Items where Author is "Langley, Kate"

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.

2012

Williams, Nigel M. and Franke, Barbara and Mick, Eric and Anney, Richard J. L. and Freitag, Christine M. and Gill, Michael and Thapar, Anita and O'Donovan, Michael C. and Owen, Michael J. and Holmans, Peter and Kent, Lindsey and Middleton, Frank and Zhang-James, Yanli and Liu, Lu and Meyer, Jobst and Nguyen, Thuy Trang and Romanos, Jasmin and Romanos, Marcel and Seitz, Christiane and Renner, Tobias J. and Walitza, Susanne and Warnke, Andreas and Palmason, Haukur and Buitelaar, Jan and Rommelse, Nanda and Vasquez, Alejandro Arias and Hawi, Ziarih and Langley, Kate and Sergeant, Joseph and Steinhausen, Hans-Christoph and Roeyers, Herbert and Biederman, Joseph and Zaharieva, Irina and Hakonarson, Hakon and Elia, Josephine and Lionel, Anath C. and Crosbie, Jennifer and Marshall, Christian R. and Schachar, Russell and Scherer, Stephen W. and Todorov, Alexandre and Smalley, Susan L. and Loo, Sandra and Nelson, Stanley and Shtir, Corina and Asherson, Philip and Reif, Andreas and Lesch, Klaus-Peter and Faraone, Stephen V.. (2012) Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder. American journal of psychiatry, Vol. 169, H. 2. pp. 195-204.

Stergiakouli, Evangelia and Hamshere, Marian and Holmans, Peter and Langley, Kate and Zaharieva, Irina and deCode Genetics, and Psychiatric Gwas Consortium, and Hawi, Ziarah and Kent, Lindsey and Gill, Michael and Williams, Nigel and Owen, Michael J. and O'Donovan, Michael and Thapar, Anita. (2012) Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American journal of psychiatry, Vol. 169, H. 2. pp. 186-194.