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Publications

Author Correction: The power of genetic diversity in genome-wide association studies of lipids.

Graham SE. et al, (2023), Nature

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

Yu M. et al, (2023), Circulation: Genomic and Precision Medicine

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

Young WJ. et al, (2023), Nature communications, 14

Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy

Aung N. et al, (2023), Circulation: Genomic and Precision Medicine

Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Wang N. et al, (2023), Journal of Translational Genetics and Genomics, 7, 1 - 2

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

Aragam KG. et al, (2022), Nat Genet

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.

Kanoni S. et al, (2022), Genome biology, 23

A saturated map of common genetic variants associated with human height.

Yengo L. et al, (2022), Nature, 610, 704 - 712

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Ramdas S. et al, (2022), American journal of human genetics, 109, 1366 - 1387

The power of genetic diversity in genome-wide association studies of lipids.

Graham SE. et al, (2021), Nature

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Lagou V. et al, (2021), Nature Communications, 12

Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.

Grace C. et al, (2021), Genet Epidemiol

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.

Lagou V. et al, (2021), Nature communications, 12

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Harper AR. et al, (2021), Nature Genetics, 53, 135 - 142

Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine, 13

Genetic variation in CADM2 as a link between psychological traits and obesity

Morris J. et al, (2019), Scientific Reports, 9

Associations of autozygosity with a broad range of human phenotypes.

Clark DW. et al, (2019), Nature communications, 10

A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction

Douglas G. et al, (2019), Cardiovascular Research

A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

Sung YJ. et al, (2019), Human Molecular Genetics, 28, 2615 - 2633

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease

Magosi LE. et al, (2019), Bioinformatics

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