Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 75 Records) |
Query Trace: TBX5[original query] |
---|
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 |
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature genetics 2018 Jul . Nielsen Jonas B, Thorolfsdottir Rosa B, Fritsche Lars G, Zhou Wei, Skov Morten W, Graham Sarah E, Herron Todd J, McCarthy Shane, Schmidt Ellen M, Sveinbjornsson Gardar, Surakka Ida, Mathis Michael R, Yamazaki Masatoshi, Crawford Ryan D, Gabrielsen Maiken E, Skogholt Anne Heidi, Holmen Oddgeir L, Lin Maoxuan, Wolford Brooke N, Dey Rounak, Dalen Håvard, Sulem Patrick, Chung Jonathan H, Backman Joshua D, Arnar David O, Thorsteinsdottir Unnur, Baras Aris, O'Dushlaine Colm, Holst Anders G, Wen Xiaoquan, Hornsby Whitney, Dewey Frederick E, Boehnke Michael, Kheterpal Sachin, Mukherjee Bhramar, Lee Seunggeun, Kang Hyun M, Holm Hilma, Kitzman Jacob, Shavit Jordan A, Jalife José, Brummett Chad M, Teslovich Tanya M, Carey David J, Gudbjartsson Daniel F, Stefansson Kari, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
[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 |
Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects. Journal of cardiovascular and thoracic research 2018 5 10 (1): 41-45. Khatami Mehri, Heidari Mohammad Mehdi, Kazeminasab Fatemeh, Zare Bidaki Razi |
[Association of single nucleotide polymorphisms of TBX5 gene and environmental exposure index with susceptibility to oral cancer]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2019 5 53 (5): 480-485. Bao X D, Lin L S, Chen F, Liu F Q, Wang J, Shi B, Yan L J, Wu J F, Lin L K, Wang R, Pan L Z, Zheng X Y, Qiu Y, Cao R K, Hu Z J, Cai L, He B |
Exploring the interaction between FGF Genes and T-box genes among chinese nonsyndromic cleft lip with or without cleft palate case-parent trios. Environmental and molecular mutagenesis 2019 Mar . Li Wenyong, Wang Mengying, Zhou Ren, Wang Siyue, Zheng Hongchen, Liu Dongjing, Zhou Zhibo, Zhu Hongping, Wu Tao, Beaty Terri |
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 |
SNP located in an AluJb repeat downstream of TMCO1, rs4657473, is protective for POAG in African Americans. The British journal of ophthalmology 2019 Mar . Verkuil Lana, Danford Ian, Pistilli Maxwell, Collins David W, Gudiseva Harini V, Trachtman Ben T, He Jie, Rathi Sonika, Haider Naqi, Ying Gui-Shuang, Chavali Venkata R M, O'Brien Joan Mar |
Identification and functional analysis of genetic variants in TBX5 gene promoter in patients with acute myocardial infarction. BMC cardiovascular disorders 2019 11 19 (1): 265. Wang Shuai, Zhang Jie, He Xiaohui, Zhang Yexin, Chen Jing, Su Qiang, Pang Shuchao, Zhang Shufang, Cui Yinghua, Yan |
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and precision medicine 2020 8 13 (5): 387-395. Weng Lu-Chen, Hall Amelia Weber, Choi Seung Hoan, Jurgens Sean J, Haessler Jeffrey, Bihlmeyer Nathan A, Grarup Niels, Lin Honghuang, Teumer Alexander, Li-Gao Ruifang, Yao Jie, Guo Xiuqing, Brody Jennifer A, Müller-Nurasyid Martina, Schramm Katharina, Verweij Niek, van den Berg Marten E, van Setten Jessica, Isaacs Aaron, Ramírez Julia, Warren Helen R, Padmanabhan Sandosh, Kors Jan A, de Boer Rudolf A, van der Meer Peter, Sinner Moritz F, Waldenberger Melanie, Psaty Bruce M, Taylor Kent D, Völker Uwe, Kanters Jørgen K, Li Man, Alonso Alvaro, Perez Marco V, Vaartjes Ilonca, Bots Michiel L, Huang Paul L, Heckbert Susan R, Lin Henry J, Kornej Jelena, Munroe Patricia B, van Duijn Cornelia M, Asselbergs Folkert W, Stricker Bruno H, van der Harst Pim, Kääb Stefan, Peters Annette, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Dörr Marcus, Felix Stephan B, Linneberg Allan, Hansen Torben, Arking Dan E, Kooperberg Charles, Benjamin Emelia J, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven |
ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block. International heart journal 2020 7 61 (4): 761-768. Zhang Yan, Sun Yu-Min, Xu Ying-Jia, Zhao Cui-Mei, Yuan Fang, Guo Xiao-Juan, Guo Yu-Han, Yang Chen-Xi, Gu Jia-Ning, Qiao Qi, Wang Jun, Yang Yi-Qi |
Identification and analysis of KLF13 variants in patients with congenital heart disease. BMC medical genetics 2020 4 21 (1): 78. Li Wenjuan, Li Baolei, Li Tingting, Zhang Ergeng, Wang Qingjie, Chen Sun, Sun K |
