Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Dan E Arking"'
Autor:
David T. Huang, Wojciech Zareba, Spencer Rosero, Kris Cutter, Ilan Goldenberg, Valentina Kutyifa, Dan E. Arking, Nona Sotoodehnia, Bronislava Polonski, Ayhan Yoruk, Mehmet K. Aktas, Scott McNitt, Arwa Younis, Peter J. Kudenchuk, Thomas D. Rea
Publikováno v:
Heart Rhythm. 19:41-48
Background Use of oral contraceptives (OCs) may modulate the clinical course of women with congenital long QT syndrome (LQTS). The safety of OC use by sex hormone content has not been assessed in women with LQTS. Objective We aimed to evaluate the as
Autor:
Mariana Lazo, Jiaqi Xie, Christian S. Alvarez, Dominick Parisi, Stephanie Yang, Alvaro Rivera‐Andrade, Maria F. Kroker‐Lobos, John D. Groopman, Eliseo Guallar, Manuel Ramirez‐Zea, Dan E. Arking, Katherine A. McGlynn
Publikováno v:
Liver Int
Autor:
Valentina Kutyifa, Anita Y. Chen, Scott McNitt, Spencer Rosero, Christopher G. Scott, Katrina B. Sorensen, Dan E. Arking, Ilan Goldenberg, David T. Huang, Nona Sotoodehnia, Ayhan Yoruk, Mehmet K. Aktas, Michael J. Ackerman, Wojciech Zareba, J. Martijn Bos, Coeli M. Lopes, Kaylie A. Briske, Arwa Younis, Peter J. Kudenchuk, Thomas D. Rea
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background We aimed to provide personalized risk estimates for cardiac events (CEs) and life‐threatening events in women with either type 1 or type 2 long QT. Methods and Results The prognostic model was derived from the Rochester Long QT Syndrome
Autor:
Alexandre C. Pereira, Jie Yao, Makoto Hirata, Ozren Polasek, Dragana Vuckovic, Mariaelisa Graff, Jing Hua Zhao, Michael R. Brown, Xuan Deng, Barbara V. Howard, Vilmundur Gudnason, Tuomo Rankinen, Yuan Shi, Timo A. Lakka, Ulrich Broeckel, Anuradhani Kasturiratne, Eric Boerwinkle, Charles Kooperberg, Hugues Aschard, Stephen S. Rich, Pamela J. Schreiner, Dan E. Arking, Hans J. Grabe, Ilaria Gandin, Mario Sims, Carl D. Langefeld, Yii-Der Ida Chen, Meian He, W. James Gauderman, Bruce M. Psaty, Kent D. Taylor, Tõnu Esko, Olli T. Raitakari, Saima Afaq, Maik Pietzner, Federica Laguzzi, Dennis O. Mook-Kanamori, Gregory P. Wilson, Xiuqing Guo, Jaspal S. Kooner, David R. Jacobs, Yajuan Wang, Raha Pazoki, Wei Zhao, Andres Metspalu, Mary F. Feitosa, Jost B. Jonas, Tin Aung, Tamara B. Harris, Karin Leander, Nancy L. Pedersen, Charles B. Eaton, Sharon L.R. Kardia, Bernardo L. Horta, Candace M. Kammerer, Terrence Forrester, Alexander P. Reiner, Paul W. Franks, Tanika N. Kelly, Igor Rudan, Ruben N. Eppinga, Melissa A. Richard, Colin A. McKenzie, Christine Williams, Christian Gieger, Joseph H. Lee, Brigitte Kühnel, Christopher P. Nelson, Wen Bin Wei, Antonietta Robino, Anne U. Jackson, E. Shyong Tai, Alisa K. Manning, Lisa R. Yanek, Paul Elliott, Lynne E. Wagenknecht, Ananda R. Wickremasinghe, José Eduardo Krieger, Peter S. Sever, Nora Franceschini, André G. Uitterlinden, Paul M. Ridker, Yun J. Sung, Karen L. Mohlke, Thomas H. Mosley, Nilesh J. Samani, Patricia B. Munroe, Jennifer A. Smith, John M. C. Connell, H. Janaka de Silva, Nicholas Y. Q. Tan, Jian'an Luan, Jennifer