HuGE Literature Finder
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| Genetic insight into sick sinus syndrome. European heart journal 2021 May 42 (20): 1959-1971. Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Genetic insight into sick sinus syndrome.
European heart journal 2021 Feb . Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, , Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
| 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, Mese Pelin, Yetmis Furkan, Mert Kadir Ugur, Görenek Bülent, Çilingir Oguz, Erzurumluoglu Gökalp Ebru, Arslan Serap, Artan Sevilhan, Aykaç Özlem, Çolak Ertugrul, Yorgun Hikmet, Canpolat Ugur, Aytemir Kudr |
| [Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2018 Jun 43 (6): 594-603. Wang Xu, Nie Yali, Ning Shuwei, Shi Yong, Zhao Yujie, Niu Siquan, Guo Chengxian, Meng Xiangguang, Yuan Yiqia |
| Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in physiology 2018 9 894. Andreasen Laura, Ghouse Jonas, Skov Morten W, Have Christian T, Ahlberg Gustav, Rasmussen Peter V, Linneberg Allan, Pedersen Oluf, Platonov Pyotr G, Haunsø Stig, Svendsen Jesper H, Hansen Torben, Kanters Jørgen K, Olesen Morten |
| Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.
Circulation. Cardiovascular genetics 2017 Aug 10 (4): . Christophersen Ingrid E, Magnani Jared W, Yin Xiaoyan, Barnard John, Weng Lu-Chen, Arking Dan E, Niemeijer Maartje N, Lubitz Steven A, Avery Christy L, Duan Qing, Felix Stephan B, Bis Joshua C, Kerr Kathleen F, Isaacs Aaron, Müller-Nurasyid Martina, Müller Christian, North Kari E, Reiner Alex P, Tinker Lesley F, Kors Jan A, Teumer Alexander, Petersmann Astrid, Sinner Moritz F, Buzkova Petra, Smith Jonathan D, Van Wagoner David R, Völker Uwe, Waldenberger Melanie, Peters Annette, Meitinger Thomas, Limacher Marian C, Wilhelmsen Kirk C, Psaty Bruce M, Hofman Albert, Uitterlinden Andre, Krijthe Bouwe P, Zhang Zhu-Ming, Schnabel Renate B, Kääb Stefan, van Duijn Cornelia, Rotter Jerome I, Sotoodehnia Nona, Dörr Marcus, Li Yun, Chung Mina K, Soliman Elsayed Z, Alonso Alvaro, Whitsel Eric A, Stricker Bruno H, Benjamin Emelia J, Heckbert Susan R, Ellinor Patrick |
| Association of SCN10A Polymorphisms with the Recurrence of Atrial Fibrillation after Catheter Ablation in a Chinese Han Population. Scientific reports 2017 Mar 7 44003. Wu Haiqing, Xu Juan, Chen Songwen, Zhou Genqing, Qi Baozhen, Wei Yong, Hu En, Tang Dongdong, Chen Gang, Li Hongli, Zhao Liqun, Shi Yongyong, Liu Shaow |
| The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population. Scientific reports 2016 Oct 6 35212. Fang Zhen, Jiang Yue, Wang Yifeng, Lin Yuan, Liu Yaowu, Zhao Liyan, Xu Yan, Toorabally Mohammad Bilaal, He Shenghu, Zhang Fengxia |
| Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Circulation. Cardiovascular genetics 2015 Feb 8 (1): 64-73. Jabbari Javad, Olesen Morten S, Yuan Lei, Nielsen Jonas B, Liang Bo, Macri Vincenzo, Christophersen Ingrid E, Nielsen Nikolaj, Sajadieh Ahmad, Ellinor Patrick T, Grunnet Morten, Haunsø Stig, Holst Anders G, Svendsen Jesper H, Jespersen Thom |
| Brugada syndrome risk loci seem protective against atrial fibrillation. European journal of human genetics : EJHG 2014 Dec 22 (12): 1357-61. Andreasen Laura, Nielsen Jonas B, Darkner Stine, Christophersen Ingrid E, Jabbari Javad, Refsgaard Lena, Thiis Jens J, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten |
| Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation 2013 Apr 127 (13): 1377-85. Ritchie Marylyn D, Denny Joshua C, Zuvich Rebecca L, Crawford Dana C, Schildcrout Jonathan S, Bastarache Lisa, Ramirez Andrea H, Mosley Jonathan D, Pulley Jill M, Basford Melissa A, Bradford Yuki, Rasmussen Luke V, Pathak Jyotishman, Chute Christopher G, Kullo Iftikhar J, McCarty Catherine A, Chisholm Rex L, Kho Abel N, Carlson Christopher S, Larson Eric B, Jarvik Gail P, Sotoodehnia Nona, , Manolio Teri A, Li Rongling, Masys Daniel R, Haines Jonathan L, Roden Dan |
| Genome-wide association study of PR interval.
Nature genetics 2010 Feb 42 (2): 153-9. Pfeufer Arne, van Noord Charlotte, Marciante Kristin D, Arking Dan E, Larson Martin G, Smith Albert Vernon, Tarasov Kirill V, Müller Martina, Sotoodehnia Nona, Sinner Moritz F, Verwoert Germaine C, Li Man, Kao W H Linda, Köttgen Anna, Coresh Josef, Bis Joshua C, Psaty Bruce M, Rice Kenneth, Rotter Jerome I, Rivadeneira Fernando, Hofman Albert, Kors Jan A, Stricker Bruno H C, Uitterlinden André G, van Duijn Cornelia M, Beckmann Britt M, Sauter Wiebke, Gieger Christian, Lubitz Steven A, Newton-Cheh Christopher, Wang Thomas J, Magnani Jared W, Schnabel Renate B, Chung Mina K, Barnard John, Smith Jonathan D, Van Wagoner David R, Vasan Ramachandran S, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Launer Lenore J, Najjar Samer S, Lakatta Edward, Schlessinger David, Uda Manuela, Abecasis Gonçalo R, Müller-Myhsok Bertram, Ehret Georg B, Boerwinkle Eric, Chakravarti Aravinda, Soliman Elsayed Z, Lunetta Kathryn L, Perz Siegfried, Wichmann H-Erich, Meitinger Thomas, Levy Daniel, Gudnason Vilmundur, Ellinor Patrick T, Sanna Serena, Kääb Stefan, Witteman Jacqueline C M, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan |
| Several common variants modulate heart rate, PR interval and QRS duration.
Nature genetics 2010 Feb 42 (2): 117-22. Holm Hilma, Gudbjartsson Daniel F, Arnar David O, Thorleifsson Gudmar, Thorgeirsson Gudmundur, Stefansdottir Hrafnhildur, Gudjonsson Sigurjon A, Jonasdottir Aslaug, Mathiesen Ellisiv B, Njølstad Inger, Nyrnes Audhild, Wilsgaard Tom, Hald Erin M, Hveem Kristian, Stoltenberg Camilla, Løchen Maja-Lisa, Kong Augustine, Thorsteinsdottir Unnur, Stefansson Ka |
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