Li Y, Du J, Deng S, Liu B, Jing X, Yan Y
Signal Transduct Target Ther. 2024; 9(1):368.
PMID: 39715759
PMC: 11666744.
DOI: 10.1038/s41392-024-02069-8.
Yang J, Wang Z, Zhou Y, Jiang S, Qin X, Xu Z
J Mol Med (Berl). 2024; 103(1):51-71.
PMID: 39528804
PMC: 11739230.
DOI: 10.1007/s00109-024-02492-y.
Prapa M, Ho S
Adv Exp Med Biol. 2024; 1441:761-775.
PMID: 38884747
DOI: 10.1007/978-3-031-44087-8_45.
Hernandez-Garcia A, Pendleton K, Kim S, Li Y, Kim B, Zaveri H
Hum Mol Genet. 2023; 32(13):2152-2161.
PMID: 37000005
PMC: 10281751.
DOI: 10.1093/hmg/ddad050.
Zhao R, Cao L, Gu W, Li L, Chen Z, Xiang J
Cell Rep Med. 2023; 4(3):100953.
PMID: 36809766
PMC: 10040382.
DOI: 10.1016/j.xcrm.2023.100953.
Genetics of congenital heart disease: a narrative review of recent advances and clinical implications.
Yasuhara J, Garg V
Transl Pediatr. 2021; 10(9):2366-2386.
PMID: 34733677
PMC: 8506053.
DOI: 10.21037/tp-21-297.
Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects.
Khatami M, Ghorbani S, Adriani M, Bahaloo S, Naeini M, Heidari M
Curr Med Sci. 2021; 42(1):129-143.
PMID: 34652630
DOI: 10.1007/s11596-021-2428-9.
Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs).
Lin H, McBride K, Garg V, Zhao M
Front Cell Dev Biol. 2021; 9:630069.
PMID: 33585486
PMC: 7873857.
DOI: 10.3389/fcell.2021.630069.
The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect.
Bu H, Sun G, Zhu Y, Yang Y, Tan Z, Zhao T
BMC Cardiovasc Disord. 2021; 21(1):12.
PMID: 33413087
PMC: 7788758.
DOI: 10.1186/s12872-020-01822-5.
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
El Bouchikhi I, Bouguenouch L, Moufid F, Belhassan K, Samri I, Chaouti A
Eurasian J Med. 2020; 52(3):283-287.
PMID: 33209082
PMC: 7651766.
DOI: 10.5152/eurasianjmed.2020.19237.
In Vivo and In Vitro Genetic Models of Congenital Heart Disease.
Majumdar U, Yasuhara J, Garg V
Cold Spring Harb Perspect Biol. 2019; 13(4).
PMID: 31818859
PMC: 7307584.
DOI: 10.1101/cshperspect.a036764.
Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated mutation.
LaHaye S, Majumdar U, Yasuhara J, Koenig S, Matos-Nieves A, Kumar R
Dis Model Mech. 2019; 12(6).
PMID: 31138536
PMC: 6602309.
DOI: 10.1242/dmm.036764.
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.
Pierpont M, Brueckner M, Chung W, Garg V, Lacro R, McGuire A
Circulation. 2018; 138(21):e653-e711.
PMID: 30571578
PMC: 6555769.
DOI: 10.1161/CIR.0000000000000606.
Gata4 potentiates second heart field proliferation and Hedgehog signaling for cardiac septation.
Zhou L, Liu J, Xiang M, Olson P, Guzzetta A, Zhang K
Proc Natl Acad Sci U S A. 2017; 114(8):E1422-E1431.
PMID: 28167794
PMC: 5338429.
DOI: 10.1073/pnas.1605137114.
c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.
Mattapally S, Nizamuddin S, Murthy K, Thangaraj K, Banerjee S
BMC Med Genet. 2015; 16:7.
PMID: 25928801
PMC: 4422155.
DOI: 10.1186/s12881-015-0152-7.
Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.
Prendiville T, Jay P, Pu W
Cold Spring Harb Perspect Med. 2014; 4(10).
PMID: 25274754
PMC: 4200204.
DOI: 10.1101/cshperspect.a013946.
Genetics of valvular heart disease.
LaHaye S, Lincoln J, Garg V
Curr Cardiol Rep. 2014; 16(6):487.
PMID: 24743897
PMC: 4531840.
DOI: 10.1007/s11886-014-0487-2.
Mutation spectrum of GATA4 associated with congenital atrial septal defects.
Yang Y, Wang J, Liu X, Chen X, Zhang W, Wang X
Arch Med Sci. 2014; 9(6):976-83.
PMID: 24482639
PMC: 3902718.
DOI: 10.5114/aoms.2013.39788.
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.
Muiya N, Wakil S, Tahir A, Hagos S, Najai M, Gueco D
Hum Genomics. 2013; 7:25.
PMID: 24330461
PMC: 3899629.
DOI: 10.1186/1479-7364-7-25.
Identification of functional mutations in GATA4 in patients with congenital heart disease.
Wang E, Sun S, Qiao B, Duan W, Huang G, An Y
PLoS One. 2013; 8(4):e62138.
PMID: 23626780
PMC: 3633926.
DOI: 10.1371/journal.pone.0062138.