HuGE Literature Finder
Records 1-30
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 |
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Nature communications 2020 05 11 (1): 2542. Ntalla Ioanna, Weng Lu-Chen, Cartwright James H, Hall Amelia Weber, Sveinbjornsson Gardar, Tucker Nathan R, Choi Seung Hoan, Chaffin Mark D, Roselli Carolina, Barnes Michael R, Mifsud Borbala, Warren Helen R, Hayward Caroline, Marten Jonathan, Cranley James J, Concas Maria Pina, Gasparini Paolo, Boutin Thibaud, Kolcic Ivana, Polasek Ozren, Rudan Igor, Araujo Nathalia M, Lima-Costa Maria Fernanda, Ribeiro Antonio Luiz P, Souza Renan P, Tarazona-Santos Eduardo, Giedraitis Vilmantas, Ingelsson Erik, Mahajan Anubha, Morris Andrew P, Del Greco M Fabiola, Foco Luisa, Gögele Martin, Hicks Andrew A, Cook James P, Lind Lars, Lindgren Cecilia M, Sundström Johan, Nelson Christopher P, Riaz Muhammad B, Samani Nilesh J, Sinagra Gianfranco, Ulivi Sheila, Kähönen Mika, Mishra Pashupati P, Mononen Nina, Nikus Kjell, Caulfield Mark J, Dominiczak Anna, Padmanabhan Sandosh, Montasser May E, O'Connell Jeff R, Ryan Kathleen, Shuldiner Alan R, Aeschbacher Stefanie, Conen David, Risch Lorenz, Thériault Sébastien, Hutri-Kähönen Nina, Lehtimäki Terho, Lyytikäinen Leo-Pekka, Raitakari Olli T, Barnes Catriona L K, Campbell Harry, Joshi Peter K, Wilson James F, Isaacs Aaron, Kors Jan A, van Duijn Cornelia M, Huang Paul L, Gudnason Vilmundur, Harris Tamara B, Launer Lenore J, Smith Albert V, Bottinger Erwin P, Loos Ruth J F, Nadkarni Girish N, Preuss Michael H, Correa Adolfo, Mei Hao, Wilson James, Meitinger Thomas, Müller-Nurasyid Martina, Peters Annette, Waldenberger Melanie, Mangino Massimo, Spector Timothy D, Rienstra Michiel, van de Vegte Yordi J, van der Harst Pim, Verweij Niek, Kääb Stefan, Schramm Katharina, Sinner Moritz F, Strauch Konstantin, Cutler Michael J, Fatkin Diane, London Barry, Olesen Morten, Roden Dan M, Benjamin Shoemaker M, Gustav Smith J, Biggs Mary L, Bis Joshua C, Brody Jennifer A, Psaty Bruce M, Rice Kenneth, Sotoodehnia Nona, De Grandi Alessandro, Fuchsberger Christian, Pattaro Cristian, Pramstaller Peter P, Ford Ian, Wouter Jukema J, Macfarlane Peter W, Trompet Stella, Dörr Marcus, Felix Stephan B, Völker Uwe, Weiss Stefan, Havulinna Aki S, Jula Antti, Sääksjärvi Katri, Salomaa Veikko, Guo Xiuqing, Heckbert Susan R, Lin Henry J, Rotter Jerome I, Taylor Kent D, Yao Jie, de Mutsert Renée, Maan Arie C, Mook-Kanamori Dennis O, Noordam Raymond, Cucca Francesco, Ding Jun, Lakatta Edward G, Qian Yong, Tarasov Kirill V, Levy Daniel, Lin Honghuang, Newton-Cheh Christopher H, Lunetta Kathryn L, Murray Alison D, Porteous David J, Smith Blair H, Stricker Bruno H, Uitterlinden André, van den Berg Marten E, Haessler Jeffrey, Jackson Rebecca D, Kooperberg Charles, Peters Ulrike, Reiner Alexander P, Whitsel Eric A, Alonso Alvaro, Arking Dan E, Boerwinkle Eric, Ehret Georg B, Soliman Elsayed Z, Avery Christy L, Gogarten Stephanie M, Kerr Kathleen F, Laurie Cathy C, Seyerle Amanda A, Stilp Adrienne, Assa Solmaz, Abdullah Said M, Yldau van der Ende M, Lambiase Pier D, Orini Michele, Ramirez Julia, Van Duijvenboden Stefan, Arnar David O, Gudbjartsson Daniel F, Holm Hilma, Sulem Patrick, Thorleifsson Gudmar, Thorolfsdottir Rosa B, Thorsteinsdottir Unnur, Benjamin Emelia J, Tinker Andrew, Stefansson Kari, Ellinor Patrick T, Jamshidi Yalda, Lubitz Steven A, Munroe Patricia |
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Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.
