about
Genome-wide associations of gene expression variation in humansThe DNA sequence of the human X chromosomeGenome-wide detection and characterization of positive selection in human populationsGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsEnsembl 2014Multiple common variants for celiac disease influencing immune gene expressionGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsAbdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Genome-wide and fine-resolution association analysis of malaria in West AfricaGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisCommon variants near MC4R are associated with fat mass, weight and risk of obesityVariants in MTNR1B influence fasting glucose levels.Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsA second generation human haplotype map of over 3.1 million SNPsGenome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A regionIdentification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association studyLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesEnsembl 2013Genome-wide association analysis identifies 13 new risk loci for schizophreniaClustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorderEnsembl 2017Ensembl 2016Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium mapsGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityA genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.Integrating common and rare genetic variation in diverse human populationsEnsembl 2015Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.An SNP map of human chromosome 22.A whole-genome mouse BAC microarray with 1-Mb resolution for analysis of DNA copy number changes by array comparative genomic hybridization.The correlation between reading and mathematics ability at age twelve has a substantial genetic component.A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.The fine-scale structure of recombination rate variation in the human genome.
P50
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P50
description
bioinformatician
@en
bioinformaticus
@nl
name
Sarah E Hunt
@es
Sarah E Hunt
@nl
Sarah E. Hunt
@en
Sarah Hunt
@fr
سارة إي. هنت
@ar
type
label
Sarah E Hunt
@es
Sarah E Hunt
@nl
Sarah E. Hunt
@en
Sarah Hunt
@fr
سارة إي. هنت
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altLabel
Sarah E Hunt
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Sarah Hunt
@en
prefLabel
Sarah E Hunt
@es
Sarah E Hunt
@nl
Sarah E. Hunt
@en
Sarah Hunt
@fr
سارة إي. هنت
@ar
P106
P21
P2456
P31
P496
0000-0002-8350-1235