E. Huffman, Anna F. Dominiczak, Carsten Oliver Schmidt, Christie M. Ballantyne, Peter J. van der Most, Anuj Goel, Jerome I. Rotter, Amy R. Bentley, Lihua Wang, Rajkumar Dorajoo, Lenore J. Launer, Yechiel Friedlander, Mickaël Canouil, Traci M. Bartz, Thomas Meitinger, Robert A. Scott, Mike A. Nalls, Xueling Sim, Sarah E. Harris, Michael A. Province, Chew-Kiat Heng, Zhe Wang, Norihiro Kato, Evangelos Evangelou, Philippe Froguel, Virginia Fisher, Leslie J. Raffel, Renée de Mutsert, Michele K. Evans, Brenda W.J.H. Penninx, Yih Chung Tham, Tin Louie, Nana Matoba, Lawrence F. Bielak, Andrea R. V. R. Horimoto, Jingmin Liu, Lynda M. Rose, Nona Sotoodehnia, Daniel I. Chasman, Jasmin Divers, John M. Starr, Patricia A. Peyser, Ervin R. Fox, Barry I. Freedman, Megan L. Grove, Jeffrey R. O'Connell, Rob M. van Dam, Michiaki Kubo, Jessica D. Faul, Fang-Chi Hsu, Yize Li, Ilja M. Nolte, Caroline Hayward, Paolo Gasparini, Chiea Chuen Khor, Changwei Li, Xu Chen, James E. Hixson, Patrik K. E. Magnusson, John C. Chambers, Yoichiro Kamatani, Sami Heikkinen, M. Abdullah Said, Martin Farrall, Alena Stančáková, Konstantin Strauch, Albert V. Smith, Yik Ying Teo, Bamidele O. Tayo, Tamar Sofer, Caizheng Yu, Maris Alver, Oscar H. Franco, Yongmei Liu, Ioanna Ntalla, Myriam Fornage, W. Craig Johnson, Dina Vojinovic, William R. Scott, David R. Weir, Yanick Hagemeijer, Raymond Noordam, Mathilde Boissel, Cornelia M. van Duijn, Karen Schwander, Jingzhong Ding, James Scott, Diana van Heemst, Ching-Yu Cheng, Woon-Puay Koh, Jianjun Liu, Kenneth J. Mukamal, Blair H. Smith, Claude Bouchard, Claudia Langenberg, Jingjing Liang, Wei Zheng, Najaf Amin, Ulf de Faire, Bing Yu, Archie Campbell, Kari E. North, Salman M. Tajuddin, Fernando Pires Hartwig, Steve B. Kritchevsky, Tibor V. Varga, Pirjo Komulainen, Hugh Watkins, Johanna Kuusisto, Kurt Lohman, Rozenn N. Lemaitre, Ani Manichaikul, Dabeeru C. Rao, Kenneth Rice, Weihua Zhang, Franco Giulianini, Reedik Mägi, Solomon K. Musani, Wanqing Wen, Nicholas J. Wareham, Charles N. Rotimi, Marzyeh Amini, Rainer Rauramaa, Nicholette D. Palmer, Annette Peters, Neil R Poulter, Benjamin Lehne, Matthias Nauck, Harold Snieder, Donald W. Bowden, M. Arfan Ikram, Lisa de las Fuentes, C. Charles Gu, Xiaofeng Zhu, Markku Laakso, Tuomas O. Kilpeläinen, Ching-Ti Liu, Michael Boehnke, Jin-Fang Chai, Lili Milani, L. Adrienne Cupples, Yuri Milaneschi, Kiang Liu, Stephen Sidney, Alan B. Zonderman, Thomas W. Winkler, Ian J. Deary, Fumihiko Takeuchi, Mary K. Wojczynski, Pim van der Harst, Leo-Pekka Lyytikäinen, Jennifer G. Robinson, Chuan Gao, Xiao-Ou Shu, Diane M. Becker, Mohsen Ghanbari, Alanna C. Morrison, Jian-Min Yuan, Tomohiro Katsuya, Ivana Kolcic, Melanie Waldenberger, Terho Lehtimäki, Heikki A. Koistinen, Erin B. Ware, Ya Xing Wang, Marie Loh, Treva Rice, Qing Duan, Aldi T. Kraja, Sabanayagam Charumathi, Tien Yin Wong, Paul S. de Vries, Yujie Wang, Muhammad Riaz
Publikováno v:
American Journal of Epidemiology, 188(6), 1033-1054. Oxford University Press
American Journal of Epidemiology, 188(6), 1033-1054. OXFORD UNIV PRESS INC
American Journal of Epidemiology
