Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and TBX20[original query] |
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| T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease. European journal of medical genetics 0 51 (6): 580-7. Liu Caixia, Shen Adong, Li Xiaofeng, Jiao Weiwei, Zhang Xingen, Li Zhongz |
| Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defects. Gene 2012 May 500 (1): 28-31. Qiao Yanli, Wanyan Hongxin, Xing Qining, Xie Wen, Pang Shuchao, Shan Jiping, Yan |
| Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates. Pediatric cardiology 2015 Apr 36 (4): 737-42. Chen Junhua, Sun Fuqiang, Fu Jia, Zhang Hongy |
A genome-wide association study of suicidal behavior.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct 168 (7): 557-63. Galfalvy Hanga, Haghighi Fatemeh, Hodgkinson Colin, Goldman David, Oquendo Maria A, Burke Ainsley, Huang Yung-Yu, Giegling Ina, Rujescu Dan, Bureau Alexandre, Turecki Gustavo, Mann J Jo |
| 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 |
| TBX20 loss-of-function mutation contributes to double outlet right ventricle. International journal of molecular medicine 2015 Apr 35 (4): 1058-66. Pan Yun, Geng Rui, Zhou Ning, Zheng Gui-Fen, Zhao Hong, Wang Juan, Zhao Cui-Mei, Qiu Xing-Biao, Yang Yi-Qing, Liu Xing-Yu |
| Relationship between TBX20 gene polymorphism and congenital heart disease. Genetics and molecular research : GMR 2016 Jun 15 (2): . Yang X F, Zhang Y F, Zhao C F, Liu M M, Si J P, Fang Y F, Xing W W, Wang F |
| Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy. International heart journal 2017 Jul . Xu Jia-Hong, Gu Jian-Yun, Guo Yu-Han, Zhang Hong, Qiu Xing-Biao, Li Ruo-Gu, Shi Hong-Yu, Liu Hua, Yang Xiao-Xiao, Xu Ying-Jia, Qu Xin-Kai, Yang Yi-Qi |
| Association Analysis of Nonsyndromic Congenital Heart Disease and Tag Single Nucleotide Polymorphisms of TBX20 and Genes in the Ras-MAPK Pathway. Genetic testing and molecular biomarkers 2017 Jul 21 (7): 440-444. Luo Zhiling, Shen Yan, Chen Wei, Ma Xuejuan, Liu Liping, Huang Xiaoqin, Yang Zhaoqing, Sun H |
| Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
| Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome. Journal of genetics 2019 6 98 (2): . Wang Enshi, Nie Yu, Fan Xuesong, Zheng Zhe, Gu Haiyong, Zhang Hao, Hu Shengsh |
| Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene. European journal of human genetics : EJHG 2019 3 27 (7): 1033-1043. Luyckx Ilse, Kumar Ajay A, Reyniers Edwin, Dekeyser Emily, Vanderstraeten Kathleen, Vandeweyer Geert, Wünnemann Florian, Preuss Christoph, Mazzella Jean-Michaël, Goudot Guillaume, Messas Emmanuel, Albuisson Juliette, Jeunemaitre Xavier, Eriksson Per, Mohamed Salah A, Kempers Marlies, Salemink Simone, Duijnhouwer Anthonie, Andelfinger Gregor, Dietz Harry C, Verstraeten Aline, Van Laer Lut, Loeys Bart L, |
| Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies. Balkan journal of medical genetics : BJMG 2021 Nov 24 (2): 39-47. Wang E, Fan X, Nie Y, Zheng Z, Hu |
| High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.
Nature genetics 2022 6 54 (6): 772-782. Tcheandjieu Catherine, Xiao Ke, Tejeda Helio, Lynch Julie A, Ruotsalainen Sanni, Bellomo Tiffany, Palnati Madhuri, Judy Renae, Klarin Derek, Kember Rachel L, Verma Shefali, , , , Palotie Aarno, Daly Mark, Ritchie Marylyn, Rader Daniel J, Rivas Manuel A, Assimes Themistocles, Tsao Philip, Damrauer Scott, Priest James |
| Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal defects: Correlation with cardiac troponin T and caspase-3. Gene 2023 7 882 147660. Mohamed Taha, Nourhan Awny, Somaia Ismail, Engy A Ashaat, Mahmoud A Senou |
| Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy. Diagnostics (Basel, Switzerland) 2023 1 13 (2): . Gu Jia-Ning, Yang Chen-Xi, Ding Yuan-Yuan, Qiao Qi, Di Ruo-Min, Sun Yu-Min, Wang Jun, Yang Ling, Xu Ying-Jia, Yang Yi-Qi |
| Genetic and functional variants of the TBX20 gene promoter in dilated cardiomyopathy. Molecular genetics & genomic medicine 2024 1 12 (1): e2355. Xue Gao, Shuchao Pang, Liangcai Ding, Han Yan, Yinghua Cui, Bo Y |
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