Zobrazeno 71 - 80
of 178
pro vyhledávání: '"Martina Müller-Nurasyid"'
Autor:
Martina Müller-Nurasyid, Stefan Kääb, Manuel Lutz, Gerhard Steinbeck, Moritz F. Sinner, Holger Reinecke
Publikováno v:
European Heart Journal
Aims Risks of catheter ablation for atrial fibrillation and flutter assessed in retrospective studies, registries, and controlled trials may underestimate ‘real world’ conditions. Methods and results To assess complications in a nationwide approa
Autor:
Olaf Wolkenhauer, Matthias Hübenthal, Tarunveer S. Ahluwalia, Markus M. Nöthen, Ulrike Wehkamp, Elke Rodriguez, Marie Standl, Stefan Schreiber, Hans Bisgaard, Natalija Novak, Andreas Arnold, Lavinia Paternoster, Carsten Oliver Schmidt, Martina Müller-Nurasyid, Gabriele Mayr, Eva Ellinghaus, Melanie Hotze, Andre Franke, Hansjörg Baurecht, Christian Gieger, Young-Ae Lee, Philip Rosenstiel, Sascha Gerdes, Sarah Grosche, Stephan Weidinger, Saptarshi Bej, Jan Christian Kässens, Frauke Degenhardt, Wolfgang Lieb, Georg Homuth, Markus Wolfien, Nick Dand, Annette Peters, David Ellinghaus, Thomas Werfel, Holger Schulz, Klaus Bønnelykke, Dora Stölzl, Melanie Waldenberger, Per Hoffmann, Sören Mucha, Hila Emmert, Ingo Marenholz, Eun Suk Jung, Lars Wienbrandt, Konstantin Strauch
Publikováno v:
2019, ' Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression ', Journal of Allergy and Clinical Immunology . https://doi.org/10.1016/j.jaci.2019.10.030
J. Allergy Clin. Immunol. 145, 1208-1218 (2020)
Journal of Allergy and Clinical Immunology
J. Allergy Clin. Immunol. 145, 1208-1218 (2020)
Journal of Allergy and Clinical Immunology
Background: Fifteen percent of atopic dermatitis (AD) liability-scale heritability could be attributed to 31 susceptibility loci identified by using genome-wide association studies, with only 3 of them (IL13, IL-6 receptor [IL6R], and filaggrin [FLG]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae597323bbc55a66411fe48c5a5e02bf
https://research-information.bris.ac.uk/en/publications/eba95c53-2a75-47b8-9708-08cba8407be3
https://research-information.bris.ac.uk/en/publications/eba95c53-2a75-47b8-9708-08cba8407be3
Autor:
Carolina Ochoa-Rosales, M. Arfan Ikram, Martina Müller-Nurasyid, Xu Gao, Alexander Teumer, Hermann Brenner, Pashupati P. Mishra, Christian Gieger, Diana L Juvinao-Quintero, Taulant Muka, Jana Nano, Marie Loh, Bruno H. Stricker, Margit Heier, Stephan B. Felix, Yan Zhang, Hans J. Grabe, Oscar L. Rueda-Ochoa, Jaspal S. Kooner, Mohsen Ghanbari, Terho Lehtimäki, Joyce B. J. van Meurs, Annette Peters, Benjamin Lehne, John C. Chambers, Eliana Portilla-Fernandez, Melanie Waldenberger, Ben Schöttker, Oscar H. Franco, Trudy Voortman, Rory P. Wilson, Weihua Zhang
Publikováno v:
Diabetes Care, 43, 875-884. American Diabetes Association Inc.