American Journal of Epidemiology, 2019, 188 (6), pp.1033-1054. ⟨10.1093/aje/kwz005⟩
American Journal of Epidemiology, Oxford University Press (OUP), 2019, 188 (6), pp.1033-1054. ⟨10.1093/aje/kwz005⟩
2019, ' Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions ', American Journal of Epidemiology . https://doi.org/10.1093/aje/kwz005
American journal of epidemiology, vol 188, iss 6
De Vries, P S, Lifelines Cohort Study, Brown, M R, Bentley, A R, Sung, Y J, Winkler, T W, Ntalla, I, Schwander, K, Kraja, A T, Guo, X, Franceschini, N, Cheng, C Y, Sim, X, Vojinovic, D, Huffman, J E, Musani, S K, Li, C, Feitosa, M F, Richard, M A, Noordam, R, Aschard, H, Bartz, T M, Bielak, L F, Deng, X, Dorajoo, R, Lohman, K K, Manning, A K, Rankinen, T, Smith, A V, Tajuddin, S M, Evangelou, E, Graff, M, Alver, M, Boissel, M, Chai, J F, Chen, X, Divers, J, Gandin, I, Gao, C, Goel, A, Hagemeijer, Y, Harris, S E, Hartwig, F P, He, M, Horimoto, A R V R, Hsu, F C, Jackson, A U, Kasturiratne, A, Komulainen, P, Kühnel, B, Laguzzi, F, Penninx, BWJH & Lifelines Cohort 2019, ' Multiancestry Genome-Wide Association study of lipid levels incorporating gene-alcohol interactions ', American Journal of Epidemiology, vol. 188, no. 6, pp. 1033-1054 . https://doi.org/10.1093/aje/kwz005
Am J Epidemiol
American journal of epidemiology, 188(6), 1033-1054. Oxford University Press
American Journal of Epidemiology, 188(6), 1033-1054. OXFORD UNIV PRESS INC
American Journal of Epidemiology
American Journal of Epidemiology, 2019, 188 (6), pp.1033-1054. ⟨10.1093/aje/kwz005⟩
American Journal of Epidemiology, Oxford University Press (OUP), 2019, 188 (6), pp.1033-1054. ⟨10.1093/aje/kwz005⟩
2019, ' Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions ', American Journal of Epidemiology . https://doi.org/10.1093/aje/kwz005
American journal of epidemiology, vol 188, iss 6
De Vries, P S, Lifelines Cohort Study, Brown, M R, Bentley, A R, Sung, Y J, Winkler, T W, Ntalla, I, Schwander, K, Kraja, A T, Guo, X, Franceschini, N, Cheng, C Y, Sim, X, Vojinovic, D, Huffman, J E, Musani, S K, Li, C, Feitosa, M F, Richard, M A, Noordam, R, Aschard, H, Bartz, T M, Bielak, L F, Deng, X, Dorajoo, R, Lohman, K K, Manning, A K, Rankinen, T, Smith, A V, Tajuddin, S M, Evangelou, E, Graff, M, Alver, M, Boissel, M, Chai, J F, Chen, X, Divers, J, Gandin, I, Gao, C, Goel, A, Hagemeijer, Y, Harris, S E, Hartwig, F P, He, M, Horimoto, A R V R, Hsu, F C, Jackson, A U, Kasturiratne, A, Komulainen, P, Kühnel, B, Laguzzi, F, Penninx, BWJH & Lifelines Cohort 2019, ' Multiancestry Genome-Wide Association study of lipid levels incorporating gene-alcohol interactions ', American Journal of Epidemiology, vol. 188, no. 6, pp. 1033-1054 . https://doi.org/10.1093/aje/kwz005
Am J Epidemiol
American journal of epidemiology, 188(6), 1033-1054. Oxford University Press
© The Author(s) 2019. A person's lipid profile is influenced by genetic variants and alcohol consumption, but the contribution of interactions between these exposures has not been studied. We therefore incorporated gene-Alcohol interactions into a m
Autor:
