Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 67 Records) |
| Query Trace: Disease and GATA4[original query] |
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| Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis. Frontiers in physiology 2017 8 612. Giusti Betti, Sticchi Elena, De Cario Rosina, Magi Alberto, Nistri Stefano, Pepe Guglielmi |
| Identification of intronic-splice site mutations in GATA4 gene in Indian patients with congenital heart disease. Mutation research 2017 8 803-805 26-34. Bose Divya, D Vaigundan, Shetty Mitesh, J Krishnappa, Kutty A V |
| 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 |
| Associations of GATA4 genetic mutations with the risk of congenital heart disease: A meta-analysis. Medicine 2017 May 96 (18): e6857. Zhang Yanwei, Ai Feng, Zheng Jiayong, Peng Bangti |
| Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease. Pediatric cardiology 2018 8 40 (1): 17-22. Yin Jie, Qian Jianhua, Dai Genyin, Wang Chunli, Qin Yuming, Xu Ting, Li Zewei, Zhang Han, Yang Shiw |
| [Association of single nucleotide polymorphisms of transcription factors with congenital heart diseases in the Chinese population: a Meta analysis]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2018 7 20 (6): 490-496. Chen Le-Tao, Yang Tu-Bao, Wang Ting-Ting, Zheng Zan, Zhao Li-Juan, Ye Zi-Wei, Zhang Sen-Mao, Qin Jia- |
| Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing. Prenatal diagnosis 2018 Jul . Kammoun Molka, Souche Erika, Brady Paul, Ding Jia, Cosemans Nele, Gratacos Eduard, Devriendt Koen, Eixarch Elisenda, Deprest Jan, Vermeesch Joris Robe |
| 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 |
| Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease. Pediatric cardiology 2018 Jan . Pulignani Silvia, Vecoli Cecilia, Borghini Andrea, Foffa Ilenia, Ait-Alì Lamia, Andreassi Maria Graz |
| 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 |
| Functional genetic variants of the GATA4 gene promoter in acute myocardial infarction. Molecular medicine reports 2019 Jan . Chen Jing, Wang Shuai, Pang Shuchao, Cui Yinghua, Yan Bo, Hawley Robert |
| Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease. Molecular genetics & genomic medicine 2020 Aug e1406. Musfee Fadi I, Guo Dongchuan, Pinard Amélie C, Hostetler Ellen M, Blue Elizabeth E, Nickerson Deborah A, , Bamshad Michael J, Milewicz Dianna M, Prakash Siddharth |
| 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 |
| Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency. PloS one 2020 10 15 (10): e0240795. França Monica M, Funari Mariana F A, Lerario Antonio M, Santos Mariza G, Nishi Mirian Y, Domenice Sorahia, Moraes Daniela R, Costalonga Everlayny F, Maciel Gustavo A R, Maciel-Guerra Andrea T, Guerra-Junior Gil, Mendonca Berenice |
| Association of NFKB1, NKX2-5, GATA4 and RANKL Gene Polymorphisms with Sporadic Congenital Heart Disease in Greek Patients. Balkan journal of medical genetics : BJMG 2021 8 24 (1): 15-20. Aidinidou L, Chatzikyriakidou A, Giannopoulos A, Karpa V, Tzimou I, Aidinidou E, Fidani |
| 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 |
| Identification and functional study of GATA4 gene regulatory variants in atrial septal defects. BMC cardiovascular disorders 2021 7 21 (1): 321. Fan Dongchen, Pang Shuchao, Chen Jing, Shan Jiping, Cheng Qianjin, Yan |
| Identification and functional study of GATA4 gene regulatory variants in type 2 diabetes mellitus. BMC endocrine disorders 2021 4 21 (1): 73. Ding Liangcai, Cai Mengdi, Chen Lu, Yan Han, Lu Shicheng, Pang Shuchao, Yan |
