Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Martina Müller-Nurasyid"'
Autor:
Cristina Sanchez-Mora, Jie Hu, Philippe Amouyel, Annette Peters, Charles C Hong, Mary Cushman, Kathleen A. Ryan, Jiang Li, Liming Li, Thomas Jaworek, Sylvia Wassertheil-Smoller, Tiina Metso, Martin Soderholm, Kathryn M. Rexrode, Nicholas L. Smith, Jane Maguire, Martina Müller-Nurasyid, Agnieszka Slowik, Marguerite R. Irvin, Adam S. Butterworth, Martin O’Donnell, Leema Reddy Peddareddygari, Rainer Malik, Ralph L. Sacco, Brady Gaynor, Christian Geiger, Debashree Ray, Anne-Katrin Giese, John W. Cole, Jon Peter Durda, Vincent Thijs, Jukka Putaala, Michiaki Kubo, O. Colin Stine, Rebecca D. Jackson, Israel Fernandez-Cadenas, Reinhold Schmidt, Aki S. Havulinna, Kuang Lin, Christopher Levi, Steven Bell, Timothy O’Connor, Daniel Woo, Jara Cárcel-Márquez, Braxton D. Mitchell, Christina Jern, Jonathan Rosand, Sharon L.R. Kardia, Pankaj Sharma, Mina A. Jacob, Masaru Koido, Vida Abedi, Yoichiro Kamatani, Kristiina Rannikmäe, Michael Chong, Nuria P. Torres-Aguila, Cathie L. M. Sudlow, Ramin Zand, Elizabeth Holliday, Tatjana Rundek, Jessica D. Faul, Leslie Lange, Gunnar Engstrom, Marc C. Hochberg, Bradford B. Worrall, Hugh S. Markus, Joanna Pera, Jordi Jimenez-Conde, Caitrin W. McDonough, Raji P. Grewal, Owen Ross, Robin G. Walters, David J. Duggan, Guillaume Paré, Turgut Tatlisumak, Laura Heitsch, Jin-Moo Lee, Natalie Fecteau, Robin Lemmens, Jennifer A. Smith, Daniel Strbian, Patrick F. McArdle, Martin Dichgans, Jan H. Veldink, Liisa Tomppo, Arne G. Lindgren, Zhengming Chen, Chikashi Terao, Ulrike Grittner, Marta Ribasés, David R. Weir, James F. Meschia, Sothear Luke, Raquel Rabionet Janssen, Tara M. Stanne, Stephanie Debette, Nicole D. Armstrong, James A. Perry, Julie A. Johnson, Huichun Xu, Christopher D. Anderson, Giorgio B. Boncoraglio, Christian Enzinger, Haley Lopez, Anil Man Tuladhar, Oscar R. Benavente, Veikko Salomaa, David-Alexandre Trégouët, John Danesh, F-E de Leeuw, John Attia, Peter M. Rothwell, Steven J. Kittner, Andreea Ilinca, Carlos Cruchaga
ObjectiveTo determine the contribution of common genetic variants to risk of early onset ischemic stroke (IS).MethodsWe performed a meta-analysis of genome-wide association studies of early onset IS, ages 18-59, using individual level data or summary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd936a9592fa06f9544ad9f7927fd356
https://doi.org/10.1101/2021.11.06.21265795
https://doi.org/10.1101/2021.11.06.21265795
Autor:
Sara M. Willems, Josée Dupuis, Martina Müller-Nurasyid, Boehnke M, Mark H, Salem, Inês Barroso, Letizia Marullo, Kari Stefansson, C Gieger, Anna Ulrich, Morris J. Brown, González Ksg, Grant W. Montgomery, Anders Hamsten, Emma Ahlqvist, Aaron Isaacs, Kay-Tee Khaw, Amy Hofman, Corrêa Ir, Inger Njølstad, L Zudina, Rona J. Strawbridge, J. Tuomilehto, E Albrecht, Jing Hua Zhao, Patrick M. Sexton, Mark I. McCarthy, Roxana Maria Rujan, Chiara Scapoli, Anne U. Jackson, Ioanna Tzoulaki, van Duijn C, Giuseppe Deganutti, Reedik Mägi, Jose C. Florez, Bernhard O. Boehm, Toby Johnson, Petar Todorov, Jones B, Inga Prokopenko, Leif Groop, Lagou, Hugh