SNP information rs3184504

Research and publications:

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

  18252225   On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.

  18311140   Newly identified genetic risk variants for celiac disease related to the immune response.

  18556337   Impact of diabetes susceptibility loci on progression from pre-diabetes to diabetes in at-risk individuals of the diabetes prevention trial-type 1 (DPT-1)

  18713140   Translational mini-review series on the immunogenetics of gut disease: immunogenetics of coeliac disease.

  18978792   Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci

  18987646   The expanding genetic overlap between multiple sclerosis and type I diabetes.

  19073967   Shared and distinct genetic variants in type 1 diabetes and celiac disease

  19168599   Type 1 diabetes in the BB rat: a polygenic disease.

  19198610   Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.

  19307593   Signals of recent positive selection in a worldwide sample of human populations.

  19430479   Genome-wide association study of blood pressure and hypertension.

  19430480   Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

  19430483   Genome-wide association study identifies eight loci associated with blood pressure.

  19648293   Replication of celiac disease UK genome-wide association study results in a US population.

  19693089   Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort.

  19820697   A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

  19860791   Genetic evidence for a role of IL33 in nasal polyposis.

  19862010   Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

  19913121   Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

  19951419   Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis.

  19956433   Genetics of coronary artery disease: focus on genome-wide association studies.

  20045101   Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.

  20112382   Confirmation of an association between rs6822844 at the Il2-Il21 region and multiple autoimmune diseases: evidence of a general susceptibility locus.

  20190752   Multiple common variants for celiac disease influencing immune gene expression.

  20224392   Blood pressure and human genetic variation in the general population.

  20425154   Genome-wide association studies: contribution of genomics to understanding blood pressure and essential hypertension.

  20440292   Early identification of cardiovascular risk using genomics and proteomics.

  20453842   Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.

  20508602   The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis.

  20526340   Common variants in FOXP1 are associated with generalized vitiligo.

  20546165   The carriage of the type 1 diabetes-associated R262W variant of human LNK correlates with increased proliferation of peripheral blood monocytes in diabetic patients.

  20560212   Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection.

  20587799   Genetics of type 1 diabetes: what next?

  20610812   The genetics of normal platelet reactivity.

  20647273   Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis.

  20729558   Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.

  20805105   Synthetic associations in the context of genome-wide association scan signals

  20838585   Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.

  20854658   Overlapping genetic susceptibility variants between three autoimmune disorders: rheumatoid arthritis, type 1 diabetes and coeliac disease.

  20885991   Advances and challenges in biomarker development for type 1 diabetes prediction and prevention using omic technologies.

  20933377   Recent findings on genetics of systemic autoimmune diseases.

  20948529   Recent findings in the genetics of blood pressure and hypertension traits.

  20971364   A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.

  21045733   Discovery and replication of new genetic loci for blood pressure in the Women's Genome Health Study.

  21060006   Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.

  21060863   Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.

  21129164   The genetics of blood pressure and hypertension: the role of rare variation.

  21153663   Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

  21193429   Determinants of platelet count in humans.

  21253569   Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?

  21266329   Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs.

  21270831   Association between type 1 diabetes and GWAS SNPs in the southeast US Caucasian population.

  21369780   Genome-wide association studies in atherosclerosis.

  21378095   Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.

  21378990   Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

  21507254   Geographic differences in allele frequencies of susceptibility SNPs for cardiovascular disease.

  21533024   Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci

  21572416   Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.

  21595938   Polymorphisms associated with rheumatoid arthritis do not protect against Alzheimer's disease.

  21738479   Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

  21765104   Evaluation of 19 autoimmune disease-associated loci with rheumatoid arthritis in a Colombian population: evidence for replication and gene-gene interaction.

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

  21829393   Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

  21852963   Pervasive sharing of genetic effects in autoimmune disease.

  21860704   Implications of discoveries from genome-wide association studies in current cardiovascular practice.

  21873553   Genetic analysis of adult-onset autoimmune diabetes.

  21875899   Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

  21909115   Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

  21952740   Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort.

  21971053   Genome-wide association study of coronary artery disease in the Japanese.

  21980299   A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.

  22025373   Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study.

  22046141   Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus.

  22057235   Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

  22087237   Improving the estimation of celiac disease sibling risk by non-HLA genes.

  22139419   New gene functions in megakaryopoiesis and platelet formation.

  22140480   SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension.

  22144573   Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

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

  22151179   Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record.

  22216278   Large scale association analysis identifies three susceptibility loci for coronary artery disease.

  22277159   Implications for health and disease in the genetic signature of the Ashkenazi Jewish population.

  22293688   1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.

  22315323   Effects of non-HLA gene polymorphisms on development of islet autoimmunity and type 1 diabetes in a population with high-risk HLA-DR,DQ genotypes.

  22328738   Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort.

  22363065   Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

  22493691   Novel associations for hypothyroidism include known autoimmune risk loci.

  22525200   Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.

  22577522   Shared HLA Class II in Six Autoimmune Diseases in Latin America: A Meta-Analysis.

  22588700   Genetics of coronary artery disease in the 21st century.

  22848412   Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

  22916186   ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

  23328882   Meta-analyses of four eosinophil related gene variants in coronary heart disease.

  23417110   Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.

  23468967   Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.

  23840476   Identification of the tyrosine-protein phosphatase non-receptor type 2 as a rheumatoid arthritis susceptibility locus in europeans.

  24219970   Common genetic variants do not associate with CAD in familial hypercholesterolemia.

  24274136   Biobanking across the phenome - at the center of chronic disease research.

  24768677   Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.