Colleen M. Sitlani, Eimear E. Kenny, Yii-Der Ida Chen, Chani J. Hodonsky, Jerome I. Rotter, Rahul Gondalia, Xiuqing Guo, Lucia A. Hindorff, Alex P. Reiner, Heather M. Highland, Charles Kooperberg, Elsayed Z. Soliman, Nona Sotoodehnia, Susan R. Heckbert, Ulrike Peters, Wendy Post, Ralph V. Shohet, Ran Tao, Kari E. North, Amanda A. Seyerle, Dan E. Arking, Genevieve L. Wojcik, Kent D. Taylor, Eric A. Whitsel, Antoine R Baldassari, Jie Yao, Robert C. Kaplan, Henry J. Lin, Mariaelisa Graff, Steven Buyske, Christy L. Avery, Dawood Darbar
Publikováno v:
Circulation. Genomic and precision medicine, vol 13, iss 4
Circ Genom Precis Med
Circ Genom Precis Med
Background: We examined how expanding electrocardiographic trait genome-wide association studies to include ancestrally diverse populations, prioritize more precise phenotypic measures, and evaluate evidence for shared genetic effects enabled the det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca17ca2bc52c085ae3d1ef0ce99c7fa6
https://escholarship.org/uc/item/70k449r8
https://escholarship.org/uc/item/70k449r8
Autor:
Carlos Iribarren, Dongwon Lee, Aravinda Chakravarti, Eric Boerwinkle, Dilrini K. Ranatunga, Georg B. Ehret, Man Li, Dan E. Arking, Priyanka Nandakumar, Pui-Yan Kwok, Catherine Schaefer, Megan L. Grove, Neil Risch, Thomas J. Hoffmann
Publikováno v:
Hum Mol Genet
Human molecular genetics, vol 29, iss 11
Human molecular genetics, vol 29, iss 11
Hundreds of loci have been associated with blood pressure traits from many genome-wide association studies. We identified an enrichment of these loci in aorta and tibial artery expression quantitative trait loci in our previous work in ∼100,000 Gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::847a80b2a082b32bcfd9b68d16be2953
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:
Avi Z. Rosenberg, Rohan X. Verma, Matthew N. McCall, Marc K. Halushka, Dan E. Arking, Tim O. Nieuwenhuis, Samuel Yang, Pillalamarri
One of the challenges of next generation sequencing (NGS) is read contamination. We used the Genotype-Tissue Expression (GTEx) project, a large, diverse, and robustly generated dataset, to understand the factors that contribute to contamination. We o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede2b5d0342556ddbbcbfce3451faedb
https://doi.org/10.1101/602367
https://doi.org/10.1101/602367
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
Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder
Autor:
Shannon E. Ellis, M. Daniele Fallin, Lisa A. Croen, Brooke Sheppard, Dan E. Arking, Irva Hertz-Picciotto, Andrew P. Feinberg, Christine Ladd-Acosta, Shan V. Andrews, Kelly M. Bakulski, Craig J. Newschaffer
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature communications, vol 8, iss 1
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature communications, vol 8, iss 1
Integration of emerging epigenetic information with autism spectrum disorder (ASD) genetic results may elucidate functional insights not possible via either type of information in isolation. Here we use the genotype and DNA methylation (DNAm) data fr