about
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseHost-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseGenetic studies of body mass index yield new insights for obesity biologyGenome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other lociReplication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.Common variants at five new loci associated with early-onset inflammatory bowel diseaseDeep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel diseaseGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociHundreds of variants clustered in genomic loci and biological pathways affect human heightGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisUlcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association studyThe role of the CD58 locus in multiple sclerosisT-bet polymorphisms are associated with asthma and airway hyperresponsivenessGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisGenome-wide association identifies multiple ulcerative colitis susceptibility lociRare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traitsInflammatory bowel disease characteristics among African Americans, Hispanics, and non-Hispanic Whites: characterization of a large North American cohortAssociation of DLG5 R30Q variant with inflammatory bowel diseaseA functional candidate screen for coeliac disease genesA genome-wide association study identifies IL23R as an inflammatory bowel disease geneGenetic variation in myosin IXB is associated with ulcerative colitisHigh-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitisFamilial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosusMeta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac diseaseTECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVTRare and low-frequency coding variants alter human adult heightRisk alleles for multiple sclerosis identified by a genomewide studyLarge-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genomeLarge-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans.Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.The promise and perils of interpreting genetic associations in Crohn's disease.Occupational and environmental exposures and risk of systemic lupus erythematosus: silica, sunlight, solvents.Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.Identification of two independent risk factors for lupus within the MHC in United Kingdom families.
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P50
description
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John D Rioux
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John D Rioux
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John D. Rioux
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John D Rioux
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John D Rioux
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John D. Rioux
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P214
P244
P269
P1053
A-9599-2015
P106
P21
P214
P244
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P269
P31
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P7859
lccn-n2014182242