BMC cardiovascular disorders 2019 Jan 19 (1): 26. Westphal Sabine, Stoppe Christian, Gruenewald Matthias, Bein Berthold, Renner Jochen, Cremer Jochen, Coburn Mark, Schaelte Gereon, Boening Andreas, Niemann Bernd, Kletzin Frank, Roesner Jan, Strouhal Ulrich, Reyher Christian, Laufenberg-Feldmann Rita, Ferner Marion, Brandes Ivo F, Bauer Martin, Kortgen Andreas, Stehr Sebastian N, Wittmann Maria, Baumgarten Georg, Struck Rafael, Meyer-Treschan Tanja, Kienbaum Peter, Heringlake Matthias, Schoen Julika, Sander Michael, Treskatsch Sascha, Smul Thorsten, Wolwender Ewa, Schilling Thomas, Degenhardt Frauke, Franke Andre, Mucha Soeren, Tittmann Lukas, Kohlhaas Madeline, Fuernau Georg, Brosteanu Oana, Hasenclever Dirk, Zacharowski Kai, Meybohm Patrick, |
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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 |
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Multi-ethnic genome-wide association study for atrial fibrillation.
Nature genetics 2018 Jun . Roselli Carolina, Chaffin Mark D, Weng Lu-Chen, Aeschbacher Stefanie, Ahlberg Gustav, Albert Christine M, Almgren Peter, Alonso Alvaro, Anderson Christopher D, Aragam Krishna G, Arking Dan E, Barnard John, Bartz Traci M, Benjamin Emelia J, Bihlmeyer Nathan A, Bis Joshua C, Bloom Heather L, Boerwinkle Eric, Bottinger Erwin B, Brody Jennifer A, Calkins Hugh, Campbell Archie, Cappola Thomas P, Carlquist John, Chasman Daniel I, Chen Lin Y, Chen Yii-Der Ida, Choi Eue-Keun, Choi Seung Hoan, Christophersen Ingrid E, Chung Mina K, Cole John W, Conen David, Cook James, Crijns Harry J, Cutler Michael J, Damrauer Scott M, Daniels Brian R, Darbar Dawood, Delgado Graciela, Denny Joshua C, Dichgans Martin, Dörr Marcus, Dudink Elton A, Dudley Samuel C, Esa Nada, Esko Tonu, Eskola Markku, Fatkin Diane, Felix Stephan B, Ford Ian, Franco Oscar H, Geelhoed Bastiaan, Grewal Raji P, Gudnason Vilmundur, Guo Xiuqing, Gupta Namrata, Gustafsson Stefan, Gutmann Rebecca, Hamsten Anders, Harris Tamara B, Hayward Caroline, Heckbert Susan R, Hernesniemi Jussi, Hocking Lynne J, Hofman Albert, Horimoto Andrea R V R, Huang Jie, Huang Paul L, Huffman Jennifer, Ingelsson Erik, Ipek Esra Gucuk, Ito Kaoru, Jimenez-Conde Jordi, Johnson Renee, Jukema J Wouter, Kääb Stefan, Kähönen Mika, Kamatani Yoichiro, Kane John P, Kastrati Adnan, Kathiresan Sekar, Katschnig-Winter Petra, Kavousi Maryam, Kessler Thorsten, Kietselaer Bas L, Kirchhof Paulus, Kleber Marcus E, Knight Stacey, Krieger Jose E, Kubo Michiaki, Launer Lenore J, Laurikka Jari, Lehtimäki Terho, Leineweber Kirsten, Lemaitre Rozenn N, Li Man, Lim Hong Euy, Lin Henry J, Lin Honghuang, Lind Lars, Lindgren Cecilia M, Lokki Marja-Liisa, London Barry, Loos Ruth J F, Low Siew-Kee, Lu Yingchang, Lyytikäinen Leo-Pekka, Macfarlane Peter W, Magnusson Patrik K, Mahajan Anubha, Malik Rainer, Mansur Alfredo J, Marcus Gregory M, Margolin Lauren, Margulies Kenneth B, März Winfried, McManus David D, Melander Olle, Mohanty Sanghamitra, Montgomery Jay A, Morley Michael P, Morris Andrew P, Müller-Nurasyid Martina, Natale Andrea, Nazarian Saman, Neumann Benjamin, Newton-Cheh Christopher, Niemeijer Maartje N, Nikus Kjell, Nilsson Peter, Noordam Raymond, Oellers Heidi, Olesen Morten S, Orho-Melander Marju, Padmanabhan Sandosh, Pak Hui-Nam, Paré Guillaume, Pedersen Nancy L, Pera Joanna, Pereira Alexandre, Porteous David, Psaty Bruce M, Pulit Sara L, Pullinger Clive R, Rader Daniel J, Refsgaard Lena, Ribasés Marta, Ridker Paul M, Rienstra Michiel, Risch Lorenz, Roden Dan M, Rosand Jonathan, Rosenberg Michael A, Rost Natalia, Rotter Jerome I, Saba Samir, Sandhu Roopinder K, Schnabel Renate B, Schramm Katharina, Schunkert Heribert, Schurman Claudia, Scott Stuart A, Seppälä Ilkka, Shaffer Christian, Shah Svati, Shalaby Alaa A, Shim Jaemin, Shoemaker M Benjamin, Siland Joylene E, Sinisalo Juha, Sinner Moritz F, Slowik Agnieszka, Smith Albert V, Smith Blair H, Smith J Gustav, Smith Jonathan D, Smith Nicholas L, Soliman Elsayed Z, Sotoodehnia Nona, Stricker Bruno H, Sun Albert, Sun Han, Svendsen Jesper H, Tanaka Toshihiro, Tanriverdi Kahraman, Taylor Kent D, Teder-Laving Maris, Teumer Alexander, Thériault Sébastien, Trompet Stella, Tucker Nathan R, Tveit Arnljot, Uitterlinden Andre G, Van Der Harst Pim, Van Gelder Isabelle C, Van Wagoner David R, Verweij Niek, Vlachopoulou Efthymia, Völker Uwe, Wang Biqi, Weeke Peter E, Weijs Bob, Weiss Raul, Weiss Stefan, Wells Quinn S, Wiggins Kerri L, Wong Jorge A, Woo Daniel, Worrall Bradford B, Yang Pil-Sung, Yao Jie, Yoneda Zachary T, Zeller Tanja, Zeng Lingyao, Lubitz Steven A, Lunetta Kathryn L, Ellinor Patrick |
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A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.
