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Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 4
Zeitschriftenartikel
Grimm, Tiemo; Garshasbi, Masoud; Puettmann, Lucia; Chen, Wei; Ullmann, Reinhard; Müller-Myhsok, Bertram; Klopocki, Eva; Herbst, Lina; Haug, Janina; Jensen, Lars R.; Fischer, Christine; Nöthen, Markus; Ludwig, Kerstin; Warnke, Andreas; Ott, Jürg; Schulte-Körne, Gerd; Ropers, Hans-Hilger und Kuss, Andreas W.
(2020):
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
In: Zeitschrift für Kinder-und Jugendpsychiatrie und Psychotherapie, Bd. 48, Nr. 6: S. 478-489
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
Freitag, Christine M.; Lempp, Thomas; Nguyen, T. Trang; Jacob, Christian P.; Weissflog, Lena; Romanos, Marcel; Renner, Tobias J.; Walitza, Susanne; Warnke, Andreas; Rujescu, Dan; Lesch, Klaus-Peter und Reif, Andreas
(2016):
The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits.
In: Journal of Neural Transmission, Bd. 123, Nr. 8: S. 849-858
Neuhoff, Nina; Bruder, Jennifer; Bartling, Jürgen; Warnke, Andreas; Remschmidt, Helmut; Müller-Myhsok, Bertram und Schulte-Körne, Gerd
(2012):
Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.
In: PLOS ONE 7(5), e34909 [PDF, 415kB]
In: PLOS ONE 7(5), e34909 [PDF, 415kB]