Jeffrey C Barrett


Ontology type: schema:Person     


Person Info

NAME

Jeffrey C

SURNAME

Barrett

Publications in SciGraph latest 50 shown

  • 2021-10-28 An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci in NATURE GENETICS
  • 2020-02-21 Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease in NATURE COMMUNICATIONS
  • 2019-12-20 Complex Disease Genes and Their Discovery in MOLECULAR GENETICS OF INFLAMMATORY BOWEL DISEASE
  • 2018-09-26 Common genetic variants contribute to risk of rare severe neurodevelopmental disorders in NATURE
  • 2018-03-21 De novo mutations in regulatory elements in neurodevelopmental disorders in NATURE
  • 2018-01-11 Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders in GENETICS IN MEDICINE
  • 2017-06-28 Fine-mapping inflammatory bowel disease loci to single-variant resolution in NATURE
  • 2017-06-26 The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability in NATURE GENETICS
  • 2017-01-09 Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7 in NATURE GENETICS
  • 2017-01-09 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease in NATURE GENETICS
  • 2016-08-01 Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing in NATURE GENETICS
  • 2016-03-14 Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders in NATURE NEUROSCIENCE
  • 2016-03-14 Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci in NATURE GENETICS
  • 2016-02-01 HLA class II sequence variants influence tuberculosis risk in populations of European ancestry in NATURE GENETICS
  • 2015-10-05 Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families in NATURE GENETICS
  • 2015-09-15 Using human genetics to make new medicines in NATURE REVIEWS GENETICS
  • 2015-09-14 The UK10K project identifies rare variants in health and disease in NATURE
  • 2015-08-05 High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping in BMC GENOMICS
  • 2015-07-20 Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations in NATURE GENETICS
  • 2015-03-16 Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration in NATURE GENETICS
  • 2015-03-09 Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers in NATURE GENETICS
  • 2015-02-10 Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer in BMC MEDICAL GENOMICS
  • 2015-01-05 High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis in NATURE GENETICS
  • 2014-10-29 Synaptic, transcriptional and chromatin genes disrupted in autism in NATURE
  • 2014-04-23 Guidelines for investigating causality of sequence variants in human disease in NATURE
  • 2014-02-11 A genome-wide association study of anorexia nervosa in MOLECULAR PSYCHIATRY
  • 2013-10-22 Response to ‘Predicting the diagnosis of autism spectrum disorder using gene pathway analysis’ in MOLECULAR PSYCHIATRY
  • 2013-08-21 Complex Disease Genes and Their Discovery in MOLECULAR GENETICS OF INFLAMMATORY BOWEL DISEASE
  • 2013-05-22 Negligible impact of rare autoimmune-locus coding-region variants on missing heritability in NATURE
  • 2013-04-17 The zebrafish reference genome sequence and its relationship to the human genome in NATURE
  • 2012-10-31 Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease in NATURE
  • 2012-09-09 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis in NATURE GENETICS
  • 2012-02-27 From HLA association to function in NATURE GENETICS
  • 2011-12-27 Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry in NATURE GENETICS
  • 2011-11-06 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease in NATURE GENETICS
  • 2011-03-02 Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-02-06 Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 in NATURE GENETICS
  • 2010-11-21 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci in NATURE GENETICS
  • 2010-02-28 Multiple common variants for celiac disease influencing immune gene expression in NATURE GENETICS
  • 2009-05-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes in NATURE GENETICS
  • 2009-04-23 Marker selection for genetic case–control association studies in NATURE PROTOCOLS
  • 2008-11-02 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci in NATURE GENETICS
  • 2008-06-29 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease in NATURE GENETICS
  • 2008-06-04 Worldwide population differentiation at disease-associated SNPs in BMC MEDICAL GENOMICS
  • 2008-04-27 Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease in NATURE GENETICS
  • 2008-01-16 To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-06-06 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility in NATURE GENETICS
  • 2006-05-21 Evaluating coverage of genome-wide association studies in NATURE GENETICS
  • 2005-12-04 Common deletion polymorphisms in the human genome in NATURE GENETICS
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