Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: GJA1[original query] |
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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 |
Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3. International journal of pediatric otorhinolaryngology 2013 Feb 77 (2): 189-93. Kooshavar Daniz, Tabatabaiefar Mohammad Amin, Farrokhi Effat, Abolhasani Marziye, Noori-Daloii Mohammad-Reza, Hashemzadeh-Chaleshtori Morte |
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 |
Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2015 Oct 272 (10): 2765-76. Beck Christopher, Pérez-Álvarez Jose Carmelo, Sigruener Alexander, Haubner Frank, Seidler Till, Aslanidis Charalampos, Strutz Jürgen, Schmitz Ge |
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 |
Mutations in MicroRNA Genes and Their Binding Sites are Infrequently Associated with Human Colorectal Cancer in the Kashmiri Population. MicroRNA (Sh?riqah, United Arab Emirates) 2014 2 (3): 219-24. Maqbool Raihana, Ismail Rehana, Hussain Mahboob- U |
In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes. Omics : a journal of integrative biology 2014 Jul 18 (7): 481-5. Bosch Jason, Lebeko Kamogelo, Nziale Jean Jacques Noubiap, Dandara Collet, Makubalo Nomlindo, Wonkam Ambroi |
No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2015 Jan 105 (1): 23-6. Wonkam A, Bosch J, Noubiap J J N, Lebeko K, Makubalo N, Dandara |
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.
PloS one 2015 10 (6): e0127791. Van Driest Sara L, McGregor Tracy L, Velez Edwards Digna R, Saville Ben R, Kitchner Terrie E, Hebbring Scott J, Brilliant Murray, Jouni Hayan, Kullo Iftikhar J, Creech C Buddy, Kannankeril Prince J, Vear Susan I, Brothers Kyle B, Bowton Erica A, Shaffer Christian M, Patel Neelam, Delaney Jessica T, Bradford Yuki, Wilson Sarah, Olson Lana M, Crawford Dana C, Potts Amy L, Ho Richard H, Roden Dan M, Denny Josh |
A novel truncation mutation in GJA1 associated with open angle glaucoma and microcornea in a large Chinese family. Eye (London, England) 2015 Jul 29 (7): 972-7. Huang X, Wang N, Xiao X, Li S, Zhang |
A known mutation in GJB6 in a large Chinese family with hidrotic ectodermal dysplasia. Journal of the European Academy of Dermatology and Venereology : JEADV 2016 May . Yang R, Hu Zl, Kong Qt, Li Ww, Zhang Ll, Du X, Huang Sy, Xia Xy, Sang |
GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population. Forensic science international 2016 Dec 270 178-182. Wu Qiuping, Wu Yeda, Zhang Liyong, Zheng Jinxiang, Tang Shuangbo, Cheng Jiandi |
Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.
Hypertension (Dallas, Tex. : 1979) 2017 Jan 69 (1): 51-59. Salvi Erika, Wang Zhiying, Rizzi Federica, Gong Yan, McDonough Caitrin W, Padmanabhan Sandosh, Hiltunen Timo P, Lanzani Chiara, Zaninello Roberta, Chittani Martina, Bailey Kent R, Sarin Antti-Pekka, Barcella Matteo, Melander Olle, Chapman Arlene B, Manunta Paolo, Kontula Kimmo K, Glorioso Nicola, Cusi Daniele, Dominiczak Anna F, Johnson Julie A, Barlassina Cristina, Boerwinkle Eric, Cooper-DeHoff Rhonda M, Turner Stephen |
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 |
A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation. The American journal of cardiology 2018 12 123 (5): 787-793. Mechakra Asma, Footz Tim, Walter Michael, Aránega Amelia, Hernández-Torres Francisco, Morel Elodie, Millat Gilles, Yang Yi-Qing, Chahine Mohamed, Chevalier Philippe, Christé Georg |
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia. Investigative ophthalmology & visual science 2018 1 59 (1): 338-348. Flitcroft D Ian, Loughman James, Wildsoet Christine F, Williams Cathy, Guggenheim Jeremy A, |
Genetics of heart rate in heart failure patients (GenHRate).
