Items where Author is "Ripke, Stephan"

2019

Demontis, Ditte and Walters, Raymond K. and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D. and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I. and Grasby, Katrina L. and Grove, Jakob and Gudmundsson, Olafur O. and Hansen, Christine S. and Hauberg, Mads Engel and Hollegaard, Mads V. and Howrigan, Daniel P. and Huang, Hailiang and Maller, Julian B. and Martin, Alicia R. and Martin, Nicholas G. and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S. and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B. and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J. and Adhd Working Group of the Psychiatric Genomics Consortium, and Early Lifecourse, and Genetic Epidemiology Consortium, and Andreassen, Ole A. and Asherson, Philip and Burton, Christie L. and Boomsma, Dorret I. and Cormand, Bru and Dalsgaard, Søren and Franke, Barbara and Gelernter, Joel and Geschwind, Daniel and Hakonarson, Hakon and Haavik, Jan and Kranzler, Henry R. and Kuntsi, Jonna and Langley, Kate and Lesch, Klaus-Peter and Middeldorp, Christel and Reif, Andreas and Rohde, Luis Augusto and Roussos, Panos and Schachar, Russell and Sklar, Pamela and Sonuga-Barke, Edmund J. S. and Sullivan, Patrick F. and Thapar, Anita and Tung, Joyce Y. and Waldman, Irwin D. and Medland, Sarah E. and Stefansson, Kari and Nordentoft, Merete and Hougaard, David M. and Werge, Thomas and Mors, Ole and Mortensen, Preben Bo and Daly, Mark J. and Faraone, Stephen V. and Børglum, Anders D. and Neale, Benjamin M.. (2019) Discovery of the First Genome-Wide Significant Risk Loci for Attention Deficit/Hyperactivity Disorder. Nature Genetics, 51 (1). pp. 63-75.

2015

Maier, Robert and Moser, Gerhard and Chen, Guo-Bo and Ripke, Stephan and Cross-Disorder Working Group of the Psychiatric Genomics Consort, and Coryell, William and Potash, James B. and Scheftner, William A. and Shi, Jianxin and Weissman, Myrna M. and Hultman, Christina M. and Landén, Mikael and Levinson, Douglas F. and Kendler, Kenneth S. and Smoller, Jordan W. and Wray, Naomi R. and Lee, S. Hong. (2015) Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. American Journal of Human Genetics, Vol. 96, H. 2. pp. 283-294.

2014

Heck, Angela and Fastenrath, Matthias and Ackermann, Sandra and Auschra, Bianca and Bickel, Horst and Coynel, David and Gschwind, Leo and Jessen, Frank and Kaduszkiewicz, Hanna and Maier, Wolfgang and Milnik, Annette and Pentzek, Michael and Riedel-Heller, Steffi G. and Ripke, Stephan and Spalek, Klara and Sullivan, Patrick and Vogler, Christian and Wagner, Michael and Weyerer, Siegfried and Wolfsgruber, Steffen and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas. (2014) Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity. Neuron, 81 (5). pp. 1203-1213.

Juraeva, Dilafruz and Haenisch, Britta and Zapatka, Marc and Frank, Josef and Group Investigators, and Psych-Gems Scz Working Group, and Witt, Stephanie H. and Muhleisen, Thomas W. and Treutlein, Jens and Strohmaier, Jana and Meier, Sandra and Degenhardt, Franziska and Giegling, Ina and Ripke, Stephan and Leber, Markus and Lange, Christoph and Schulze, Thomas G. and Mössner, Rainald and Nenadic, Igor and Sauer, Heinrich and Rujescu, Dan and Maier, Wolfgang and Borglum, Anders and Ophoff, Roel A. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Mattheisen, Manuel and Brors, Benedikt. (2014) Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS Genetics, 10 (6). e1004345.

2011

Kohli, Martin A. and Lucae, Susanne and Saemann, Philipp G. and Schmidt, Mathias V. and Demirkan, Ayse and Hek, Karin and Czamara, Darina and Alexander, Michael and Salyakina, Daria and Ripke, Stephan and Hoehn, David and Specht, Michael and Menke, Andreas and Hennings, Johannes and Heck, Angela and Wolf, Christiane and Ising, Marcus and Schreiber, Stefan and Czisch, Michael and Müller, Marianne B. and Uhr, Manfred and Bettecken, Thomas and Becker, Albert and Schramm, Johannes and Rietschel, Marcella and Maier, Wolfgang and Bradley, Bekh and Ressler, Kerry J. and Nöthen, Markus M. and Cichon, Sven and Craig, Ian W. and Breen, Gerome and Lewis, Cathryn M. and Hofman, Albert and Tiemeier, Henning and van Duijn, Cornelia M. and Holsboer, Florian and Müller-Myhsok, Bertram and Binder, Elisabeth B.. (2011) The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron, 70 (2). pp. 252-265.

2010

Neale, Benjamin M. and Medland, Sarah and Ripke, Stephan and Anney, Richard J. L. and Asherson, Philip and Buitelaar, Jan and Franke, Barbara and Gill, Michael and Kent, Lindsey and Holmans, Peter and Middleton, Frank and Thapar, Anita and Lesch, Klaus-Peter and Faraone, Stephen V. and Daly, Mark and Nguyen, Thuy Trang and Schäfer, Helmut and Steinhausen, Hans-Christoph and Reif, Andreas and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Warnke, Andreas and Walitza, Susanne and Freitag, Christine and Meyer, Jobst and Palmason, Haukur and Rothenberger, Aribert and Hawi, Ziarih and Sergeant, Joseph and Roeyers, Herbert and Mick, Eric and Biederman, Joseph and Image II Consortium Group, . (2010) Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49 (9). pp. 906-920.

Neale, Benjamin M. and Medland, Sarah E. and Ripke, Stephan and Asherson, Philip and Franke, Barbara and Lesch, Klaus-Peter and Faraone, Stephen V. and Nguyen, Thuy Trang and Schäfer, Helmut and Holmans, Peter and Daly, Mark and Steinhausen, Hans-Christoph and Freitag, Christine and Reif, Andreas and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Walitza, Susanne and Warnke, Andreas and Meyer, Jobst and Palmason, Haukur and Buitelaar, Jan and Vasquez, Alejandro Arias and Lambregts-Rommelse, Nanda and Gill, Michael and Anney, Richard J. L. and Langely, Kate and O'Donovan, Michael and Williams, Nigel and Owen, Michael and Thapar, Anita and Kent, Lindsey and Sergeant, Joseph and Roeyers, Herbert and Mick, Eric and Biederman, Joseph and Doyle, Alysa and Smalley, Susan and Loo, Sandra and Hakonarson, Hakon and Elia, Josephine and Todorov, Alexandre and Miranda, Ana and Mulas, Fernando and Ebstein, Richard P. and Rothenberger, Aribert and Banaschewski, Tobias and Oades, Robert D. and Sonuga-Barke, Edmund and McGough, James and Nisenbaum, Laura and Middleton, Frank and Hu, Xiaolan and Nelson, Stan and Psychiatric Gwas Consortium: Adhd Subgroup, . (2010) Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49 (9). pp. 884-897.

2009

Unschuld, Paul G. and Ising, Marcus and Specht, Michael and Erhardt, Angelika and Ripke, Stephan and Heck, Angela and Kloiber, Stefan and Straub, Verica and Brueckl, Tanja and Müller-Myhsok, Bertram and Holsboer, Florian and Binder, Elisabeth B.. (2009) Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders. American Journal of Medical Genetics, 150B (8). pp. 1100-1109.