SNP information rs11171739

Research and publications:

  17554260   Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

  18224312   Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment

  18533027   Worldwide population differentiation at disease-associated SNPs

  18846218   Evolutionary signatures of common human cis-regulatory haplotypes.

  19361613   Genetic control of human brain transcript expression in Alzheimer disease.

  20088021   Screen and clean: a tool for identifying interactions in genome-wide association studies.

  20351726   Whole-genome association mapping of gene expression in the human prefrontal cortex.

  20668683   Genetically dependent ERBB3 expression modulates antigen presenting cell function and type 1 diabetes risk.

  21036813   A variable selection method for genome-wide association studies.

  21129726   Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals.

  21829388   Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA.

  21850031   Evidence for two independent associations with type 1 diabetes at the 12q13 locus.

  22140419   BLOCK-BASED BAYESIAN EPISTASIS ASSOCIATION MAPPING WITH APPLICATION TO WTCCC TYPE 1 DIABETES DATA.

  22144904   Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.

  22446964   Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.

  22496761   Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis.

  23036011   Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

  23804261   From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era.

  24592274   Genomic architecture of sickle cell disease in West African children.

  25010687   Cis and trans effects of human genomic variants on gene expression.

  26019233   Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

  26320593   A single-nucleotide polymorphism of CCL21 rs951005 T>C is associated with susceptibility of polymyositis and such patients with interstitial lung disease in a Chinese Han population.

  27047549   A rare nonsynonymous variant in the lipid metabolic gene HELZ2 related to primary biliary cirrhosis in Chinese Han.

  27153677   Assessing statistical significance in multivariable genome wide association analysis.

  27892471   Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.

  30888520   Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune Diabetes.