Johnson AD

No ORCID on file · 3 papers in corpus
other 2017
Rare coding variants pinpoint genes that control human hematological traits
PLoS genetics ·doi:10.1371/journal.pgen.1006925

The identification of rare coding or splice site variants remains the most straightforward strategy to link genes with human phenotypes. Here, we analyzed the association between 137,086 rare (minor allele frequency (MAF) <1%) coding or spl…

2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.
Journal of the American College of Cardiology ·doi:10.1016/j.jacc.2016.11.056

BackgroundGenome-wide association studies have so far identified 56 loci associated with risk of coronary artery disease (CAD). Many CAD loci show pleiotropy; that is, they are also associated with other diseases or traits.ObjectivesThis st…

2014
GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database.
Bioinformatics (Oxford, England) ·doi:10.1093/bioinformatics/btu273

SummaryWe created a deeply extracted and annotated database of genome-wide association studies (GWAS) results. GRASP v1.0 contains >6.2 million SNP-phenotype association from among 1390 GWAS studies. We re-annotated GWAS results with 16 ann…