European heart journal 2018 Mar . Bjornsson Thorsteinn, Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Sulem Patrick, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Magnusdottir Audur, Danielsen Ragnar, Sigurdsson Emil L, Adalsteinsdottir Berglind, Gunnarsson Sverrir I, Jonsdottir Ingileif, Arnar David O, Helgason Hrodmar, Gudbjartsson Tomas, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Stefansson Ka |
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Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
American journal of human genetics 2018 Jan 102 (1): 103-115. Nielsen Jonas B, Fritsche Lars G, Zhou Wei, Teslovich Tanya M, Holmen Oddgeir L, Gustafsson Stefan, Gabrielsen Maiken E, Schmidt Ellen M, Beaumont Robin, Wolford Brooke N, Lin Maoxuan, Brummett Chad M, Preuss Michael H, Refsgaard Lena, Bottinger Erwin P, Graham Sarah E, Surakka Ida, Chu Yunhan, Skogholt Anne Heidi, Dalen Håvard, Boyle Alan P, Oral Hakan, Herron Todd J, Kitzman Jacob, Jalife José, Svendsen Jesper H, Olesen Morten S, Njølstad Inger, Løchen Maja-Lisa, Baras Aris, Gottesman Omri, Marcketta Anthony, O'Dushlaine Colm, Ritchie Marylyn D, Wilsgaard Tom, Loos Ruth J F, Frayling Timothy M, Boehnke Michael, Ingelsson Erik, Carey David J, Dewey Frederick E, Kang Hyun M, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
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A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
European heart journal 2018 11 39 (44): 3961-3969. Ashar Foram N, Mitchell Rebecca N, Albert Christine M, Newton-Cheh Christopher, Brody Jennifer A, Müller-Nurasyid Martina, Moes Anna, Meitinger Thomas, Mak Angel, Huikuri Heikki, Junttila M Juhani, Goyette Philippe, Pulit Sara L, Pazoki Raha, Tanck Michael W, Blom Marieke T, Zhao XiaoQing, Havulinna Aki S, Jabbari Reza, Glinge Charlotte, Tragante Vinicius, Escher Stefan A, Chakravarti Aravinda, Ehret Georg, Coresh Josef, Li Man, Prineas Ronald J, Franco Oscar H, Kwok Pui-Yan, Lumley Thomas, Dumas Florence, McKnight Barbara, Rotter Jerome I, Lemaitre Rozenn N, Heckbert Susan R, O'Donnell Christopher J, Hwang Shih-Jen, Tardif Jean-Claude, VanDenburgh Martin, Uitterlinden André G, Hofman Albert, Stricker Bruno H C, de Bakker Paul I W, Franks Paul W, Jansson Jan-Hakan, Asselbergs Folkert W, Halushka Marc K, Maleszewski Joseph J, Tfelt-Hansen Jacob, Engstrøm Thomas, Salomaa Veikko, Virmani Renu, Kolodgie Frank, Wilde Arthur A M, Tan Hanno L, Bezzina Connie R, Eijgelsheim Mark, Rioux John D, Jouven Xavier, Kääb Stefan, Psaty Bruce M, Siscovick David S, Arking Dan E, Sotoodehnia No |
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PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.
