1. A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect
   Yi-Meng Zhou et al, 2016, Molecular Medicine Reports CrossRef
2. Functional characterization of GATA6 genetic variants associated with mild congenital heart defects
   Haoran Wu et al, 2023, Biochemical and Biophysical Research Communications CrossRef
3. An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations
   Yan-Jie Li et al, 2017, Expert Review of Molecular Diagnostics CrossRef
4. GATA5 loss-of-function mutation in familial dilated cardiomyopathy
   XIAN-LING ZHANG et al, 2015, International Journal of Molecular Medicine CrossRef
5. TBX20 loss-of-function mutation contributes to double outlet right ventricle
   YUN PAN et al, 2015, International Journal of Molecular Medicine CrossRef
6. Peculiarities of alleles and genotypes distribution of genes CRELD1 and GATA6 in mothers of children with sporadic congenital heart diseases
   A. V. Shabaldin et al, 2018, Problemy reproduktsii CrossRef
7. Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block
   Ying-Jia Xu et al, 2017, Molecular Medicine Reports CrossRef
8. Evaluating High‐Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses
   Martin M. C. Chui et al, 2023, Journal of the American Heart Association CrossRef
9. Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa
   Nicholas Ekow Thomford et al, 2018, OMICS: A Journal of Integrative Biology CrossRef
10. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot
    CAI-XIA LU et al, 2016, International Journal of Molecular Medicine CrossRef
11. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population
    Enshi Wang et al, 2019, DNA and Cell Biology CrossRef
12. Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects
    Erge Zhang et al, 2018, Gene CrossRef
13. Unique functions of Gata4 in mouse liver induction and heart development
    Matthew J. Borok et al, 2016, Developmental Biology CrossRef
14. Novel mutation of GATA4 gene in Kurdish population of Iran with nonsyndromic congenital heart septals defects
    Fariborz Soheili et al, 2018, Congenital Heart Disease CrossRef
15. GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum
    Doris Škorić‐Milosavljević et al, 2019, American Journal of Medical Genetics Part A CrossRef
16. GATA transcription factors in development and disease
    Mathieu Tremblay et al, 2018, Development CrossRef
17. TBX1 loss‑of‑function mutation contributes to congenital conotruncal defects
    Min Zhang et al, 2017, Experimental and Therapeutic Medicine CrossRef
18. MESP1 loss-of-function mutation contributes to double outlet right ventricle
    Min Zhang et al, 2017, Molecular Medicine Reports CrossRef
19. Gene expression and transcriptional regulation driven by transcription factors involved in congenital heart defects
    Hira Mubeen et al, 2023, Irish Journal of Medical Science (1971 -) CrossRef
20. An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract
    Naoko Yamaguchi et al, 2023, Circulation CrossRef