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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

by Cartwright, James H, Amelia Weber Hall, Sveinbjornsson, Gardar, Tucker, Nathan R, Choi, Seung Hoan, Chaffin, Mark D, Roselli, Carolina, Barnes, Michael R, Warren, Helen R, Hayward, Caroline, Marten, Jonathan, Cranley, James J, Boutin, Thibaud, Araujo, Nathalia M, Souza, Renan P, Giedraitis, Vilmantas, Ingelsson, Erik, Morris, Andrew P, Fabiola Del Greco M, Foco, Luisa, Cook, James P, Lind, Lars, Lindgren, Cecilia M, Sundstrom, Johan, Nelson, Christopher P, Samani, Nilesh J, Ulivi, Sheila, Kahonen, Mika, Mishra, Pashupati P, Nikus, Kjell, Caulfield, Mark J, O'connell, Jeff R, Aeschbacher, Stefanie, Theriault, Sebastien, Campbell, Harry, Joshi, Peter K, Wilson, James F, Huang, Paul L, Gudnason, Vilmundur, Launer, Lenore J, Bottinger, Erwin P, Loos, Ruth J F, Hao Mei, Wilson, James, Muller-Nurasyid, Martina, Waldenberger, Melanie, Mangino, Massimo, Spector, Timothy D, Rienstra, Michiel, Yordi J Van De Vegte, Pim Van Der Harst, Strauch, Konstantin, Fatkin, Diane, Olesen, Morten, Shoemaker, M Benjamin, Bis, Joshua C, Sotoodehnia, Nona, De Grandi, Alessandro, Fuchsberger, Christian, Pramstaller, Peter P, d, Ian, Jukema, J Wouter, Felix, Stephan B, Weiss, Stefan, Havulinna, Aki S, Salomaa, Veikko, Heckbert, Susan R, Rotter, Jerome I, Yao, Jie, De Mutsert, Renee, Maan, Arie C, Noordam, Raymond, Ding, Jun, Lakatta, Edward G, Tarasov, Kirill V, Lin, Honghuang, Newton-Cheh, Christopher H, Porteous, David J, Smith, Blair H, Marten E Van Den Berg, Jackson, Rebecca D, Whitsel, Eric A, Arking, Dan E, Gogarten, Stephanie M, Kerr, Kathleen F, Laurie, Cathy C, Seyerle, Amanda A, Assa, Solmaz, Lambiase, Pier D, Ramirez, Julia, Stefan Van Duijvenboden, Gudbjartsson, Daniel F, Holm, Hilma, Sulem, Patrick, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Benjamin, Emelia J, Ellinor, Patrick T, Lubitz, Steven A, Munroe, Patricia B
Published in bioRxiv (30.07.2019)

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

by Shah, Sonia, Roselli, Carolina, Lin, Honghuang, Hedman, Åsa K, Morley, Michael P, Chaffin, Mark D, Helgadottir, Anna, Dehghan, Abbas, Almgren, Peter, Anderson, Charlotte, Ärnlöv, Johan, Biggs, Mary L, Bloom, Heather L, Brandimarto, Jeffrey, Broad Af Investigators, Carey, David J, Center, Regeneron Genetics, Chen, Xu, Chung, Jonathan, Chutkow, William, Cook, James P, Delgado, Graciela E, Doney, Alexander S, Dörr, Marcus, Dudley, Samuel C, Consortium, Echogen, Engström, Gunnar, Tõnu Esko, Felix, Stephan B, Ghanbari, Mohsen, Giedraitis, Vilmantas, Gottdiener, John S, Gross, Stefan, Gutmann, Rebecca, Ingelsson, Erik, Jukema, J Wouter, Kavousi, Maryam, Kay-Tee Khaw, Køber, Lars, Koekemoer, Andrea, Lindgren, Cecilia M, London, Barry, Lotta, Luca A, Magnusson, Patrik, Margulies, Kenneth B, März, Winfried, Melander, Olle, Mordi, Ify R, Morgan, Thomas, Morris, Andrew P, Morrison, Alanna C, Nelson, Christopher P, Niessner, Alexander, O'donoghue, Michelle L, Owens, Anjali T, Palmer, Colin N A, Parry, Helen M, Portilla-Fernandez, Eliana, Psaty, Bruce M, Rice, Kenneth M, Romaine, Simon P R, Rotter, Jerome I, Salo, Perttu, Salomaa, Veikko, Jessica Van Setten, Shalaby, Alaa A, Smelser, Diane T, Stender, Steen, Svensson, Per, Maris Teder-Laving, Teumer, Alexander, Thorgeirsson, Guðmundur, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Benoit Tyl, Veluchamy, Abirami, Voors, Adriaan A, Wareham, Nicholas J, Weeke, Peter E, Weiss, Raul, Heming Xing, Yerges-Armstrong, Laura M, Yu, Bing, Zhao, Jing Hua, Samani, Nilesh J, Yang, Jian, Visscher, Peter M, Newton-Cheh, Christopher, Malarstig, Anders, Lubitz, Steven A, Sattar, Naveed, Holmes, Michael V, Cappola, Thomas P, Hingorani, Aroon Dinesh, Lang, Chim C, Stefansson, Kari, Smith, J Gustav, Vasan, Ramachandran S, Lumbers, R Thomas
Published in bioRxiv (10.07.2019)

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