Genetics of atrial fibrillation: from families to genomes von Christophersen, Ingrid E, Ellinor, Patrick T

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A comparison of the CHARGE–AF and the CHA2DS2-VASc risk scores for prediction of atrial fibrillation in the Framingham Heart Study von Christophersen, Ingrid E., Yin, Xiaoyan, Larson, Martin G., Lubitz, Steven A., Magnani, Jared W., McManus, David D., Ellinor, Patrick T., Benjamin, Emelia J.

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Atrial Fibrillation Genetics Update: Toward Clinical Implementation von Kalstø, Silje Madeleine, Siland, Joylene Elisabeth, Rienstra, Michiel, Christophersen, Ingrid E.

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes von Chauhan, Ganesh, Traylor, Matthew, Sargurupremraj, Muralidharan, Okada, Yukinori, Mishra, Aniket, Giese, Anne-Katrin, van der Laan, Sander W., Gretarsdottir, Solveig, Anderson, Christopher D., Almgren, Peter, Amouyel, Philippe, Bartz, Traci M., Benavente, Oscar R., Boncoraglio, Giorgio B., Butterworth, Adam S., Carrera, Caty, Chasman, Daniel I., Cotlarciuc, Ioana, Cruchaga, Carlos, de Bakker, Paul I. W., Duan, Qing, Gottesman, Rebecca F., Harris, Tamara B., Hassan, Ahamad, Havulinna, Aki S., Heckbert, Susan R., Hyacinth, Hyacinth I., Ikram, M. Arfan, Ingelsson, Erik, Jian, Xueqiu, Jukema, J. Wouter, Kanai, Masahiro, Keene, Keith L., Kissela, Brett M., Kleindorfer, Dawn O., Kooperberg, Charles, Lange, Leslie A., Langenberg, Claudia, Launer, Lenore J., Lemmens, Robin, Lewis, Cathryn M., Lin, Wei-Yu, Lorentzen, Erik, Magnusson, Patrik K., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., O’Donnell, Martin J., Pulit, Sara L., Reiner, Alexander P., Ridker, Paul M., Rothwell, Peter M., Rotter, Jerome I., Sale, Michele M., Salomaa, Veikko, Sapkota, Bishwa R., Schmidt, Reinhold, Schmidt, Carsten O., Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie L. M., Tanislav, Christian, Thijs, Vincent N. S., Thorsteinsdottir, Unnur, Tiedt, Steffen, Trompet, Stella, Wareham, Nicholas J., Wassertheil-Smoller, Sylvia, Wilson, James G., Pastinen, Tomi, Ruusalepp, Arno, Koplev, Simon, Björkegren, Johan L. M., Codoni, Veronica, Civelek, Mete, Christophersen, Ingrid E., Roselli, Carolina, Ellinor, Patrick T., Kato, Norihiro, van der Harst, Pim, Elliott, Paul, Takeuchi, Fumihiko, Johnson, Andrew D., Sanghera, Dharambir K., Melander, Olle, Strbian, Daniel, Fernandez-Cadenas, Israel, Rolfs, Arndt, Hata, Jun, Woo, Daniel, Pare, Guillaume, Hopewell, Jemma C., Saleheen, Danish, Stefansson, Kari, Worrall, Bradford B., Seshadri, Sudha, Markus, Hugh S., Debette, Stephanie, Dichgans, Martin

