Sarah Hunt

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2016-12 The Ensembl Variant Effect Predictor in GENOME BIOLOGY
  • 2015-10 A global reference for human genetic variation in NATURE
  • 2014-12 The correlation between reading and mathematics ability at age twelve has a substantial genetic component in NATURE COMMUNICATIONS
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2013-11 Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis in NATURE GENETICS
  • 2013-10 Genome-wide association analysis identifies 13 new risk loci for schizophrenia in NATURE GENETICS
  • 2013-06 Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis in NATURE GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-02 Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis in NATURE GENETICS
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-12 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis in NATURE GENETICS
  • 2012-10 Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus in NATURE GENETICS
  • 2012-09 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes in NATURE GENETICS
  • 2012-03 Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke in NATURE GENETICS
  • 2012-01 Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry in NATURE GENETICS
  • 2011-12 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease in NATURE GENETICS
  • 2011-08 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis in NATURE
  • 2011-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility in NATURE GENETICS
  • 2011-07 The GENCODE exome: sequencing the complete human exome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-03-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease in NATURE GENETICS
  • 2011-02 Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes in NATURE GENETICS
  • 2010-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 in NATURE GENETICS
  • 2010-09 Integrating common and rare genetic variation in diverse human populations in NATURE
  • 2010-04 Multiple common variants for celiac disease influencing immune gene expression in NATURE GENETICS
  • 2010-04 Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls in NATURE
  • 2009-12 Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region in NATURE GENETICS
  • 2009-06 Genome-wide and fine-resolution association analysis of malaria in West Africa in NATURE GENETICS
  • 2009-01 Variants in MTNR1B influence fasting glucose levels in NATURE GENETICS
  • 2008-06 Common variants near MC4R are associated with fat mass, weight and risk of obesity in NATURE GENETICS
  • 2008-06 Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease in NATURE GENETICS
  • 2007-11 Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants in NATURE GENETICS
  • 2007-10-18 A second generation human haplotype map of over 3.1 million SNPs in NATURE
  • 2007-10-18 Genome-wide detection and characterization of positive selection in human populations in NATURE
  • 2007-06-07 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls in NATURE
  • 2006-05 The DNA sequence and biological annotation of human chromosome 1 in NATURE
  • 2005-08 Common VKORC1 and GGCX polymorphisms associated with warfarin dose in THE PHARMACOGENOMICS JOURNAL
  • 2005-03 The DNA sequence of the human X chromosome in NATURE
  • 2004-05 DNA sequence and analysis of human chromosome 9 in NATURE
  • 2004-05 The DNA sequence and comparative analysis of human chromosome 10 in NATURE
  • 2004-04 The DNA sequence and analysis of human chromosome 13 in NATURE
  • 2003-10 The DNA sequence and analysis of human chromosome 6 in NATURE
  • 2002-08 A first-generation linkage disequilibrium map of human chromosome 22 in NATURE
  • 2002-02 The genome sequence of Schizosaccharomyces pombe in NATURE
  • 2001-12 The DNA sequence and comparative analysis of human chromosome 20 in NATURE
  • 2001-02 The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X in NATURE
  • 2001-02 A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms in NATURE
  • 2000-09 An SNP map of human chromosome 22 in NATURE
  • 1999-12 The DNA sequence of human chromosome 22 in NATURE
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