OBJECTIVE To investigate the role of epigenetics in statins’ diabetogenic effect comparing DNA methylation (DNAm) between statin users and nonusers in an epigenome-wide association study in blood. RESEARCH DESIGN AND METHODS Five cohort studies’
Autor:
Barbara McKnight, Martina Müller-Nurasyid, Raha Pazoki, Michael W.T. Tanck, Thomas Engstrøm, Arthur A.M. Wilde, Man Li, Martin VanDenburgh, Marieke T. Blom, Reza Jabbari, Thomas Meitinger, Philippe Goyette, Anna Moes, Rebecca N. Mitchell, Christine M. Albert, Aravinda Chakravarti, Dan E. Arking, Jean-Claude Tardif, Rozenn N. Lemaitre, Foram N. Ashar, Pui-Yan Kwok, Frank D. Kolodgie, Jacob Tfelt-Hansen, Renu Virmani, Susan R. Heckbert, Angel C.Y. Mak, David S. Siscovick, Vinicius Tragante, Xavier Jouven, Hanno L. Tan, John D. Rioux, Mark Eijgelsheim, Ronald J. Prineas, Nona Sotoodehnia, Xiaoqing Zhao, Stefan A. Escher, Heikki V. Huikuri, Bruce M. Psaty, Charlotte Glinge, Albert Hofman, Oscar H. Franco, Florence Dumas, Bruno H. Stricker, M. Juhani Junttila, Folkert W. Asselbergs, Josef Coresh, Christopher J. O'Donnell, Paul W. Franks, Shih-Jen Hwang, Veikko Salomaa, Jan-Håkan Jansson, Stefan Kääb, Christopher Newton-Cheh, Joseph J. Maleszewski, Paul I.W. de Bakker, Jennifer A. Brody, Aki S. Havulinna, André G. Uitterlinden, Georg Ehret, Jerome I. Rotter, Thomas Lumley, Connie R. Bezzina, Marc K. Halushka, Sara L. Pulit
Publikováno v:
Ashar, F N, Mitchell, R N, Albert, C M, Newton-Cheh, C, Brody, J A, Müller-Nurasyid, M, Moes, A, Meitinger, T, Mak, A, Huikuri, H, Junttila, M J, Goyette, P, Pulit, S L, Pazoki, R, Tanck, M W, Blom, M T, Zhao, X, Havulinna, A S, Jabbari, R, Glinge, C, Tragante, V, Escher, S A, Chakravarti, A, Ehret, G, Coresh, J, Li, M, Prineas, R J, Franco, O H, Kwok, P Y, Lumley, T, Dumas, F, McKnight, B, Rotter, J I, Lemaitre, R N, Heckbert, S R, O'Donnell, C J, Hwang, S J, Tardif, J C, VanDenburgh, M, Uitterlinden, A G, Hofman, A, Stricker, B H C, De Bakker, P I W, Franks, P W, Jansson, J H, Asselbergs, F W, Halushka, M K, Maleszewski, J J, Tfelt-Hansen, J, Engstrøm, T, Salomaa, V, Virmani, R, Kolodgie, F, Wilde, A A M, Tan, H L, Bezzina, C R, Eijgelsheim, M, Rioux, J D, Jouven, X, Kääb, S, Psaty, B M, Siscovick, D S, Arking, D E & Sotoodehnia, N 2018, ' A comprehensive evaluation of the genetic architecture of sudden cardiac arrest ', European Heart Journal, vol. 39, no. 44, pp. 3961-3969 . https://doi.org/10.1093/eurheartj/ehy474
European Heart Journal
European Heart Journal, 39(44), 3961. Oxford University Press
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; ... (2018). A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. European Heart Journal, 39(44), pp. 3961-3969. Oxford University Press 10.1093/eurheartj/ehy474
European Heart Journal, 39(44), 3961-3969. Oxford University Press
European Heart Journal, 39(44), 3961-+. Oxford University Press
European Heart Journal, Vol. 39, No 44 (2018) pp. 3961-3969
European heart journal, vol 39, iss 44
European heart journal, 39(44), 3961-3969. Oxford University Press
European Heart Journal
European Heart Journal, 39(44), 3961. Oxford University Press
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; ... (2018). A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. European Heart Journal, 39(44), pp. 3961-3969. Oxford University Press 10.1093/eurheartj/ehy474
