Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 21 (of 21 Records) |
Query Trace: Sudden Cardiac Death[original query] |
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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
![]() Nature communications 2022 9 13 (1): 5144. Young William J, Lahrouchi Najim, Isaacs Aaron, Duong ThuyVy, Foco Luisa, Ahmed Farah, Brody Jennifer A, Salman Reem, Noordam Raymond, Benjamins Jan-Walter, Haessler Jeffrey, Lyytikäinen Leo-Pekka, Repetto Linda, Concas Maria Pina, van den Berg Marten E, Weiss Stefan, Baldassari Antoine R, Bartz Traci M, Cook James P, Evans Daniel S, Freudling Rebecca, Hines Oliver, Isaksen Jonas L, Lin Honghuang, Mei Hao, Moscati Arden, Müller-Nurasyid Martina, Nursyifa Casia, Qian Yong, Richmond Anne, Roselli Carolina, Ryan Kathleen A, Tarazona-Santos Eduardo, Thériault Sébastien, van Duijvenboden Stefan, Warren Helen R, Yao Jie, Raza Dania, Aeschbacher Stefanie, Ahlberg Gustav, Alonso Alvaro, Andreasen Laura, Bis Joshua C, Boerwinkle Eric, Campbell Archie, Catamo Eulalia, Cocca Massimiliano, Cutler Michael J, Darbar Dawood, De Grandi Alessandro, De Luca Antonio, Ding Jun, Ellervik Christina, Ellinor Patrick T, Felix Stephan B, Froguel Philippe, Fuchsberger Christian, Gögele Martin, Graff Claus, Graff Mariaelisa, Guo Xiuqing, Hansen Torben, Heckbert Susan R, Huang Paul L, Huikuri Heikki V, Hutri-Kähönen Nina, Ikram M Arfan, Jackson Rebecca D, Junttila Juhani, Kavousi Maryam, Kors Jan A, Leal Thiago P, Lemaitre Rozenn N, Lin Henry J, Lind Lars, Linneberg Allan, Liu Simin, MacFarlane Peter W, Mangino Massimo, Meitinger Thomas, Mezzavilla Massimo, Mishra Pashupati P, Mitchell Rebecca N, Mononen Nina, Montasser May E, Morrison Alanna C, Nauck Matthias, Nauffal Victor, Navarro Pau, Nikus Kjell, Pare Guillaume, Patton Kristen K, Pelliccione Giulia, Pittman Alan, Porteous David J, Pramstaller Peter P, Preuss Michael H, Raitakari Olli T, Reiner Alexander P, Ribeiro Antonio Luiz P, Rice Kenneth M, Risch Lorenz, Schlessinger David, Schotten Ulrich, Schurmann Claudia, Shen Xia, Shoemaker M Benjamin, Sinagra Gianfranco, Sinner Moritz F, Soliman Elsayed Z, Stoll Monika, Strauch Konstantin, Tarasov Kirill, Taylor Kent D, Tinker Andrew, Trompet Stella, Uitterlinden André, Völker Uwe, Völzke Henry, Waldenberger Melanie, Weng Lu-Chen, Whitsel Eric A, Wilson James G, Avery Christy L, Conen David, Correa Adolfo, Cucca Francesco, Dörr Marcus, Gharib Sina A, Girotto Giorgia, Grarup Niels, Hayward Caroline, Jamshidi Yalda, Järvelin Marjo-Riitta, Jukema J Wouter, Kääb Stefan, Kähönen Mika, Kanters Jørgen K, Kooperberg Charles, Lehtimäki Terho, Lima-Costa Maria Fernanda, Liu Yongmei, Loos Ruth J F, Lubitz Steven A, Mook-Kanamori Dennis O, Morris Andrew P, O'Connell Jeffrey R, Olesen Morten Salling, Orini Michele, Padmanabhan Sandosh, Pattaro Cristian, Peters Annette, Psaty Bruce M, Rotter Jerome I, Stricker Bruno, van der Harst Pim, van Duijn Cornelia M, Verweij Niek, Wilson James F, Arking Dan E, Ramirez Julia, Lambiase Pier D, Sotoodehnia Nona, Mifsud Borbala, Newton-Cheh Christopher, Munroe Patricia |
Genetically Determined Serum Calcium Levels and Markers of Ventricular Repolarization: A Mendelian Randomization Study in the UK Biobank.