Nature communications 2018 07 9 (1): 2904. van Setten Jessica, Brody Jennifer A, Jamshidi Yalda, Swenson Brenton R, Butler Anne M, Campbell Harry, Del Greco Fabiola M, Evans Daniel S, Gibson Quince, Gudbjartsson Daniel F, Kerr Kathleen F, Krijthe Bouwe P, Lyytikäinen Leo-Pekka, Müller Christian, Müller-Nurasyid Martina, Nolte Ilja M, Padmanabhan Sandosh, Ritchie Marylyn D, Robino Antonietta, Smith Albert V, Steri Maristella, Tanaka Toshiko, Teumer Alexander, Trompet Stella, Ulivi Sheila, Verweij Niek, Yin Xiaoyan, Arnar David O, Asselbergs Folkert W, Bader Joel S, Barnard John, Bis Josh, Blankenberg Stefan, Boerwinkle Eric, Bradford Yuki, Buckley Brendan M, Chung Mina K, Crawford Dana, den Hoed Marcel, Denny Josh C, Dominiczak Anna F, Ehret Georg B, Eijgelsheim Mark, Ellinor Patrick T, Felix Stephan B, Franco Oscar H, Franke Lude, Harris Tamara B, Holm Hilma, Ilaria Gandin, Iorio Annamaria, Kähönen Mika, Kolcic Ivana, Kors Jan A, Lakatta Edward G, Launer Lenore J, Lin Honghuang, Lin Henry J, Loos Ruth J F, Lubitz Steven A, Macfarlane Peter W, Magnani Jared W, Leach Irene Mateo, Meitinger Thomas, Mitchell Braxton D, Munzel Thomas, Papanicolaou George J, Peters Annette, Pfeufer Arne, Pramstaller Peter P, Raitakari Olli T, Rotter Jerome I, Rudan Igor, Samani Nilesh J, Schlessinger David, Silva Aldana Claudia T, Sinner Moritz F, Smith Jonathan D, Snieder Harold, Soliman Elsayed Z, Spector Timothy D, Stott David J, Strauch Konstantin, Tarasov Kirill V, Thorsteinsdottir Unnur, Uitterlinden Andre G, Van Wagoner David R, Völker Uwe, Völzke Henry, Waldenberger Melanie, Jan Westra Harm, Wild Philipp S, Zeller Tanja, Alonso Alvaro, Avery Christy L, Bandinelli Stefania, Benjamin Emelia J, Cucca Francesco, Dörr Marcus, Ferrucci Luigi, Gasparini Paolo, Gudnason Vilmundur, Hayward Caroline, Heckbert Susan R, Hicks Andrew A, Jukema J Wouter, Kääb Stefan, Lehtimäki Terho, Liu Yongmei, Munroe Patricia B, Parsa Afshin, Polasek Ozren, Psaty Bruce M, Roden Dan M, Schnabel Renate B, Sinagra Gianfranco, Stefansson Kari, Stricker Bruno H, van der Harst Pim, van Duijn Cornelia M, Wilson James F, Gharib Sina A, de Bakker Paul I W, Isaacs Aaron, Arking Dan E, Sotoodehnia No |
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Heritability of Atrial Fibrillation.
Circulation. Cardiovascular genetics 2017 Dec 10 (6): . Weng Lu-Chen, Choi Seung Hoan, Klarin Derek, Smith J Gustav, Loh Po-Ru, Chaffin Mark, Roselli Carolina, Hulme Olivia L, Lunetta Kathryn L, Dupuis Josée, Benjamin Emelia J, Newton-Cheh Christopher, Kathiresan Sekar, Ellinor Patrick T, Lubitz Steven |
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The Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
Circulation research 2017 Dec . van der Harst Pim, Verweij Ni |
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Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2.
Heart (British Cardiac Society) 2017 Nov . Seyerle Amanda A, Lin Henry J, Gogarten Stephanie M, Stilp Adrienne, Méndez Giráldez Raul, Soliman Elsayed, Baldassari Antoine, Graff Mariaelisa, Heckbert Susan, Kerr Kathleen F, Kooperberg Charles, Rodriguez Carlos, Guo Xiuqing, Yao Jie, Sotoodehnia Nona, Taylor Kent D, Whitsel Eric A, Rotter Jerome I, Laurie Cathy C, Avery Chris |
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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 |
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nature genetics 2017 Jun 49 (6): 946-952. Christophersen Ingrid E, Rienstra Michiel, Roselli Carolina, Yin Xiaoyan, Geelhoed Bastiaan, Barnard John, Lin Honghuang, Arking Dan E, Smith Albert V, Albert Christine M, Chaffin Mark, Tucker Nathan R, Li Molong, Klarin Derek, Bihlmeyer Nathan A, Low Siew-Kee, Weeke Peter E, Müller-Nurasyid Martina, Smith J Gustav, Brody Jennifer A, Niemeijer Maartje N, Dörr Marcus, Trompet Stella, Huffman Jennifer, Gustafsson Stefan, Schurmann Claudia, Kleber Marcus E, Lyytikäinen Leo-Pekka, Seppälä Ilkka, Malik Rainer, Horimoto Andrea R V R, Perez Marco, Sinisalo Juha, Aeschbacher Stefanie, Thériault Sébastien, Yao Jie, Radmanesh Farid, Weiss Stefan, Teumer Alexander, Choi