Watkins, Balkhiyarova Z, Tomas A, Longda Jiang, Oddgeir L. Holmen, Tan Tm, Barbara Thorand, Andre G. Uitterlinden, Wolfgang Koenig, He Gao, Sodbo Zh Sharapov, Claudia Langenberg, D Rybin, Ayse Demirkan, H Grallert, Christine Meisinger, Eric F, Denise Wootten, Heinz Erich Wichmann, Wolfgang Kratzer, Paul Elliott, Tune H. Pers, Beben Benyamin, Yurii S. Aulchenko, Robert A. Scott, Marika Kaakinen, Alessia David, Tom Wilsgaard, John Whitfield, Patricia B. Munroe, Chen S, Karen L. Mohlke, Alessia Faggian, Evangelos Evangelou, Philippe Froguel, Nicholas J. Wareham, Unnur Thorsteinsdottir, N. G. Martin, Christopher A. Reynolds, Steinthorsdottir, Heather M. Stringham, Mark J. Caulfield, Gudmar Thorleifsson, James B. Meigs, Anuj Goel, Kristian Hveem, Evan L. Brittain, Julian S
Homeostatic control of blood glucose requires different physiological responses in the fasting and post-prandial states. We reasoned that glucose measurements under non-standardised conditions (random glucose; RG) may capture diverse glucoregulatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78e4d80872e2445f49e7123f3fd68633
https://doi.org/10.1101/2021.04.17.21255471
https://doi.org/10.1101/2021.04.17.21255471
Autor:
Céline Besse, François Cambien, Folkert W. Asselbergs, Robert Olaso, Jeanette Erdman, Benjamin Meder, Stephan B. Felix, Stefan Weiss, Laurent Fauchier, Konstantin Strauch, Luigi Tavazzi, Anne Boland, Gérard Roizès, Pascal DeGroote, Renee Maas, Melanie Waldenberger, Ganapathi Varma Saripella, Pablo García-Pavía, Brendan J. Keating, Vera Regitz-Zagrosek, Marine Germain, Stefan Blankenberg, Jessica van Setten, Eloisa Arbustini, Pierre Boutouyrie, Carole Proust, Delphine Bacq-Daian, Hemerich Daiane, Sophie Garnier, Michal Mokry, Richard Dorent, Martina Müller-Nurasyid, Philippe Charron, Maurizia Grasso, Steven Mc Ginn, Vincent Fontaine, Uwe Völker, Patrick Lacolley, Thomas Meitinger, Christine E. Seidman, Ibticem Raji, David-Alexandre Trégouët, Jean-Noël Trochu, Thomas Wichter, Jörg Callis, Alain van Mil, Jean-François Deleuze, Declan P. O'Regan, Xavier Jouven, Jin Li, Klaus Stark, Eric Villard, Stuart A. Cook, Hakon Hakonarson, Michael Morley, Kenneth B. Marguiles, Sanjay K Prasad, Volker Ruppert, Jean-François Aupetit, Jean-Philippe Empana, Marcus Dörr, Thomas P. Cappola, Michel Komajda, Magdalena Harakalova, Christian Hengstenberg, Hélène Blanché, Angélique Curjol, L. Duboscq-Bidot, Richard Isnard, Olivier Dubourg, K Lehnert
SummaryWe present the results of the largest genome wide association study (GWAS) performed so far in dilated cardiomyopathy (DCM), a leading cause of systolic heart failure and cardiovascular death, with 2,719 cases and 4,440 controls in the discove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fc3119dd5f3a16ea14b94c575d999ba
https://doi.org/10.1101/2020.02.28.969147
https://doi.org/10.1101/2020.02.28.969147
Autor:
Helmut Küchenhoff, Katrin Horn, Christina Kiel, F. Rauscher, Bernhard H. F. Weber, Ruth E Hogg, Marisa Cañadas-Garre, Klaus Stark, Annette Peters, Caroline Brandl, Thomas W. Winkler, Lorraine Weidner, Alicia Poplawski, Nicola Quinn, Tobias Strunz, Martina E. Zimmermann, Amy Jayne McKnight, Tobias Elze, Felix Grassmann, Felix Günther, Markus Scholz, Alexander K. Schuster, Martina Müller-Nurasyid, Iris M. Heid, Christina Korb