![]() Circulation. Genomic and precision medicine 2021 4 14 (3): e003231. Young William J, Warren Helen R, Mook-Kanamori Dennis O, Ramírez Julia, van Duijvenboden Stefan, Orini Michele, Tinker Andrew, van Heemst Diana, Lambiase Pier D, Jukema J Wouter, Munroe Patricia B, Noordam Raymo |
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.
![]() PloS one 2009 4 (7): e6138. Nolte Ilja M, Wallace Chris, Newhouse Stephen J, Waggott Daryl, Fu Jingyuan, Soranzo Nicole, Gwilliam Rhian, Deloukas Panos, Savelieva Irina, Zheng Dongling, Dalageorgou Chrysoula, Farrall Martin, Samani Nilesh J, Connell John, Brown Morris, Dominiczak Anna, Lathrop Mark, Zeggini Eleftheria, Wain Louise V, , , Newton-Cheh Christopher, Eijgelsheim Mark, Rice Kenneth, de Bakker Paul I W, , Pfeufer Arne, Sanna Serena, Arking Dan E, , Asselbergs Folkert W, Spector Tim D, Carter Nicholas D, Jeffery Steve, Tobin Martin, Caulfield Mark, Snieder Harold, Paterson Andrew D, Munroe Patricia B, Jamshidi Yal |
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
![]() Nature genetics 2009 Apr 41 (4): 4. Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A |
Common variants at ten loci influence QT interval duration in the QTGEN Study.
![]() Nature genetics 2009 Apr 41 (4): 4. Newton-Cheh C, Eijgelsheim M, Rice KM, de Bakker PI, Yin X, Estrada K, Bis JC, Marciante K, Rivadeneira F, Noseworthy PA, Sotoodehnia N, Smith NL, Rotter JI, Kors JA, Witteman JC, Hofman A, Heckbert SR, O'Donnell CJ, Uitterlinden AG, Psaty BM, Lumley T, Larson MG, Stricker BH |
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.
![]() PLoS genetics 2011 Jun 7 (6): e1002158. Arking Dan E, Junttila M Juhani, Goyette Philippe, Huertas-Vazquez Adriana, Eijgelsheim Mark, Blom Marieke T, Newton-Cheh Christopher, Reinier Kyndaron, Teodorescu Carmen, Uy-Evanado Audrey, Carter-Monroe Naima, Kaikkonen Kari S, Kortelainen Marja-Leena, Boucher Gabrielle, Lagacé Caroline, Moes Anna, Zhao XiaoQing, Kolodgie Frank, Rivadeneira Fernando, Hofman Albert, Witteman Jacqueline C M, Uitterlinden André G, Marsman Roos F, Pazoki Raha, Bardai Abdennasser, Koster Rudolph W, Dehghan Abbas, Hwang Shih-Jen, Bhatnagar Pallav, Post Wendy, Hilton Gina, Prineas Ronald J, Li Man, Köttgen Anna, Ehret Georg, Boerwinkle Eric, Coresh Josef, Kao W H Linda, Psaty Bruce M, Tomaselli Gordon F, Sotoodehnia Nona, Siscovick David S, Burke Greg L, Marbán Eduardo, Spooner Peter M, Cupples L Adrienne, Jui Jonathan, Gunson Karen, Kesäniemi Y Antero, Wilde Arthur A M, Tardif Jean-Claude, O'Donnell Christopher J, Bezzina Connie R, Virmani Renu, Stricker Bruno H C H, Tan Hanno L, Albert Christine M, Chakravarti Aravinda, Rioux John D, Huikuri Heikki V, Chugh Sumeet |
A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.
![]() American journal of human genetics 2012 Jul 91 (1): 180-4. Kim Jong Wook, Hong Kyung-Won, Go Min Jin, Kim Sung Soo, Tabara Yasuharu, Kita Yoshikuni, Tanigawa Takeshi, Cho Yoon Shin, Han Bok-Ghee, Oh Bermse |
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.
