Pages that link to "Q36843011"

The following pages link to Molecular genetics of myocardial infarction (Q36843011):

Displaying 15 items.

• Cardiovascular genomics (Q26995980) (← links)
• Identification of STXBP2 as a novel susceptibility locus for myocardial infarction in Japanese individuals by an exome-wide association study (Q33779544) (← links)
• The association between variants on chromosome 9p21 and inflammatory biomarkers in ethnically diverse women with coronary heart disease: a pilot study (Q33986857) (← links)
• Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis (Q34170897) (← links)
• Glutathione S-transferase M1 (GSTM1) null genotype and coronary artery disease risk: a meta-analysis. (Q34547917) (← links)
• MiRNA and TF co-regulatory network analysis for the pathology and recurrence of myocardial infarction (Q35386890) (← links)
• Prothrombotic gene variants as risk factors of acute myocardial infarction in young women (Q36527065) (← links)
• Lack of association of chromosome 9p21.3 genotype with cardiovascular structure and function in persons with stable coronary artery disease: The Heart and Soul Study (Q37279049) (← links)
• The logic of the hepatic methionine metabolic cycle (Q37456645) (← links)
• A multiclass likelihood ratio approach for genetic risk prediction allowing for phenotypic heterogeneity (Q37566380) (← links)
• Predictive genetic testing for coronary artery disease (Q37643740) (← links)
• Translating genomic analyses into improved management of coronary artery disease (Q37770573) (← links)
• Bioinformatic screening for key miRNAs and genes associated with myocardial infarction. (Q55383851) (← links)
• Variants in MEF2A gene in relation with coronary artery disease in Saudi population (Q89376625) (← links)
• Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis (Q99400049) (← links)