Publikováno v:
BMC Med. Genomics 13:120 (2020)
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-18 (2020)
BMC Medical Genomics
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-18 (2020)
BMC Medical Genomics
Background Advanced age-related macular degeneration (AMD) is a leading cause of blindness. While around half of the genetic contribution to advanced AMD has been uncovered, little is known about the genetic architecture of early AMD. Methods To iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b54583b59cba9c40278282f803e03177
https://doi.org/10.1101/2019.12.20.883801
https://doi.org/10.1101/2019.12.20.883801
Autor:
Shahram Bahrami, Gregor K. Wenning, J. Raphael Gibbs, Antonio Heras-Garvin, Sonja W. Scholz, Stefan Schreiber, Wassilios G. Meissner, John Hardy, Andrew B. Singleton, Monia B. Hammer, Markus M. Nöthen, Manu Sharma, Olivier Rascol, Ole A. Andreassen, Cornelis Blauwendraat, Oleksandr Frei, Martina Müller-Nurasyid, Ashwin Ashok Kumar Sreelatha, Andreas Arnold, Thomas Gasser, David Ellinghaus, Carsten Oliver Schmidt, Jinhui Ding, Nadia Stefanova, Andre Franke, Kevin S. O’Connell, Anne Pavy-Le Traon, Alexey A. Shadrin, Wolfgang Lieb, Georg Homuth, Mary B. Makarious, Christian Gieger, Per Hoffmann, Alexandra Foubert-Samier, Sören Mucha, Henry Houlden
We aimed to identify shared genetic background between multiple system atrophy (MSA) and autoimmune diseases by using the conjFDR approach. Our study showed significant genetic overlap between MSA and inflammatory bowel disease and identified DENND1B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589f88e504d22f1e0fb8d82a01e8c4a9
Autor:
Lorenz Risch, Igor Rudan, Hilma Holm, Christopher P. Nelson, Jan A. Kors, Stefanie Aeschbacher, Stefan Kääb, Peter W. Macfarlane, Lars Lind, Amanda A. Seyerle, Ozren Polasek, Daniel F. Gudbjartsson, Xiuqing Guo, Nilesh J. Samani, Bruce M. Psaty, Rosa B. Thorolfsdottir, Elsayed Z. Soliman, Yong Qian, Mary L. Biggs, Antti Jula, Vilmundur Gudnason, Paul L. Huang, Tamara B. Harris, Gianfranco Sinagra, Luisa Foco, Anubha Mahajan, Mika Kähönen, Lu-Chen Weng, Borbala Mifsud, Stefan van Duijvenboden, Terho Lehtimäki, Jennifer A. Brody, Paolo Gasparini, Kathleen A. Ryan, Marten E. van den Berg, James J. Cranley, Eric Boerwinkle, Cathy C. Laurie, Annette Peters, Joshua C. Bis, Raymond Noordam, Andrew P. Morris, Johan Sundström, Lenore J. Launer, Stefan Weiss, Rebecca D. Jackson, Alison D. Murray, Jeffrey R. O'Connell, Aki S. Havulinna, Dennis O. Mook-Kanamori, Sheila Ulivi, Renée de Mutsert, Eric A. Whitsel, Adrienne M. Stilp, James P. Cook, Nona Sotoodehnia, Antonio Luiz Pinho Ribeiro, Seung Hoan Choi, Mark J. Caulfield, Sébastien Thériault, Henry J. Lin, Dan M. Roden, J. Wouter Jukema, James F. Wilson, Veikko Salomaa, Honghuang Lin, Andrew A. Hicks, Christy L. Avery, Nina Mononen, Dan E. Arking, Ruth J. F. Loos, Yalda Jamshidi, André G. Uitterlinden, Nina Hutri-Kähönen, Andrew Tinker, Gudmar Thorleifsson, Daniel