![]() Heart rhythm : the official journal of the Heart Rhythm Society 2012 Oct 9 (10): 1627-34. Sinner Moritz F, Porthan Kimmo, Noseworthy Peter A, Havulinna Aki S, Tikkanen Jani T, Müller-Nurasyid Martina, Peloso Gina, Ulivi Sheila, Beckmann Britt Maria, Brockhaus A Catharina, Cooper Rebecca R, Gasparini Paolo, Hengstenberg Christian, Hwang Shih-Jen, Iorio Annamaria, Junttila M Juhani, Klopp Norman, Kähönen Mika, Laaksonen Maarit A, Lehtimäki Terho, Lichtner Peter, Lyytikäinen Leo-Pekka, Martens Eimo, Meisinger Christa, Meitinger Thomas, Merchant Faisal M, Nieminen Markku S, Peters Annette, Pietilä Arto, Perz Siegfried, Oikarinen Lasse, Raitakari Olli, Reinhard Wibke, Silander Kaisa, Thorand Barbara, Wichmann H-Erich, Sinagra Gianfranco, Viikari Jorma, O'Donnell Christopher J, Ellinor Patrick T, Huikuri Heikki V, Kääb Stefan, Newton-Cheh Christopher, Salomaa Veik |
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, |
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
![]() Nature genetics 2013 Sep 45 (9): 1044-9. Bezzina Connie R, Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O, Schwartz Peter J, Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Borggrefe Martin, Schimpf Rainer, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R, Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M, Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J, Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L, Roden Dan M, Christoffels Vincent M, Le Marec Hervé, Wilde Arthur A, Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richa |
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.
![]() PloS one 2013 8 (4): e59905. Huertas-Vazquez Adriana, Nelson Christopher P, Guo Xiuqing, Reinier Kyndaron, Uy-Evanado Audrey, Teodorescu Carmen, Ayala Jo, Jerger Katherine, Chugh Harpriya, , Braund Peter S, Deloukas Panos, Hall Alistair S, Balmforth Anthony J, Jones Michelle, Taylor Kent D, Pulit Sara L, Newton-Cheh Christopher, Gunson Karen, Jui Jonathan, Rotter Jerome I, Albert Christine M, Samani Nilesh J, Chugh Sumeet |
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 |
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.
![]() Human molecular genetics 2014 Dec 23 (24): 6659-67. Hong Kyung-Won, Lim Ji Eun, Kim Jong Wook, Tabara Yasuharu, Ueshima Hirotsugu, Miki Tetsuro, Matsuda Fumihiko, Cho Yoon Shin, Kim Yeonjung, Oh Bermse |
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
![]() Nature genetics 2014 Aug 46 (8): 826-36. Arking Dan E, Pulit Sara L, Crotti Lia, van der Harst Pim, Munroe Patricia B, Koopmann Tamara T, Sotoodehnia Nona, Rossin Elizabeth J, Morley Michael, Wang Xinchen, Johnson Andrew D, Lundby Alicia, Gudbjartsson Daníel F, Noseworthy Peter A, Eijgelsheim Mark, Bradford Yuki, Tarasov Kirill V, Dörr Marcus, Müller-Nurasyid Martina, Lahtinen Annukka M, Nolte Ilja M, Smith Albert Vernon, Bis Joshua C, Isaacs Aaron, Newhouse Stephen J, Evans Daniel S, Post Wendy S, Waggott Daryl, Lyytikäinen Leo-Pekka, Hicks Andrew A, Eisele Lewin, Ellinghaus David, Hayward Caroline, Navarro Pau, Ulivi Sheila, Tanaka Toshiko, Tester David J, Chatel Stéphanie, Gustafsson Stefan, Kumari Meena, Morris Richard W, Naluai Åsa T, Padmanabhan Sandosh, Kluttig Alexander, Strohmer Bernhard, Panayiotou