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Anzahl der Publikationen: 4
Zeitschriftenartikel
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
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; 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
Kogelman, Lisette J. A.; Esserlind, Ann-Louise; Christensen, Anne Francke; Awasthi, Swapnil; Ripke, Stephan; Ingason, Andres; Davidsson, Olafur B.; Erikstrup, Christian; Hjalgrim, Henrik; Ullum, Henrik; Olesen, Jes; Hansen, Thomas Folkmann; Gudbjartsson, Daniel; Gastafsson, Omar; Stefansson, Kari; Stefansson, Hreinn; Porsteinsdottir, Unnur; Andersen, Steffen; Banasik, Karina; Brunak, Soren; Buil, Alfonso; Burgdorf, Kristoffer; Gregor, Jemec; Jennum, Poul; Nielsen, Kasper Rene; Nyegaard, Mette; Paarup, Helene Mariana; Pedersen, Ole Birger; Sorensen, Erik; Werge, Thomas; Anttila, Verneri; Artto, Ville; Belin, Andrea Carmine; de Boer, Irene; Boomsma, Dorret; Borte, Sigrid; Chasman, Daniel; Cherkas, Lynn; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; Dichgans, Martin; van Duijn, Cornelia; Esko, Tonu; Ferrari, Michel; Frants, Rune R.; Freilinger, Tobias; Furlotte, Nick; Gormley, Padhraig; Griffiths, Lyn; Hamalainen, Eija; Hiekkala, Marjo; Ikram, M. Arfan; Jarvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimaki, Terho; Lessel, Davor; Ligthart, Lannie; Litterman, Nadia; van den Maagdenberg, Arn; Macaya, Alfons; Malik, Rainer; Mangino, Massimo; McMahon, George; Muller-Myhsok, Bertram; Neale, Benjamin M.; Northover, Carrie; Nyholt, Dale R.; Palotie, Aarno; Palta, Priit; Pedersen, Linda; Pedersen, Nancy; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Schurks, Markus; Sintas, Celia; Steinberg, Stacy; Strachan, David; Terwindt, Gisela; Vila-Pueyo, Marta; Wessman, Maija; Winsvold, Bendik S.; Zhao, Huiying und Zwart, John-Anker
(2019):
Migraine polygenic risk score associates with efficacy of migraine-specific drugs.
In: Neurology-Genetics, Bd. 5, Nr. 6, e364
de Vries, Boukje; Freilinger, Tobias; Anttila, Verneri; Malik, Rainer; Kallela, Mikko; Terwindt, Gisela M.; Pozo-Rosich, Patricia; Winsvold, Bendik; Nyholt, Dale R.; van Oosterhout, Willebrordus P. J.; Artto, Ville; Todt, Unda; Hamalainen, Eija; Fernandez-Morales, Jessica; Louter, Mark A.; Kaunisto, Mari A.; Schoenen, Jean; Raitakari, Olli; Lehtimaki, Terho; Vila-Pueyo, Marta; Goebel, Hartmut; Wichmann, Erich; Sintas, Celia; Uitterlinden, Andre G.; Hofman, Albert; Rivadeneira, Fernando; Heinze, Axel; Tronvik, Erling; Van Duijn, Cornelia M.; Kaprio, Jaakko; Cormand, Bru; Wessman, Maija; Frants, Rune R.; Meitinger, Thomas; Mueller-Myhsok, Bertram; Zwart, John-Anker; Farkkila, Markus; Macaya, Alfons; Ferrari, Michel D.; Kubisch, Christian; Palotie, Aarno; Dichgans, Martin und van den Maagdenberg, Arn M. J. M.
(2013):
Migraine without aura: genome-wide association analysis identifies several novel susceptibility.
In: The Journal of Headache and Pain, Bd. 14, P18
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