European Heart Journal, 39(44), 3961-3969. Oxford University Press
European Heart Journal, 39(44), 3961-+. Oxford University Press
European Heart Journal, Vol. 39, No 44 (2018) pp. 3961-3969
European heart journal, vol 39, iss 44
European heart journal, 39(44), 3961-3969. Oxford University Press
BackgroundSudden cardiac arrest (SCA) accounts for 10% of adult mortality in Western populations. While several risk factors are observationally associated with SCA, the genetic architecture of SCA in the general population remains unknown. Furthermo
Autor:
Myriam Fornage, Thomas Meitinger, Elena Carnero-Montoro, Donna K. Arnett, Rory P. Wilson, Steve Horvath, Mina A. Jhun, Tao Zhang, Elias Salfati, Devin Absher, Marguerite R. Irvin, Melanie Waldenberger, Nona Sotoodehnia, Mohsen Ghanbari, Klodian Dhana, Christian Gieger, Stefan Gustafsson, Wei Chen, Andrea A. Baccarelli, Lifang Hou, Jeffrey R. O'Connell, Rui Xia, Jordana T. Bell, Bruce M. Psaty, Lars Lind, Yii-Der Ida Chen, Mohammad Arfan Ikram, May E. Montasser, Weihua Guan, Paula Singmann, Jincheng Shen, Eric Boerwinkle, Martina Müller-Nurasyid, Anh N. Do, Shengxu Li, Traci M. Bartz, Dianjianyi Sun, Eric A. Whitsel, Erik Ingelsson, Annette Peters, Jennifer A. Smith, Daniel Levy, Coleen M. Damcott, Xiaoping Zhao, Wei Zhao, Philip S. Tsao, Alan R. Shuldiner, Themistocles L. Assimes, Michael M. Mendelson, Tim D. Spector, Åsa K. Hedman, Chen Yao, Pfeiffer Liliane, Joyce B. J. van Meurs, Rahul Gondalia, Abbas Dehghan, Kim Valeska Emilie Braun, Roby Joehanes, Sharon L.R. Kardia, Erin B. Ware, Deugi Zhi, Megan L. Grove, Jennifer A. Brody, André G. Uitterlinden
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-1 (2021)
Nature Communications
Nature Communications
Here we examine the association between DNA methylation in circulating leukocytes and blood lipids in a multi-ethnic sample of 16,265 subjects. We identify 148, 35, and 4 novel associations among Europeans, African Americans, and Hispanics, respectiv
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:
Niek Verweij, Iva Miljkovic, Peter Vollenweider, Denis Rybin, Aaron Isaacs, Arthur W. Musk, Eero Kajantie, Sara M. Willems, Ronan Roussel, Martina Müller-Nurasyid, Inês Barroso, Beverley Balkau, Stephan J. L. Bakker, Tamara B. Harris, Ching-Ti Liu, Jennie Hui, Letizia Marullo, Joseph Hung, John Beilby, Annette Peters, Cornelia M. van Duijn, Zoltán Kutalik, Kelly S. Benke, Mickaël Canouil, Johan G. Eriksson, Nicole Vogelzangs, James B. Meigs, Loic Yengo, Philippe Froguel, Rico Rueedi, Wolfgang Rathmann, Jennifer L. Bragg-Gresham, Daniel DiCorpo, Maryam Kavousi, Harald Grallert, Chiara Scapoli, Laura J. Rasmussen-Torvik, Jose C. Florez, Pim van der Harst, Nabila Bouatia-Naji, Jordi Merino, Carola Marzi, Tanguy Corre, Alan James, Lyle J. Palmer, Ghislain Rocheleau, Inga Prokopenko, Josée Dupuis, Jari Lahti, Sven Bergmann
Publikováno v:
Scientific Reports, 9:9439. Nature Publishing Group
Scientific Reports
Scientific reports, vol. 9, no. 1, pp. 9439
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Sci. Rep. 9:9439 (2019)
Scientific Reports, 9(1):9439. Nature Publishing Group
Scientific Reports
Scientific reports, vol. 9, no. 1, pp. 9439
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Sci. Rep. 9:9439 (2019)
