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rdfs:label	ASSOCIATION STUDIES ARTICLES
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is Subject of	Pathway and network-based analysis of genome-wide association studies in multiple sclerosis Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis Genome-wide association of anthropometric traits in African- and African-derived populations Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study Support for the involvement of large copy number variants in the pathogenesis of schizophrenia Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation Association of HY-restricting HLA class II alleles with pregnancy outcome in patients with recurrent miscarriage subsequent to a firstborn boy The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations Sarcoidosis HLA class II genotyping distinguishes differences of clinical phenotype across ethnic groups The COPD genetic association compendium: a comprehensive online database of COPD genetic associations Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects Genome-wide association identifies ATOH7 as a major gene determining human optic disc size A comprehensive analysis of common IGF1, IGFBP1 and IGFBP3 genetic variation with prospective IGF-I and IGFBP-3 blood levels and prostate cancer risk among Caucasians Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves’ disease Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count Genome-wide association study of circulating vitamin D levels Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes Genome-wide association analysis identifies multiple loci related to resting heart rate Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15 Common body mass index-associated variants confer risk of extreme obesity Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk Common and different genetic background for rheumatoid arthritis and coeliac disease Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden ADH single nucleotide polymorphism associations with alcohol metabolism in vivo Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease Admixture mapping of quantitative trait loci for blood lipids in African-Americans Large replication study and meta-analyses of DVWA as an osteoarthritis susceptibility locus in European and Asian populations A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci Association of variants in the PCSK1 gene with obesity in the EPIC-Norfolk study Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate α-secretase activity Common variants in the region around Osterix are associated with bone mineral density and growth in childhood Common variants in CASP3 confer susceptibility to Kawasaki disease Refining the association of MHC with multiple sclerosis in African Americans Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes A variant in the gene FUT9 is associated with susceptibility to placental malaria infection A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12 New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8 Life course variations in the associations between FTO and MC4R gene variants and body size Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk Genome-wide association meta-analysis for total serum bilirubin levels Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl Copy number, linkage disequilibrium and disease association in the FCGR locus A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population A large genome scan for rare CNVs in amyotrophic lateral sclerosis ITPKC gene SNP rs28493229 and Kawasaki disease in Taiwanese children Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk A functional variant in the 3′-UTR of angiopoietin-1 might reduce stroke risk by interfering with the binding efficiency of microRNA 211 Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus Genetic determinants of HSP70 gene expression following heat shock Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer Involvement of SMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5 Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15 Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis Genome-wide association of serum bilirubin levels in Korean population A genome-wide scan for common alleles affecting risk for autism

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