Search Results - "MORRIS, Andrew P"
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Transethnic meta-analysis of genomewide association studies
Published in Genetic epidemiology (01-12-2011)“…The detection of loci contributing effects to complex human traits, and their subsequent fine‐mapping for the location of causal variants, remains a…”
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GWAMA: software for genome-wide association meta-analysis
Published in BMC bioinformatics (28-05-2010)“…Despite the recent success of genome-wide association studies in identifying novel loci contributing effects to complex human traits, such as type 2 diabetes…”
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An evaluation of statistical approaches to rare variant analysis in genetic association studies
Published in Genetic epidemiology (01-02-2010)“…Genome‐wide association (GWA) studies have proved to be extremely successful in identifying novel common polymorphisms contributing effects to the genetic…”
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Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution
Published in Human molecular genetics (15-09-2017)“…Trans-ethnic meta-analysis of genome-wide association studies (GWAS) across diverse populations can increase power to detect complex trait loci when the…”
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Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility
Published in European journal of human genetics : EJHG (01-08-2016)“…Genome-wide association studies (GWAS) have traditionally been undertaken in homogeneous populations from the same ancestry group. However, with the increasing…”
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Data quality control in genetic case-control association studies
Published in Nature protocols (01-09-2010)“…This protocol details the steps for data quality assessment and control that are typically carried out during case-control association studies. The steps…”
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Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework
Published in Nature communications (21-02-2020)“…In Mendelian randomization (MR) analysis, variants that exert horizontal pleiotropy are typically treated as a nuisance. However, they could be valuable in…”
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Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease
Published in PLoS genetics (03-04-2017)“…Recent advances in highly multiplexed immunoassays have allowed systematic large-scale measurement of hundreds of plasma proteins in large cohort studies. In…”
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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
Published in Nature genetics (01-04-2012)“…Peter Visscher and colleagues report a new method for approximate conditional and joint association analysis that makes use of summary statistics from…”
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Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel
Published in European journal of human genetics : EJHG (01-06-2017)“…Genetic imputation is a cost-efficient way to improve the power and resolution of genome-wide association (GWA) studies. Current publicly accessible imputation…”
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Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets
Published in Human reproduction update (01-09-2014)“…Endometriosis is a heritable common gynaecological condition influenced by multiple genetic and environmental factors. Genome-wide association studies (GWASs)…”
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Basic statistical analysis in genetic case-control studies
Published in Nature protocols (01-02-2011)“…This protocol describes how to perform basic statistical analysis in a population-based genetic association case-control study. The steps described involve the…”
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Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis
Published in Nature communications (02-09-2020)“…Genome-wide association studies have identified genetic variation contributing to complex disease risk. However, assigning causal genes and mechanisms has been…”
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Leveraging information between multiple population groups and traits improves fine-mapping resolution
Published in Nature communications (10-11-2023)“…Statistical fine-mapping helps to pinpoint likely causal variants underlying genetic association signals. Its resolution can be improved by (i) leveraging…”
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Evaluating the Performance of Fine-Mapping Strategies at Common Variant GWAS Loci
Published in PLoS genetics (01-09-2015)“…The growing availability of high-quality genomic annotation has increased the potential for mechanistic insights when the specific variants driving common…”
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Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease
Published in International journal of epidemiology (06-01-2022)“…Abstract Background This study was to systematically test whether previously reported risk factors for chronic kidney disease (CKD) are causally related to CKD…”
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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
Published in American journal of human genetics (07-02-2013)“…Several lines of evidence suggest that genome-wide association studies (GWASs) have the potential to explain more of the “missing heritability” of common…”
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A Genome‐wide Association Study of Circulating Levels of Atorvastatin and Its Major Metabolites
Published in Clinical pharmacology and therapeutics (01-08-2020)“…Atorvastatin (ATV) is frequently prescribed and generally well tolerated, but can lead to myotoxicity, especially at higher doses. A genome‐wide association…”
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Functional genomics atlas of synovial fibroblasts defining rheumatoid arthritis heritability
Published in Genome Biology (25-08-2021)“…Genome-wide association studies have reported more than 100 risk loci for rheumatoid arthritis (RA). These loci are shown to be enriched in immune…”
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Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS
Published in International journal of molecular sciences (01-02-2023)“…Amyotrophic lateral sclerosis (ALS) is a fatal late-onset motor neuron disease characterized by the loss of the upper and lower motor neurons. Our…”
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