Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and GATA6[original query] |
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| 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 |
| Identification of GATA6 sequence variants in patients with congenital heart defects. Pediatric research 2010 Oct 68 (4): 281-5. Maitra Meenakshi, Koenig Sara N, Srivastava Deepak, Garg Vi |
| A novel GATA6 mutation associated with congenital ventricular septal defect. International journal of molecular medicine 2012 Jun 29 (6): 1065-71. Zheng Gui-Fen, Wei Dong, Zhao Hong, Zhou Ning, Yang Yi-Qing, Liu Xing-Yu |
| 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 |
| Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot. International journal of molecular medicine 2013 Jan 31 (1): 1. Huang RT, Xue S, Xu YJ, Yang YQ |
| GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy. International journal of molecular medicine 2014 Nov 34 (5): 1315-22. Xu Lei, Zhao Lan, Yuan Fang, Jiang Wei-Feng, Liu Hua, Li Ruo-Gu, Xu Ying-Jia, Zhang Min, Fang Wei-Yi, Qu Xin-Kai, Yang Yi-Qing, Qiu Xing-Bi |
| Novel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects. International journal of molecular sciences 2014 15 (7): 12677-87. Li Chunyu, Li Xianke, Pang Shuchao, Chen Wei, Qin Xianyun, Huang Wenhui, Zeng Changqing, Yan |
| Two functional sequence variants of the GATA6 gene promoter in patients with indirect inguinal hernia. Gene 2014 Aug 547 (1): 86-90. Qiao Yuangang, Zhang Zhiping, Huang Wenhui, Pang Shuchao, Xing Qining, Yan |
| Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects. Molecular medicine reports 2014 Aug 10 (2): 743-8. Wang Xike, Ji Wei, Wang Jian, Zhao Pengjun, Guo Ying, Xu Rang, Chen Sun, Sun K |
| Genome, Exome, and Targeted Next-Generation Sequencing in Neonatal Diabetes. Pediatric clinics of North America 2015 Aug 62 (4): 1037-53. De Franco Elisa, Ellard Si |
| Integrated Genomic Analysis of Pancreatic Ductal Adenocarcinomas Reveals Genomic Rearrangement Events as Significant Drivers of Disease. Cancer research 2015 Dec . Murphy Stephen J, Hart Steven N, Halling Geoffrey, Johnson Sarah H, Smadbeck James B, Drucker Travis, Felipe Lima Joema, Rakhshan Rohakhtar Fariborz, Harris Faye R, Kosari Farhad, Subramanian Subbaya, Petersen Gloria M, Wiltshire Timothy D, Kipp Benjamin R, Truty Mark J, McWilliams Robert R, Couch Fergus J, Vasmatzis Geor |
| Lack of APC somatic mutation is associated with early-onset colorectal cancer in African Americans. Carcinogenesis 2018 Sep . Xicola Rosa M, Manojlovic Zarko, Augustus Gaius J, Kupfer Sonia S, Emmadi Rajyasree, Alagiozian-Angelova Victoria, Triche Tim, Salhia Bodour, Carpten John, Llor Xavier, Ellis Nathan |
| GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve. Gene 2018 4 663 115-120. Xu Ying-Jia, Di Ruo-Min, Qiao Qi, Li Xiu-Mei, Huang Ri-Tai, Xue Song, Liu Xing-Yuan, Wang Juan, Yang Yi-Qi |
| Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ?43% of 35 Families With Midaortic Syndrome. Hypertension (Dallas, Tex. : 1979) 2018 2 71 (4): 691-699. Warejko Jillian K, Schueler Markus, Vivante Asaf, Tan Weizhen, Daga Ankana, Lawson Jennifer A, Braun Daniela A, Shril Shirlee, Amann Kassaundra, Somers Michael J G, Rodig Nancy M, Baum Michelle A, Daouk Ghaleb, Traum Avram Z, Kim Heung Bae, Vakili Khashayar, Porras Diego, Lock James, Rivkin Michael J, Chaudry Gulraiz, Smoot Leslie B, Singh Michael N, Smith Edward R, Mane Shrikant M, Lifton Richard P, Stein Deborah R, Ferguson Michael A, Hildebrandt Friedhe |
| Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
| 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 |
| Genetic and Functional Variants Analysis of the GATA6 Gene Promoter in Acute Myocardial Infarction. Frontiers in genetics 2019 11 10 1100. Sun Zhaoqing, Pang Shuchao, Cui Yinghua, Yan |
| [Gene variant analysis of a child presented with neonatal diabetes and multiple organ malformations]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 12 37 (12): 1371-1375. Wu Jing, Meng Ge, Dou Binghua, Xu Yanlei, Cheng Xiuyong, Zhang Haohao, Zhang Ji |
| Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes. Journal of human genetics 2021 Sep . Williams Simon G, Byrne Dominic J F, Keavney Bernard |
| Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
| Molecular genetic study on GATA5 gene promoter in acute myocardial infarction. PloS one 2021 3 16 (3): e0248203. Song Zhipeng, Chen Lu, Pang Shuchao, Yan |
| Molecular Landscape and Prognostic Biomarker Analysis of Advanced Pancreatic Cancer and Predictors of Treatment Efficacy of AG Chemotherapy. Frontiers in oncology 2022 12 844527. Du Juan, Qiu Xin, Lu Changchang, Zhu Yahui, Kong Weiwei, Xu Mian, Zhang Xin, Tang Min, Chen Jun, Li Qi, Li Aimei, He Jian, Gu Qing, Wang Lei, Qiu Yudong, Liu Baor |
| Association of Angio-LncRNAs MIAT rs1061540/MALAT1 rs3200401 Molecular Variants with Gensini Score in Coronary Artery Disease Patients Undergoing Angiography. Biomolecules 2022 01 12 (1): . Elwazir Mohamed Y, Hussein Mohammad H, Toraih Eman A, Al Ageeli Essam, Esmaeel Safya E, Fawzy Manal S, Faisal Sal |
| Evaluating High-Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses. Journal of the American Heart Association 2023 2 12 (4): e028226. Chui Martin M C, Mak Christopher C Y, Yu Mullin H C, Wong Sandra Y Y, Lun Kin-Shing, Yung Tak-Cheung, Kwong Anna K Y, Chow Pak-Cheong, Chung Brian H |
| Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
- Page last reviewed:Feb 1, 2024
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