| 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 |
| Implication of rare genetic variants of NODAL and ACVR1B in congenital heart disease patients from Indian population. Experimental cell research 2021 10 409 (1): 112869. Yadav Manohar Lal, Ranjan Prashant, Das Parimal, Jain Dharmendra, Kumar Ashok, Mohapatra Bhagyalax |
| Molecular profiles of response to neoadjuvant chemoradiotherapy in oesophageal cancers to develop personalized treatment strategies. Molecular oncology 2021 Jan . de Klerk Leonie K, Goedegebuure Ruben S A, van Grieken Nicole C T, van Sandick Johanna W, Cats Annemieke, Stiekema Jurrien, van der Kaaij Rosa T, Farina Sarasqueta Arantza, van Engeland Manon, Jacobs Maarten A J M, van Wanrooij Roy L J, van der Peet Donald L, Thorner Aaron R, Verheul Henk M W, Thijssen Victor L J L, Bass Adam J, Derks Sar |
| Pathological and Comprehensive Genetic Investigation of Autopsy Cases of Idiopathic Bradyarrhythmia. Circulation journal : official journal of the Japanese Circulation Society 2022 9 87 (1): 111-119. Hata Yukiko, Ichimata Shojiro, Hirono Keiichi, Yamaguchi Yoshiaki, Oku Yuko, Ichida Fukiko, Nishida Nao |
Elucidation of the genetic causes of bicuspid aortic valve disease.
Cardiovascular research 2022 Jun . Gehlen Jan, Stundl Anja, Debiec Radoslaw, Fontana Federica, Krane Markus, Sharipova Dinara, Nelson Christopher P, Al-Kassou Baravan, Giel Ann Sophie, Sinning Jan Malte, Bruenger Christopher Mh, Zelck Carolin F, Koebbe Laura L, Braund Peter S, Webb Thomas R, Hetherington Simon, Ensminger Stephan, Fujita Buntaro, Mohamed Salah A, Shrestha Malakh, Krueger Heike, Siepe Matthias, Kari Fabian Alexander, Nordbeck Peter, Buravezky Larissa, Kelm Malte, Veulemans Verena, Adam Matti, Baldus Stephan, Laugwitz Karl Ludwig, Haas Yannick, Karck Matthias, Mehlhorn Uwe, Conzelmann Lars Oliver, Breitenbach Ingo, Lebherz Corinna, Urbanski Paul, Kim Won Keun, Kandels Joscha, Ellinghaus David, Nowak-Goettl Ulrike, Hoffmann Per, Wirth Felix, Doppler Stefanie, Lahm Harald, Dreßen Martina, von Scheidt Moritz, Knoll Katharina, Kessler Thorsten, Hengstenberg Christian, Schunkert Heribert, Nickenig Georg, Nöthen Markus M, Bolger Aidan P, Abdelilah-Seyfried Salim, Samani Nilesh J, Erdmann Jeanette, Trenkwalder Teresa, Schumacher Johann |
| MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations. BMC cardiovascular disorders 2022 6 22 (1): 278. Lin Li-Rong, Hu Xue-Qun, Lu Li-Hong, Dai Jia-Zhen, Lin Ning-Ning, Wang Re-Hua, Xie Zhang-Xin, Chen Xue-M |
| Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510. Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl |
| Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve. medRxiv : the preprint server for health sciences 2023 11 . Steven G Carlisle, Hasan Albasha, Hector Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dong-Chuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Kim L McBride, , , Dianna M Milewicz, Simon C Body, Siddharth K Praka |
| Relationships between Maternal Folic Acid Supplementation and GATA4 Gene Polymorphisms in Patients with Non-Chromosomal Congenital Heart Disease: A Hospital-Based Case-Control Study in China. Nutrients 2023 10 15 (20): . Letao Chen, Tubao Yang, Tingting Wang, Mengting Sun, Jiabi Q |
| Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve. PloS one 2024 9 19 (9): e0304514. Steven G Carlisle, Hasan Albasha, Hector I Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Kim L McBride, Dianna M Milewicz, Simon C Body, Siddharth K Prakash, , |
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