMartin Dichgans, Rainer Malik, Inke R König, et al.
Circulation. Cardiovascular Genetics|October 7, 2010
Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controlsMichael Preuss, Inke R König, John R Thompson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 28, 2013
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemiaNathan O Stitziel, Sigrid W Fouchier, Barbara Sjouke, et al.
Journal of the American College of Cardiology|June 4, 2013
Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort)Jane F Ferguson, Gregory J Matthews, Raymond R Townsend, et al.
Nature Medicine|June 8, 2021
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infectionSeyedeh M Zekavat, Shu-Hong Lin, Alexander G Bick, et al.
Nature Genetics|April 27, 2007
A variant in CDKAL1 influences insulin response and risk of type 2 diabetesValgerdur Steinthorsdottir, Gudmar Thorleifsson, Inga Reynisdottir, et al.
Plos Genetics|September 21, 2011
Genetic association for renal traits among participants of African ancestry reveals new loci for renal functionChing-Ti Liu, Maija K Garnaas, Adrienne Tin, et al.
Pageof 30