Scientific Reports, 9(1):9439. Nature Publishing Group
Type 2 diabetes (T2D) affects the health of millions of people worldwide. The identification of genetic determinants associated with changes in glycemia over time might illuminate biological features that precede the development of T2D. Here we condu
Autor:
Yalda Jamshidi, Paul I.W. de Bakker, J. Wouter Jukema, Ilaria Gandin, Monika Stoll, Christopher P. Nelson, Moritz F. Sinner, Eco J. C. de Geus, André G. Uitterlinden, Jan A. Kors, Vilmundur Gudnason, Sheila Ulivi, Jouke-Jan Hottenga, Terho Lehtimäki, Antonietta Robino, Mark Eijgelsheim, Annamaria Iorio, Niek Verweij, Martina Müller-Nurasyid, Ian Ford, Hao Mei, James G. Wilson, Albert V. Smith, Thomas Meitinger, Gianfranco Sinagra, Claudia T. Silva Aldana, Maartje N. Niemeijer, Torben Hansen, Allan Linneberg, Jennifer A. Brody, Pim van der Harst, Stella Trompet, Paolo Gasparini, Bram P. Prins, Stefan Kääb, Hamdi Mbarek, Alvaro Alonso, Leanne M. Hall, Helen R. Warren, Dan E. Arking, Peter W. Macfarlane, Annette Peters, Olli T. Raitakari, Daiane Hemerich, Mark J. Caulfield, Folkert W. Asselbergs, Dorret I. Boomsma, Aaron Isaacs, Bruno H. Stricker, Tamara B. Harris, Susan R. Heckbert, Jessica van Setten, Niels Grarup, Patricia B. Munroe, Leo-Pekka Lyytikäinen, Nilesh J. Samani, Cornelia M. van Duijn, Elsayed Z. Soliman, Nona Sotoodehnia, Jørgen K. Kanters, Melanie Waldenberger
Publikováno v:
European Journal of Human Genetics, 27(6), 952-962. Nature Publishing Group
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
European Journal of Human Genetics
van Setten, J, Verweij, N, Mbarek, H, Niemeijer, M N, Trompet, S, Arking, D E, Brody, J A, Gandin, I, Grarup, N, Hall, L M, Hemerich, D, Lyytikäinen, L-P, Mei, H, Müller-Nurasyid, M, Prins, B P, Robino, A, Smith, A V, Warren, H R, Asselbergs, F W, Boomsma, D I, Caulfield, M J, Eijgelsheim, M, Ford, I, Hansen, T, Harris, T B, Heckbert, S R, Hottenga, J-J, Iorio, A, Kors, J A, Linneberg, A, MacFarlane, P W, Meitinger, T, Nelson, C P, Raitakari, O T, Silva Aldana, C T, Sinagra, G, Sinner, M, Soliman, E Z, Stoll, M, Uitterlinden, A, van Duijn, C M, Waldenberger, M, Alonso, A, Gasparini, P, Gudnason, V, Jamshidi, Y, Kääb, S, Kanters, J K, Lehtimäki, T, Munroe, P B, Peters, A, Samani, N J, Sotoodehnia, N, Ulivi, S, Wilson, J G, de Geus, E J C, Jukema, J W, Stricker, B, van der Harst, P, de Bakker, P I W & Isaacs, A 2019, ' Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits ', European Journal of Human Genetics, vol. 27, pp. 952-962 . https://doi.org/10.1038/s41431-018-0295-z
Eur. J. Hum. Genet. 27, 952-962 (2019)
European Journal of Human Genetics, 27(6), 952-962. NATURE PUBLISHING GROUP
van Setten, J, Verweij, N, Mbarek, H, Niemeijer, M N, Trompet, S, Arking, D E, Brody, J A, Gandin, I, Grarup, N, Hall, L M, Hemerich, D, Lyytikäinen, L P, Mei, H, Müller-Nurasyid, M, Prins, B P, Robino, A, Smith, A V, Warren, H R, Asselbergs, F W, Boomsma, D I, Caulfield, M J, Eijgelsheim, M, Ford, I, Hansen, T, Harris, T B, Heckbert, S R, Hottenga, J J, Iorio, A, Kors, J A, Linneberg, A, MacFarlane, P W, Meitinger, T, Nelson, C P, Raitakari, O T, Silva Aldana, C T, Sinagra, G, Sinner, M, Soliman, E Z, Stoll, M, Uitterlinden, A, van Duijn, C M, Waldenberger, M, Alonso, A, Gasparini, P, Gudnason, V, Jamshidi, Y, Kääb, S, Kanters, J K, Lehtimäki, T, Munroe, P B, Peters, A, Samani, N J, Sotoodehnia, N, Ulivi, S, Wilson, J G, de Geus, E J C, Jukema, J W, Stricker, B, van der Harst, P, de Bakker, P I W & Isaacs, A 2019, ' Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits ', European Journal of Human Genetics, vol. 27, no. 6, pp. 952-962 . https://doi.org/10.1038/s41431-018-0295-z