Human genomics 2019 May 13 (1): 22. Evans Kaleigh L, Wirtz Heidi S, Li Jia, She Ruicong, Maya Juan, Gui Hongsheng, Hamer Andrew, Depre Christophe, Lanfear David |
Functional variation of SLC52A3 rs13042395 predicts survival of Chinese gastric cancer patients. Journal of cellular and molecular medicine 2020 9 24 (21): 12550-12559. Qu Xiaofei, Cheng Lei, Zhao Liqin, Qiu Lixin, Guo Weiji |
GJA1 Gene Polymorphisms and Topographic Distribution of Cranial MRI Lesions in Cerebral Small Vessel Disease. Frontiers in neurology 2020 12 11 583974. Zhang Jing, You Qian, Shu Junlong, Gang Qiang, Jin Haiqiang, Yu Meng, Sun Wei, Zhang Wei, Huang Yini |
Association Between GJA1 rs13216675 T>C Polymorphism and Risk of Atrial Fibrillation: A Systematic Review and Meta-Analysis. Frontiers in cardiovascular medicine 2020 11 7 585268. Chen Xuejiao, Li Guowei, Zhang Junguo, Huang Xin, Ye Zebing, Zhao Yaho |
Impact of a Gap Junction Protein Alpha 4 Variant on Clinical Disease Phenotype in F508del Homozygous Patients With Cystic Fibrosis. Frontiers in genetics 2020 11 11 570403. Horn Tabea, Ludwig Michael, Eickmeier Olaf, Neerinex Anne H, Maitland-van der Zee Anke H, Smaczny Christina, Wagner Thomas O F, Schubert Ralf, Zielen Stefan, Majoor Christof, Bos Lieuwe D, Schmitt-Grohé Sabi |
Hypomyelinating leukodystrophies in adults: Clinical and genetic features. European journal of neurology 2020 11 28 (3): 934-944. Di Bella Daniela, Magri Stefania, Benzoni Chiara, Farina Laura, Maccagnano Carmelo, Sarto Elisa, Moscatelli Marco, Baratta Silvia, Ciano Claudia, Piacentini Sylvie H M J, Draghi Lara, Mauro Elena, Pareyson Davide, Gellera Cinzia, Taroni Franco, Salsano Etto |
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel, Switzerland) 2020 10 10 (11): . Adadey Samuel Mawuli, Wonkam-Tingang Edmond, Twumasi Aboagye Elvis, Nayo-Gyan Daniel Wonder, Boatemaa Ansong Maame, Quaye Osbourne, Awandare Gordon A, Wonkam Ambroi |
GJA1 rs2071165 A?>?G Variant Increased Gastric Cancer Risk in Females of Northwest China: A Case-Control Study. Journal of oncology 2021 2021 5556303. Yuan Lijuan, Yang Ping, Wei Gang, Lu Jianguo, Yang Zhengyu, Yang Lin, Peng Shujia, He Xianli, Bao Guoqia |
Heterozygous GJA1 variants with ocular phenotype: Missense in domain but truncation out of domain. Molecular vision 2021 5 27 309-322. Li Xueqing, Xiao Xueshan, Li Shiqiang, Ouyang Jiamin, Sun Wenmin, Liu Xing, Zhang Qingjio |
Minor allele of GJA1 gene polymorphism is associated with higher heart rate during atrial fibrillation. Scientific reports 2021 Jan 11 (1): 2549. Okamura Sho, Onohara Yuko, Ochi Hidenori, Tokuyama Takehito, Hironobe Naoya, Okubo Yosaku, Ikeuchi Yoshihiro, Miyauchi Shunsuke, Chayama Kazuaki, Kihara Yasuki, Nakano Yuki |
Identification of Cx43 variants predisposing to ventricular fibrillation in the acute phase of ST-elevation myocardial infarction. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 8 25 (1): 101-111. Chevalier Philippe, Moreau Adrien, Bessière Francis, Richard Sylvain, Chahine Mohamed, Millat Gilles, Morel Elodie, Paganelli Franck, Lesavre Nathalie, Placide Leslie, Montestruc François, Ankou Bénédicte, Puertas Rosa Doñate, Asatryan Babken, Delinière Antoine, |
GJA1 gene polymorphism is a genetic predictor of recurrence after pulmonary vein isolation in patients with paroxysmal atrial fibrillation. Heart rhythm 2022 Aug . Okamura Sho, Ochi Hidenori, Onohara Yuko, Nakashima Mika, Akiyama Rie, Tokuyama Takehito, Okubo Yousaku, Ikeuchi Yoshihiro, Miyauchi Shunsuke, Miyamoto Shogo, Oguri Naoto, Uotani Yukimi, Odake Yodo, Chayama Kazuaki, Kihara Yasuki, Nakano Yuki |
Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders. Pediatric dermatology 2022 7 39 (6): 903-907. Atzmony Lihi, Ugwu Nelson, Hamilton Claire, Paller Amy S, Zech Loren, Antaya Richard J, Choate Keith |
Connexin 43, Bcl-2, Bax, Ki67, and E-cadherin patterns in oral squamous cell carcinoma and its relationship with GJA1 rs12197797 C/G. Medicina oral, patologia oral y cirugia bucal 2022 Jul 27 (4): e366-e374. Segura I-G, Secchi D-G, Galíndez M-F, Carrica A, Bologna-Molina R, Brunotto M, Centeno V |
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- Page last updated:Apr 22, 2024
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