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death. American journal of medical genetics. Part A 2020 12 185 (3): 923-929. Markunas Alexandra M, Manivannan Perathu K R, Ezekian Jordan E, Agarwal Agnim, Eisner William, Alsina Katherina, Allen Hugh D, Wray Gregory A, Kim Jeffrey J, Wehrens Xander H T, Landstrom Andrew |
The Effects of Single Nucleotide Polymorphisms in Korean Patients with Early-onset Atrial Fibrillation after Catheter Ablation. Journal of Korean medical science 2020 Dec 35 (49): e411. Park Yae Min, Roh Seung Young, Lee Dae In, Shim Jaemin, Choi Jong Il, Park Sang Weon, Kim Young Ho |
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve. Genetics and molecular biology 2020 12 43 (4): e20200142. Jiang Wei-Feng, Xu Ying-Jia, Zhao Cui-Mei, Wang Xin-Hua, Qiu Xing-Biao, Liu Xu, Wu Shao-Hui, Yang Yi-Qi |
USF3 modulates osteoporosis risk by targeting WNT16, RANKL, RUNX2, and two GWAS lead SNPs rs2908007 and rs4531631. Human mutation 2020 10 42 (1): 37-49. Ye Weiyuan, Wang Ya, Hou Sasa, Mei Bing, Liu Xinhong, Huang Han, Zhou Qian, Niu Yajing, Chen Yuanyuan, Zhang Manling, Huang Qingya |
Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative. Female pelvic medicine & reconstructive surgery 2021 May . Cox Caroline K, Pandit Anita, Zawistowski Matthew, Dutta Diptavo, Narla Goutham, Swenson Carolyn |
Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2021 5 85 (9): 1469-1478. Nguyen Thuy Vy, Tran Vu Minh Thu, Do Thi Nam Phuong, Tran Thi Huynh Nga, Do Thi Hao, Nguyen Thi My Hanh, Tran Huynh Bao Nam, Le Lan Anh, Nguyen Pham Ngoc Thieu, Nguyen Thi Dieu Ai, Nguyen Thi My Nuong, Le Ngoc Hong Phuong, Pham Nguyen Vinh, Ho Huynh Thuy Duo |
The Classification of VACTERL Association into 3 Groups According to the Limb Defect. Plastic and reconstructive surgery. Global open 2021 3 9 (2): e3360. Al-Qattan Mohammad |
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients. Anatolian journal of cardiology 2021 02 25 (2): 129-138. Ulus Taner, Dural Muhammet, Me?e Pelin, Yetmi? Furkan, Mert Kadir U?ur, Görenek Bülent, Çilingir O?uz, Erzurumluoglu Gökalp Ebru, Arslan Serap, Artan Sevilhan, Aykaç Özlem, Çolak Ertu?rul, Yorgun Hikmet, Canpolat U?ur, Aytemir Kudr |
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 |
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population. Italian journal of pediatrics 2022 7 48 (1): 124. Sarwar Sumbal, Shabana , Tahir Amna, Liaqat Zainab, Naseer Saher, Seme Rani Summeya, Mehmood Sabahat, Shahid Saleem Ullah, Hasnain Shahi |
Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves.
eLife 2022 9 11 . Chan Melanie M Y, Sadeghi-Alavijeh Omid, Lopes Filipa M, Hilger Alina C, Stanescu Horia C, Voinescu Catalin D, Beaman Glenda M, Newman William G, Zaniew Marcin, Weber Stefanie, Ho Yee Mang, Connolly John O, Wood Dan, Maj Carlo, Stuckey Alexander, Kousathanas Athanasios, , Kleta Robert, Woolf Adrian S, Bockenhauer Detlef, Levine Adam P, Gale Daniel |
Prioritizing Cardiovascular Disease-Associated Variants Altering NKX2-5 Binding through an Integrative Computational Approach. medRxiv : the preprint server for health sciences 2023 9 . Edwin G Peña-Martínez, Diego A Pomales-Matos, Alejandro Rivera-Madera, Jean L Messon-Bird, Joshua G Medina-Feliciano, Leandro Sanabria-Alberto, Adriana C Barreiro-Rosario, Jessica M Rodriguez-Rios, José A Rodríguez-Martín |
Genetic Risk Score Constructed from Polymorphisms in the VEGFA, TBX5, and SMAD7 Genes Provides Novel Insights into the Molecular Mechanisms of the Tetralogy of Fallot and Ventricular Septal Defect (Case-Control Study from the Pakistani Population). The American journal of cardiology 2023 7 203 368-375. Sana Ashiq, Muhammad Farooq Sabar, Syed Najam Hyd |
TBX5 Variants are Associated with Susceptibility to and the Incidence of Liver Cirrhosis and Hepatocellular Carcinoma in the Chinese Population: A Multicenter and Follow-Up Study. Infection and drug resistance 2023 5 16 2653-2665. JinJian Yao, Xiaochun Mao, Qigang Sun, Biao Wu, Weiling Yu, Yanjing Huang, Shuai Luo, Jia Zeng, Jusheng L |
Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs). BMC pediatrics 2023 2 23 (1): 67. Sarwar Sumbal, Shabana , Sajjad Khadija, Hasnain Shahi |
A genome-wide and candidate gene association study of preterm birth in Korean pregnant women. PloS one 2023 11 18 (11): e0294948. Young Min Hur, Jae Young Yoo, Young Ah You, Sunwha Park, Soo Min Kim, Gain Lee, Young Ju K |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: