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Anuj Goel

Showing results (41-50 of 120) with videos related to

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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.
Nature Genetics|February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settingsSean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
Atherosclerosis|October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisationRona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Journal of the American College of Cardiology|January 30, 2016
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization StudyTanya Keenan, Wei Zhao, Asif Rasheed, et al.
Research Square|February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathiesDaria Kramarenko, Poeya Haydarlou, George Powell, et al.
Journal of the American College of Cardiology|January 29, 2013
Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysisKenneth Chan, Riyaz S Patel, Paul Newcombe, et al.
Circulation. Genomic and Precision Medicine|December 15, 2020
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes MellitusNatalie R van Zuydam, Claes Ladenvall, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|July 18, 2017
Association analyses based on false discovery rate implicate new loci for coronary artery diseaseChristopher P Nelson, Anuj Goel, Adam S Butterworth, et al.
Pageof 12

Showing results (41-50 of 120) with videos related to

Sort By:
Pageof 12
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.
Nature Genetics|February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settingsSean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
Atherosclerosis|October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisationRona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Journal of the American College of Cardiology|January 30, 2016
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization StudyTanya Keenan, Wei Zhao, Asif Rasheed, et al.
Research Square|February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathiesDaria Kramarenko, Poeya Haydarlou, George Powell, et al.
Journal of the American College of Cardiology|January 29, 2013
Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysisKenneth Chan, Riyaz S Patel, Paul Newcombe, et al.
Circulation. Genomic and Precision Medicine|December 15, 2020
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes MellitusNatalie R van Zuydam, Claes Ladenvall, Benjamin F Voight, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|July 18, 2017
Association analyses based on false discovery rate implicate new loci for coronary artery diseaseChristopher P Nelson, Anuj Goel, Adam S Butterworth, et al.
Pageof 12