Pages that link to "Q28199426"

The following pages link to Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study (Q28199426):

Displaying 31 items.

• Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease (Q24649709) (← links)
• Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias (Q28731901) (← links)
• A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (Q29417111) (← links)
• The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies (Q33514659) (← links)
• Genome-wide association studies: progress and potential for drug discovery and development (Q33784699) (← links)
• Lack of an association between connexin-37, stromelysin-1, plasminogen activator-inhibitor type 1 and lymphotoxin-alpha genes and acute coronary syndrome in Czech Caucasians (Q34194254) (← links)
• Genomic approaches to coronary artery disease (Q34530017) (← links)
• Lack of association between LTA and LGALS2 polymorphisms and myocardial infarction in Japanese and Korean populations (Q34627081) (← links)
• Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants (Q34851773) (← links)
• Identifying the genotype behind the phenotype: a role model found in VKORC1 and its association with warfarin dosing (Q35037456) (← links)
• Tumor necrosis factor B (TNFB) genetic variants and its increased expression are associated with vitiligo susceptibility (Q35060678) (← links)
• Four genetic polymorphisms of lymphotoxin-alpha gene and cancer risk: a systematic review and meta-analysis (Q35070335) (← links)
• Role of TNF block genetic variants in HIV-associated sensory neuropathy in black Southern Africans (Q35079928) (← links)
• Polymorphisms of the LTA gene may contribute to the risk of myocardial infarction: a meta-analysis (Q35124031) (← links)
• Genetics of stress response and stress-related disorders (Q35236890) (← links)
• Genetic and genomic insights into the molecular basis of atherosclerosis (Q36155114) (← links)
• Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke (Q36839359) (← links)
• Molecular genetics of myocardial infarction (Q36843011) (← links)
• Calibration of credibility of agnostic genome-wide associations (Q37117080) (← links)
• Genetics of premature myocardial infarction (Q37167765) (← links)
• Genome-wide association studies: progress in identifying genetic biomarkers in common, complex diseases. (Q37280930) (← links)
• The involvement of multiple thrombogenic and atherogenic markers in premature coronary artery disease (Q37342485) (← links)
• Creating a genetic risk score for coronary artery disease (Q37441260) (← links)
• Susceptibility genes for coronary heart disease and myocardial infarction (Q37923933) (← links)
• The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions (Q38910344) (← links)
• Tumor necrosis factor and lymphotoxin-alpha polymorphisms and severe malaria in African populations (Q42111238) (← links)
• IL-1ra anti-inflammatory cytokine polymorphism is associated with risk of gastric cancer and chronic gastritis in a Brazilian population, but the TNF-β pro-inflammatory cytokine is not. (Q44962067) (← links)
• Association of LT-alpha Ala252Gly gene polymorphism and the genetic predisposition of coronary heart disease in Chinese (Q46051718) (← links)
• SNPs in BRAP associated with risk of myocardial infarction in Asian populations. (Q51836575) (← links)
• Lymphotoxin-α and galectin-2 SNPs are not associated with myocardial infarction in two different German populations (Q57251847) (← links)
• The exon 1–8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population (Q57611309) (← links)