Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Atrial Fibrillation and Synpo2l[original query] |
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| The rs3807989 G/A polymorphism in CAV1 is associated with the risk of atrial fibrillation in Chinese Han populations. Pacing and clinical electrophysiology : PACE 2015 Feb 38 (2): 164-70. Liu Yaowu, Ni Bixian, Lin Yuan, Chen Xin-Guang, Chen Minglong, Hu Zhibin, Zhang Fengxia |
| Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling. Cardiovascular research 2015 Aug . Lozano-Velasco Estefanía, Hernández-Torres Francisco, Daimi Houria, Serra Selma A, Herraiz Adela, Hove-Madsen Leif, Aránega Amelia, Franco Die |
| Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. Journal of the American Heart Association 2015 May 4 (5): . Chen Shanshan, Wang Chuchu, Wang Xiaojing, Xu Chengqi, Wu Manman, Wang Pengxia, Tu Xin, Wang Qing |
| Whole Exome Sequencing in Atrial Fibrillation. PLoS genetics 2016 Sep 12 (9): e1006284. Lubitz Steven A, Brody Jennifer A, Bihlmeyer Nathan A, Roselli Carolina, Weng Lu-Chen, Christophersen Ingrid E, Alonso Alvaro, Boerwinkle Eric, Gibbs Richard A, Bis Joshua C, , Cupples L Adrienne, Mohler Peter J, Nickerson Deborah A, Muzny Donna, Perez Marco V, Psaty Bruce M, Soliman Elsayed Z, Sotoodehnia Nona, Lunetta Kathryn L, Benjamin Emelia J, Heckbert Susan R, Arking Dan E, Ellinor Patrick T, Lin Honghua |
| 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 |
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nature communications 2020 01 11 (1): 163. Shah Sonia, Henry Albert, Roselli Carolina, Lin Honghuang, Sveinbjörnsson Garðar, Fatemifar Ghazaleh, Hedman Åsa K, Wilk Jemma B, Morley Michael P, Chaffin Mark D, Helgadottir Anna, Verweij Niek, Dehghan Abbas, Almgren Peter, Andersson Charlotte, Aragam Krishna G, Ärnlöv Johan, Backman Joshua D, Biggs Mary L, Bloom Heather L, Brandimarto Jeffrey, Brown Michael R, Buckbinder Leonard, Carey David J, Chasman Daniel I, Chen Xing, Chen Xu, Chung Jonathan, Chutkow William, Cook James P, Delgado Graciela E, Denaxas Spiros, Doney Alexander S, Dörr Marcus, Dudley Samuel C, Dunn Michael E, Engström Gunnar, Esko Tõnu, Felix Stephan B, Finan Chris, Ford Ian, Ghanbari Mohsen, Ghasemi Sahar, Giedraitis Vilmantas, Giulianini Franco, Gottdiener John S, Gross Stefan, Guðbjartsson Daníel F, Gutmann Rebecca, Haggerty Christopher M, van der Harst Pim, Hyde Craig L, Ingelsson Erik, Jukema J Wouter, Kavousi Maryam, Khaw Kay-Tee, Kleber Marcus E, Køber Lars, Koekemoer Andrea, Langenberg Claudia, Lind Lars, Lindgren Cecilia M, London Barry, Lotta Luca A, Lovering Ruth C, Luan Jian'an, Magnusson Patrik, Mahajan Anubha, Margulies Kenneth B, März Winfried, Melander Olle, Mordi Ify R, Morgan Thomas, Morris Andrew D, Morris Andrew P, Morrison Alanna C, Nagle Michael W, Nelson Christopher P, Niessner Alexander, Niiranen Teemu, O'Donoghue Michelle L, Owens Anjali T, Palmer Colin N A, Parry Helen M, Perola Markus, Portilla-Fernandez Eliana, Psaty Bruce M, , Rice Kenneth M, Ridker Paul M, Romaine Simon P R, Rotter Jerome I, Salo Perttu, Salomaa Veikko, van Setten Jessica, Shalaby Alaa A, Smelser Diane T, Smith Nicholas L, Stender Steen, Stott David J, Svensson Per, Tammesoo Mari-Liis, Taylor Kent D, Teder-Laving Maris, Teumer Alexander, Thorgeirsson Guðmundur, Thorsteinsdottir Unnur, Torp-Pedersen Christian, Trompet Stella, Tyl Benoit, Uitterlinden Andre G, Veluchamy Abirami, Völker Uwe, Voors Adriaan A, Wang Xiaosong, Wareham Nicholas J, Waterworth Dawn, Weeke Peter E, Weiss Raul, Wiggins Kerri L, Xing Heming, Yerges-Armstrong Laura M, Yu Bing, Zannad Faiez, Zhao Jing Hua, Hemingway Harry, Samani Nilesh J, McMurray John J V, Yang Jian, Visscher Peter M, Newton-Cheh Christopher, Malarstig Anders, Holm Hilma, Lubitz Steven A, Sattar Naveed, Holmes Michael V, Cappola Thomas P, Asselbergs Folkert W, Hingorani Aroon D, Kuchenbaecker Karoline, Ellinor Patrick T, Lang Chim C, Stefansson Kari, Smith J Gustav, Vasan Ramachandran S, Swerdlow Daniel I, Lumbers R Thom |
| Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation. Frontiers in cardiovascular medicine 2021 8 650667. Clausen Alexander Guldmann, Vad Oliver Bundgaard, Andersen Julie Husted, Olesen Morten Salli |
| Transcriptomic Insights into the Atrial Fibrillation Susceptibility Locus near the MYOZ1 and SYNPO2L Genes. International journal of molecular sciences 2024 10 25 (19): . Sojin Y Wass, Han Sun, Gregory Tchou, Nana Liu, David R Van Wagoner, Mina K Chung, John Barnard, Jonathan D Smi |
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