Levy, Martina Müller-Nurasyid, Alexander P. Reiner, Bruno H. Stricker, Caroline Hayward, Yordi J. van de Vegte, Ioanna Ntalla, Tim D. Spector, Niek Verweij, Michael R. Barnes, Martin Gögele, Nathan R. Tucker, Arie C. Maan, Eduardo Tarazona-Santos, Katri Sääksjärvi, Maria Pina Concas, Pim van der Harst, Georg Ehret, Cecilia M. Lindgren, David Conen, Cornelia M. van Duijn, Muhammad B. Riaz, Leo-Pekka Lyytikäinen, Amelia W. Hall, Peter P. Pramstaller, Maria Fernanda Lima-Costa, Vilmantas Giedraitis, Emelia J. Benjamin, M. Fabiola Del Greco, Thomas Meitinger, Erwin P. Bottinger, Francesco Cucca, Aaron Isaacs, Carolina Roselli, James H. Cartwright, Massimo Mangino, Adolfo Correa, Patrick Sulem, Thibaud Boutin, Michiel Rienstra, Stephan B. Felix, Julia Ramirez, Kathleen F. Kerr, Jonathan Marten, David J. Porteous, Kent D. Taylor, Patrick T. Ellinor, Michele Orini, Susan R. Heckbert, Olli T. Raitakari, Girish N. Nadkarni, Edward G. Lakatta, Anna F. Dominiczak, Jie Yao, Erik Ingelsson, Christopher Newton-Cheh, Katharina Schramm, Jerome I. Rotter, Michael J. Cutler, Pashupati P. Mishra, Diane Fatkin, Marcus Dörr, Ulrike Peters, Solmaz Assa, Christian Fuchsberger, M. Abdullah Said, Catriona L. K. Barnes, Peter K. Joshi, M. Yldau van der Ende, Alvaro Alonso, James G. Wilson, Jun Ding, Kathryn L. Lunetta, Kjell Nikus, Helen R. Warren, Charles Kooperberg, Moritz F. Sinner, Sandosh Padmanabhan, Patricia B. Munroe, Jeffrey Haessler, Albert V. Smith, Alan R. Shuldiner, Morten S. Olesen, Konstantin Strauch, Steven A. Lubitz, J. Gustav Smith, Renan P. Souza, Michael Preuss, Kirill V. Tarasov, M. Benjamin Shoemaker, Barry London, Melanie Waldenberger, Cristian Pattaro, David O. Arnar, Gardar Sveinbjornsson, Alessandro De Grandi, Ian Ford, Kenneth Rice, Mark Chaffin, Kari Stefansson, Hao Mei, Uwe Völker, Blair H. Smith, Nathalia M. Araujo, Harry Campbell, Pier D. Lambiase, Stephanie M. Gogarten, May E. Montasser, Unnur Thorsteinsdottir, Ivana Kolcic, Stella Trompet
The electrocardiographic PR interval reflects atrioventricular conduction, and is associated with conduction abnormalities, pacemaker implantation, atrial fibrillation (AF), and cardiovascular mortality1,2. We performed multi-ancestry (N=293,051) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3776ecad4a8ada2d09b3d886a3e960fe
https://doi.org/10.1101/712398
https://doi.org/10.1101/712398
Autor:
Dmitreva J, van Iterson M, Brenda W.J.H. Penninx, Reyhan Sonmez, Michel Georges, Tõnu Esko, Matthias Nauck, Eline Slagboom, Bruce M. Psaty, Urko M. Marigorta, Michel G. Nivard, C Wijmenga, Markus Perola, Joost Verlouw, Jaanika Kronberg-Guzman, Bastiaan T. Heijmans, van Dongen J, Martina Müller-Nurasyid, Yukihide Momozawa, Silva Kasela, Joseph E. Powell, Sina Rüeger, Brandon L. Pierce, Sven Bergmann, van Meurs J, Lude Franke, Uwe Völker, Futao Zhang, Marc Jan Bonder, Z. Kutalik, Frank Beutner, Ilkka Seppälä, Jarno Kettunen, Morris A. Swertz, Harm-Jan Westra, Jan H. Veldink, Hailiang Mei, Joachim Thiery, Jian Yang, Anand Kumar Andiappan, Grant W. Montgomery, Wibowo Arindrarto, Julian C. Knight, Markus Scholz, Mark W. Christiansen, Alexander