about
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseMeta-analysis and imputation refines the association of 15q25 with smoking quantityMonoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsGenome-wide association meta-analysis identifies new endometriosis risk lociGenome-wide association study identifies a locus at 7p15.2 associated with endometriosisGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociDense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosisGenome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A regionHeterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsGeneration of primary human intestinal T cell transcriptomes reveals differential expression at genetic risk loci for immune-mediated diseaseGenome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosisSequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibilityDense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.A reference panel of 64,976 haplotypes for genotype imputation.Data quality control in genetic case-control association studies.Synthetic associations are unlikely to account for many common disease genome-wide association signalsInvestigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variantsClass II HLA interactions modulate genetic risk for multiple sclerosis.Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway.Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.Genetic studies of Crohn's disease: past, present and future.Fine-mapping inflammatory bowel disease loci to single-variant resolution.Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines.Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidismCombined Influence of B-Cell Receptor Rearrangement and Somatic Hypermutation on B-Cell Class-Switch Fate in Health and in Chronic Lymphocytic LeukemiaAmino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitisConsequences of Identifying XIAP Deficiency in an Adult Patient With Inflammatory Bowel DiseaseIncomplete genetic reconstitution of B cell pools contributes to prolonged immunosuppression after measles
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P50
description
onderzoeker
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researcher
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հետազոտող
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name
Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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Carl A Anderson
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P106
P31
P496
0000-0003-1719-7009