Andrie G, Torres Maria, Knoflach Michael, Hubacek Jaroslav A, Slowikowski Kamil, Raychaudhuri Soumya, Kumar Runjun D, Harris Tamara B, Launer Lenore J, Shuldiner Alan R, Alonso Alvaro, Bader Joel S, Ehret Georg, Huang Hailiang, Kao W H Linda, Strait James B, Macfarlane Peter W, Brown Morris, Caulfield Mark J, Samani Nilesh J, Kronenberg Florian, Willeit Johann, , , Smith J Gustav, Greiser Karin H, Meyer Zu Schwabedissen Henriette, Werdan Karl, Carella Massimo, Zelante Leopoldo, Heckbert Susan R, Psaty Bruce M, Rotter Jerome I, Kolcic Ivana, Polašek Ozren, Wright Alan F, Griffin Maura, Daly Mark J, , Arnar David O, Hólm Hilma, Thorsteinsdottir Unnur, , Denny Joshua C, Roden Dan M, Zuvich Rebecca L, Emilsson Valur, Plump Andrew S, Larson Martin G, O'Donnell Christopher J, Yin Xiaoyan, Bobbo Marco, D'Adamo Adamo P, Iorio Annamaria, Sinagra Gianfranco, Carracedo Angel, Cummings Steven R, Nalls Michael A, Jula Antti, Kontula Kimmo K, Marjamaa Annukka, Oikarinen Lasse, Perola Markus, Porthan Kimmo, Erbel Raimund, Hoffmann Per, Jöckel Karl-Heinz, Kälsch Hagen, Nöthen Markus M, , den Hoed Marcel, Loos Ruth J F, Thelle Dag S, Gieger Christian, Meitinger Thomas, Perz Siegfried, Peters Annette, Prucha Hanna, Sinner Moritz F, Waldenberger Melanie, de Boer Rudolf A, Franke Lude, van der Vleuten Pieter A, Beckmann Britt Maria, Martens Eimo, Bardai Abdennasser, Hofman Nynke, Wilde Arthur A M, Behr Elijah R, Dalageorgou Chrysoula, Giudicessi John R, Medeiros-Domingo Argelia, Barc Julien, Kyndt Florence, Probst Vincent, Ghidoni Alice, Insolia Roberto, Hamilton Robert M, Scherer Stephen W, Brandimarto Jeffrey, Margulies Kenneth, Moravec Christine E, del Greco M Fabiola, Fuchsberger Christian, O'Connell Jeffrey R, Lee Wai K, Watt Graham C M, Campbell Harry, Wild Sarah H, El Mokhtari Nour E, Frey Norbert, Asselbergs Folkert W, Mateo Leach Irene, Navis Gerjan, van den Berg Maarten P, van Veldhuisen Dirk J, Kellis Manolis, Krijthe Bouwe P, Franco Oscar H, Hofman Albert, Kors Jan A, Uitterlinden André G, Witteman Jacqueline C M, Kedenko Lyudmyla, Lamina Claudia, Oostra Ben A, Abecasis Gonçalo R, Lakatta Edward G, Mulas Antonella, Orrú Marco, Schlessinger David, Uda Manuela, Markus Marcello R P, Völker Uwe, Snieder Harold, Spector Timothy D, Ärnlöv Johan, Lind Lars, Sundström Johan, Syvänen Ann-Christine, Kivimaki Mika, Kähönen Mika, Mononen Nina, Raitakari Olli T, Viikari Jorma S, Adamkova Vera, Kiechl Stefan, Brion Maria, Nicolaides Andrew N, Paulweber Bernhard, Haerting Johannes, Dominiczak Anna F, Nyberg Fredrik, Whincup Peter H, Hingorani Aroon D, Schott Jean-Jacques, Bezzina Connie R, Ingelsson Erik, Ferrucci Luigi, Gasparini Paolo, Wilson James F, Rudan Igor, Franke Andre, Mühleisen Thomas W, Pramstaller Peter P, Lehtimäki Terho J, Paterson Andrew D, Parsa Afshin, Liu Yongmei, van Duijn Cornelia M, Siscovick David S, Gudnason Vilmundur, Jamshidi Yalda, Salomaa Veikko, Felix Stephan B, Sanna Serena, Ritchie Marylyn D, Stricker Bruno H, Stefansson Kari, Boyer Laurie A, Cappola Thomas P, Olsen Jesper V, Lage Kasper, Schwartz Peter J, Kääb Stefan, Chakravarti Aravinda, Ackerman Michael J, Pfeufer Arne, de Bakker Paul I W, Newton-Cheh Christoph |
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.