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
European Journal of Human Genetics
van Setten, J, Verweij, N, Mbarek, H, Niemeijer, M N, Trompet, S, Arking, D E, Brody, J A, Gandin, I, Grarup, N, Hall, L M, Hemerich, D, Lyytikäinen, L-P, Mei, H, Müller-Nurasyid, M, Prins, B P, Robino, A, Smith, A V, Warren, H R, Asselbergs, F W, Boomsma, D I, Caulfield, M J, Eijgelsheim, M, Ford, I, Hansen, T, Harris, T B, Heckbert, S R, Hottenga, J-J, Iorio, A, Kors, J A, Linneberg, A, MacFarlane, P W, Meitinger, T, Nelson, C P, Raitakari, O T, Silva Aldana, C T, Sinagra, G, Sinner, M, Soliman, E Z, Stoll, M, Uitterlinden, A, van Duijn, C M, Waldenberger, M, Alonso, A, Gasparini, P, Gudnason, V, Jamshidi, Y, Kääb, S, Kanters, J K, Lehtimäki, T, Munroe, P B, Peters, A, Samani, N J, Sotoodehnia, N, Ulivi, S, Wilson, J G, de Geus, E J C, Jukema, J W, Stricker, B, van der Harst, P, de Bakker, P I W & Isaacs, A 2019, ' Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits ', European Journal of Human Genetics, vol. 27, pp. 952-962 . https://doi.org/10.1038/s41431-018-0295-z
Eur. J. Hum. Genet. 27, 952-962 (2019)
European Journal of Human Genetics, 27(6), 952-962. NATURE PUBLISHING GROUP
van Setten, J, Verweij, N, Mbarek, H, Niemeijer, M N, Trompet, S, Arking, D E, Brody, J A, Gandin, I, Grarup, N, Hall, L M, Hemerich, D, Lyytikäinen, L P, Mei, H, Müller-Nurasyid, M, Prins, B P, Robino, A, Smith, A V, Warren, H R, Asselbergs, F W, Boomsma, D I, Caulfield, M J, Eijgelsheim, M, Ford, I, Hansen, T, Harris, T B, Heckbert, S R, Hottenga, J J, Iorio, A, Kors, J A, Linneberg, A, MacFarlane, P W, Meitinger, T, Nelson, C P, Raitakari, O T, Silva Aldana, C T, Sinagra, G, Sinner, M, Soliman, E Z, Stoll, M, Uitterlinden, A, van Duijn, C M, Waldenberger, M, Alonso, A, Gasparini, P, Gudnason, V, Jamshidi, Y, Kääb, S, Kanters, J K, Lehtimäki, T, Munroe, P B, Peters, A, Samani, N J, Sotoodehnia, N, Ulivi, S, Wilson, J G, de Geus, E J C, Jukema, J W, Stricker, B, van der Harst, P, de Bakker, P I W & Isaacs, A 2019, ' Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits ', European Journal of Human Genetics, vol. 27, no. 6, pp. 952-962 . https://doi.org/10.1038/s41431-018-0295-z
Publisher's version (útgefin grein)
Genome-wide association studies (GWAS) of quantitative electrocardiographic (ECG) traits in large consortia have identified more than 130 loci associated with QT interval, QRS duration, PR interval, and heart
Genome-wide association studies (GWAS) of quantitative electrocardiographic (ECG) traits in large consortia have identified more than 130 loci associated with QT interval, QRS duration, PR interval, and heart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bec5734bbaae3105adbbaea038bf1b3
https://research.vu.nl/en/publications/28706f57-bfc4-450a-b581-9338a887dea5
https://research.vu.nl/en/publications/28706f57-bfc4-450a-b581-9338a887dea5
Autor:
