HuGE Literature Finder
Records 1-14
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Association of Cx43 rs2071166 polymorphism with an increased risk for atrial septal defect.
Cardiology in the young 2018 Mar 28 (3): 397-402. Gu Ruoyi, Sheng Wei, Ma Xiaojing, Huang Guoyi |
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Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.
Scientific reports 2018 Feb 8 (1): 3297. Wang Pengxia, Qin Weixi, Wang Pengyun, Huang Yufeng, Liu Ying, Zhang Rongfeng, Li Sisi, Yang Qin, Wang Xiaojing, Chen Feifei, Liu Jingqiu, Yang Bo, Cheng Xiang, Liao Yuhua, Wu Yanxia, Ke Tie, Tu Xin, Ren Xiang, Yang Yanzong, Xia Yunlong, Luo Xiaoping, Liu Mugen, Li He, Liu Jingyu, Xiao Yi, Chen Qiuyun, Xu Chengqi, Wang Qing |
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Association of connexin gene polymorphism with essential hypertension in Kazak and Han Chinese in Xinjiang, China.
Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2017 Apr 37 (2): 197-203. Wang Li-Jie, Zhang Wen-Wen, Zhang Liang, Shi Wen-Yan, Wang Ying-Zi, Ma Ke-Tao, Liu Wei-Dong, Zhao Lei, Li Li, Si Jun-Qia |
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Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease.
Gene 2016 Aug 588 (1): 86-94. Tong Yi-F |
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Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general population.
European journal of human genetics : EJHG 2015 Aug . Christensen Alex Hørby, Kamstrup Pia Rørbœk, Gandjbakhch Estelle, Benn Marianne, Jensen Jan Skov, Bundgaard Henning, Villard Eric, Tybjærg-Hansen An |
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Connexin40 abnormalities and atrial fibrillation in the human heart.
Journal of molecular and cellular cardiology 2014 Nov 76 159-68. Gemel Joanna, Levy Andrew E, Simon Adria R, Bennett Katherine B, Ai Xun, Akhter Shahab, Beyer Eric |
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Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.
Circulation 2014 Oct 130 (15): 1225-35. Sinner Moritz F, Tucker Nathan R, Lunetta Kathryn L, Ozaki Kouichi, Smith J Gustav, Trompet Stella, Bis Joshua C, Lin Honghuang, Chung Mina K, Nielsen Jonas B, Lubitz Steven A, Krijthe Bouwe P, Magnani Jared W, Ye Jiangchuan, Gollob Michael H, Tsunoda Tatsuhiko, Müller-Nurasyid Martina, Lichtner Peter, Peters Annette, Dolmatova Elena, Kubo Michiaki, Smith Jonathan D, Psaty Bruce M, Smith Nicholas L, Jukema J Wouter, Chasman Daniel I, Albert Christine M, Ebana Yusuke, Furukawa Tetsushi, Macfarlane Peter W, Harris Tamara B, Darbar Dawood, Dörr Marcus, Holst Anders G, Svendsen Jesper H, Hofman Albert, Uitterlinden Andre G, Gudnason Vilmundur, Isobe Mitsuaki, Malik Rainer, Dichgans Martin, Rosand Jonathan, Van Wagoner David R, , , Benjamin Emelia J, Milan David J, Melander Olle, Heckbert Susan R, Ford Ian, Liu Yongmei, Barnard John, Olesen Morten S, Stricker Bruno H C, Tanaka Toshihiro, Kääb Stefan, Ellinor Patrick |
Common genetic variation near the Connexin-43 gene is associated with resting heart rate in African Americans: A Genome-wide Association Study of 13,372 participants.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Nov . Deo R, Nalls MA, Avery CL, Gustav Smith J, Evans DS, Keller MF, Butler AM, Buxbaum SG, Guo Li P, Miguel Quibrera P, Smith EN, Tanaka T, Akylbekova EL, Alonso A, Arking DE, Benjamin EM, Berenson GS, Bis JC, Chen LY, Chen W, Cummings SR, Ellinor PT, Evans MK, Ferrucci L, Fox ER, Heckbert SR, Heiss G, Hsueh WC, Kerr KF, Limacher MC, Liu Y, Lubitz SA, Magnani JW, Mehra R, Marcus GM, Murray SS, Newman AB, Njajou O, North KE, Paltoo DN, Psaty BM, Redline SS, Reiner AP, Robinson JG, Rotter JI, Samdarshi TE, Schnabel RB, Schork NJ, Singleton AB, Siscovick D, Soliman EZ, Sotoodehnia N, Srinivasan SR, Taylor HA, Trevisan M, Zhang ZM, Zonderman AB, Newton-Cheh C, Whitsel EA |
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Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population.
Genomics & informatics 2012 Jun 10 (2): 2. Kim NH, Kim YJ, Oh JH, Cho YS |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.
International journal of cardiology 2010 Dec 145 (3): 487-9. Wang Binbin, Wen Qiaolian, Xie XiaoDong, Liu Shiguo, Liu Mugen, Tao You, Li Zhongzhi, Suo Peisu, Shen Adong, Wang Jing, Ma |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Mutations of connexin43 in fetuses with congenital heart malformations.
Chinese medical journal 2005 Jun 118 (12): 971-6. Chen Ping, Xie Li-jian, Huang Guo-ying, Zhao Xiao-qing, Chang C |
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Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).
Mutation research 2001 Aug 479 (1-2): 173-86. Dasgupta C, Martinez AM, Zuppan CW, Shah MM, Bailey LL, Fletcher WH |
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- Page last updated:Jan 16, 2020
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