Items where Author is "Stefansson, Hreinn"

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.

2011

Jacquemont, Sébastien and Reymond, Alexandre and Zufferey, Flore and Harewood, Louise and Walters, Robin G. and Kutalik, Zoltán and Martinet, Danielle and Shen, Yiping and Valsesia, Armand and Beckmann, Noam D. and Thorleifsson, Gudmar and Belfiore, Marco and Bouquillon, Sonia and Campion, Dominique and de Leeuw, Nicole and de Vries, Bert B. A. and Esko, Tõnu and Fernandez, Bridget A. and Fernández-Aranda, Fernando and Fernández-Real, José Manuel and Gratacòs, Mònica and Guilmatre, Audrey and Hoyer, Juliane and Jarvelin, Marjo-Riitta and Kooy, R. Frank and Kurg, Ants and Le Caignec, Cédric and Männik, Katrin and Platt, Orah S. and Sanlaville, Damien and Van Haelst, Mieke M. and Villatoro Gomez, Sergi and Walha, Faida and Wu, Bai-Lin and Yu, Yongguo and Aboura, Azzedine and Addor, Marie-Claude and Alembik, Yves and Antonarakis, Stylianos E. and Arveiler, Benoît and Barth, Magalie and Bednarek, Nathalie and Béna, Frédérique and Bergmann, Sven and Beri, Mylène and Bernardini, Laura and Blaumeiser, Bettina and Bonneau, Dominique and Bottani, Armand and Boute, Odile and Brunner, Han G. and Cailley, Dorothée and Callier, Patrick and Chiesa, Jean and Chrast, Jacqueline and Coin, Lachlan and Coutton, Charles and Cuisset, Jean-Marie and Cuvellier, Jean-Christophe and David, Albert and de Freminville, Bénédicte and Delobel, Bruno and Delrue, Marie-Ange and Demeer, Bénédicte and Descamps, Dominique and Didelot, Gérard and Dieterich, Klaus and Disciglio, Vittoria and Doco-Fenzy, Martine and Drunat, Séverine and Duban-Bedu, Bénédicte and Dubourg, Christèle and El-Sayed Moustafa, Julia S. and Elliott, Paul and Faas, Brigitte H. W. and Faivre, Laurence and Faudet, Anne and Fellmann, Florence and Ferrarini, Alessandra and Fisher, Richard and Flori, Elisabeth and Forer, Lukas and Gaillard, Dominique and Gerard, Marion and Gieger, Christian and Gimelli, Stefania and Gimelli, Giorgio and Grabe, Hans J. and Guichet, Agnès and Guillin, Olivier and Hartikainen, Anna-Liisa and Heron, Délphine and Hippolyte, Loyse and Holder, Muriel and Homuth, Georg and Isidor, Bertrand and Jaillard, Sylvie and Jaros, Zdenek and Jiménez-Murcia, Susana and Helas, Géraldine Joly and Jonveaux, Philippe and Kaksonen, Satu and Keren, Boris and Kloss-Brandstätter, Anita and Knoers, Nine V. A. M. and Koolen, David A. and Kroisel, Peter M. and Kronenberg, Florian and Labalme, Audrey and Landais, Emilie and Lapi, Elisabetta and Layet, Valérie and Legallic, Solenn and Leheup, Bruno and Leube, Barbara and Lewis, Suzanne and Lucas, Josette and MacDermot, Kay D. and Magnusson, Pall and Marshall, Christian and Mathieu-Dramard, Michèle and McCarthy, Mark I. and Meitinger, Thomas and Mencarelli, Maria Antonietta and Merla, Giuseppe and Moerman, Alexandre and Mooser, Vincent and Morice-Picard, Fanny and Mucciolo, Mafalda and Nauck, Matthias and Ndiaye, Ndeye Coumba and Nordgren, Ann and Pasquier, Laurent and Petit, Florence and Pfundt, Rolph and Plessis, Ghislaine and Rajcan-Separovic, Evica and Ramelli, Gian Paolo and Rauch, Anita and Ravazzolo, Roberto and Reis, Andre and Renieri, Alessandra and Richart, Cristobal and Ried, Janina S. and Rieubland, Claudine and Roberts, Wendy and Roetzer, Katharina M. and Rooryck, Caroline and Rossi, Massimiliano and Saemundsen, Evald and Satre, Véronique and Schurmann, Claudia and Sigurdsson, Engilbert and Stavropoulos, Dimitri J. and Stefansson, Hreinn and Tengström, Carola and Thorsteinsdóttir, Unnur and Tinahones, Francisco J. and Touraine, Renaud and Vallée, Louis and van Binsbergen, Ellen and Van der Aa, Nathalie and Vincent-Delorme, Catherine and Visvikis-Siest, Sophie and Vollenweider, Peter and Völzke, Henry and Vulto-van Silfhout, Anneke T. and Waeber, Gérard and Wallgren-Pettersson, Carina and Witwicki, Robert M. and Zwolinksi, Simon and Andrieux, Joris and Estivill, Xavier and Gusella, James F. and Gustafsson, Omar and Metspalu, Andres and Scherer, Stephen W. and Stefansson, Kari and Blakemore, Alexandra I. F. and Beckmann, Jacques S. and Froguel, Philippe. (2011) Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature, Vol. 478, H. 7367. pp. 97-102.