Michael Boehnke, Anke R. Hammerschlag, Stavroula Kanoni, Nilesh J. Samani, Stefan Blankenberg, Arpana Agrawal, Ersin Yavas, Chris Hsu, Dominique Arveiler, Giovanni Veronesi, Sarah E. Harris, Guillaume Lettre, Leah Wetherill, Helen R. Warren, M Samuel, Manav Kapoor, Praveen Surendran, Mengzhen Liu, Massimo Mangino, Abdulla Al Shafi Majumder, Chiara Batini, Jeff Haessler, Anton J. M. De Craen, Matt McGue, Laura J. Bierut, Yi Ling Chou, Markku Laakso, Ian J. Deary, Rebecca Rohde, Nhung Le, David Schlessinger, J. Dylan Weissenkampen, Claudia Langenberg, Tim D. Spector, Paul W. Franks, John P. Rice, Philippe M. Frossard, Hanieh Yaghootkar, Janie Corley, Frank Kee, J. Wouter Jukema, Pim van der Harst, Dermot F. Reily, Jenny Chang-Claude, Nicholas G. Martin, Tatiana Foroud, Sune F. Nielsen, Charles Kooperberg, Rudolf A. de Boer, Francesco Cucca, Paul D.P. Pharoah, Alex P. Reiner, Daniel R. Barnes, Anders Mälarstig, Jonathan Marten, Henry Völzke, Yu Jiang, Jukka Kontto, J Danesh, Antonis C. Antoniou, Andrew C. Heath, Nicholas J. Wareham, Joanna M. M. Howson, Alison Goate, Olov Rolandsson, Frida Renström, Chu Chen, Vinicius Tragante, Matt J. Neville, Kathleen Stirrups, Clemens Baumbach, Colin N. A. Palmer, Adam S. Butterworth, William G. Iacono, Naveed Sattar, Ian P. Hall, Daniel O. Stram, Giorgio Pistis, Jan-Håkan Jansson, Jaakko Kaprio, David R. Weir, David P. Strachan, Martin D. Tobin, Folkert W. Asselbergs, John M. Starr, Stefan Weiss, Thomas F. Vogt, Riccardo E. Marioni, Maarten Hoek, Jessica Tyrrell, Hilary A. Tindle, Alison M. Dunning, Anu Loukola, Joe Dennis, Victoria E. Jackson, Louise V. Wain, Eleftheria Zeggini, Weihua Zhang, Yaming Shao, Kari Kuulasmaa, Elisabeth Altmaier, Jean-Claude Tardif, Jian Gong, A. Mesut Erzurumluoglu, Andries R. van der Leij, Kari E. North, Anna F. Dominiczak, Martina Müller-Nurasyid, Scott I. Vrieze, Sarah Bertelsen, Markus Perola, Evangelos Evangelou, Chris J. Packard, Gonçalo R. Abecasis, Robert A. Scott, S. Trompet, Jennifer A. Smith, H. Steven Scholte, Timothy M. Frayling, Danielle Posthuma, Ian Ford, Douglas F. Easton, Børge Grønne Nordestgaard, Michiel L. Bots, Charles B. Eaton, Sharon L.R. Kardia, Dewan S. Alam, Xiaowei Zhan, Sean P. David, Maria Uria-Nickelsen, Dongbing Lai, Ilonca Vaartjes, Mark J. Caulfield, Valérie Turcot, Jean Ferrières, Emanuele Di Angelantonio, Robin Young, Pamela A. F. Madden, Tibor V. Varga, Asif Rasheed, Peter van der Meer, Dajiang J. Liu, Ioanna Tachmazidou, Panos Deloukas, Danish Saleheen, Evelin Mihailov, Caroline Hayward, Patricia B. Munroe, Beenish Qaiser, Jessica D. Faul, John C. Chambers, Matthias Nauck, Niek Verweij, Jordan M. Hughey, Christopher A. Haiman, Hans J. Grabe, Muriel Caslake, Saima Afaq, Jaspal S. Kooner, Tinca J. C. Polderman, Philippe Amouyel, Wei Zhao, Göran Hallmans, Andres Metspalu, Jarmo Virtamo, Carl A. Melbourne, Kaixin Zhou, Christiaan de Leeuw, Peter S. Sever, Eirini Marouli, Neil Poulter, Rajiv Chowdhury, Jian'an Luan, Deborah J. Thompson, F Karpe, Kyriaki Michailidou, David M. Brazel, Heather M. Stringham
Publikováno v:
Biological Psychiatry, 85(11), 946-955. Elsevier
Biological Psychiatry, 85(11), 946-955. Elsevier USA
Biological Psychiatry, 85(11), 946-955. ELSEVIER SCIENCE INC