Seung Hoan, Weng Lu-Chen, Clauss Sebastian, Deo Rajat, Rader Daniel J, Shah Svati H, Sun Albert, Hopewell Jemma C, Debette Stephanie, Chauhan Ganesh, Yang Qiong, Worrall Bradford B, Paré Guillaume, Kamatani Yoichiro, Hagemeijer Yanick P, Verweij Niek, Siland Joylene E, Kubo Michiaki, Smith Jonathan D, Van Wagoner David R, Bis Joshua C, Perz Siegfried, Psaty Bruce M, Ridker Paul M, Magnani Jared W, Harris Tamara B, Launer Lenore J, Shoemaker M Benjamin, Padmanabhan Sandosh, Haessler Jeffrey, Bartz Traci M, Waldenberger Melanie, Lichtner Peter, Arendt Marina, Krieger Jose E, Kähönen Mika, Risch Lorenz, Mansur Alfredo J, Peters Annette, Smith Blair H, Lind Lars, Scott Stuart A, Lu Yingchang, Bottinger Erwin B, Hernesniemi Jussi, Lindgren Cecilia M, Wong Jorge A, Huang Jie, Eskola Markku, Morris Andrew P, Ford Ian, Reiner Alex P, Delgado Graciela, Chen Lin Y, Chen Yii-Der Ida, Sandhu Roopinder K, Li Man, Boerwinkle Eric, Eisele Lewin, Lannfelt Lars, Rost Natalia, Anderson Christopher D, Taylor Kent D, Campbell Archie, Magnusson Patrik K, Porteous David, Hocking Lynne J, Vlachopoulou Efthymia, Pedersen Nancy L, Nikus Kjell, Orho-Melander Marju, Hamsten Anders, Heeringa Jan, Denny Joshua C, Kriebel Jennifer, Darbar Dawood, Newton-Cheh Christopher, Shaffer Christian, Macfarlane Peter W, Heilmann-Heimbach Stefanie, Almgren Peter, Huang Paul L, Sotoodehnia Nona, Soliman Elsayed Z, Uitterlinden Andre G, Hofman Albert, Franco Oscar H, Völker Uwe, Jöckel Karl-Heinz, Sinner Moritz F, Lin Henry J, Guo Xiuqing, , , Dichgans Martin, Ingelsson Erik, Kooperberg Charles, Melander Olle, Loos Ruth J F, Laurikka Jari, Conen David, Rosand Jonathan, van der Harst Pim, Lokki Marja-Liisa, Kathiresan Sekar, Pereira Alexandre, Jukema J Wouter, Hayward Caroline, Rotter Jerome I, März Winfried, Lehtimäki Terho, Stricker Bruno H, Chung Mina K, Felix Stephan B, Gudnason Vilmundur, Alonso Alvaro, Roden Dan M, Kääb Stefan, Chasman Daniel I, Heckbert Susan R, Benjamin Emelia J, Tanaka Toshihiro, Lunetta Kathryn L, Lubitz Steven A, Ellinor Patrick T, |
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Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nature genetics 2017 Apr . Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, , Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihi |
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Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci.
European heart journal 2017 Apr . Lee Ji-Young, Kim Tae-Hoon, Yang Pil-Sung, Lim Hong Euy, Choi Eue-Keun, Shim Jaemin, Shin Eunsoon, Uhm Jae-Sun, Kim Jin-Seok, Joung Boyoung, Oh Seil, Lee Moon-Hyoung, Kim Young-Hoon, Pak Hui-N |
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Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery.
American heart journal 2015 Sep 170 (3): 580-90.e28. Kertai Miklos D, Li Yi-Ju, Ji Yunqi, Qi Wenjing, Lombard Frederick W, Shah Svati H, Kraus William E, Stafford-Smith Mark, Newman Mark F, Milano Carmelo A, Waldron Nathan, Podgoreanu Mihai V, Mathew Joseph P, |
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Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
Human molecular genetics 2014 Oct 23 (20): 5505-17. Zhan Ming, Chen Gang, Pan Chun-Ming, Gu Zhao-Hui, Zhao Shuang-Xia, Liu Wei, Wang Hai-Ning, Ye Xiao-Ping, Xie Hui-Jun, Yu Sha-Sha, Liang Jun, Gao Guan-Qi, Yuan Guo-Yue, Zhang Xiao-Mei, Zuo Chun-Lin, Su Bin, Huang Wei, Ning Guang, Chen Sai-Juan, Chen Jia-Lun, Song Huai-Dong, |
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Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Nature genetics 2013 Jun 45 (6): 621-31. den Hoed Marcel, Eijgelsheim Mark, Esko Tõnu, Brundel Bianca J J M, Peal David S, Evans David M, Nolte Ilja M, Segrè Ayellet V, Holm Hilma, Handsaker Robert E, Westra Harm-Jan, Johnson Toby, Isaacs Aaron, Yang Jian, Lundby Alicia, Zhao Jing Hua, Kim Young Jin, Go Min Jin, Almgren Peter, Bochud Murielle, Boucher Gabrielle, Cornelis Marilyn C, Gudbjartsson Daniel, Hadley David, van der Harst Pim, Hayward Caroline, den Heijer Martin, Igl Wilmar, Jackson Anne U, Kutalik Zoltán, Luan Jian'an, Kemp John P, Kristiansson Kati, Ladenvall