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Open AccessJournal ArticleDOI

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.

TLDR
The genomic score developed and evaluated here substantially advances the concept of using genomic information to stratify individuals with different trajectories of CAD risk and highlights the potential for genomic screening in early life to complement conventional risk prediction.
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This article is published in Journal of the American College of Cardiology.The article was published on 2018-10-16 and is currently open access. It has received 522 citations till now. The article focuses on the topics: Framingham Risk Score.

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Citations
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Journal ArticleDOI

Comprehensive Analysis of ceRNA Regulation Network Involved in the Development of Coronary Artery Disease.

TL;DR: In this paper, a CAD-specific endogenous RNA (ceRNA) regulation network was successfully constructed, contributing to the understanding of the relationship among lncRNAs, miRNAs and mRNAs.
Posted ContentDOI

An integrative analysis of genomic and exposomic data for complex traits and phenotypic prediction

TL;DR: A linear mixed model approach is proposed, which jointly models the random effects of the two omics layers on phenotypes of complex traits and shows that integrating genomic and exposomic data is essential to attaining a clinically meaningful level of prediction accuracy for disease traits.
References
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Journal ArticleDOI

ROCR: visualizing classifier performance in R

TL;DR: UNLABELLED ROCR is a package for evaluating and visualizing the performance of scoring classifiers in the statistical language R that features over 25 performance measures that can be freely combined to create two-dimensional performance curves.
Journal ArticleDOI

A reference panel of 64,976 haplotypes for genotype imputation

Shane A. McCarthy, +117 more
- 22 Aug 2016 - 
TL;DR: A reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly European ancestry leads to accurate genotype imputation at minor allele frequencies as low as 0.1% and a large increase in the number of SNPs tested in association studies.
Journal ArticleDOI

Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.

TL;DR: UK Biobank is not representative of the sampling population; there is evidence of a “healthy volunteer” selection bias; valid assessment of exposure-disease relationships may be widely generalizable and does not require participants to be Representative of the population at large.
Journal ArticleDOI

A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease

Majid Nikpay, +167 more
- 07 Sep 2015 - 
TL;DR: This article conducted a meta-analysis of coronary artery disease (CAD) cases and controls, interrogating 6.7 million common (minor allele frequency (MAF) > 0.05) and 2.7 millions low-frequency (0.005 < MAF < 0.5) variants.
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A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease

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