Search Results - "Staley, James R."
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PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
Published in Bioinformatics (01-11-2019)“…Abstract Summary PhenoScanner is a curated database of publicly available results from large-scale genetic association studies in humans. This online tool…”
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A robust and efficient method for Mendelian randomization with hundreds of genetic variants
Published in Nature communications (17-01-2020)“…Mendelian randomization (MR) is an epidemiological technique that uses genetic variants to distinguish correlation from causation in observational data. The…”
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PhenoScanner: a database of human genotype-phenotype associations
Published in Bioinformatics (Oxford, England) (15-10-2016)“…PhenoScanner is a curated database of publicly available results from large-scale genetic association studies. This tool aims to facilitate 'phenome scans',…”
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A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits
Published in Nature communications (03-02-2021)“…Genome-wide association studies (GWAS) have identified thousands of genomic regions affecting complex diseases. The next challenge is to elucidate the causal…”
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The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Published in Cell (17-11-2016)“…Many common variants have been associated with hematological traits, but identification of causal genes and pathways has proven challenging. We performed a…”
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Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases
Published in Nature genetics (01-10-2020)“…The human proteome is a major source of therapeutic targets. Recent genetic association analyses of the plasma proteome enable systematic evaluation of the…”
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The EWAS Catalog: a database of epigenome-wide association studies
Published in Wellcome open research (2022)“…Epigenome-wide association studies (EWAS) seek to quantify associations between traits/exposures and DNA methylation measured at thousands or millions of CpG…”
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Coding and regulatory variants are associated with serum protein levels and disease
Published in Nature communications (25-01-2022)“…Circulating proteins can be used to diagnose and predict disease-related outcomes. A deep serum proteome survey recently revealed close associations between…”
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DNA methylation signatures of adolescent victimization: analysis of a longitudinal monozygotic twin sample
Published in Epigenetics (02-11-2021)“…Accumulating evidence suggests that individuals exposed to victimization at key developmental stages may have different epigenetic fingerprints compared to…”
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Semiparametric methods for estimation of a nonlinear exposure‐outcome relationship using instrumental variables with application to Mendelian randomization
Published in Genetic epidemiology (01-05-2017)“…ABSTRACT Mendelian randomization, the use of genetic variants as instrumental variables (IV), can test for and estimate the causal effect of an exposure on an…”
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Associations of Blood Pressure in Pregnancy With Offspring Blood Pressure Trajectories During Childhood and Adolescence: Findings From a Prospective Study
Published in Journal of the American Heart Association (01-05-2015)“…Background Hypertensive disorders of pregnancy are related to higher offspring blood pressure (BP), but it is not known whether this association strengthens or…”
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MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data
Published in Wellcome open research (2020)“…The MendelianRandomization package is a software package written for the R software environment that implements methods for Mendelian randomization based on…”
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Genomic atlas of the human plasma proteome
Published in Nature (London) (01-06-2018)“…Although plasma proteins have important roles in biological processes and are the direct targets of many drugs, the genetic factors that control…”
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The EWAS Catalog: a database of epigenome-wide association studies
Published in Wellcome open research (01-01-2022)“…Epigenome-wide association studies (EWAS) seek to quantify associations between traits/exposures and DNA methylation measured at thousands or millions of CpG…”
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Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses
Published in BMJ (Online) (26-03-2019)“…AbstractObjectiveTo investigate the shape of the causal relation between body mass index (BMI) and mortality.DesignLinear and non-linear mendelian…”
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The Effect of Attention Deficit/Hyperactivity Disorder on Physical Health Outcomes: A 2-Sample Mendelian Randomization Study
Published in American journal of epidemiology (01-06-2021)“…Attention-deficit/hyperactivity disorder (ADHD) is associated with a broad range of physical health problems. Using different research designs to test whether…”
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Published in Nature genetics (01-10-2016)“…Patricia Munroe, Joanna Howson and colleagues genotype ∼350,000 individuals and identify 30 new blood pressure– or hypertension-associated risk loci. Their…”
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A robust mean and variance test with application to high-dimensional phenotypes
Published in European journal of epidemiology (01-04-2022)“…Most studies of continuous health-related outcomes examine differences in mean levels (location) of the outcome by exposure. However, identifying effects on…”
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Sclerostin Downregulation Globally by Naturally Occurring Genetic Variants, or Locally in Atherosclerotic Plaques, Does Not Associate With Cardiovascular Events in Humans
Published in Journal of bone and mineral research (01-07-2021)“…ABSTRACT Inhibition of sclerostin increases bone formation and decreases bone resorption, leading to increased bone mass, bone mineral density, and bone…”
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