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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2022
Mattheisen, Manuel; Grove, Jakob; Als, Thomas D.; Martin, Joanna; Voloudakis, Georgios; Meier, Sandra; Demontis, Ditte; Bendl, Jaroslav; Walters, Raymond; Carey, Caitlin E.; Rosengren, Anders; Strom, Nora I.; Hauberg, Mads Engel; Zeng, Biao; Hoffman, Gabriel; Zhang, Wen; Bybjerg-Grauholm, Jonas; Baekvad-Hansen, Marie; Agerbo, Esben; Cormand, Bru; Nordentoft, Merete; Werge, Thomas; Mors, Ole; Hougaard, David M.; Buxbaum, Joseph D.; Faraone, Stephen V.; Franke, Barbara; Dalsgaard, Soren; Mortensen, Preben B.; Robinson, Elise B.; Roussos, Panos; Neale, Benjamin M.; Daly, Mark J. und Borglum, Anders D.
(2022):
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.
In: Nature Genetics, Bd. 54, Nr. 10: S. 1470-1478
2019
Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gisli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Baekvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Olafur O.; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads V.; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian B.; Martin, Alicia R.; Martin, Nicholas G.; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bocker; Pedersen, Marianne Giortz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; Andreassen, Ole A.; Asherson, Philip; Burton, Christie L.; Boomsma, Dorret I.; Cormand, Bru; Dalsgaard, Soren; Franke, Barbara; Gelernter, Joel; Geschwind, Daniel; Hakonarson, Hakon; Haavik, Jan; Kranzler, Henry R.; Kuntsi, Jonna; Langley, Kate; Lesch, Klaus-Peter; Middeldorp, Christel; Reif, Andreas; Rohde, Luis Augusto; Roussos, Panos; Schachar, Russell; Sklar, Pamela; Sonuga-Barke, Edmund J. S.; Sullivan, Patrick F.; Thapar, Anita; Tung, Joyce Y.; Waldman, Irwin D.; Medland, Sarah E.; Stefansson, Kari; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen V.; Borglum, Anders D.; Neale, Benjamin M.; Albayrak, Ozgur; Anney, Richard J. L.; Arranz, Maria Jesus; Banaschewski, Tobias J.; Bau, Claiton; Biederman, Joseph; Buitelaar, Jan K.; Casas, Miguel; Charach, Alice; Crosbie, Jennifer; Dempfle, Astrid; Doyle, Alysa E.; Ebstein, Richard P.; Elia, Josephine; Freitag, Christine; Focker, Manuel; Gill, Michael; Grevet, Eugenio; Hawi, Ziarih; Hebebrand, Johannes; Herpertz-Dahlmann, Beate; Hervas, Amaia; Hinney, Anke; Hohmann, Sarah; Holmans, Peter; Hutz, Mara; Ickowitz, Abel; Johansson, Stefan; Kent, Lindsey; Kittel-Schneider, Sarah; Lambregts-Rommelse, Nanda; Lehmkuhl, Gerd; Loo, Sandra K.; McGough, James J.; Meyer, Jobst; Mick, Eric; Middletion, Frank; Miranda, Ana; Mota, Nina Roth; Mulas, Fernando; Mulligan, Aisling; Nelson, Freimer; Nguyen, T. Trang; Oades, Robert D.; O'Donovan, Michael C.; Owen, Michael J.; Palmason, Haukur; Ramos-Quiroga, Josep Antoni; Renner, Tobias J.; Ribases, Marta; Rietschel, Marcella; Rivero, Olga; Romanos, Jasmin; Romanos, Marcel; Rothenberger, Aribert; Royers, Herbert; Sanchez-Mora, Christina; Scherag, Andre; Schimmelmann, Benno G.; Schafer, Helmut; Sergeant, Joseph; Sinzig, Judith; Smalley, Susan L.; Steinhausen, Hans-Christoph; Thompson, Margaret; Todorov, Alexandre; Vasquez, Alejandro Arias; Walitza, Susanne; Wang, Yufeng; Warnke, Andreas; Williams, Nigel; Witt, Stephanie H.; Yang, Li; Zayats, Tetyana; Zhang-James, Yanli; Smith, George Davey; Davies, Gareth E.; Ehli, Erik A.; Evans, David M.; Fedko, Iryna O.; Greven, Corina U.; Groen-Blokhuis, Maria M.; Guxens, Monica; Hammerschlag, Anke R.; Hartman, Catharina A.; Heinrich, Joachim 
ORCID: https://orcid.org/0000-0002-9620-1629; Hottenga, Jouke Jan; Hudziak, James; Jugessur, Astanand; Kemp, John P.; Krapohl, Eva; Murcia, Mario; Myhre, Ronny; Nolte, Ilja M.; Nyholt, Dale R.; Ormel, Johan; Ouwens, Klaasjan G.; Pappa, Irene; Pennell, Craig E.; Plomin, Robert; Ring, Susan; Standl, Marie; Stergiakouli, Evie; St Pourcain, Beate; Stoltenberg, Camilla; Sunyer, Jordi; Thiering, Elisabeth; Tiemeier, Henning; Tiesler, Carla M. T.; Timpson, Nicholas J.; Trzaskowski, Maciej; van der Most, Peter Johannes; Vilor-Tejedor, Natalia; Wang, Carol A.; Whitehouse, Andrew J. O.; Zhao, Huiying; Agee, Michelle; Alipanahi, Babak; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna; Elson, Sarah L.; Fontanillas, Pierre; Furlotte, Nicholas A.; Hinds, David A.; Hromatka, Bethann S.; Huber, Karen E.; Kleinman, Aaron; Litterman, Nadia K.; McIntyre, Matthew H.; Mountain, Joanna L.; Northover, Carrie A. M.; Pitts, Steven J.; Sathirapongsasuti, J. Fah; Sazonova, Olga V.; Shelton, Janie F.; Shringarpure, Suyash; Tian, Chao; Vacic, Vladimir und Wilson, Catherine H.
(2019):
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
In: Nature Genetics, Bd. 51, Nr. 1
ORCID: https://orcid.org/0000-0002-9620-1629; Hottenga, Jouke Jan; Hudziak, James; Jugessur, Astanand; Kemp, John P.; Krapohl, Eva; Murcia, Mario; Myhre, Ronny; Nolte, Ilja M.; Nyholt, Dale R.; Ormel, Johan; Ouwens, Klaasjan G.; Pappa, Irene; Pennell, Craig E.; Plomin, Robert; Ring, Susan; Standl, Marie; Stergiakouli, Evie; St Pourcain, Beate; Stoltenberg, Camilla; Sunyer, Jordi; Thiering, Elisabeth; Tiemeier, Henning; Tiesler, Carla M. T.; Timpson, Nicholas J.; Trzaskowski, Maciej; van der Most, Peter Johannes; Vilor-Tejedor, Natalia; Wang, Carol A.; Whitehouse, Andrew J. O.; Zhao, Huiying; Agee, Michelle; Alipanahi, Babak; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna; Elson, Sarah L.; Fontanillas, Pierre; Furlotte, Nicholas A.; Hinds, David A.; Hromatka, Bethann S.; Huber, Karen E.; Kleinman, Aaron; Litterman, Nadia K.; McIntyre, Matthew H.; Mountain, Joanna L.; Northover, Carrie A. M.; Pitts, Steven J.; Sathirapongsasuti, J. Fah; Sazonova, Olga V.; Shelton, Janie F.; Shringarpure, Suyash; Tian, Chao; Vacic, Vladimir und Wilson, Catherine H.
(2019):
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
In: Nature Genetics, Bd. 51, Nr. 1
Grove, Jakob; Ripke, Stephan; Als, Thomas D.; Mattheisen, Manuel; Walters, Raymond K.; Won, Hyejung; Pallesen, Jonatan; Agerbo, Esben; Andreassen, Ole A.; Anney, Richard; Awashti, Swapnil; Belliveau, Rich; Bettella, Francesco; Buxbaum, Joseph D.; Bybjerg-Grauholm, Jonas; Baekvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Christensen, Jane H.; Churchhouse, Claire; Dellenvall, Karin; Demontis, Ditte; De Rubeis, Silvia; Devlin, Bernie; Djurovic, Srdjan; Dumont, Ashley L.; Goldstein, Jacqueline; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads; Hope, Sigrun; Howrigan, Daniel P.; Huang, Hailiang; Hultman, Christina M.; Klei, Lambertus; Maller, Julian; Martin, Joanna; Martin, Alicia R.; Moran, Jennifer L.; Nyegaard, Mette; Naerland, Terje; Palmer, Duncan S.; Palotie, Aarno; Pedersen, Carsten Bocker; Pedersen, Marianne Giortz; dPoterba, Timothy; Poulsen, Jesper Buchhave; St Pourcain, Beate; Qvist, Per; Rehnstrom, Karola; Reichenberg, Abraham; Reichert, Jennifer; Robinson, Elise B.; Roeder, Kathryn; Roussos, Panos; Saemundsen, Evald; Sandin, Sven; Satterstrom, F. Kyle; Smith, George Davey; Stefansson, Hreinn; Steinberg, Stacy; Stevens, Christine R.; Sullivan, Patrick F.; Turley, Patrick; Walters, G. Bragi; Xu, Xinyi; Stefansson, Kari; Geschwind, Daniel H.; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Neale, Benjamin M.; Daly, Mark J.; Borglum, Anders D.; Wray, Naomi R.; Trzaskowski, Maciej; Byrne, Enda M.; Abdellaoui, Abdel; Adams, Mark J.; Air, Tracy M.; Andlauer, Till F. M.; Bacanu, Silviu-Alin; Beekman, Aartjan T. F.; Bigdeli, Tim B.; Binder, Elisabeth B.; Blackwood, Douglas H. R.; Bryois, Julien; Buttenschon, Henriette N.; Cai, Na; Castelao, Enrique; Clarke, Toni-Kim; Coleman, Jonathan R.; Colodro-Conde, Lucia; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E.; Davies, Gail; Deary, Ian J.; Degenhardt, Franziska; Derks, Eske M.; Direk, Nese; Dolan, Conor; Dunn, Erin C.; Eley, Thalia C.; Escott-Price, Valentina; Kiadeh, Farnush Farhadi Hassan; Finucane, Hilary K.; Forstner, Andreas J.; Frank, Josef; Gaspar, Helena A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Hall, Lynsey S.; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Ising, Marcus; Jansen, Rick; Jörgenson, Eric; Knowles, James A.; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; Krogh, Jesper; Kutalik, Zoltan; Li, Yihan; Lind, Penelope A.; MacIntyre, Donald J.; MacKinnon, Dean F.; Maier, Robert M.; Maier, Wolfgang; Marchini, Jonathan; Mbarek, Hamdi; McGrath, Patrick; McGuffin, Peter; Medland, Sarah E.; Mehta, Divya; Middeldorp, Christel M.; Mihailov, Evelin; Milaneschi, Yuri; Milani, Lili; Mondimore, Francis M.; Montgomery, Grant W.; Mostafavi, Sara; Mullins, Niamh; Nauck, Matthias; Ng, Bernard; Nivard, Michel G.; Nyholt, Dale R.; O'Reilly, Paul F.; Oskarsson, Hogni; Owen, Michael J.; Painter, Jodie N.; Peterson, Roseann E.; Pettersson, Erik; Peyrot, Wouter J.; Pistis, Giorgio; Posthuma, Danielle; Quiroz, Jörge A.; Rice, John P.; Riley, Brien P.; Rivera, Margarita; Mirza, Saira Saeed; Schoevers, Robert; Schulte, Eva C.; Shen, Ling; Shi, Jianxin; Shyn, Stanley; Sigurdsson, Engilbert; Sinnamon, Grant C. B.; Smit, Johannes H.; Smith, Daniel J.; Streit, Fabian; Strohmaier, Jana; Tansey, Katherine E.; Teismann, Henning; Teumer, Alexander; Thompson, Wesley; Thomson, Pippa A.; Thorgeirsson, Thorgeir E.; Traylor, Matthew; Treutlein, Jens; Trubetskoy, Vassily; Uitterlinden, Andr G.; Umbricht, Daniel; Van Der Auwera, Sandra; van Hemert, Albert M.; Viktorin, Alexander; Visscher, Peter M.; Wang, Yunpeng; Webb, Bradley T.; Weinsheimer, Shantel Marie; Wellmann, Jürgen; Willemsen, Gonneke; Witt, Stephanie H.; Wu, Yang; Xi, Hualin S.; Yang, Jian; Zhang, Futao; Arolt, Volker; Baune, Bernhard T.; Berger, Klaus; Boomsma, Dorret; Cichon, Sven; Dannlowski, Udo; de Geus, E. J. C.; DePaulo, J. Raymond; Domenici, Enrico; Domschke, Katharina; Esko, Tonu; Grabe, Hans J.; Hamilton, Steven P.; Hayward, Caroline; Heath, Andrew C.; Kendler, Kenneth S.; Kloiber, Stefan; Lewis, Glyn; Li, Qingqin S.; Lucae, Susanne; Madden, Pamela A. F.; Magnusson, Patrik K.; Martin, Nicholas G.; McIntosh, Andrew M.; Metspalu, Andres; Müller-Myhsok, Bertram; Noethen, Markus M.; O'Donovan, Michael C.; Paciga, Sara A.; Pedersen, Nancy L.; Penninx, Brenda W. J. H.; Perlis, Roy H.; Porteous, David J.; Potash, James B.; Preisig, Martin; Rietschel, Marcella; Schäfer, Catherine; Schulze, Thomas G.; Smoller, Jordan W.; Tiemeier, Henning; Uher, Rudolf; Voelzke, Henry; Weissman, Myrna M.; Lewis, Cathryn M.; Levinson, Douglas F.; Breen, Gerome; Agee, Michelle; Alipanahi, Babak; Auton, Adam; Bell, Robert K.; Bryc, Katarzyna; Elson, Sarah L.; Fontanillas, Pierre; Furlotte, Nicholas A.; Hromatka, Bethann S.; Huber, Karen E.; Kleinman, Aaron; Litterman, Nadia K.; McIntyre, Matthew H.; Mountain, Joanna L.; Noblin, Elizabeth S.; Northover, Carrie A. M.; Pitts, Steven J.; Sathirapongsasuti, J. Fah; Sazonova, Olga; Shelton, Janie F.; Shringarpure, Suyash; Tung, Joyce Y.; Vacic, Vladimir und Wilson, Catherine H.
(2019):
Identification of common genetic risk variants for autism spectrum disorder.
In: Nature Genetics, Bd. 51, Nr. 3
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