Search Results - "Wallace, Chris"
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A more accurate method for colocalisation analysis allowing for multiple causal variants
Published in PLoS genetics (29-09-2021)“…In genome-wide association studies (GWAS) it is now common to search for, and find, multiple causal variants located in close proximity. It has also become…”
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Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses
Published in PLoS genetics (01-04-2020)“…Horizontal integration of summary statistics from different GWAS traits can be used to evaluate evidence for their shared genetic causality. One popular method…”
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Statistical Testing of Shared Genetic Control for Potentially Related Traits
Published in Genetic epidemiology (01-12-2013)“…ABSTRACT Integration of data from genome‐wide single nucleotide polymorphism (SNP) association studies of different traits should allow researchers to…”
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Accurate detection of shared genetic architecture from GWAS summary statistics in the small-sample context
Published in PLoS genetics (16-08-2023)“…Assessment of the genetic similarity between two phenotypes can provide insight into a common genetic aetiology and inform the use of pleiotropy-informed,…”
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Bayesian test for colocalisation between pairs of genetic association studies using summary statistics
Published in PLoS genetics (01-05-2014)“…Genetic association studies, in particular the genome-wide association study (GWAS) design, have provided a wealth of novel insights into the aetiology of a…”
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A pleiotropy-informed Bayesian false discovery rate adapted to a shared control design finds new disease associations from GWAS summary statistics
Published in PLoS genetics (01-02-2015)“…Genome-wide association studies (GWAS) have been successful in identifying single nucleotide polymorphisms (SNPs) associated with many traits and diseases…”
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Improving the coverage of credible sets in Bayesian genetic fine-mapping
Published in PLoS computational biology (13-04-2020)“…Genome Wide Association Studies (GWAS) have successfully identified thousands of loci associated with human diseases. Bayesian genetic fine-mapping studies aim…”
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fcfdr: an R package to leverage continuous and binary functional genomic data in GWAS
Published in BMC bioinformatics (30-07-2022)“…Genome-wide association studies (GWAS) are limited in power to detect associations that exceed the stringent genome-wide significance threshold. This…”
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Consensus clustering for Bayesian mixture models
Published in BMC bioinformatics (21-07-2022)“…Cluster analysis is an integral part of precision medicine and systems biology, used to define groups of patients or biomolecules. Consensus clustering is an…”
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Widespread seasonal gene expression reveals annual differences in human immunity and physiology
Published in Nature communications (12-05-2015)“…Seasonal variations are rarely considered a contributing component to human tissue function or health, although many diseases and physiological process display…”
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The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
Published in Cell (17-11-2016)“…The International Human Epigenome Consortium (IHEC) coordinates the generation of a catalog of high-resolution reference epigenomes of major primary human cell…”
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Leveraging auxiliary data from arbitrary distributions to boost GWAS discovery with Flexible cFDR
Published in PLoS genetics (20-10-2021)“…Genome-wide association studies (GWAS) have identified thousands of genetic variants that are associated with complex traits. However, a stringent significance…”
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Sharing GWAS summary statistics results in more citations
Published in Communications biology (28-01-2023)“…Rates of sharing of genome-wide association studies (GWAS) summary statistics are historically low, limiting potential for scientific discovery. Here we show,…”
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Central bank communication design in a Lucas-Phelps economy
Published in Journal of monetary economics (01-04-2014)“…In a Lucas-Phelps island economy, an island has access to many informative signals about demand conditions. Each signal incorporates both public and private…”
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Early versus persistent Complex Regional Pain Syndrome: Is there a difference in patient reported outcomes following rehabilitation?
Published in European journal of pain (01-03-2024)“…Background Expert consensus asserts that early treatment of Complex Regional Pain Syndrome (CRPS) leads to better outcomes. Yet no evidence supports this…”
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CoPheScan: phenome-wide association studies accounting for linkage disequilibrium
Published in Nature communications (12-07-2024)“…Phenome-wide association studies (PheWAS) facilitate the discovery of associations between a single genetic variant with multiple phenotypes. For variants…”
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Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls
Published in Nature genetics (01-07-2015)“…Mary Fortune, Chris Wallace and colleagues report a new method that allows statistical colocalization of genetic risk variants for related autoimmune diseases…”
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A Type I Interferon Transcriptional Signature Precedes Autoimmunity in Children Genetically at Risk for Type 1 Diabetes
Published in Diabetes (New York, N.Y.) (01-07-2014)“…Diagnosis of the autoimmune disease type 1 diabetes (T1D) is preceded by the appearance of circulating autoantibodies to pancreatic islets. However, almost…”
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Vascularized Groin Lymph Node Transfer Using the Wrist as a Recipient Site for Management of Postmastectomy Upper Extremity Lymphedema
Published in Plastic and reconstructive surgery (1963) (01-04-2009)“…Restoring the continuity of lymphatic drainage by lymphaticovenous or lymphaticolymphatic anastomosis was observed in the short term to be patent but…”
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Stochastic search and joint fine-mapping increases accuracy and identifies previously unreported associations in immune-mediated diseases
Published in Nature communications (19-07-2019)“…Thousands of genetic variants are associated with human disease risk, but linkage disequilibrium (LD) hinders fine-mapping the causal variants. Both lack of…”
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