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Multi-ethnic genome-wide association study for atrial fibrillation von Roselli, Carolina, Chaffin, Mark D., Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M., Alonso, Alvaro, Anderson, Christopher D., Arking, Dan E., Bartz, Traci M., Benjamin, Emelia J., Bihlmeyer, Nathan A., Bis, Joshua C., Bloom, Heather L., Brody, Jennifer A., Chen, Lin Y., Choi, Eue-Keun, Christophersen, Ingrid E., Conen, David, Cook, James, Damrauer, Scott M., Denny, Joshua C., Dudley, Samuel C., Esko, Tonu, Felix, Stephan B., Franco, Oscar H., Geelhoed, Bastiaan, Grewal, Raji P., Gutmann, Rebecca, Harris, Tamara B., Hofman, Albert, Huang, Jie, Huang, Paul L., Ito, Kaoru, Johnson, Renee, Kääb, Stefan, Kamatani, Yoichiro, Kastrati, Adnan, Katschnig-Winter, Petra, Kessler, Thorsten, Kirchhof, Paulus, Kleber, Marcus E., Kubo, Michiaki, Lin, Henry J., Lindgren, Cecilia M., Loos, Ruth J. F., Lu, Yingchang, Lyytikäinen, Leo-Pekka, Magnusson, Patrik K., Malik, Rainer, Mansur, Alfredo J., Marcus, Gregory M., März, Winfried, Melander, Olle, Müller-Nurasyid, Martina, Nazarian, Saman, Neumann, Benjamin, Newton-Cheh, Christopher, Nilsson, Peter, Noordam, Raymond, Oellers, Heidi, Pak, Hui-Nam, Pedersen, Nancy L., Psaty, Bruce M., Pulit, Sara L., Pullinger, Clive R., Ribasés, Marta, Rienstra, Michiel, Rosand, Jonathan, Rost, Natalia, Saba, Samir, Schramm, Katharina, Schurman, Claudia, Scott, Stuart A., Shaffer, Christian, Shah, Svati, Shalaby, Alaa A., Shim, Jaemin, Shoemaker, M. Benjamin, Sinner, Moritz F., Smith, Albert V., Smith, Blair H., Sun, Han, Tanaka, Toshihiro, Tanriverdi, Kahraman, Taylor, Kent D., Thériault, Sébastien, Trompet, Stella, Tucker, Nathan R., Tveit, Arnljot, Uitterlinden, Andre G., Van Der Harst, Pim, Van Wagoner, David R., Wang, Biqi, Wong, Jorge A., Woo, Daniel, Yoneda, Zachary T., Zeller, Tanja, Zeng, Lingyao, Lubitz, Steven A.

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Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study von Anjum, Mariam, Ariansen, Inger, Hjellvik, Vidar, Selmer, Randi, Kjerpeseth, Lars J, Skovlund, Eva, Myrstad, Marius, Ellekjær, Hanne, Christophersen, Ingrid E, Tveit, Arnljot, Berge, Trygve

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Identification of six new genetic loci associated with atrial fibrillation in the Japanese population von 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, Toshihiro

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Rare Variants in GJA5 Are Associated With Early-Onset Lone Atrial Fibrillation von Christophersen, Ingrid E., MD, Holmegard, Haya N., MScPharm, Jabbari, Javad, MSc, Haunsø, Stig, MD, DMSc, Tveit, Arnljot, MD, DMSc, Svendsen, Jesper H., MD, DMSc, Olesen, Morten S., MSc, PhD

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation von Rienstra, Michiel, Roselli, Carolina, Yin, Xiaoyan, Geelhoed, Bastiaan, Lin, Honghuang, Arking, Dan E, Smith, Albert V, Albert, Christine M, Chaffin, Mark, Tucker, Nathan R, Li, Molong, Klarin, Derek, Low, Siew-Kee, Müller-Nurasyid, Martina, Dörr, Marcus, Trompet, Stella, Gustafsson, Stefan, Kleber, Marcus E, Lyytikäinen, Leo-Pekka, Seppälä, Ilkka, Malik, Rainer, Perez, Marco, Sinisalo, Juha, Thériault, Sébastien, Radmanesh, Farid, Teumer, Alexander, Weng, Lu-Chen, Deo, Rajat, Rader, Daniel J, Shah, Svati H, Yang, Qiong, Worrall, Bradford B, Kamatani, Yoichiro, Hagemeijer, Yanick P, Siland, Joylene E, Kubo, Michiaki, Smith, Jonathan D, 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, Kähönen, Mika, Risch, Lorenz, Mansur, Alfredo J, Smith, Blair H, Lu, Yingchang, Bottinger, Erwin B, Hernesniemi, Jussi, Lindgren, Cecilia M, Huang, Jie, Ford, Ian, Delgado, Graciela, Chen, Lin Y, Chen, Yii-Der Ida, Li, Man, Lannfelt, Lars, Rost, Natalia, Taylor, Kent D, Campbell, Archie, Porteous, David, Hocking, Lynne J, Nikus, Kjell, Orho-Melander, Marju, Hamsten, Anders, Denny, Joshua C, Kriebel, Jennifer, Newton-Cheh, Christopher, Shaffer, Christian, Macfarlane, Peter W, Heilmann-Heimbach, Stefanie, Huang, Paul L, Sotoodehnia, Nona, Soliman, Elsayed Z, Uitterlinden, Andre G, Hofman, Albert, Franco, Oscar H, Völker, Uwe, Lin, Henry J, Ingelsson, Erik, Kooperberg, Charles, Conen, David, Rosand, Jonathan, van der Harst, Pim, Kathiresan, Sekar, Stricker, Bruno H, Chung, Mina K, Felix, Stephan B, Gudnason, Vilmundur, Alonso, Alvaro, Kääb, Stefan, Chasman, Daniel I, Benjamin, Emelia J, Tanaka, Toshihiro, Lunetta, Kathryn L

