Items where Author is "Hakonarson, Hakon"

Yes

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.

Li, Dalin and Achkar, Jean-Paul and Haritunians, Talin and Jacobs, Jonathan P. and Hui, Ken Y. and D'Amato, Mauro and Brand, Stephan and Radford-Smith, Graham and Halfvarson, Jonas and Niess, Jan-Hendrik and Kugathasan, Subra and Buning, Carsten and Schumm, Philip and Klei, Lambertus and Ananthakrishnan, Ashwin and Aumais, Guy and Baidoo, Leonardo and Dubinsky, Marla and Fiocchi, Claudio and Glas, Jürgen and Milgrom, Raquel and Proctor, Deborah D. and Regueiro, Miguel and Simms, Lisa A. and Stempak, Joanne M. and Targan, Stephan R. and Torkvist, Leif and Sharma, Yashoda and Devlin, Bernie and Borneman, James and Hakonarson, Hakon and Xavier, Ramnik J. and Daly, Mark and Brant, Steven R. and Rioux, John D. and Silverberg, Mark S. and Cho, Judy H. and Braun, Jonathan and McGovern, Dermot P. and Duerr, Richard H.. (2016) A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition. Gastroenterology, 151 (4). pp. 724-732.

Marenholz, Ingo and Esparza-Gordillo, Jorge and Rüschendorf, Franz and Bauerfeind, Anja and Strachan, David P. and Spycher, Ben D. and Baurecht, Hansjörg and Margaritte-Jeannin, Patricia and Sääf, Annika and Kerkhof, Marjan and Ege, Markus and Baltic, Svetlana and Matheson, Melanie C. and Li, Jin and Michel, Sven and Ang, Wei Q. and McArdle, Wendy and Arnold, Andreas and Homuth, Georg and Demenais, Florence and Bouzigon, Emmanuelle and Söderhäll, Cilla and Pershagen, Göran and de Jongste, Johan C. and Postma, Dirkje S. and Braun-Fahrländer, Charlotte and Horak, Elisabeth and Ogorodova, Ludmila M. and Puzyrev, Valery P. and Bragina, Elena Yu and Hudson, Thomas J. and Morin, Charles and Duffy, David L. and Marks, Guy B. and Robertson, Colin F. and Montgomery, Grant W. and Musk, Bill and Thompson, Philip J. and Martin, Nicholas G. and James, Alan and Sleiman, Patrick and Toskala, Elina and Rodriguez, Elke and Fölster-Holst, Regina and Franke, Andre and Lieb, Wolfgang and Gieger, Christian and Heinzmann, Andrea and Rietschel, Ernst and Keil, Thomas and Cichon, Sven and Nöthen, Markus M. and Pennell, Craig E. and Sly, Peter D. and Schmidt, Carsten O. and Matanovic, Anja and Schneider, Valentin and Heinig, Matthias and Hübner, Norbert and Holt, Patrick G. and Lau, Susanne and Kabesch, Michael and Weidinger, Stefan and Hakonarson, Hakon and Ferreira, Manuel A. R. and Laprise, Catherine and Freidin, Maxim B. and Genuneit, Jon and Koppelman, Gerard H. and Melén, Erik and Dizier, Marie-Hélène and Henderson, A. John and Lee, Young Ae. (2015) Meta-analysis identifies seven susceptibility loci involved in the atopic march. Nature communications, 6. p. 8804.

Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456.

Boraska, Vesna and Franklin, Christopher S. and Floyd, James A.B. and Thornton, Laura M. and Huckins, Laura M. and Southam, Lorraine and Rayner, N. William and Tachmazidou, Ioanna and Klumpp, Kelly and Treasure, Janet and Lewis, Cathryn M. and Schmidt, Ulrike and Tozzi, Federica and Kiezebrink, Kirsty and Hebebrand, Johannes and Gorwood, Philip and Adan, Roger A. H. and Kas, Martin J. H. and Favaro, Angela and Santonastaso, Paolo and Fernández-Aranda, Fernando and Gratacòs, Mònica and Rybakowski, Filip and Dmitrzak-Weglarz, Monika and Kaprio, Jaakko and Keski-Rahkonen, Anna and Raevuori, Anu and Van Furth, Eric F. and Slof-Op 't Landt, Margarita and Hudson, James I. and Reichborn-Kjennerud, Ted and Knudsen, Gun Peggy S. and Monteleone, Palmiero and Kaplan, Allan S. and Karwautz, Andreas and Hakonarson, Hakon and Berrettini, Wade H. and Guo, Yiran and Li, Dong and Schork, Nicholas and Komaki, Gen and Ando, Tetsuya and Inoko, Hidetoshi and Esko, Tõnu and Fischer, Krista and Männik, Katrin and Metspalu, Andres and Baker, Jessica H. and Cone, Roger D. and Dackor, Jennifer and DeSocio, Janiece E. and Hilliard, Christopher E. and O'Toole, Julie K. and Pantel, Jacques and Szatkiewicz, Jin P. and Taico, Chrysecolla and Zerwas, Stephanie and Trace, Sara E. and Davis, Oliver S. P. and Helder, Sietske and Buhren, Katherina and Burghardt, Roland and de Zwaan, Martina and Egberts, Karin and Ehrlich, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Imgart, Hartmut and Scherag, André and Scherag, Susann and Zipfel, Stephan and Boni, Claudette and Ramoz, Nicolas and Versini, Audrey and Brandys, Marek K. and Danner, Unna N. and de Kovel, Carolien and Hendriks, Judith and Koeleman, Bobby P. C. and Ophoff, Roel A. and Strengman, Eric and van Elburg, Annemarie A. and Bruson, Alice and Clementi, Maurizio and Degortes, Daniela and Forzan, Monica and Tenconi, Elena and Docampo, Elisa and Escaramis, Georgia and Jiménez-Murcia, Susana and Lissowska, Jolanta and Rajewski, Andrzej and Szeszenia-Dabrowska, Neonila and Slopien, Agnieszka and Hauser, Joanna and Karhunen, Leila and Meulenbelt, Ingrid and Slagboom, P. