Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sigurdur H, Magnusson"'
Autor:
Guanglu Li, Shaojie Duan, International Headache Genetics Consortium (IHGC), Tao Zheng, Tiantian Zhu, Baoquan Qu, Lei Liu, Zunjing Liu, Verneri Anttila, Ville Artto, Andrea C Belin, Anna Bjornsdottir, Gyda Bjornsdottir, Dorret I Boomsma, Sigrid Børte, Mona A Chalmer, Daniel I Chasman, Bru Cormand, Ester Cuenca-Leon, George Davey-Smith, Irene de Boer, Martin Dichgans, Tonu Esko, Tobias Freilinger, Padhraig Gormley, Lyn R Griffiths, Eija Hämäläinen, Thomas F Hansen, Aster VE Harder, Heidi Hautakangas, Marjo Hiekkala, Maria G Hrafnsdottir, M. Arfan Ikram, Marjo-Riitta Järvelin, Risto Kajanne, Mikko Kallela, Jaakko Kaprio, Mari Kaunisto, Lisette JA Kogelman, Espen S Kristoffersen, Christian Kubisch, Mitja Kurki, Tobias Kurth, Lenore Launer, Terho Lehtimäki, Davor Lessel, Lannie Ligthart, Sigurdur H Magnusson, Rainer Malik, Bertram Müller-Myhsok, Carrie Northover, Dale R Nyholt, Jes Olesen, Aarno Palotie, Priit Palta, Linda M Pedersen, Nancy Pedersen, Matti Pirinen, Danielle Posthuma, Patricia Pozo-Rosich, Alice Pressman, Olli Raitakari, Caroline Ran, Gudrun R Sigurdardottir, Hreinn Stefansson, Kari Stefansson, Olafur A Sveinsson, Gisela M Terwindt, Thorgeir E Thorgeirsson, Arn MJM vanden Maagdenberg, Cornelia van Duijn, Maija Wessman, Bendik S Winsvold, John-Anker Zwart.
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundMigraine has an increased prevalence in several immune disorders, but genetic cause-effect relationships remain unclear. Mendelian randomization (MR) was used in this study to explore whether immune diseases are causally associated with mig
Externí odkaz:
https://doaj.org/article/a30f6c7b567e43149a0c5afd66373445
Autor:
Astros Th. Skuladottir, Gyda Bjornsdottir, Egil Ferkingstad, Gudmundur Einarsson, Lilja Stefansdottir, Muhammad Sulaman Nawaz, Asmundur Oddsson, Thorunn A. Olafsdottir, Saedis Saevarsdottir, G. Bragi Walters, Sigurdur H. Magnusson, Anna Bjornsdottir, Olafur A. Sveinsson, Arnor Vikingsson, Thomas Folkmann Hansen, Rikke Louise Jacobsen, Christian Erikstrup, Michael Schwinn, Søren Brunak, Karina Banasik, Sisse Rye Ostrowski, Anders Troelsen, Cecilie Henkel, Ole Birger Pedersen, DBDS Genetic Consortium, Ingileif Jonsdottir, Daniel F. Gudbjartsson, Patrick Sulem, Thorgeir E. Thorgeirsson, Hreinn Stefansson, Kari Stefansson
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
The underlying genetics of carpal tunnel syndrome is not well understood. Here, the authors perform a GWAS meta-analysis for carpal tunnel syndrome finding variants at 50 loci with connections to the extracellular matrix discovered through various fu
Externí odkaz:
https://doaj.org/article/569badaaffdf4538b77e6ebdcc046111
Autor:
Astros Th. Skuladottir, Gyda Bjornsdottir, Gudmar Thorleifsson, G. Bragi Walters, Muhammad Sulaman Nawaz, Kristjan Helgi Swerford Moore, Pall I. Olason, Thorgeir E. Thorgeirsson, Brynja Sigurpalsdottir, Gardar Sveinbjornsson, Hannes P. Eggertsson, Sigurdur H. Magnusson, Asmundur Oddsson, Anna Bjornsdottir, Arnor Vikingsson, Olafur A. Sveinsson, Maria G. Hrafnsdottir, Gudrun R. Sigurdardottir, Bjarni V. Halldorsson, Thomas Folkmann Hansen, Helene Paarup, Christian Erikstrup, Kaspar Nielsen, Mads Klokker, Mie Topholm Bruun, Erik Sorensen, Karina Banasik, Kristoffer S. Burgdorf, Ole Birger Pedersen, Henrik Ullum, Ingileif Jonsdottir, Hreinn Stefansson, Kari Stefansson
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract Bell’s palsy is the most common cause of unilateral facial paralysis and is defined as an idiopathic and acute inability to control movements of the facial muscles on the affected side. While the pathogenesis remains unknown, previous stud
Externí odkaz:
https://doaj.org/article/3d2fc42f3e4e427a80a49c09b7408bbb
Autor:
Maria Didriksen, Muhammad Sulaman Nawaz, Joseph Dowsett, Steven Bell, Christian Erikstrup, Ole B. Pedersen, Erik Sørensen, Poul J. Jennum, Kristoffer S. Burgdorf, Brendan Burchell, Adam S. Butterworth, Nicole Soranzo, David B. Rye, Lynn Marie Trotti, Prabhjyot Saini, Lilja Stefansdottir, Sigurdur H. Magnusson, Gudmar Thorleifsson, Thordur Sigmundsson, Albert P. Sigurdsson, Katja Van Den Hurk, Franke Quee, Michael W. T. Tanck, Willem H. Ouwehand, David J. Roberts, Eric J. Earley, Michael P. Busch, Alan E. Mast, Grier P. Page, John Danesh, Emanuele Di Angelantonio, Hreinn Stefansson, Henrik Ullum, Kari Stefansson
Publikováno v:
Communications Biology, Vol 3, Iss 1, Pp 1-9 (2020)
Didriksen, Nawaz, et al. identify three novel genetic risk variants for restless legs syndrome and confirm 19 out of 20 previously reported variants through a genome-wide association meta-analysis including nearly half a million individuals. Using ex
Externí odkaz:
https://doaj.org/article/b804eef352554c768c94ad94c5a8a74a
Autor:
Thorgeir E. Thorgeirsson, Sigurdur H. Magnusson, Helene M. Paarup, Astros Skuladottir, Erik Elgaard Sørensen, Olafur A. Sveinsson, Gardar Sveinbjornsson, Brynja D. Sigurpalsdottir, Hreinn Stefansson, Christian Erikstrup, Muhammad Sulaman Nawaz, Gyda Bjornsdottir, Maria Gudlaug Hrafnsdottir, Gudrun R. Sigurdardottir, Pall I. Olason, G. Bragi Walters, Mie Topholm Bruun, Ingileif Jonsdottir, Thomas Hansen, Gudmar Thorleifsson, Bjarni V. Halldorsson, Kristoffer Sølvsten Burgdorf, Anna Bjornsdottir, Ole Birger Pedersen, Karina Banasik, Asmundur Oddsson, Henrik Ullum, Mads Klokker, Kari Stefansson, Kaspar René Nielsen, Arnor Vikingsson, Hannes P. Eggertsson, Kristjan H. S. Moore
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sørensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Scientific Reports
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sorensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Skuladottir, A T, Bjornsdottir, G, Thorleifsson, G, Walters, G B, Nawaz, M S, Moore, K H S, Olason, P I, Thorgeirsson, T E, Sigurpalsdottir, B, Sveinbjornsson, G, Eggertsson, H P, Magnusson, S H, Oddsson, A, Bjornsdottir, A, Vikingsson, A, Sveinsson, O A, Hrafnsdottir, M G, Sigurdardottir, G R, Halldorsson, B V, Hansen, T F, Paarup, H, Erikstrup, C, Nielsen, K, Klokker, M, Bruun, M T, Sørensen, E, Banasik, K, Burgdorf, K S, Pedersen, O B, Ullum, H, Jonsdottir, I, Stefansson, H & Stefansson, K 2021, ' A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy ', Scientific Reports, vol. 11, no. 1, 4188 . https://doi.org/10.1038/s41598-021-82736-w
Bell’s palsy is the most common cause of unilateral facial paralysis and is defined as an idiopathic and acute inability to control movements of the facial muscles on the affected side. While the pathogenesis remains unknown, previous studies have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262d073983b206e4c093749e018eebbe
https://doaj.org/article/3d2fc42f3e4e427a80a49c09b7408bbb
https://doaj.org/article/3d2fc42f3e4e427a80a49c09b7408bbb
Autor:
Muhammad Sulaman Nawaz, Gudmundur Einarsson, Mariana Bustamante, Rosa S Gisladottir, G Bragi Walters, Gudrun A Jonsdottir, Astros Th Skuladottir, Gyda Bjornsdottir, Sigurdur H Magnusson, Bergrun Asbjornsdottir, Unnur Unnsteinsdottir, Engilbert Sigurdsson, Palmi V Jonsson, Vala Kolbrun Palmadottir, Sigurjon A Gudjonsson, Gisli H Halldorsson, Egil Ferkingstad, Ingileif Jonsdottir, Gudmar Thorleifsson, Hilma Holm, Unnur Thorsteinsdottir, Patrick Sulem, Daniel F Gudbjartsson, Hreinn Stefansson, Thorgeir E Thorgeirsson, Magnus O Ulfarsson, Kari Stefansson
Publikováno v:
Brain Communications
Intracranial volume, measured through magnetic resonance imaging and/or estimated from head circumference, is heritable and correlates with cognitive traits and several neurological disorders. We performed a genome-wide association study meta-analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e14463d7bfdb808351c6a36bd85aa5d1
https://pubmed.ncbi.nlm.nih.gov/36415660
https://pubmed.ncbi.nlm.nih.gov/36415660
Autor:
Niamh Mullins, JooEun Kang, Adrian I. Campos, Jonathan R.I. Coleman, Alexis C. Edwards, Hanga Galfalvy, Daniel F. Levey, Adriana Lori, Andrey Shabalin, Anna Starnawska, Mei-Hsin Su, Hunna J. Watson, Mark Adams, Swapnil Awasthi, Michael Gandal, Jonathan D. Hafferty, Akitoyo Hishimoto, Minsoo Kim, Satoshi Okazaki, Ikuo Otsuka, Stephan Ripke, Erin B. Ware, Andrew W. Bergen, Wade H. Berrettini, Martin Bohus, Harry Brandt, Xiao Chang, Wei J. Chen, Hsi-Chung Chen, Steven Crawford, Scott Crow, Emily DiBlasi, Philibert Duriez, Fernando Fernández-Aranda, Manfred M. Fichter, Steven Gallinger, Stephen J. Glatt, Philip Gorwood, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Hai-Gwo Hwu, Sonia Jain, Stéphane Jamain, Susana Jiménez-Murcia, Craig Johnson, Allan S. Kaplan, Walter H. Kaye, Pamela K. Keel, James L. Kennedy, Kelly L. Klump, Dong Li, Shih-Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Chih-Min Liu, Pierre J. Magistretti, Christian R. Marshall, James E. Mitchell, Eric T. Monson, Richard M. Myers, Dalila Pinto, Abigail Powers, Nicolas Ramoz, Stefan Roepke, Vsevolod Rozanov, Stephen W. Scherer, Christian Schmahl, Marcus Sokolowski, Michael Strober, Laura M. Thornton, Janet Treasure, Ming T. Tsuang, Stephanie H. Witt, D. Blake Woodside, Zeynep Yilmaz, Lea Zillich, Rolf Adolfsson, Ingrid Agartz, Tracy M. Air, Martin Alda, Lars Alfredsson, Ole A. Andreassen, Adebayo Anjorin, Vivek Appadurai, María Soler Artigas, Sandra Van der Auwera, M. Helena Azevedo, Nicholas Bass, Claiton H.D. Bau, Bernhard T. Baune, Frank Bellivier, Klaus Berger, Joanna M. Biernacka, Tim B. Bigdeli, Elisabeth B. Binder, Michael Boehnke, Marco P. Boks, Rosa Bosch, David L. Braff, Richard Bryant, Monika Budde, Enda M. Byrne, Wiepke Cahn, Miguel Casas, Enrique Castelao, Jorge A. Cervilla, Boris Chaumette, Sven Cichon, Aiden Corvin, Nicholas Craddock, David Craig, Franziska Degenhardt, Srdjan Djurovic, Howard J. Edenberg, Ayman H. Fanous, Jerome C. Foo, Andreas J. Forstner, Mark Frye, Janice M. Fullerton, Justine M. Gatt, Pablo V. Gejman, Ina Giegling, Hans J. Grabe, Melissa J. Green, Eugenio H. Grevet, Maria Grigoroiu-Serbanescu, Blanca Gutierrez, Jose Guzman-Parra, Steven P. Hamilton, Marian L. Hamshere, Annette Hartmann, Joanna Hauser, Stefanie Heilmann-Heimbach, Per Hoffmann, Marcus Ising, Ian Jones, Lisa A. Jones, Lina Jonsson, René S. Kahn, John R. Kelsoe, Kenneth S. Kendler, Stefan Kloiber, Karestan C. Koenen, Manolis Kogevinas, Bettina Konte, Marie-Odile Krebs, Mikael Landén, Jacob Lawrence, Marion Leboyer, Phil H. Lee, Douglas F. Levinson, Calwing Liao, Jolanta Lissowska, Susanne Lucae, Fermin Mayoral, Susan L. McElroy, Patrick McGrath, Peter McGuffin, Andrew McQuillin, Sarah E. Medland, Divya Mehta, Ingrid Melle, Yuri Milaneschi, Philip B. Mitchell, Esther Molina, Gunnar Morken, Preben Bo Mortensen, Bertram Müller-Myhsok, Caroline Nievergelt, Vishwajit Nimgaonkar, Markus M. Nöthen, Michael C. O’Donovan, Roel A. Ophoff, Michael J. Owen, Carlos Pato, Michele T. Pato, Brenda W.J.H. Penninx, Jonathan Pimm, Giorgio Pistis, James B. Potash, Robert A. Power, Martin Preisig, Digby Quested, Josep Antoni Ramos-Quiroga, Andreas Reif, Marta Ribasés, Vanesa Richarte, Marcella Rietschel, Margarita Rivera, Andrea Roberts, Gloria Roberts, Guy A. Rouleau, Diego L. Rovaris, Dan Rujescu, Cristina Sánchez-Mora, Alan R. Sanders, Peter R. Schofield, Thomas G. Schulze, Laura J. Scott, Alessandro Serretti, Jianxin Shi, Stanley I. Shyn, Lea Sirignano, Pamela Sklar, Olav B. Smeland, Jordan W. Smoller, Edmund J.S. Sonuga-Barke, Gianfranco Spalletta, John S. Strauss, Beata Świątkowska, Maciej Trzaskowski, Gustavo Turecki, Laura Vilar-Ribó, John B. Vincent, Henry Völzke, James T.R. Walters, Cynthia Shannon Weickert, Thomas W. Weickert, Myrna M. Weissman, Leanne M. Williams, Naomi R. Wray, Clement C. Zai, Allison E. Ashley-Koch, Jean C. Beckham, Elizabeth R. Hauser, Michael A. Hauser, Nathan A. Kimbrel, Jennifer H. Lindquist, Benjamin McMahon, David W. Oslin, Xuejun Qin, Esben Agerbo, Anders D. Børglum, Gerome Breen, Annette Erlangsen, Tõnu Esko, Joel Gelernter, David M. Hougaard, Ronald C. Kessler, Henry R. Kranzler, Qingqin S. Li, Nicholas G. Martin, Andrew M. McIntosh, Ole Mors, Merete Nordentoft, Catherine M. Olsen, David Porteous, Robert J. Ursano, Danuta Wasserman, Thomas Werge, David C. Whiteman, Cynthia M. Bulik, Hilary Coon, Ditte Demontis, Anna R. Docherty, Po-Hsiu Kuo, Cathryn M. Lewis, J. John Mann, Miguel E. Rentería, Daniel J. Smith, Eli A. Stahl, Murray B. Stein, Fabian Streit, Virginia Willour, Douglas M. Ruderfer, Manuel Mattheisen, Abdel Abdellaoui, Mark J. Adams, Till F.M. Andlauer, Silviu-Alin Bacanu, Marie Bækvad-Hansen, Aartjan T.F. Beekman, Julien Bryois, Henriette N. Buttenschøn, Jonas Bybjerg-Grauholm, Na Cai, Jane Hvarregaard Christensen, Toni-Kim Clarke, Lucía Colodro-Conde, Baptiste Couvy-Duchesne, Nick Craddock, Gregory E. Crawford, Gail Davies, Eske M. Derks, Nese Direk, Conor V. Dolan, Erin C. Dunn, Thalia C. Eley, Valentina Escott-Price, Farnush Farhadi Hassan Kiadeh, Hilary K. Finucane, Josef Frank, Héléna A. Gaspar, Michael Gill, Fernando S. Goes, Scott D. Gordon, Shantel Marie Weinsheimer, Jürgen Wellmann, Gonneke Willemsen, Yang Wu, Hualin S. Xi, Jian Yang, Futao Zhang, Volker Arolt, Dorret I. Boomsma, Udo Dannlowski, E.J.C. de Geus, J. Raymond Depaulo, Enrico Domenici, Katharina Domschke, Jakob Grove, Lynsey S. Hall, Christine Søholm Hansen, Thomas F. Hansen, Stefan Herms, Ian B. Hickie, Georg Homuth, Carsten Horn, Jouke-Jan Hottenga, David M. Howard, Rick Jansen, Eric Jorgenson, James A. Knowles, Isaac S. Kohane, Julia Kraft, Warren W. Kretzschmar, Zoltán Kutalik, Yihan Li, Penelope A. Lind, Donald J. MacIntyre, Dean F. MacKinnon, Robert M. Maier, Wolfgang Maier, Jonathan Marchini, Hamdi Mbarek, Christel M. Middeldorp, Evelin Mihailov, Lili Milani, Francis M. Mondimore, Grant W. Montgomery, Sara Mostafavi, Matthias Nauck, Bernard Ng, Michel G. Nivard, Dale R. Nyholt, Paul F. O’Reilly, Hogni Oskarsson, Caroline Hayward, Andrew C. Heath, Glyn Lewis, Pamela A.F. Madden, Patrik K. Magnusson, Andres Metspalu, Sara A. Paciga, Nancy L. Pedersen, Jodie N. Painter, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Roseann E. Peterson, Wouter J. Peyrot, Danielle Posthuma, Jorge A. Quiroz, Per Qvist, John P. Rice, Brien P. Riley, Saira Saeed Mirza, Robert Schoevers, Eva C. Schulte, Ling Shen, Engilbert Sigurdsson, Grant C.B. Sinnamon, Johannes H. Smit, Hreinn Stefansson, Stacy Steinberg, Jana Strohmaier, Katherine E. Tansey, Henning Teismann, Alexander Teumer, Wesley Thompson, Pippa A. Thomson, Thorgeir E. Thorgeirsson, Matthew Traylor, Jens Treutlein, Vassily Trubetskoy, André G. Uitterlinden, Daniel Umbricht, Albert M. van Hemert, Alexander Viktorin, Peter M. Visscher, Yunpeng Wang, Bradley T. Webb, Roy H. Perlis, David J. Porteous, Catherine Schaefer, Kari Stefansson, Henning Tiemeier, Rudolf Uher, Patrick F. Sullivan, Kevin S. O’Connell, Brandon Coombes, Zhen Qiao, Thomas D. Als, Sigrid Børte, Alexander W. Charney, Ole Kristian Drange, Michael J. Gandal, Saskia P. Hagenaars, Masashi Ikeda, Nolan Kamitaki, Kristi Krebs, Georgia Panagiotaropoulou, Brian M. Schilder, Laura G. Sloofman, Bendik S. Winsvold, Hong-Hee Won, Liliya Abramova, Kristina Adorjan, Mariam Al Eissa, Diego Albani, Ney Alliey-Rodriguez, Verneri Antilla, Anastasia Antoniou, Ji Hyun Baek, Michael Bauer, Eva C. Beins, Sarah E. Bergen, Armin Birner, Erlend Bøen, Murielle Brum, Ben M. Brumpton, Nathalie Brunkhorst-Kanaan, William Byerley, Murray Cairns, Miquel Casas, Pablo Cervantes, Cristiana Cruceanu, Alfredo Cuellar-Barboza, Julie Cunningham, David Curtis, Piotr M. Czerski, Anders M. Dale, Nina Dalkner, Friederike S. David, Amanda L. Dobbyn, Athanassios Douzenis, Torbjørn Elvsåshagen, I. Nicol Ferrier, Alessia Fiorentino, Tatiana M. Foroud, Liz Forty, Oleksandr Frei, Nelson B. Freimer, Louise Frisén, Katrin Gade, Julie Garnham, Ian R. Gizer, Katherine Gordon-Smith, Tiffany A. Greenwood, José Guzman-Parra, Kyooseob Ha, Magnus Haraldsson, Martin Hautzinger, Urs Heilbronner, Dennis Hellgren, Peter A. Holmans, Laura Huckins, Jessica S. Johnson, Janos L. Kalman, Yoichiro Kamatani, Sarah Kittel-Schneider, Maria Koromina, Thorsten M. Kranz, Michiaki Kubo, Ralph Kupka, Steven A. Kushner, Catharina Lavebratt, Markus Leber, Heon-Jeong Lee, Shawn E. Levy, Catrin Lewis, Martin Lundberg, Sigurdur H. Magnusson, Adam Maihofer, Dolores Malaspina, Eirini Maratou, Lina Martinsson, Nathaniel W. McGregor, James D. McKay, Helena Medeiros, Vincent Millischer, Jennifer L. Moran, Derek W. Morris, Thomas W. Mühleisen, Niamh O’Brien, Claire O’Donovan, Loes M. Olde Loohuis, Lilijana Oruc, Sergi Papiol, Antonio F. Pardiñas, Amy Perry, Andrea Pfennig, Evgenia Porichi, Towfique Raj, Mark H. Rapaport, J. Raymond DePaulo, Eline J. Regeer, Fabio Rivas, Julian Roth, Panos Roussos, Fanny Senner, Sally Sharp, Paul D. Shilling, Claire Slaney, Janet L. Sobell, Maria Soler Artigas, Anne T. Spijker, Dan J. Stein, Chikashi Terao, Claudio Toma, Paul Tooney, Evangelia-Eirini Tsermpini, Marquis P. Vawter, Helmut Vedder, Simon Xi, Wei Xu, Jessica Mei Kay Yang, Allan H. Young, Hannah Young, Peter P. Zandi, Hang Zhou, null HUNT All-In Psychiatry, Gulja Babadjanova, Lena Backlund, Susanne Bengesser, Douglas H.R. Blackwood, Vaughan J. Carr, Stanley Catts, Dimitris Dikeos, Bruno Etain, Panagiotis Ferentinos, Micha Gawlik, Elliot S. Gershon, Frans Henskens, Jan Hillert, Kyung Sue Hong, Christina M. Hultman, Kristian Hveem, Nakao Iwata, Assen V. Jablensky, George Kirov, Christine Lochner, Carmel Loughland, Carol A. Mathews, Francis J. McMahon, Patricia Michie, Bryan Mowry, Benjamin M. Neale, Caroline M. Nievergelt, Ketil J. Oedegaard, Tomas Olsson, Chris Pantelis, George P. Patrinos, Eva Z. Reininghaus, Takeo Saito, Ulrich Schall, Martin Schalling, Rodney J. Scott, Eystein Stordal, Arne E. Vaaler, Eduard Vieta, Irwin D. Waldman, John-Anker Zwart, John I. Nurnberger, Arianna Di Florio, Roger A.H. Adan, Tetsuya Ando, Harald Aschauer, Jessica H. Baker, Vladimir Bencko, Andreas Birgegård, Joseph M. Boden, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Katharina Buehren, Roland Burghardt, Laura Carlberg, Matteo Cassina, Maurizio Clementi, Roger D. Cone, Philippe Courtet, James J. Crowley, Unna N. Danner, Oliver S.P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Christian Dina, Monika Dmitrzak-Weglarz, Elisa Docampo Martinez, Laramie E. Duncan, Karin Egberts, Morten Mattingsdal, Sara McDevitt, Ingrid Meulenbelt, Nadia Micali, James Mitchell, Karen Mitchell, Palmiero Monteleone, Alessio Maria Monteleone, Melissa A. Munn-Chernoff, Benedetta Nacmias, Marie Navratilova, Ioanna Ntalla, Julie K. O’Toole, Leonid Padyukov, Aarno Palotie, Jacques Pantel, Hana Papezova, Richard Parker, John F. Pearson, Stefan Ehrlich, Geòrgia Escaramís, Thomas Espeseth, Xavier Estivill, Anne Farmer, Angela Favaro, Krista Fischer, James A.B. Floyd, Manuel Föcker, Lenka Foretova, Monica Forzan, Christopher S. Franklin, Giovanni Gambaro, Johanna Giuranna, Paola Giusti-Rodríquez, Fragiskos Gonidakis, Scott Gordon, Monica Gratacos Mayora, Sébastien Guillaume, Ken B. Hanscombe, Konstantinos Hatzikotoulas, Johannes Hebebrand, Sietske G. Helder, Anjali K. Henders, Beate Herpertz-Dahlmann, Wolfgang Herzog, Anke Hinney, L. John Horwood, Christopher Hübel, Liselotte V. Petersen, Kirstin L. Purves, Anu Raevuori, Ted Reichborn-Kjennerud, Valdo Ricca, Samuli Ripatti, Franziska Ritschel, Marion Roberts, Filip Rybakowski, Paolo Santonastaso, André Scherag, Ulrike Schmidt, Nicholas J. Schork, Alexandra Schosser, Jochen Seitz, Lenka Slachtova, P. Eline Slagboom, Margarita C.T. Slof-Op ‘t Landt, Agnieszka Slopien, Nicole Soranzo, Sandro Sorbi, Lorraine Southam, Vidar W. Steen, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimir Janout, Jennifer Jordan, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J.H. Kas, Martin A. Kennedy, Anna Keski-Rahkonen, Kirsty Kiezebrink, Youl-Ri Kim, Katherine M. Kirk, Lars Klareskog, Gun Peggy S. Knudsen, Janne T. Larsen, Stephanie Le Hellard, Virpi M. Leppä, Paul Lichtenstein, Bochao Danae Lin, Astri Lundervold, Jurjen Luykx, Mario Maj, Katrin Mannik, Sara Marsal, Garret D. Stuber, Jin P. Szatkiewicz, Ioanna Tachmazidou, Elena Tenconi, Alfonso Tortorella, Federica Tozzi, Artemis Tsitsika, Marta Tyszkiewicz-Nwafor, Konstantinos Tziouvas, Annemarie A. van Elburg, Eric F. van Furth, Tracey D. Wade, Gudrun Wagner, Esther Walton, H. Erich Wichmann, Elisabeth Widen, Shuyang Yao, Eleftheria Zeggini, Stephanie Zerwas, Stephan Zipfel, Martin Jungkunz, Lydie Dietl, Cornelia E. Schwarze, Norbert Dahmen, Björn H. Schott, Arian Mobascher, Silvia Crivelli, Michelle F. Dennis, Phillip D. Harvey, Bruce W. Carter, Jennifer E. Huffman, Daniel Jacobson, Ravi Madduri, Maren K. Olsen, John Pestian, J. Michael Gaziano, Sumitra Muralidhar, Rachel Ramoni, Jean Beckham, Kyong-Mi Chang, Christopher J. O’Donnell, Philip S. Tsao, James Breeling, Grant Huang, J.P. Casas Romero, Jennifer Moser, Stacey B. Whitbourne, Jessica V. Brewer, Mihaela Aslan, Todd Connor, Dean P. Argyres, Brady Stephens, Mary T. Brophy, Donald E. Humphries, Luis E. Selva, Nhan Do, Shahpoor Shayan, Kelly Cho, Saiju Pyarajan, Elizabeth Hauser, Yan Sun, Hongyu Zhao, Peter Wilson, Rachel McArdle, Louis Dellitalia, Kristin Mattocks, John Harley, Clement J. Zablocki, Jeffrey Whittle, Frank Jacono, Salvador Gutierrez, Gretchen Gibson, Kimberly Hammer, Laurence Kaminsky, Gerardo Villareal, Scott Kinlay, Junzhe Xu, Mark Hamner, Roy Mathew, Sujata Bhushan, Pran Iruvanti, Michael Godschalk, Zuhair Ballas, Douglas Ivins, Stephen Mastorides, Jonathan Moorman, Saib Gappy, Jon Klein, Nora Ratcliffe, Hermes Florez, Olaoluwa Okusaga, Maureen Murdoch, Peruvemba Sriram, Shing Shing Yeh, Neeraj Tandon, Darshana Jhala, Samuel Aguayo, David Cohen, Satish Sharma, Suthat Liangpunsakul, Kris Ann Oursler, Mary Whooley, Sunil Ahuja, Joseph Constans, Paul Meyer, Jennifer Greco, Michael Rauchman, Richard Servatius, Melinda Gaddy, Agnes Wallbom, Timothy Morgan, Todd Stapley, Scott Sherman, George Ross, Philip Tsao, Patrick Strollo, Edward Boyko, Laurence Meyer, Samir Gupta, Mostaqul Huq, Joseph Fayad, Adriana Hung, Jack Lichy, Robin Hurley, Brooks Robey, Robert Striker
Publikováno v:
Biological Psychiatry 91(3), 313-327 (2022). doi:10.1016/j.biopsych.2021.05.029 special issue: "Novel Neuromodulators of Anxiety"
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium, MVP Suicide Exemplar Workgroup & VA Million Veteran Program 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biol. Psychiatry 91, 313-327 (2022)
Biological psychiatry 91(3), 313-327 (2022). doi:10.1016/j.biopsych.2021.05.029
Mullins, N, Kang, J E, Campos, A I, Coleman, J R I, Ruderfer, D M, VA Million Veteran Program, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium, MVP Suicide Exemplar Workgroup, Abdellaoui, A, Derks, E M, Dolan, C, Willemsen, G, Boomsma, D, de Geus, E J C, Hottenga, J J, Jansen, R, Mbarek, H, Middeldorp, C M, Milaneschi, Y, Nivard, M, Peyrot, W, Posthuma, D, W J H Penninx, B & Lin, B 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biological Psychiatry, 91(3), 313-327. Elsevier Inc.
Dipòsit Digital de la UB
Universidad de Barcelona
Biological Psychiatry
Mullins, N, Kang, J E, Campos, A I, Coleman, J R I, Edwards, A C, Galfalvy, H, Levey, D F, Lori, A, Shabalin, A, Starnawska, A, Su, M H, Watson, H J, Adams, M, Awasthi, S, Gandal, M, Hafferty, J D, Hishimoto, A, Kim, M, Okazaki, S, Otsuka, I, Ripke, S, Ware, E B, Bergen, A W, Berrettini, W H, Bohus, M, Brandt, H, Chang, X, Chen, W J, Chen, H C, Crawford, S, Crow, S, DiBlasi, E, Duriez, P, Fernández-Aranda, F, Fichter, M M, Gallinger, S, Glatt, S J, Gorwood, P, Guo, Y, Hakonarson, H, Halmi, K A, Hwu, H G, Jain, S, Li, D, Røpke, S, Appadurai, V, Jonsson, L, Schofield, P R, Nordentoft, M, Werge, T, VA Million Veteran Program, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium & MVP Suicide Exemplar Workgroup 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biological psychiatry, 91(3), 313-327. Elsevier USA
Biological Psychiatry, 91(3), 313-327. Elsevier USA
Online: 0006-3223
2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Mullins, N, Kang, J, Campos, A, Coleman, J R, Edwards, A C, Galfalvy, H, Levey, D F, Lori, A, Shabalin, A, Starnawska, A, Su, M-H, Watson, H J, Adams, M, Awasthi, S, Ganda, M, Hafferty, J D, Hishimoto, A, Kim, M, Okazaki, S, Otsuka, I, Ripke, S, Ware, E B, Bergen, A W, Berrettini, W H, Bohus, M, Brandt, H, Chang, X, Chen, W J, Chen, H-C, Crawford, S, Crow, S, DiBlasi, E, Duriez, P, Fernandez-Aranda, F, Fichter, M M, Gallinger, S, Glatt, S J, Gorwood, P, Guo, Y, Hakonarson, H, Halmi, K A, Yilmaz, Z, Byrne, E M, Mortensen, P B, Sonuga-Barke, E J S, Vilar-Ribo, L, Psychiat Genomics Consortium, German Borderline Genomics Consort, MVP Suicide Exemplar Workgrp & VA Million Vet Program 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium, MVP Suicide Exemplar Workgroup & VA Million Veteran Program 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biol. Psychiatry 91, 313-327 (2022)
Biological psychiatry 91(3), 313-327 (2022). doi:10.1016/j.biopsych.2021.05.029
Mullins, N, Kang, J E, Campos, A I, Coleman, J R I, Ruderfer, D M, VA Million Veteran Program, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium, MVP Suicide Exemplar Workgroup, Abdellaoui, A, Derks, E M, Dolan, C, Willemsen, G, Boomsma, D, de Geus, E J C, Hottenga, J J, Jansen, R, Mbarek, H, Middeldorp, C M, Milaneschi, Y, Nivard, M, Peyrot, W, Posthuma, D, W J H Penninx, B & Lin, B 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biological Psychiatry, 91(3), 313-327. Elsevier Inc.
Dipòsit Digital de la UB
Universidad de Barcelona
Biological Psychiatry
Mullins, N, Kang, J E, Campos, A I, Coleman, J R I, Edwards, A C, Galfalvy, H, Levey, D F, Lori, A, Shabalin, A, Starnawska, A, Su, M H, Watson, H J, Adams, M, Awasthi, S, Gandal, M, Hafferty, J D, Hishimoto, A, Kim, M, Okazaki, S, Otsuka, I, Ripke, S, Ware, E B, Bergen, A W, Berrettini, W H, Bohus, M, Brandt, H, Chang, X, Chen, W J, Chen, H C, Crawford, S, Crow, S, DiBlasi, E, Duriez, P, Fernández-Aranda, F, Fichter, M M, Gallinger, S, Glatt, S J, Gorwood, P, Guo, Y, Hakonarson, H, Halmi, K A, Hwu, H G, Jain, S, Li, D, Røpke, S, Appadurai, V, Jonsson, L, Schofield, P R, Nordentoft, M, Werge, T, VA Million Veteran Program, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium & MVP Suicide Exemplar Workgroup 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Biological psychiatry, 91(3), 313-327. Elsevier USA
Biological Psychiatry, 91(3), 313-327. Elsevier USA
Online: 0006-3223
2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Mullins, N, Kang, J, Campos, A, Coleman, J R, Edwards, A C, Galfalvy, H, Levey, D F, Lori, A, Shabalin, A, Starnawska, A, Su, M-H, Watson, H J, Adams, M, Awasthi, S, Ganda, M, Hafferty, J D, Hishimoto, A, Kim, M, Okazaki, S, Otsuka, I, Ripke, S, Ware, E B, Bergen, A W, Berrettini, W H, Bohus, M, Brandt, H, Chang, X, Chen, W J, Chen, H-C, Crawford, S, Crow, S, DiBlasi, E, Duriez, P, Fernandez-Aranda, F, Fichter, M M, Gallinger, S, Glatt, S J, Gorwood, P, Guo, Y, Hakonarson, H, Halmi, K A, Yilmaz, Z, Byrne, E M, Mortensen, P B, Sonuga-Barke, E J S, Vilar-Ribo, L, Psychiat Genomics Consortium, German Borderline Genomics Consort, MVP Suicide Exemplar Workgrp & VA Million Vet Program 2022, ' Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors ', Biological Psychiatry, vol. 91, no. 3, pp. 313-327 . https://doi.org/10.1016/j.biopsych.2021.05.029
Statistical analyses were carried out on the NL Genetic Cluster Computer (http://www.geneticcluster.org) hosted by SURFsara and the Mount Sinai high performance computing cluster (http://hpc.mssm.edu), which is supported by the Office of Research Inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bcd507be0bf88fb1a330841764a3372
Autor:
Steinunn Thordardottir, Kristian Hveem, Per Selnes, Silke Kern, Wei Zhou, Srdjan Djurovic, Iris E. Jansen, Ole A. Andreassen, Petroula Proitsi, Linda M. Pedersen, Tormod Fladby, Tore Wergeland Meisingset, Chandra A. Reynolds, Angela Hodges, Ingmar Skoog, Alexey A. Shadrin, Bendik S. Winsvold, Margda Waern, Geir Bråthen, Danielle Posthuma, Lavinia Athanasiu, Richard Dobson, Adam Auton, Shahram Bahrami, Anna Zettergren, Maiken Elvestad Gabrielsen, Henrik Zetterberg, Eystein Stordal, Geir Selbæk, John-Anker Zwart, Laurent F. Thomas, Amy E Martinsen, Ingun Ulstein, Jonas B. Nielsen, Kari Stefansson, Ole Kristian Drange, Arvid Rongve, Anne Heidi Skogholt, Julia M. Sealock, Sigrid Botne Sando, Palmi V. Jonsson, Jon Snaedal, Kaj Blennow, Ingvild Saltvedt, Lars G. Fritsche, Karl Heilbron, Jeanne E. Savage, Sigurdur H. Magnusson, Ingunn Bosnes, Stephan Ripke, Marianne Bakke Johnsen, Ida K. Karlsson, Lea K. Davis, Latha Velayudhan, Nancy L. Pedersen, Dag Aarsland, Cristen J. Willer, Hreinn Stefansson, Dominic Holland, Sigrid Børte, Douglas P Wightman
Publikováno v:
Nature Genetics, 53(9), 1276-1282. Nature Publishing Group
Nat Genet
23andMe Research team 2021, ' A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease ', Nature Genetics, vol. 53, no. 9, pp. 1276-1282 . https://doi.org/10.1038/s41588-021-00921-z
23Andme Research Team 2021, ' A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease ', Nature genetics, vol. 53, no. 9, pp. 1276-1282 . https://doi.org/10.1038/s41588-021-00921-z
Nature genetics, 53(9), 1276-1282. Nature Publishing Group
Nat Genet
23andMe Research team 2021, ' A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease ', Nature Genetics, vol. 53, no. 9, pp. 1276-1282 . https://doi.org/10.1038/s41588-021-00921-z
23Andme Research Team 2021, ' A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease ', Nature genetics, vol. 53, no. 9, pp. 1276-1282 . https://doi.org/10.1038/s41588-021-00921-z
Nature genetics, 53(9), 1276-1282. Nature Publishing Group
Late-onset Alzheimer’s disease is a prevalent age-related polygenic disease that accounts for 50–70% of dementia cases. Currently, only a fraction of the genetic variants underlying Alzheimer’s disease have been identified. Here we show that in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c969ce931bb5be93e81bb040c5f9b03a
https://research.vumc.nl/en/publications/7e6cd206-c9e8-41c3-aa48-064cc8f9d961
https://research.vumc.nl/en/publications/7e6cd206-c9e8-41c3-aa48-064cc8f9d961
Autor:
Tobias Kurth, Nadine Pelzer, Hautakangas H, Artto, O T Raitakari, Julie E. Buring, Penninx Bwjh., Christian Erikstrup, Mikko Kallela, Matti Pirinen, Christian Benner, Daniel I. Chasman, Kristian Hveem, Kristoffersen Es, Torben Hansen, Olafur A. Sveinsson, Mika Kähönen, van den Maagdenberg Amjm., Mona Ameri Chalmer, Aarno Palotie, Elisabeth Widen, Thorgeir E. Thorgeirsson, Hreinn Stefansson, Lighart L, Paul M. Ridker, de Boer I, Gisela M. Terwindt, Garbrielsen Me, Jouke J. Hottenga, Kogelman Lja., Arpo Aromaa, Bendik S. Winsvold, Dale R. Nyholt, Ikram Ma, van Dijk Kw, Harder Ave, Martin Dichgans, Rainer Malik, Mohsen Ghanbari, Marianne Bakke Johnsen, Marjo-Ritta Jarvelin, Samuli Ripatti, Paavo Häppölä, Gyda Bjornsdottir, Martti Färkkilä, Anne Heidi Skogholt, Terho Lehtimäki, Sanni Ruotsalainen, Frits R. Rosendaal, Gudrun R. Sigurdardottir, Headache Ha, Gormley P, Kari Stefansson, J.A. Zwart, Oluf Pedersen, Raymond Noordam, Ben Michael Brumpton, Laurent F. Thomas, Karina Banasik, M.G. Hrafnsdottir, Lisanne S. Vijfhuizen, Sølvsten Burgdorf K, Jes Olesen, Sigurdur H. Magnusson, T. Freilinger, Kristen Hagen, Andrea Carmine Belin, Dorret I. Boomsma, Henrik Ullum, Maija Wessman, Ran C, Anna Bjornsdottir
Migraine affects over a billion individuals worldwide but its genetic underpinning remains largely unknown. This genome-wide association study (GWAS) of 102,084 migraine cases and 771,257 controls identified 123 loci of which 86 are novel. The loci p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e64e0da2e2c833014db37279373369e
https://doi.org/10.1101/2021.01.20.21249647
https://doi.org/10.1101/2021.01.20.21249647
Autor:
Inês Barroso, Gail Davies, H.-Erich Wichmann, Bjarke Feenstra, Peter Vollenweider, Nicholas J. Timpson, Alan F. Wright, Frank Geller, Gérard Waeber, John M. Starr, Benjamin M. Neale, George Davey Smith, Tõnu Esko, Ruth J. F. Loos, Andrew A. Hicks, Pedro Marques-Vidal, Dorret I. Boomsma, Harry Campbell, Zoltán Kutalik, David M. Evans, Scott D. Gordon, Eva Albrecht, Peter P. Pramstaller, Leena Peltonen, Jing Hua Zhao, Lavinia Paternoster, Thomas Hansen, Massimo Mangino, Fazil Aliev, Beate St Pourcain, Panos Deloukas, Heather A. Boyd, Guillaume Paré, Marco P. Boks, Monique M.B. Breteler, Jouke-Jan Hottenga, Xin Li, Kari Stefansson, Ian J. Deary, Jari Lahti, Inga Prokopenko, Nicholas Eriksson, Lili Milani, Nicholas J. Wareham, Jordan W. Smoller, Norman Klopp, Lynn Cherkas, Reedik Mägi, Margaret J. Wright, Peter Kraft, Jacques S. Beckmann, Brenda W.J.H. Penninx, Gabriel Cuellar-Partida, André G. Uitterlinden, Fernando Rivadeneira, Wendy L. McArdle, Johan G. Eriksson, Jiali Han, Jennifer E. Huffman, Andres Metspalu, J.M. Vink, Frank J. A. van Rooij, Christian Gieger, M. Arfan Ikram, Cecilia M. Lindgren, Aarno Palotie, Daniel I. Chasman, Joyce Y. Tung, Liang-Dar Hwang, David A. Hinds, Elisabeth Widen, Caroline Hayward, Michelle Luciano, Johannes H. Smit, Gonneke Willemsen, Dale R. Nyholt, Carolina Medina-Gomez, Nicole M. Warrington, Teemu Palviainen, Stacy Steinberg, Kay-Tee Khaw, Kevin S. O’Connell, Bettina Konte, Gudmar Thorleifsson, Eco J. C. de Geus, John P. Kemp, Mads Melbye, Mark I. McCarthy, Sarah E. Medland, Jaakko Kaprio, Cameron D. Palmer, Joel N. Hirschhorn, Ina Giegling, Scott Melville, Thomas Werge, Nicole Soranzo, Sigurdur H. Magnusson, Maris Teder-Laving, Hreinn Stefansson, Kauko Heikkilä, Cornelia M. van Duijn, David L. Duffy, Samuli Ripatti, Igor Rudan, Annette M. Hartmann, Ole A. Andreassen, Mari Nelis, Ozren Polasek, Vincent Mooser, Mousheng Xu, Eero Vuoksimaa, Katri Räikkönen, Nicholas G. Martin, Dan Rujescu, Tim D. Spector, Dawn M. Waterworth, Danielle M. Dick, Roel A. Ophoff
Publikováno v:
Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkila, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O'Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefansson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Partida, G C, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M MB, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E JC, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R JF, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B WJH, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, St Pourcain, B, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F JA, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour . https://doi.org/10.1038/s41562-020-00956-y
Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J J, Huffman, J E, Hwang, L D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefánsson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Mägi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, no. 1, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Nature Human Behaviour, 5, 1, pp. 59-70
Nature Human Behaviour, 5(1), 59-70. Nature Publishing Group
Nat Hum Behav
Nature Human Behaviour, 5(1), 59-70. Springer Nature
Nature Human Behaviour
Nat. Hum. Behav. 5, 59–70 (2021)
Nature Human Behaviour, 5, 59-70
Nature human behaviour 5(1), 59-70 (2021). doi:10.1038/s41562-020-00956-y
Cuellar-Partida, G, Deloukas, P, Kemp, J P, McArdle, W L, Paternoster, L, Davey Smith, G, Timpson, N J, Medland, S E & al., E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59–70 . https://doi.org/10.1038/s41562-020-00956-y
Partida, G C, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M MB, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E JC, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J-J, Huffman, J E, Hwang, L-D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K-T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R JF, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B WJH, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, St Pourcain, B, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefansson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F JA, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H-E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Magi, R, Neale, B M, Evans, D M & Medland, S E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour . https://doi.org/10.1038/s41562-020-00956-y
Cuellar-Partida, G, Tung, J Y, Eriksson, N, Albrecht, E, Aliev, F, Andreassen, O A, Barroso, I, Beckmann, J S, Boks, M P, Boomsma, D I, Boyd, H A, Breteler, M M B, Campbell, H, Chasman, D I, Cherkas, L F, Davies, G, de Geus, E J C, Deary, I J, Deloukas, P, Dick, D M, Duffy, D L, Eriksson, J G, Esko, T, Feenstra, B, Geller, F, Gieger, C, Giegling, I, Gordon, S D, Han, J, Hansen, T F, Hartmann, A M, Hayward, C, Heikkilä, K, Hicks, A A, Hirschhorn, J N, Hottenga, J J, Huffman, J E, Hwang, L D, Ikram, M A, Kaprio, J, Kemp, J P, Khaw, K T, Klopp, N, Konte, B, Kutalik, Z, Lahti, J, Li, X, Loos, R J F, Luciano, M, Magnusson, S H, Mangino, M, Marques-Vidal, P, Martin, N G, McArdle, W L, McCarthy, M I, Medina-Gomez, C, Melbye, M, Melville, S A, Metspalu, A, Milani, L, Mooser, V, Nelis, M, Nyholt, D R, O’Connell, K S, Ophoff, R A, Palmer, C, Palotie, A, Palviainen, T, Pare, G, Paternoster, L, Peltonen, L, Penninx, B W J H, Polasek, O, Pramstaller, P P, Prokopenko, I, Raikkonen, K, Ripatti, S, Rivadeneira, F, Rudan, I, Rujescu, D, Smit, J H, Smith, G D, Smoller, J W, Soranzo, N, Spector, T D, Pourcain, B S, Starr, J M, Stefánsson, H, Steinberg, S, Teder-Laving, M, Thorleifsson, G, Stefánsson, K, Timpson, N J, Uitterlinden, A G, van Duijn, C M, van Rooij, F J A, Vink, J M, Vollenweider, P, Vuoksimaa, E, Waeber, G, Wareham, N J, Warrington, N, Waterworth, D, Werge, T, Wichmann, H E, Widen, E, Willemsen, G, Wright, A F, Wright, M J, Xu, M, Zhao, J H, Kraft, P, Hinds, D A, Lindgren, C M, Mägi, R, Neale, B M, Evans, D M & Medland, S E 2021, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, no. 1, pp. 59-70 . https://doi.org/10.1038/s41562-020-00956-y
Nature Human Behaviour, 5, 1, pp. 59-70
Nature Human Behaviour, 5(1), 59-70. Nature Publishing Group
Nat Hum Behav
Nature Human Behaviour, 5(1), 59-70. Springer Nature
Nature Human Behaviour
Nat. Hum. Behav. 5, 59–70 (2021)
Nature Human Behaviour, 5, 59-70
Nature human behaviour 5(1), 59-70 (2021). doi:10.1038/s41562-020-00956-y
Cuellar-Partida, G, Deloukas, P, Kemp, J P, McArdle, W L, Paternoster, L, Davey Smith, G, Timpson, N J, Medland, S E & al., E 2020, ' Genome-wide association study identifies 48 common genetic variants associated with handedness ', Nature Human Behaviour, vol. 5, pp. 59–70 . https://doi.org/10.1038/s41562-020-00956-y
Handedness, a consistent asymmetry in skill or use of the hands, has been studied extensively because of its relationship with language and the over-representation of left-handers in some neurodevelopmental disorders. Using data from the UK Biobank,
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986a1504a38fc87e9588fa425872923b
https://curis.ku.dk/portal/da/publications/genomewide-association-study-identifies-48-common-genetic-variants-associated-with-handedness(3aa476e7-e13d-48f1-af0d-544a2ee787fd).html
https://curis.ku.dk/portal/da/publications/genomewide-association-study-identifies-48-common-genetic-variants-associated-with-handedness(3aa476e7-e13d-48f1-af0d-544a2ee787fd).html