1. The rs599839 A>G Variant Disentangles Cardiovascular Risk and Hepatocellular Carcinoma in NAFLD Patients
    Marica Meroni et al, 2021, Cancers CrossRef
  2. Imaging modalities for congenital heart disease and genetic polymorphism associated with coronary artery and cardiovascular diseases
    Gowtham Kumar Subbaraj et al, 2023, Cardiovascular and Coronary Artery Imaging CrossRef
  3. Post-Transcriptional Regulation of Molecular Determinants during Cardiogenesis
    Estefania Lozano-Velasco et al, 2022, International Journal of Molecular Sciences CrossRef
  4. The Role of Transcription Factor 21 in Epicardial Cell Differentiation and the Development of Coronary Heart Disease
    Haochang Hu et al, 2020, Frontiers in Cell and Developmental Biology CrossRef
  5. LDL-receptor gene polymorphism as a predictor of coronary artery disease: an Egyptian pilot study: relation to lipid profile and angiographic findings
    Kefaya El-Sayed et al, 2024, The Egyptian Heart Journal CrossRef
  6. Variants in the SMARCA4 gene was associated with coronary heart disease susceptibility in Chinese han population
    Xuan Guo et al, 2017, Oncotarget CrossRef
  7. Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia
    Caitlin J. Smith et al, 2016, American Journal of Hypertension CrossRef
  8. A Systematically Assembled Signature of Genes to be Deep-Sequenced for Their Associations with the Blood Pressure Response to Exercise
    Linda S. Pescatello et al, 2019, Genes CrossRef
  9. A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death
    Thomas Svensson et al, 2017, PLOS ONE CrossRef
  10. Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next-generation sequencing data analysis
    Basavaraj Vastrad et al, 2024, Egyptian Journal of Medical Human Genetics CrossRef
  11. Impact and influence of “omics” technology on hyper tension studies
    Alzenira Costa et al, 2017, International Journal of Cardiology CrossRef
  12. TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population
    Liping Yang et al, 2017, Genetic Testing and Molecular Biomarkers CrossRef
  13. Possible role of intronic polymorphisms in the PHACTR1 gene on the development of cardiovascular disease
    José Manuel Rodríguez-Pérez et al, 2016, Medical Hypotheses CrossRef
  14. Evaluation of 17 genetic variants in association with leukemia in the north Indian population using MassARRAY Sequenom
    Amrita Bhat et al, 2021, Journal of Biochemical and Molecular Toxicology CrossRef
  15. CXCL12 promotes atherosclerosis by downregulating ABCA1 expression via the CXCR4/GSK3β/β-cateninT120/TCF21 pathway
    Jia-Hui Gao et al, 2019, Journal of Lipid Research CrossRef
  16. Transcription Factor 21: A Transcription Factor That Plays an Important Role in Cardiovascular Disease
    Yaqian Luo et al, 2024, Pharmacology CrossRef
  17. Haplotype-based genome-wide association studies for carcass and growth traits in chicken
    Hui Zhang et al, 2020, Poultry Science CrossRef
  18. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
    Jingjing Liang et al, 2017, PLOS Genetics CrossRef
  19. Tissue-Specific Variations in Transcription Factors Elucidate Complex Immune System Regulation
    Hengwei Lu et al, 2022, Genes CrossRef
  20. Genetic and clinical predictors of CD4 lymphocyte recovery during suppressive antiretroviral therapy: Whole exome sequencing and antiretroviral therapy response phenotypes
    Ruth Greenblatt et al, 2019, PLOS ONE CrossRef
  21. Association of genetic variants with atrial fibrillation
    YUICHIRO YAMASE et al, 2016, Biomedical Reports CrossRef
  22. Genetics of Coronary Disease
    Brian G. Kral et al, 2016, Translational Research in Coronary Artery Disease CrossRef
  23. A Study of Associations Between rs9349379 (PHACTR1), rs2891168 (CDKN2B-AS), rs11838776 (COL4A2) and rs4880 (SOD2) Polymorphic Variants and Coronary Artery Disease in Iranian Population
    Abolfazl Yari et al, 2022, Biochemical Genetics CrossRef
  24. The association between TCF21 rs12190287 polymorphism and cardiovascular diseases risk: The first meta-analysis
    Mohammad Sarowar Uddin et al, 2022, Human Gene CrossRef
  25. PHACTR1 genotype predicts coronary artery disease in patients with familial hypercholesterolemia
    Martine Paquette et al, 2018, Journal of Clinical Lipidology CrossRef
  26. Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis
    Rosa Giannina Castillo-Avila et al, 2023, Journal of Cardiovascular Development and Disease CrossRef
  27. Coronary artery disease associated gene Phactr1 modulates severity of vascular calcification in vitro
    Redouane Aherrahrou et al, 2017, Biochemical and Biophysical Research Communications CrossRef
  28. PHACTR1 Gene Polymorphism Is Associated with Increased Risk of Developing Premature Coronary Artery Disease in Mexican Population
    Nonanzit Pérez-Hernández et al, 2016, International Journal of Environmental Research and Public Health CrossRef
  29. TCF21: a critical transcription factor in health and cancer
    Xiang Ao et al, 2020, Journal of Molecular Medicine CrossRef
  30. Correlation of SMARCA4 rs1122608 and ZFHX3 rs2106261 polymorphisms with acute myocardial infarction susceptibility in Egyptian population
    Shaimaa Elsayed Ramadan Genena et al, 2023, Human Gene CrossRef
  31. Associations between PHACTR1 gene polymorphisms and pulse pressure in Chinese Han population
    Kunfang Gu et al, 2020, Bioscience Reports CrossRef
  32. Maternal rearing styles and loneliness: The moderating role of the COMT Val158Met polymorphism
    Wen Wei et al, 2023, Current Psychology CrossRef
  33. TCF21 is related to testis growth and development in broiler chickens
    Hui Zhang et al, 2017, Genetics Selection Evolution CrossRef
  34. Molecular mechanisms of coronary disease revealed using quantitative trait loci for TCF21 binding, chromatin accessibility, and chromosomal looping
    Quanyi Zhao et al, 2020, Genome Biology CrossRef
  35. The genetic polymorphisms of ZC3HC1 and SMARCA4 are associated with hypertension risk
    Huijun Ma et al, 2019, Molecular Genetics & Genomic Medicine CrossRef