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Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years von Olesen, Morten S., MSc, PhD, Holst, Anders G., MD, Jabbari, Javad, MSc, Nielsen, Jonas B., MD, Christophersen, Ingrid E., MD, Sajadieh, Ahmad, MD, DMSc, Haunsø, Stig, MD, DMSci, Svendsen, Jesper H., MD, DMSci

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Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation von Christophersen, Ingrid E, Olesen, Morten S, Liang, Bo, Andersen, Martin N, Larsen, Anders P, Nielsen, Jonas B, Haunsø, Stig, Olesen, Søren-Peter, Tveit, Arnljot, Svendsen, Jesper H, Schmitt, Nicole

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Genetic testing in early-onset atrial fibrillation von Kany, Shinwan, Jurgens, Sean J, Rämö, Joel T, Christophersen, Ingrid E, Rienstra, Michiel, Chung, Mina K, Olesen, Morten S, Ackerman, Michael J, McNally, Elizabeth M, Semsarian, Christopher, Schnabel, Renate B, Wilde, Arthur A M, Benjamin, Emelia J, Rehm, Heidi L, Kirchhof, Paulus, Bezzina, Connie R, Roden, Dan M, Shoemaker, M Benjamin, Ellinor, Patrick T

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Atrial fibrillation in women: treatment von Ko, Darae, Rahman, Faisal, Martins, Maria A. P., Hylek, Elaine M., Ellinor, Patrick T., Schnabel, Renate B., Benjamin, Emelia J., Christophersen, Ingrid E.

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Genetic Modifier of the QTc Interval Associated With Early-Onset Atrial Fibrillation von Andreasen, Laura, BM, Nielsen, Jonas B., MD, Christophersen, Ingrid E., MD, Holst, Anders Gaarsdal, MD, PhD, Sajadieh, Ahmad, MD, DMSc, Tveit, Arnljot, MD, DMSc, Haunsø, Stig, MD, DMSc, Svendsen, Jesper H., MD, DMSc, Schmitt, Nicole, MSc, PhD, Olesen, Morten S., MSc, PhD

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Whole Exome Sequencing in Atrial Fibrillation von 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, Honghuang

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Systematic screening for atrial fibrillation in a 65-year-old population with risk factors for stroke: data from the Akershus Cardiac Examination 1950 study von Berge, Trygve, Brynildsen, Jon, Larssen, Hege K Netmangen, Onarheim, Sophia, Jenssen, Gaute R, Ihle-Hansen, Haakon, Christophersen, Ingrid E, Myrstad, Marius, Røsjø, Helge, Smith, Pål, Tveit, Arnljot

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Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation von 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, Thomas

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Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation von Vad, Oliver B., Angeli, Elisavet, Liss, Martin, Ahlberg, Gustav, Andreasen, Laura, Christophersen, Ingrid E., Hansen, Camilla C., Møller, Sophie, Hellsten, Ylva, Haunsoe, Stig, Tveit, Arnljot, Svendsen, Jesper H., Gotthardt, Michael, Lundegaard, Pia R., Olesen, Morten S.

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 von Schmidt, Amand F, Holmes, Michael V, Preiss, David, Swerdlow, Daniel I, Denaxas, Spiros, Fatemifar, Ghazaleh, Faraway, Rupert, Finan, Chris, Valentine, Dennis, Fairhurst-Hunter, Zammy, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Lill, Christina M, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Willeit, Karin, Mason, Dan, Wright, John, Morris, Richard, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Price, Jackie F, Kivimaki, Mika, Welch, Catherine, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N Charlotte, van der Schouw, Yvonne T, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Langenberg, Claudia, Scott, Robert A, Luan, Jian'an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Linneberg, Allan, Jess, Tine, Cooper, Jackie, Humphries, Steve E, Brilliant, Murray, Kitchner, Terrie, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Lester, Kirchner H, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Roden, Dan M, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Attia, John, Holliday, Elizabeth, Scott, Rodney, Schofield, Peter, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, Pare, Guillaume, van der Harst, Pim, Said, M Abdullah, Eppinga, Ruben N, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, D O, Gustafsson, Stefan, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas

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Fifteen Genetic Loci Associated With the Electrocardiographic P Wave von 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 T

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