Human Genome Epidemiology Literature Finder
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Query Trace: Tetralogy of Fallot and GATA4[original query] |
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GATA4 sequence variants in patients with congenital heart disease. Journal of medical genetics 2007 Dec 44 (12): 779-83. Tomita-Mitchell A, Maslen C L, Morris C D, Garg V, Goldmuntz |
GATA4 mutations in 486 Chinese patients with congenital heart disease. European journal of medical genetics 0 51 (6): 527-35. Zhang Weimin, Li Xiaofeng, Shen Adong, Jiao Weiwei, Guan Xiaolei, Li Zhongz |
Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects. Cardiology in the young 2009 Sep 19 (5): 482-5. Hamanoue Haruka, Rahayuningsih Sri Endah, Hirahara Yuya, Itoh Junko, Yokoyama Utako, Mizuguchi Takeshi, Saitsu Hirotomo, Miyake Noriko, Hirahara Fumiki, Matsumoto Naomic |
GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease. Chinese medical journal 2009 Feb 122 (4): 4. Zhang WM, Li XF, Ma ZY, Zhang J, Zhou SH, Li T, Shi L, Li ZZ |
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. Clinical genetics 2011 Aug 80 (2): 184-90. De Luca Alessandro, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici M L, Vergara P, De Zorzi A, Versacci P, Digilio M C, Marino B, Dallapiccola |
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease. Disease markers 2010 28 (5): 287-92. Guida Valentina, Lepri Francesca, Vijzelaar Raymon, De Zorzi Andrea, Versacci Paolo, Digilio Maria Cristina, Marino Bruno, De Luca Alessandro, Dallapiccola Bru |
A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect. Journal of human genetics 2010 Oct 55 (10): 662-7. Lin Xiaoping, Huo Zhaoxia, Liu Xingyuan, Zhang Yangyang, Li Li, Zhao Hong, Yan Biao, Liu Ying, Yang Yiqing, Chen Yi-H |
Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease. Genetica 2010 Dec 138 (11-12): 1231-40. Peng Ting, Wang Li, Zhou Shu-Feng, Li Xiaoti |
Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot. Pathology 2011 Jun 43 (4): 322-6. Wang Jian, Lu Yanan, Chen Huiwen, Yin Minzhi, Yu Tingting, Fu Qih |
Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease. Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 0 22 (2): 141-5. Xiong Fu, Li Qian, Zhang Cuimei, Chen Youming, Li Ping, Wei Xiaofeng, Li Qiang, Zhou Wanjun, Li Liang, Shang Xuan, Xu Xiangm |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects. American journal of medical genetics. Part A 2014 Feb 164A (2): 397-406. Osoegawa Kazutoyo, Iovannisci David M, Lin Bin, Parodi Christina, Schultz Kathleen, Shaw Gary M, Lammer Edward |
Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. American journal of medical genetics. Part A 2014 Dec 164A (12): 3100-7. Baban Anwar, Postma Alex Vincent, Marini Monica, Trocchio Gianluca, Santilli Antonella, Pelegrini Monica, Sirleto Pietro, Lerone Margherita, Albanese Sonia Bernadette, Barnett Phil, Boogerd Cornelis Job, Dallapiccola Bruno, Digilio Maria Cristina, Ravazzolo Roberto, Pongiglione Giaco |
Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4. PloS one 2014 9 (7): e102379. Zhang Wenwen, Shen Li, Deng Zhantao, Ding Yibing, Mo Xuming, Xu Zhengfeng, Gao Qian, Yi Lo |
A novel mutation of GATA4 (K300T) associated with familial atrial septal defect. Gene 2015 Sep . Chen Jia, Qi Bingyang, Zhao Juan, Liu Wei, Duan Ranhui, Zhang Mingq |
Identification of Copy Number Variations in Isolated Tetralogy of Fallot. Pediatric cardiology 2015 Jun . Aguayo-Gómez Adolfo, Arteaga-Vázquez Jazmín, Svyryd Yevgeniya, Calderón-Colmenero Juan, Zamora-González Carlos, Vargas-Alarcón Gilberto, Mutchinick Osvaldo |
c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. BMC medical genetics 2015 16 7. Mattapally Saidulu, Nizamuddin Sheikh, Murthy Kona Samba, Thangaraj Kumarasamy, Banerjee Sanjay |
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of human genetics 2015 Oct . Yoshida Akiko, Morisaki Hiroko, Nakaji Mai, Kitano Masataka, Kim Ki-Sung, Sagawa Koichi, Ishikawa Shiro, Satokata Ichiro, Mitani Yoshihide, Kato Hitoshi, Hamaoka Kenji, Echigo Shigeyuki, Shiraishi Isao, Morisaki Takayu |
Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot. Human mutation 2018 8 39 (12): 1957-1972. Dixit Ritu, Narasimhan Chitra, Balekundri Vijyalakshmi I, Agrawal Damyanti, Kumar Ashok, Mohapatra Bhagyalax |
The Functional Polymorphism R129W in the BVES Gene Is Associated with Sporadic Tetralogy of Fallot in the Han Chinese Population. Genetic testing and molecular biomarkers 2019 8 23 (9): 601-609. Shi Yan, Li Yongqing, Wang Yuequn, Zhuang Jian, Wang Heng, Hu Min, Mo Xiaoyang, Yue Shusheng, Chen Yu, Fan Xiongwei, Chen Jimei, Cai Wanwan, Zhu Xiaolan, Wan Yongqi, Zhong Ying, Ye Xiangli, Li Fang, Zhou Zuoqiong, Dai Guo, Luo Rong, Ocorr Karen, Jiang Zhigang, Li Xiaoping, Zhu Ping, Wu Xiushan, Yuan Wuzh |
Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population. DNA and cell biology 2019 Apr . Wang Enshi, Nie Yu, Fan Xuesong, Zheng Zhe, Hu Shengsh |
Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot. African health sciences 2019 2 18 (4): 922-930. El Bouchikhi Ihssane, Belhassan Khadija, Moufid Fatima Zohra, Houssaini Mohammed Iraqui, Bouguenouch Laila, Samri Imane, Bouhrim Mohamed, Ouldim Karim, Atmani Sam |
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. The Eurasian journal of medicine 2020 Oct 52 (3): 283-287. El Bouchikhi Ihssane, Bouguenouch Laila, Moufid Fatima Zohra, Belhassan Khadija, Samri Imane, Chaouti Amal, Houssaïni Mohammed Iraqui, Atmani Samir, Ouldim Kar |
Somatic GATA4 mutation contributes to tetralogy of Fallot. Experimental and therapeutic medicine 2024 1 27 (2): 91. Pradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, Xing-Yuan Liu, Jia-Ning Gu, Chen-Xi Yang, Ying-Jia Xu, Juan Wang, Yi-Qing Ya |
- Page last reviewed:Feb 1, 2024
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