SNP information rs9272346

Research and publications:

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

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

  20369022   Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

  20549515   Genome-wide searching of rare genetic variants in WTCCC data.

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

  21304891   A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.

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

  22253788   Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.

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

  22554139   Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis.

  22972380   Investigation of genetic risk factors for chronic adult diseases for association with preterm birth

  23181788   HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.

  23509613   Genome-wide association study of antiphospholipid antibodies.

  24926413   Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.

  26406233   Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.

  26829749   HLA class II sequence variants influence tuberculosis risk in populations of European ancestry.

  27153677   Assessing statistical significance in multivariable genome wide association analysis.

  27291710   Association of human leukocyte antigen DP/DQ gene polymorphisms with chronic hepatitis B in Chinese Han and Uygur populations.

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

  28056976   A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.

  29954342   LPG: A four-group probabilistic approach to leveraging pleiotropy in genome-wide association studies.

  30154825   To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

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