SNPStats: a web tool for the analysis of association studies.
about
Role of key TYMS polymorphisms on methotrexate therapeutic outcome in portuguese rheumatoid arthritis patientsUGT1A and TYMS genetic variants predict toxicity and response of colorectal cancer patients treated with first-line irinotecan and fluorouracil combination therapyPolymorphisms in Telomere Length Associated TERC and TERT predispose for Ischemic Stroke in a Chinese Han populationAssociation between RTEL1, PHLDB1, and TREH Polymorphisms and Glioblastoma Risk: A Case-Control StudyA 3'-UTR Polymorphism in Soluble Epoxide Hydrolase Gene Is Associated with Acute Rejection in Renal Transplant RecipientsDeath receptor (DR4) haplotypes are associated with increased susceptibility of gallbladder carcinoma in north Indian populationThe maternal ITPK1 gene polymorphism is associated with neural tube defects in a high-risk Chinese populationPolymorphisms in the TLR4 and TLR5 gene are significantly associated with inflammatory bowel disease in German shepherd dogsDisseminated cysticercosis: clinical spectrum, Toll-like receptor-4 gene polymorphisms and role of albendazole: A prospective follow-up of 60 cases with a review of 56 published casesLow-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibilityInflammatory response gene polymorphisms and their relationship with colorectal cancer risk.SNPAnalyzer 2.0: a web-based integrated workbench for linkage disequilibrium analysis and association analysis.Effects of methylenetetrahydrofolate reductase gene polymorphisms on toxicities during consolidation therapy in pediatric acute lymphoblastic leukemia in a Chinese population.A at single nucleotide polymorphism-358 is required for G at -420 to confer the highest plasma resistin in the general Japanese populationGenetic Polymorphisms of IL17 and Chagas Disease in the South and Southeast of BrazilMAVEN: a tool for visualization and functional analysis of genome-wide association results.No association between polymorphisms of WNT2 and schizophrenia in a Korean populationGenetic influences on hand osteoarthritis in Finnish women--a replication study of candidate genesKinase insert domain receptor/vascular endothelial growth factor receptor 2 (KDR) genetic variation is associated with ovarian hyperstimulation syndromeMatrix Metallopeptidase 2 Gene Polymorphism is Associated with Obesity in Korean Population.Analysis of Serum Cytokines and Single-Nucleotide Polymorphisms of SOD1, SOD2, and CAT in Erysipelas Patients.Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian SampleImpact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study.Xenobiotic and folate pathway gene polymorphisms and risk of childhood acute lymphoblastic leukaemia in Javanese children.Associations between Interleukin-31 Gene Polymorphisms and Dilated Cardiomyopathy in a Chinese Population.DNA repair genes polymorphisms and genetic susceptibility to Philadelphia-negative myeloproliferative neoplasms in a Portuguese population: The role of base excision repair genes polymorphisms.Association analysis of telomere length related gene ACYP2 with the gastric cancer risk in the northwest Chinese Han populationPolymorphisms in dopaminergic system genes; association with criminal behavior and self-reported aggression in violent prison inmates from PakistanThe association of six single nucleotide polymorphisms and their haplotypes in CDH13 with T2DM in a Han Chinese population.GADD45a promoter regulation by a functional genetic variant associated with acute lung injury.Replication of genome-wide discovered breast cancer risk loci in the Cypriot population.Inherited Variation in Cytokine, Acute Phase Response, and Calcium Metabolism Genes Affects Susceptibility to Infective Endocarditis.CTLA4 variants and haplotype contribute genetic susceptibility to myasthenia gravis in northern Chinese population.Multiple sclerosis susceptibility alleles in African Americans.Interferon-related genetic markers of necroinflammatory activity in chronic hepatitis CFunctional prostacyclin synthase promoter polymorphisms. Impact in pulmonary arterial hypertension.Toll-like receptor 9 polymorphisms influence mother-to-child transmission of human immunodeficiency virus type 1.MDM2 polymorphism associated with the development of cervical lesions in women infected with Human papillomavirus and using of oral contraceptivesAssociation of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.
P2860
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P2860
SNPStats: a web tool for the analysis of association studies.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
SNPStats: a web tool for the analysis of association studies.
@en
SNPStats: a web tool for the analysis of association studies.
@nl
type
label
SNPStats: a web tool for the analysis of association studies.
@en
SNPStats: a web tool for the analysis of association studies.
@nl
prefLabel
SNPStats: a web tool for the analysis of association studies.
@en
SNPStats: a web tool for the analysis of association studies.
@nl
P50
P356
P1433
P1476
SNPStats: a web tool for the analysis of association studies
@en
P2093
Raquel Iniesta
P304
P356
10.1093/BIOINFORMATICS/BTL268
P407
P577
2006-05-23T00:00:00Z