Claes, Lorentzon Mattias, Montasser May E, Njajou Omer T, O'Reilly Paul F, Padmanabhan Sandosh, St Pourcain Beate, Rankinen Tuomo, Salo Perttu, Tanaka Toshiko, Timpson Nicholas J, Vitart Veronique, Waite Lindsay, Wheeler William, Zhang Weihua, Draisma Harmen H M, Feitosa Mary F, Kerr Kathleen F, Lind Penelope A, Mihailov Evelin, Onland-Moret N Charlotte, Song Ci, Weedon Michael N, Xie Weijia, Yengo Loic, Absher Devin, Albert Christine M, Alonso Alvaro, Arking Dan E, de Bakker Paul I W, Balkau Beverley, Barlassina Cristina, Benaglio Paola, Bis Joshua C, Bouatia-Naji Nabila, Brage Søren, Chanock Stephen J, Chines Peter S, Chung Mina, Darbar Dawood, Dina Christian, Dörr Marcus, Elliott Paul, Felix Stephan B, Fischer Krista, Fuchsberger Christian, de Geus Eco J C, Goyette Philippe, Gudnason Vilmundur, Harris Tamara B, Hartikainen Anna-Liisa, Havulinna Aki S, Heckbert Susan R, Hicks Andrew A, Hofman Albert, Holewijn Suzanne, Hoogstra-Berends Femke, Hottenga Jouke-Jan, Jensen Majken K, Johansson Asa, Junttila Juhani, Kääb Stefan, Kanon Bart, Ketkar Shamika, Khaw Kay-Tee, Knowles Joshua W, Kooner Angrad S, Kors Jan A, Kumari Meena, Milani Lili, Laiho Päivi, Lakatta Edward G, Langenberg Claudia, Leusink Maarten, Liu Yongmei, Luben Robert N, Lunetta Kathryn L, Lynch Stacey N, Markus Marcello R P, Marques-Vidal Pedro, Mateo Leach Irene, McArdle Wendy L, McCarroll Steven A, Medland Sarah E, Miller Kathryn A, Montgomery Grant W, Morrison Alanna C, Müller-Nurasyid Martina, Navarro Pau, Nelis Mari, O'Connell Jeffrey R, O'Donnell Christopher J, Ong Ken K, Newman Anne B, Peters Annette, Polasek Ozren, Pouta Anneli, Pramstaller Peter P, Psaty Bruce M, Rao Dabeeru C, Ring Susan M, Rossin Elizabeth J, Rudan Diana, Sanna Serena, Scott Robert A, Sehmi Jaban S, Sharp Stephen, Shin Jordan T, Singleton Andrew B, Smith Albert V, Soranzo Nicole, Spector Tim D, Stewart Chip, Stringham Heather M, Tarasov Kirill V, Uitterlinden André G, Vandenput Liesbeth, Hwang Shih-Jen, Whitfield John B, Wijmenga Cisca, Wild Sarah H, Willemsen Gonneke, Wilson James F, Witteman Jacqueline C M, Wong Andrew, Wong Quenna, Jamshidi Yalda, Zitting Paavo, Boer Jolanda M A, Boomsma Dorret I, Borecki Ingrid B, van Duijn Cornelia M, Ekelund Ulf, Forouhi Nita G, Froguel Philippe, Hingorani Aroon, Ingelsson Erik, Kivimaki Mika, Kronmal Richard A, Kuh Diana, Lind Lars, Martin Nicholas G, Oostra Ben A, Pedersen Nancy L, Quertermous Thomas, Rotter Jerome I, van der Schouw Yvonne T, Verschuren W M Monique, Walker Mark, Albanes Demetrius, Arnar David O, Assimes Themistocles L, Bandinelli Stefania, Boehnke Michael, de Boer Rudolf A, Bouchard Claude, Caulfield W L Mark, Chambers John C, Curhan Gary, Cusi Daniele, Eriksson Johan, Ferrucci Luigi, van Gilst Wiek H, Glorioso Nicola, de Graaf Jacqueline, Groop Leif, Gyllensten Ulf, Hsueh Wen-Chi, Hu Frank B, Huikuri Heikki V, Hunter David J, Iribarren Carlos, Isomaa Bo, Jarvelin Marjo-Riitta, Jula Antti, Kähönen Mika, Kiemeney Lambertus A, van der Klauw Melanie M, Kooner Jaspal S, Kraft Peter, Iacoviello Licia, Lehtimäki Terho, Lokki Marja-Liisa L, Mitchell Braxton D, Navis Gerjan, Nieminen Markku S, Ohlsson Claes, Poulter Neil R, Qi Lu, Raitakari Olli T, Rimm Eric B, Rioux John D, Rizzi Federica, Rudan Igor, Salomaa Veikko, Sever Peter S, Shields Denis C, Shuldiner Alan R, Sinisalo Juha, Stanton Alice V, Stolk Ronald P, Strachan David P, Tardif Jean-Claude, Thorsteinsdottir Unnur, Tuomilehto Jaako, van Veldhuisen Dirk J, Virtamo Jarmo, Viikari Jorma, Vollenweider Peter, Waeber Gérard, Widen Elisabeth, Cho Yoon Shin, Olsen Jesper V, Visscher Peter M, Willer Cristen, Franke Lude, , , Erdmann Jeanette, Thompson John R, , Pfeufer Arne, , Sotoodehnia Nona, , Newton-Cheh Christopher, , Ellinor Patrick T, Stricker Bruno H Ch, Metspalu Andres, Perola Markus, Beckmann Jacques S, Smith George Davey, Stefansson Kari, Wareham Nicholas J, Munroe Patricia B, Sibon Ody C M, Milan David J, Snieder Harold, Samani Nilesh J, Loos Ruth J |
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Genetic determinants of dabigatran plasma levels and their relation to bleeding.