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Barnes, D R, Bertelsen, S, Chou, Y-L, Erzurumluoglu, A M, Faul, J D, Haessler, J, Hammerschlag, A R, Hsu, C, Kapoor, M, Lai, D, Le, N, de Leeuw, C A, Loukola, A, Mangino, M, Melbourne, C A, Pistis, G, Qaiser, B, Rohde, R, Shao, Y, Stringham, H, Wetherill, L, Zhao, W, Agrawal, A, Bierut, L, Chen, C, Eaton, C B, Goate, A, Haiman, C, Heath, A, Iacono, W G, Martin, N G, Polderman, T J, Reiner, A, Rice, J, Schlessinger, D, Scholte, H S, Smith, J A, Tardif, J-C, Tindle, H A, van der Leij, A R, Boehnke, M, Chang-Claude, J, Cucca, F, David, S P, Foroud, T, Howson, J M M, Kardia, S L R, Kooperberg, C, Laakso, M, Lettre, G, Madden, P, Mcgue, M, North, K, Posthuma, D, Spector, T, Stram, D, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, Di Ange-Lantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrieres, J, Kee, F, Kuulasmaa, K, Mueller-Nurasyid, M, Veronesi, G, Virtamo, J, Frossard, P, Nordestgaard, B G, Saleheen, D, Danesh, J, Butterworth, A S, Howson, J M M, Erzurumluoglu, A M, Jackson, V E, Melbourne, C A, Varga, T V, Warren, H R, Tragante, V, Tachmazidou, I, Harris, S E, Evangelou, E, Marten, J, Zhang, W, Altmaier, E, Luan, J, Langenberg, C, Scott, R A, Yaghootkar, H, Stirrups, K, Kanoni, S, Marouli, E, Karpe, F, Dominiczak, A F, Sever, P, Poulter, N, Rolandsson, O, Baumbach, C, Afaq, S, Chambers, J C, Kooner, J S, Wareham, N J, Renstrom, F, Hallmans, G, Marioni, R E, Corley, J, Starr, J M, Verweij, N, de Boer, R A, van der Meer, P, Yavas, E, Vaartjes, I, Bots, M L, Asselbergs, F W, Grabe, H J, Volzke, H, Nauck, M, Weiss, S, Pharoah, P D P, Dunning, A M, Dennis, J G, Thompson, D J, Michailidou, K, Easton, D F, Antoniou, A C, Tyrrell, J, Mihailov, E, Samani, N J, Zhou, K, Neville, M J, Metspalu, A, Palmer, C N A, Hall, I P, Strachan, D P, Deary, I J, Frayling, T M, Hayward, C, van der Harst, P, Zeggini, E, Munroe, P B, Jansson, J-H, Franks, P W, Deloukas, P, Caulfield, M J, Wain, L V & Tobin, M D 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
Biological Psychiatry, 85(11), 946. Elsevier USA
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, di Angelantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, EPIC-CVD Consortium, Frossard, P, Nordestgaard, B R G, Saleheen, D, Danesh, J, Hammerschlag, A R, Posthuma, D, Spector, T, Stram, D O, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S & CHD Exome+ Consortium 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
Biological psychiatry. Elsevier USA
CHD Exome+ Consortium & Consortium for Genetics of Smoking Behaviour 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
Biological Psychiatry, 85(11), 946-955. Elsevier USA
Biological Psychiatry, 85(11), 946-955. ELSEVIER SCIENCE INC
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Barnes, D R, Bertelsen, S, Chou, Y-L, Erzurumluoglu, A M, Faul, J D, Haessler, J, Hammerschlag, A R, Hsu, C, Kapoor, M, Lai, D, Le, N, de Leeuw, C A, Loukola, A, Mangino, M, Melbourne, C A, Pistis, G, Qaiser, B, Rohde, R, Shao, Y, Stringham, H, Wetherill, L, Zhao, W, Agrawal, A, Bierut, L, Chen, C, Eaton, C B, Goate, A, Haiman, C, Heath, A, Iacono, W G, Martin, N G, Polderman, T J, Reiner, A, Rice, J, Schlessinger, D, Scholte, H S, Smith, J A, Tardif, J-C, Tindle, H A, van der Leij, A R, Boehnke, M, Chang-Claude, J, Cucca, F, David, S P, Foroud, T, Howson, J M M, Kardia, S