Teumer, Bernett Lee, Patrick Deelen, Willem H. Ouwehand, Roman Kreuzhuber, Ashis Saha, Andrew A. Brown, Marie-Julie Favé, Eleonora Porcu, Mawusse Agbessi, Samuli Ripatti, Terho Lehtimäki, Jonathan K. Pritchard, Lili Milani, Alexis Battle, Holger Kirsten, Sina A. Gharib, Natalia Pervjakova, Annique Claringbould, Patrick F. Sullivan, Habibul Ahsan, Katharina Schramm, Hanieh Yaghootkar, Oliver Stegle, D.I. Boomsma, Anette Kalnapenkis, Mika Kähönen, Harm Brugge, Lin Tong, Biao Zeng, Holger Prokisch, Kate Downes, Rick Jansen, Peter M. Visscher, Benjamin P. Fairfax, Shuang Li, Urmo Võsa, Emmanouil T. Dermitzakis, Michael Stumvoll, Markus Loeffler, Alvaes I, Rotzchke O, Philip Awadalla, Coen D.A. Stehouwer, Olli T. Raitakari, Gibran Hemani, Peter Kovacs, Peter A C 't Hoen, Timothy M. Frayling, Anke Tönjes, Greg Gibson, Yungil Kim, Kukushkina, Mahmoud Elansary, Knut Krohn
SummaryWhile many disease-associated variants have been identified through genome-wide association studies, their downstream molecular consequences remain unclear.To identify these effects, we performedcis-andtrans-expressionquantitative trait locus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd96588979ac114fdb2e0e0219588ef0
https://doi.org/10.1101/447367
https://doi.org/10.1101/447367
Autor:
Harold Snieder, Moritz F. Sinner, Daniel F. Gudbjartsson, Niek Verweij, PM Pramstaller, B. D. Mitchell, Stephan B. Felix, Elsayed Z. Soliman, R. J. F. Loos, T.B. Harris, Mika Kähönen, Philipp S. Wild, Christy L. Avery, Kirill V. Tarasov, Stefania Bandinelli, Stefan Kääb, Tim D. Spector, Patrick T. Ellinor, David J. Stott, Renate B. Schnabel, Igor Rudan, O Polasekd, Brendan M. Buckley, Thomas Meitinger, James F. Wilson, Honghuang Lin, Gandin Ilaria, CM Duijn van, James P. Brody, L. J. Launer, Xiaoyan Yin, Ritchie, CT Aldana Silva, Paolo Gasparini, Dan M. Roden, Diane M. Crawford, Eric Boerwinkle, Davíð O. Arnar, Annette Peters, Caroline Hayward, Ilja M. Nolte, Terho Lehtimäki, Joop Jukema, Pi Bakker de, Thomas Münzel, Steven R. Cummings, Henry Völzke, Peter W. Macfarlane, John Barnard, Fabiola M Del Greco, Dan E. Arking, Anna F. Dominiczak, Patricia B. Munroe, Jonathan D. Smith, Anne M. Butler, Bruno H. Stricker, Stefan Blankenberg, Pv Harst der, S. Ulivi, Jerome I. Rotter, Hilma Holm, Alvaro Alonso, Haonan Lin, Gianfranco Sinagra, Alexander Teumer, Q Gibson, Bruce M. Psaty, Uwe Völker, Olli T. Raitakari, Annamaria Iorio, Bouwe P. Krijthe, Lude Franke, Folkert W. Asselbergs, Jared W. Magnani, G. Ehret, Susan R. Heckbert, L Ferrucci, Edward G. Lakatta, N. Sotoodehnia, Harry Campbell, Toshiko Tanaka, Wagoner van, JS Baderab, Yalda Jamshidi, Daniel S. Evans, David Schlessinger, Kari Stefansson, Nilesh J. Samani, Martina Müller-Nurasyid, Mark Eijgelsheim, Vilmundar Gudnason, Brenton R. Swenson, Sina A. Gharib, Kathleen F. Kerr, Josh C. Denny, Maristella Steri, E J Benjamin, George J. Papanicolaou, Unnur Thorsteinsdottir, Ivana Kolcic, Yuki Bradford, Mina K. Chung, Yongmei Liu, M. Waldenberger, Stella Trompet, Hoed, Jv Setten, Tanja Zeller, Jan A. Kors, Francesco Cucca, Irene Mateo Leach, A.G. Uitterlinden, Albert V. Smith, Craig Muller, Andrew A. Hicks, A Isaacs, Leo-Pekka Lyytikäinen, Konstantin Strauch, Steven A. Lubitz, Antonietta Robino, J Zhana, A. Pfeufer, Sandosh Padmanabhan, Afshin Parsa, Harm-Jan Westra, Marcus Dörr, J. C. Bis