Circulation 2013 Apr 127 (13): 1404-12. Paré Guillaume, Eriksson Niclas, Lehr Thorsten, Connolly Stuart, Eikelboom John, Ezekowitz Michael D, Axelsson Tomas, Haertter Sebastian, Oldgren Jonas, Reilly Paul, Siegbahn Agneta, Syvanen Ann-Christine, Wadelius Claes, Wadelius Mia, Zimdahl-Gelling Heike, Yusuf Salim, Wallentin La |
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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 |
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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
PLoS genetics 2013 9 (2): e1003266. Porcu Eleonora, Medici Marco, Pistis Giorgio, Volpato Claudia B, Wilson Scott G, Cappola Anne R, Bos Steffan D, Deelen Joris, den Heijer Martin, Freathy Rachel M, Lahti Jari, Liu Chunyu, Lopez Lorna M, Nolte Ilja M, O'Connell Jeffrey R, Tanaka Toshiko, Trompet Stella, Arnold Alice, Bandinelli Stefania, Beekman Marian, Böhringer Stefan, Brown Suzanne J, Buckley Brendan M, Camaschella Clara, de Craen Anton J M, Davies Gail, de Visser Marieke C H, Ford Ian, Forsen Tom, Frayling Timothy M, Fugazzola Laura, Gögele Martin, Hattersley Andrew T, Hermus Ad R, Hofman Albert, Houwing-Duistermaat Jeanine J, Jensen Richard A, Kajantie Eero, Kloppenburg Margreet, Lim Ee M, Masciullo Corrado, Mariotti Stefano, Minelli Cosetta, Mitchell Braxton D, Nagaraja Ramaiah, Netea-Maier Romana T, Palotie Aarno, Persani Luca, Piras Maria G, Psaty Bruce M, Räikkönen Katri, Richards J Brent, Rivadeneira Fernando, Sala Cinzia, Sabra Mona M, Sattar Naveed, Shields Beverley M, Soranzo Nicole, Starr John M, Stott David J, Sweep Fred C G J, Usala Gianluca, van der Klauw Melanie M, van Heemst Diana, van Mullem Alies, Vermeulen Sita H, Visser W Edward, Walsh John P, Westendorp Rudi G J, Widen Elisabeth, Zhai Guangju, Cucca Francesco, Deary Ian J, Eriksson Johan G, Ferrucci Luigi, Fox Caroline S, Jukema J Wouter, Kiemeney Lambertus A, Pramstaller Peter P, Schlessinger David, Shuldiner Alan R, Slagboom Eline P, Uitterlinden André G, Vaidya Bijay, Visser Theo J, Wolffenbuttel Bruce H R, Meulenbelt Ingrid, Rotter Jerome I, Spector Tim D, Hicks Andrew A, Toniolo Daniela, Sanna Serena, Peeters Robin P, Naitza Silv |
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Impact of ancestry and common genetic variants on QT interval in African Americans.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 647-55. Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, |
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Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Nature genetics 2012 Jun 44 (6): 670-5. Ellinor Patrick T, Lunetta Kathryn L, Albert Christine M, Glazer Nicole L, Ritchie Marylyn D, Smith Albert V, Arking Dan E, Müller-Nurasyid Martina, Krijthe Bouwe P, Lubitz Steven A, Bis Joshua C, Chung Mina K, Dörr Marcus, Ozaki Kouichi, Roberts Jason D, Smith J Gustav, Pfeufer Arne, Sinner Moritz F, Lohman Kurt, Ding Jingzhong, Smith Nicholas L, Smith Jonathan D, Rienstra Michiel, Rice Kenneth M, Van Wagoner David R, Magnani Jared W, Wakili Reza, Clauss Sebastian, Rotter Jerome I, Steinbeck Gerhard, Launer Lenore J, Davies Robert W, Borkovich Matthew, Harris Tamara B, Lin Honghuang, Völker Uwe, Völzke Henry, Milan David J, Hofman Albert, Boerwinkle Eric, Chen Lin Y, Soliman Elsayed Z, Voight Benjamin F, Li Guo, Chakravarti Aravinda, Kubo Michiaki, Tedrow Usha B, Rose Lynda M, Ridker Paul M, Conen David, Tsunoda Tatsuhiko, Furukawa Tetsushi, Sotoodehnia Nona, Xu Siyan, Kamatani Naoyuki, Levy Daniel, Nakamura Yusuke, Parvez Babar, Mahida Saagar, Furie Karen L, Rosand Jonathan, Muhammad Raafia, Psaty Bruce M, Meitinger Thomas, Perz Siegfried, Wichmann H-Erich, Witteman Jacqueline C M, Kao W H Linda, Kathiresan Sekar, Roden Dan M, Uitterlinden Andre G, Rivadeneira Fernando, McKnight Barbara, Sjögren Marketa, Newman Anne B, Liu Yongmei, Gollob Michael H, Melander Olle, Tanaka Toshihiro, Stricker Bruno H Ch, Felix Stephan B, Alonso Alvaro, Darbar Dawood, Barnard John, Chasman Daniel I, Heckbert Susan R, Benjamin Emelia J, Gudnason Vilmundur, Kääb Stef |
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Common variants in KCNN3 are associated with lone atrial fibrillation.