L R, Kooperberg, C, Laakso, M, Lettre, G, Madden, P, Mcgue, M, North, K, Posthuma, D, Spector, T, Stram, D, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, Di Ange-Lantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrieres, J, Kee, F, Kuulasmaa, K, Mueller-Nurasyid, M, Veronesi, G, Virtamo, J, Frossard, P, Nordestgaard, B G, Saleheen, D, Danesh, J, Butterworth, A S, Howson, J M M, Erzurumluoglu, A M, Jackson, V E, Melbourne, C A, Varga, T V, Warren, H R, Tragante, V, Tachmazidou, I, Harris, S E, Evangelou, E, Marten, J, Zhang, W, Altmaier, E, Luan, J, Langenberg, C, Scott, R A, Yaghootkar, H, Stirrups, K, Kanoni, S, Marouli, E, Karpe, F, Dominiczak, A F, Sever, P, Poulter, N, Rolandsson, O, Baumbach, C, Afaq, S, Chambers, J C, Kooner, J S, Wareham, N J, Renstrom, F, Hallmans, G, Marioni, R E, Corley, J, Starr, J M, Verweij, N, de Boer, R A, van der Meer, P, Yavas, E, Vaartjes, I, Bots, M L, Asselbergs, F W, Grabe, H J, Volzke, H, Nauck, M, Weiss, S, Pharoah, P D P, Dunning, A M, Dennis, J G, Thompson, D J, Michailidou, K, Easton, D F, Antoniou, A C, Tyrrell, J, Mihailov, E, Samani, N J, Zhou, K, Neville, M J, Metspalu, A, Palmer, C N A, Hall, I P, Strachan, D P, Deary, I J, Frayling, T M, Hayward, C, van der Harst, P, Zeggini, E, Munroe, P B, Jansson, J-H, Franks, P W, Deloukas, P, Caulfield, M J, Wain, L V & Tobin, M D 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
Biological Psychiatry, 85(11), 946. Elsevier USA
Brazel, D M, Jiang, Y, Hughey, J M, Turcot, V, Zhan, X, Gong, J, Batini, C, Weissenkampen, J D, Liu, M, Surendran, P, Young, R, Barnes, D R, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Kontto, J, Perola, M, Caslake, M, de Craen, A J M, Trompet, S, Uria-Nickelsen, M, Malarstig, A, Reily, D F, Hoek, M, Vogt, T, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Alam, D S, Majumder, A A S, di Angelantonio, E, Chowdhury, R, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, EPIC-CVD Consortium, Frossard, P, Nordestgaard, B R G, Saleheen, D, Danesh, J, Hammerschlag, A R, Posthuma, D, Spector, T, Stram, D O, Tobin, M D, Weir, D R, Kaprio, J, Abecasis, G R, Liu, D J, Vrieze, S & CHD Exome+ Consortium 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
Biological psychiatry. Elsevier USA
CHD Exome+ Consortium & Consortium for Genetics of Smoking Behaviour 2019, ' Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use ', Biological Psychiatry, vol. 85, no. 11, pp. 946-955 . https://doi.org/10.1016/j.biopsych.2018.11.024
BackgroundSmoking and alcohol use have been associated with common genetic variants in multiple loci. Rare variants within these loci hold promise in the identification of biological mechanisms in substance use. Exome arrays and genotype imputation c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c4c6686918e3fb0cec91a0a7423b4f4
https://dare.uva.nl/personal/pure/en/publications/exome-chip-metaanalysis-fine-maps-causal-variants-and-elucidates-the-genetic-architecture-of-rare-coding-variants-in-smoking-and-alcohol-use(5b2dcbfd-0c32-47f3-869f-1ff60f676314).html
https://dare.uva.nl/personal/pure/en/publications/exome-chip-metaanalysis-fine-maps-causal-variants-and-elucidates-the-genetic-architecture-of-rare-coding-variants-in-smoking-and-alcohol-use(5b2dcbfd-0c32-47f3-869f-1ff60f676314).html