![]() Genome biology 2018 07 19 (1): 87. Prins Bram P, Mead Timothy J, Brody Jennifer A, Sveinbjornsson Gardar, Ntalla Ioanna, Bihlmeyer Nathan A, van den Berg Marten, Bork-Jensen Jette, Cappellani Stefania, Van Duijvenboden Stefan, Klena Nikolai T, Gabriel George C, Liu Xiaoqin, Gulec Cagri, Grarup Niels, Haessler Jeffrey, Hall Leanne M, Iorio Annamaria, Isaacs Aaron, Li-Gao Ruifang, Lin Honghuang, Liu Ching-Ti, Lyytikäinen Leo-Pekka, Marten Jonathan, Mei Hao, Müller-Nurasyid Martina, Orini Michele, Padmanabhan Sandosh, Radmanesh Farid, Ramirez Julia, Robino Antonietta, Schwartz Molly, van Setten Jessica, Smith Albert V, Verweij Niek, Warren Helen R, Weiss Stefan, Alonso Alvaro, Arnar David O, Bots Michiel L, de Boer Rudolf A, Dominiczak Anna F, Eijgelsheim Mark, Ellinor Patrick T, Guo Xiuqing, Felix Stephan B, Harris Tamara B, Hayward Caroline, Heckbert Susan R, Huang Paul L, Jukema J W, Kähönen Mika, Kors Jan A, Lambiase Pier D, Launer Lenore J, Li Man, Linneberg Allan, Nelson Christopher P, Pedersen Oluf, Perez Marco, Peters Annette, Polasek Ozren, Psaty Bruce M, Raitakari Olli T, Rice Kenneth M, Rotter Jerome I, Sinner Moritz F, Soliman Elsayed Z, Spector Tim D, Strauch Konstantin, Thorsteinsdottir Unnur, Tinker Andrew, Trompet Stella, Uitterlinden André, Vaartjes Ilonca, van der Meer Peter, Völker Uwe, Völzke Henry, Waldenberger Melanie, Wilson James G, Xie Zhijun, Asselbergs Folkert W, Dörr Marcus, van Duijn Cornelia M, Gasparini Paolo, Gudbjartsson Daniel F, Gudnason Vilmundur, Hansen Torben, Kääb Stefan, Kanters Jørgen K, Kooperberg Charles, Lehtimäki Terho, Lin Henry J, Lubitz Steven A, Mook-Kanamori Dennis O, Conti Francesco J, Newton-Cheh Christopher H, Rosand Jonathan, Rudan Igor, Samani Nilesh J, Sinagra Gianfranco, Smith Blair H, Holm Hilma, Stricker Bruno H, Ulivi Sheila, Sotoodehnia Nona, Apte Suneel S, van der Harst Pim, Stefansson Kari, Munroe Patricia B, Arking Dan E, Lo Cecilia W, Jamshidi Yal |
Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study).
![]() Journal of the American Heart Association 2018 Apr 7 (8): . Tereshchenko Larisa G, Sotoodehnia Nona, Sitlani Colleen M, Ashar Foram N, Kabir Muammar, Biggs Mary L, Morley Michael P, Waks Jonathan W, Soliman Elsayed Z, Buxton Alfred E, Biering-Sørensen Tor, Solomon Scott D, Post Wendy S, Cappola Thomas P, Siscovick David S, Arking Dan |
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern.
![]() JCI insight 2019 Dec 4 (23): . Teumer Alexander, Trenkwalder Teresa, Kessler Thorsten, Jamshidi Yalda, van den Berg Marten E, Kaess Bernhard, Nelson Christopher P, Bastiaenen Rachel, De Bortoli Marzia, Rossini Alessandra, Deisenhofer Isabel, Stark Klaus, Assa Solmaz, Braund Peter S, Cabrera Claudia, Dominiczak Anna F, Gögele Martin, Hall Leanne M, Ikram M Arfan, Kavousi Maryam, Lackner Karl J, , Müller Christian, Münzel Thomas, Nauck Matthias, Padmanabhan Sandosh, Pfeiffer Norbert, Spector Tim D, Uitterlinden Andre G, Verweij Niek, Völker Uwe, Warren Helen R, Zafar Mobeen, Felix Stephan B, Kors Jan A, Snieder Harold, Munroe Patricia B, Pattaro Cristian, Fuchsberger Christian, Schmidt Georg, Nolte Ilja M, Schunkert Heribert, Pramstaller Peter P, Wild Philipp S, van der Harst Pim, Stricker Bruno H, Schnabel Renate B, Samani Nilesh J, Hengstenberg Christian, Dörr Marcus, Behr Elijah R, Reinhard Wib |
Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
![]() JAMA cardiology 2020 May . Turley Tamiel N, O'Byrne Megan M, Kosel Matthew L, de Andrade Mariza, Gulati Rajiv, Hayes Sharonne N, Tweet Marysia S, Olson Timothy |
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
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Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval.
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Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
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