Pages that link to "Q37348739"
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The following pages link to Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population (Q37348739):
Displaying 32 items.
- Genetic polymorphisms in ZFHX3 are associated with atrial fibrillation in a Chinese Han population (Q33830921) (← links)
- Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans (Q34182560) (← links)
- Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study (Q34297198) (← links)
- The role of transcription factors in atrial fibrillation (Q35062042) (← links)
- Global epidemiology of atrial fibrillation (Q35223184) (← links)
- Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons (Q35674988) (← links)
- Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation (Q35743953) (← links)
- Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population (Q36141457) (← links)
- Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success (Q36141607) (← links)
- Heterozygous deletion of Atbf1 by the Cre-loxP system in mice causes preweaning mortality (Q36237302) (← links)
- Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction (Q36609517) (← links)
- Association of Small-Conductance Calcium-Activated Potassium Channels and Atrial Fibrillation - How Far Have We Gone? (Q36721250) (← links)
- Polymorphism rs2200733 at chromosome 4q25 is associated with atrial fibrillation recurrence after radiofrequency catheter ablation in the Chinese Han population (Q36841224) (← links)
- Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis (Q37148981) (← links)
- Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease. (Q37633533) (← links)
- Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations (Q37680345) (← links)
- BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3. (Q37705173) (← links)
- Common variants for atrial fibrillation: results from genome-wide association studies (Q37898563) (← links)
- Looking into a conceptual framework of ROS-miRNA-atrial fibrillation (Q38272306) (← links)
- A complex insertion/deletion polymorphism in the compositionally biased region of the ZFHX3 gene in patients with coronary heart disease in a Chinese population. (Q38979971) (← links)
- Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci (Q40220287) (← links)
- De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia (Q41628411) (← links)
- Ethnic differences in atrial fibrillation identified using implanted cardiac devices. (Q45001870) (← links)
- Lack of association between the APLNR variant rs9943582 with ischemic stroke in the Chinese Han GeneID population (Q47161538) (← links)
- Present Status and Future Challenges of New Therapeutic Targets in Preclinical Models of Stroke in Aged Animals with/without Comorbidities (Q47712203) (← links)
- Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation (Q49830787) (← links)
- Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke. (Q52368614) (← links)
- Integrative Analysis Reveals Key Circular RNA in Atrial Fibrillation (Q64228721) (← links)
- Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia (Q90291333) (← links)
- Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation (Q92033377) (← links)
- Altered DNA methylation in children born to mothers with rheumatoid arthritis during pregnancy (Q92380102) (← links)
- Association between gene variants and the recurrence of atrial fibrillation: An updated meta-analysis (Q92559555) (← links)