SNP information rs1800750

Research and publications:

  16846490   Lemierre's syndrome and genetic polymorphisms: case report

  16872485   Three allele combinations associated with multiple sclerosis

  17216494   Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF-LTA) and breast cancer risk

  18194515   Polymorphisms of TNF-enhancer and gene for FcgammaRIIa correlate with the severity of falciparum malaria in the ethnically diverse Indian population

  18513389   New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background

  18676870   Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China

  18805939   Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis

  18936436   Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994

  19131662   A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

  19143814   Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1.

  19167443   Family-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia

  19281305   Tumor necrosis factor and lymphotoxin-alpha polymorphisms and severe malaria in African populations

  19330901   Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study

  19505919   Toll-like receptor signaling pathway variants and prostate cancer mortality

  19559392   A candidate gene association study of 77 polymorphisms in migraine

  19619703   Association of genetic variants with metabolic syndrome in 20,806 white women: The Women's Health Genome Study.

  20054343   Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes.

  20078877   Gene polymorphisms in association with emerging cardiovascular risk markers in adult women

  20417488   Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years

  20459604   Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes.

  20459687   Candidate malaria susceptibility/protective SNPs in hospital and population-based studies: the effect of sub-structuring

  21029472   A study of the TNF/LTA/LTB locus and susceptibility to severe malaria in highland papuan children and adults.

  21054877   Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994

  21149504   Common variations in genes encoding C-reactive protein, tumor necrosis factor-alpha, and interleukin-6 and risk of clinical diabetes in the Women's Health Initiative observational study.

  21385363   Polymorphisms in genes controlling inflammation and tissue repair in rheumatoid arthritis: a case control study

  21430300   Genetic polymorphisms in inflammation pathway genes and prostate cancer risk.

  21708280   Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis

  21773006   Studies of gene variants related to inflammation, oxidative stress, dyslipidemia, and obesity: implications for a nutrigenetic approach.

  21867552   Host candidate gene polymorphisms and clearance of drug-resistant Plasmodium falciparum parasites.

  21985478   TNFA-863 polymorphism is associated with a reduced risk of chronic obstructive pulmonary disease: a replication study.

  22001640   Tumour necrosis factor gene polymorphisms and migraine: a systematic review and meta-analysis.

  22172537   A pilot study of host genetic variants associated with influenza-associated deaths among children and young adults.

  22190997   Characterization of Single-Nucleotide Polymorphisms in the Tumor Necrosis Factor α Promoter Region and in Lymphotoxin α in Squamous Intraepithelial Lesions, Precursors of Cervical Cancer.

  22363536   DRB1*03:01 haplotypes: differential contribution to multiple sclerosis risk and specific association with the presence of intrathecal IgM bands.

  22615793   Investigation of host candidate malaria-associated risk/protective SNPs in a Brazilian Amazonian population.

  22711844   SNP in the TNF-α gene promoter associated with Behçet's disease in Moroccan patients.

  22808100   Functional differences exist between TNFα promoters encoding the common -237G SNP and the rarer HLA-B*5701-linked A variant.

  22844404   Evidence of associations between cytokine genes and subjective reports of sleep disturbance in oncology patients and their family caregivers.

  22957039   Candidate polymorphisms and severe malaria in a Malian population.

  23049672   Top Three Pharmacogenomics and Personalized Medicine Applications at the Nexus of Renal Pathophysiology and Cardiovascular Medicine.

  23057767   Inflammatory gene variants and the risk of biliary tract cancers and stones: a population-based study in China.

  23119005   HLA and celiac disease susceptibility: new genetic factors bring open questions about the HLA influence and gene-dosage effects.

  23133455   TNF-α Polymorphisms in Juvenile Idiopathic Arthritis: Which Potential Clinical Implications?

  23144702   Candidate human genetic polymorphisms and severe malaria in a Tanzanian population.

  23148654   Pandemic influenza A/H1N1 virus infection and TNF, LTA, IL1B, IL6, IL8, and CCL polymorphisms in Mexican population: a case-control study.

  24151497   Analysis of the association of IL10, TNF-β and IL23R-IL12RB2 SNPs with the risk of Behçet's disease in Western Algeria.

  24502445   Cytokine candidate genes predict the development of secondary lymphedema following breast cancer surgery.

  25589894   High producing tumor necrosis factor alpha gene alleles in protection against severe manifestations of dengue.

  26088606   Tumour necrosis factor allele variants and their association with the occurrence and severity of malaria in African children: a longitudinal study.

  26448013   High Incidence of Malaria Along the Sino-Burmese Border Is Associated With Polymorphisms of CR1, IL-1A, IL-4R, IL-4, NOS, and TNF, But Not With G6PD Deficiency.

  26657940   TNF, IL6, and IL1B Polymorphisms Are Associated with Severe Influenza A (H1N1) Virus Infection in the Mexican Population.

  26791477   The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study.

  27417569   Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases.

  27616475   Gene variants as risk factors for gastroschisis.

  27713886   The role of genetics and antibodies in sepsis.

  29054398   Association of TNF-Alpha gene polymorphisms and susceptibility to hepatitis B virus infection in Egyptians.

  29373769   [Variants in the TNFA, IL6 and IFNG genes are associated with the dengue severity in a sample from Colombian population].

  29404828   Tumor necrosis factor (TNF) and TNFR1 polymorphisms are not risk factors for rheumatoid arthritis in a Mexican population.

  29497291   TNF promoter polymorphisms are associated with genetic susceptibility in COPD secondary to tobacco smoking and biomass burning.

  29611038   Tumor necrosis factor gene polymorphisms are associated with systemic lupus erythematosus susceptibility or lupus nephritis in Mexican patients.

  29940817   The Correlation Between TNF-α Promoter Gene Polymorphism and Genetic Susceptibility to Cervical Cancer.

  31354816   Polymorphisms in Adipokines in Mexican Children with Obesity.

  31373163   Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia.

  31936215   Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis.