These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
166 related articles for article (PubMed ID: 30152191)
1. Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot. Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B Hum Mutat; 2018 Dec; 39(12):1957-1972. PubMed ID: 30152191 [TBL] [Abstract][Full Text] [Related]
2. GATA4 loss-of-function mutations underlie familial tetralogy of fallot. Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169 [TBL] [Abstract][Full Text] [Related]
3. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692 [TBL] [Abstract][Full Text] [Related]
4. Congenital heart diseases and their association with the variant distribution features on susceptibility genes. Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723 [TBL] [Abstract][Full Text] [Related]
5. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot. Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287 [TBL] [Abstract][Full Text] [Related]
6. GATA4 sequence variants in patients with congenital heart disease. Tomita-Mitchell A; Maslen CL; Morris CD; Garg V; Goldmuntz E J Med Genet; 2007 Dec; 44(12):779-83. PubMed ID: 18055909 [TBL] [Abstract][Full Text] [Related]
7. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595 [TBL] [Abstract][Full Text] [Related]
8. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot. El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556 [TBL] [Abstract][Full Text] [Related]
9. c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. Mattapally S; Nizamuddin S; Murthy KS; Thangaraj K; Banerjee SK BMC Med Genet; 2015 Feb; 16():7. PubMed ID: 25928801 [TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. Nemer G; Fadlalah F; Usta J; Nemer M; Dbaibo G; Obeid M; Bitar F Hum Mutat; 2006 Mar; 27(3):293-4. PubMed ID: 16470721 [TBL] [Abstract][Full Text] [Related]
11. Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. Baban A; Postma AV; Marini M; Trocchio G; Santilli A; Pelegrini M; Sirleto P; Lerone M; Albanese SB; Barnett P; Boogerd CJ; Dallapiccola B; Digilio MC; Ravazzolo R; Pongiglione G Am J Med Genet A; 2014 Dec; 164A(12):3100-7. PubMed ID: 25263169 [TBL] [Abstract][Full Text] [Related]
12. GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease. Zhang WM; Li XF; Ma ZY; Zhang J; Zhou SH; Li T; Shi L; Li ZZ Chin Med J (Engl); 2009 Feb; 122(4):416-9. PubMed ID: 19302747 [TBL] [Abstract][Full Text] [Related]
13. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164 [TBL] [Abstract][Full Text] [Related]
14. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects. Hamanoue H; Rahayuningsih SE; Hirahara Y; Itoh J; Yokoyama U; Mizuguchi T; Saitsu H; Miyake N; Hirahara F; Matsumoto N Cardiol Young; 2009 Sep; 19(5):482-5. PubMed ID: 19678963 [TBL] [Abstract][Full Text] [Related]
15. The Functional Polymorphism R129W in the Shi Y; Li Y; Wang Y; Zhuang J; Wang H; Hu M; Mo X; Yue S; Chen Y; Fan X; Chen J; Cai W; Zhu X; Wan Y; Zhong Y; Ye X; Li F; Zhou Z; Dai G; Luo R; Ocorr K; Jiang Z; Li X; Zhu P; Wu X; Yuan W Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585 [No Abstract] [Full Text] [Related]
16. Identification and functional study of GATA4 gene regulatory variants in atrial septal defects. Fan D; Pang S; Chen J; Shan J; Cheng Q; Yan B BMC Cardiovasc Disord; 2021 Jun; 21(1):321. PubMed ID: 34193080 [TBL] [Abstract][Full Text] [Related]
17. Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease. Peng T; Wang L; Zhou SF; Li X Genetica; 2010 Dec; 138(11-12):1231-40. PubMed ID: 21110066 [TBL] [Abstract][Full Text] [Related]
18. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart. Esposito G; Butler TL; Blue GM; Cole AD; Sholler GF; Kirk EP; Grossfeld P; Perryman BM; Harvey RP; Winlaw DS Am J Med Genet A; 2011 Oct; 155A(10):2416-21. PubMed ID: 22043484 [TBL] [Abstract][Full Text] [Related]
19. Screening of 99 Danish patients with congenital heart disease for GATA4 mutations. Zhang L; Tümer Z; Jacobsen JR; Andersen PS; Tommerup N; Larsen LA Genet Test; 2006; 10(4):277-80. PubMed ID: 17253934 [TBL] [Abstract][Full Text] [Related]
20. Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5. Kinnunen S; Välimäki M; Tölli M; Wohlfahrt G; Darwich R; Komati H; Nemer M; Ruskoaho H PLoS One; 2015; 10(12):e0144145. PubMed ID: 26642209 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]