Nature genetics 2010 Mar 42 (3): 240-4. Ellinor Patrick T, Lunetta Kathryn L, Glazer Nicole L, Pfeufer Arne, Alonso Alvaro, Chung Mina K, Sinner Moritz F, de Bakker Paul I W, Mueller Martina, Lubitz Steven A, Fox Ervin, Darbar Dawood, Smith Nicholas L, Smith Jonathan D, Schnabel Renate B, Soliman Elsayed Z, Rice Kenneth M, Van Wagoner David R, Beckmann Britt-M, van Noord Charlotte, Wang Ke, Ehret Georg B, Rotter Jerome I, Hazen Stanley L, Steinbeck Gerhard, Smith Albert V, Launer Lenore J, Harris Tamara B, Makino Seiko, Nelis Mari, Milan David J, Perz Siegfried, Esko Tõnu, Köttgen Anna, Moebus Susanne, Newton-Cheh Christopher, Li Man, Möhlenkamp Stefan, Wang Thomas J, Kao W H Linda, Vasan Ramachandran S, Nöthen Markus M, MacRae Calum A, Stricker Bruno H Ch, Hofman Albert, Uitterlinden André G, Levy Daniel, Boerwinkle Eric, Metspalu Andres, Topol Eric J, Chakravarti Aravinda, Gudnason Vilmundur, Psaty Bruce M, Roden Dan M, Meitinger Thomas, Wichmann H-Erich, Witteman Jacqueline C M, Barnard John, Arking Dan E, Benjamin Emelia J, Heckbert Susan R, Kääb Stef |
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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 |
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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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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
Nature genetics 2009 Jul . Gudbjartsson DF, Holm H, Gretarsdottir S, Thorleifsson G, Walters GB, Thorgeirsson G, Gulcher J, Mathiesen EB, Njølstad I, Nyrnes A, Wilsgaard T, Hald EM, Hveem K, Stoltenberg C, Kucera G, Stubblefield T, Carter S, Roden D, Ng MC, Baum L, So WY, Wong KS, Chan JC, Gieger C, Wichmann HE, Gschwendtner A, Dichgans M, Kuhlenbäumer G, Berger K, Ringelstein EB, Bevan S, Markus HS, Kostulas K, Hillert J, Sveinbjörnsdóttir S, Valdimarsson EM, Løchen ML, Ma RC, Darbar D, Kong A, Arnar DO, Thorsteinsdottir U, Stefansson K |
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Nature genetics 2009 Jul . Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino Sr RB, Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M, Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK, Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S, Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S, Ellinor PT, Witteman JC |
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Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.
Annals of neurology 2008 Oct 64 (4): 402-9. Gretarsdottir Solveig, Thorleifsson Gudmar, Manolescu Andrei, Styrkarsdottir Unnur, Helgadottir Anna, Gschwendtner Andreas, Kostulas Konstantinos, Kuhlenbäumer Gregor, Bevan Steve, Jonsdottir Thorbjorg, Bjarnason Hjordis, Saemundsdottir Jona, Palsson Stefan, Arnar David O, Holm Hilma, Thorgeirsson Gudmundur, Valdimarsson Einar Mar, Sveinbjörnsdottir Sigurlaug, Gieger Christian, Berger Klaus, Wichmann H-Erich, Hillert Jan, Markus Hugh, Gulcher Jeffrey Robert, Ringelstein E Bernd, Kong Augustine, Dichgans Martin, Gudbjartsson Daniel Fannar, Thorsteinsdottir Unnur, Stefansson Ka |
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