MotivationGenome-wide association studies have had great success in identifying human genetic variants associated with disease, disease risk factors, and other biomedical phenotypes. Many variants are associated with multiple traits, even after corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65cf9baa34e7b6179a637df32f0b4ee7
https://doi.org/10.1101/273540
https://doi.org/10.1101/273540
Autor:
Aaron Isaacs, Sina A. Gharib, Kathleen F. Kerr, Lenore J. Launer, Yuki Bradford, J. Wouter Jukema, Stefan Kääb, Ruth J. F. Loos, Philipp S. Wild, Igor Rudan, Moritz F. Sinner, Annamaria Iorio, David J. Stott, Sheila Ulivi, Martina Müller-Nurasyid, Jerome I. Rotter, Andrew A. Hicks, Leo-Pekka Lyytikäinen, Vilmundur Gudnason, Dan M. Roden, Dana C. Crawford, James F. Wilson, Renate B. Schnabel, Eric Boerwinkle, Mina K. Chung, M. Fabiola Del Greco, Jan A. Kors, Honghuang Lin, Dan E. Arking, Annette Peters, Daniel S. Evans, Kari Stefansson, Francesco Cucca, Harold Snieder, Nona Sotoodehnia, Claudia T. Silva Aldana, Paul I.W. de Bakker, David Schlessinger, Pim van der Harst, Irene Mateo Leach, Kirill V. Tarasov, Marylyn D. Ritchie, Xiaoyan Yin, Marcus Dörr, Jennifer A. Brody, Patrick T. Ellinor, Olli T. Raitakari, Christy L. Avery, Peter W. Macfarlane, Paolo Gasparini, Susan R. Heckbert, John Barnard, Jessica van Setten, Anna F. Dominiczak, Henry Völzke, Edward G. Lakatta, Nilesh J. Samani, Tamara B. Harris, Brenton R. Swenson, Joel S. Bader, Thomas Münzel, Patricia B. Munroe, Hilma Holm, Stefania Bandinelli, Christian Müller, Bruno H. Stricker, Oscar H. Franco, Yongmei Liu, Ivana Kolcic, Peter P. Pramstaller, Josh C. Denny, Maristella Steri, Henry J. Lin, Luigi Ferrucci, Arne Pfeufer, Antonietta Robino, Bruce M. Psaty, Niek Verweij, Lude Franke, Mark Eijgelsheim, Afshin Parsa, Toshiko Tanaka, Folkert W. Asselbergs, Terho Lehtimäki, Stella Trompet, Alvaro Alonso, Harm-Jan Westra, David O. Arnar, Jared W. Magnani, Bouwe P. Krijthe, Cornelia M. van Duijn, Brendan M. Buckley, Jonathan D. Smith, Tim D. Spector, George J. Papanicolaou, Anne M. Butler, Emelia J. Benjamin, Tanja Zeller, Quince Gibson, David R. Van Wagoner, André G. Uitterlinden, Albert V. Smith, Stephan B. Felix, Uwe Völker, Yalda Jamshidi, Ozren Polasek, Daniel F. Gudbjartsson, Harry Campbell, Caroline Hayward, Ilja M. Nolte, Elsayed Z. Soliman, Georg Ehret, Mika Kähönen, Konstantin Strauch, Steven A. Lubitz, Melanie Waldenberger, Alexander Teumer, Sandosh Padmanabhan, Braxton D. Mitchell, Gianfranco Sinagra, Gandin Ilaria, Thomas Meitinger, Marcel den Hoed, Stefan Blankenberg, J. C. Bis
Electrocardiographic PR interval measures atrial and atrioventricular depolarization and conduction, and abnormal PR interval is a risk factor for atrial fibrillation and heart block. We performed a genome-wide association study in over 92,000 indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb22d230f9bdc7f9fb11ee1ccbf12f6e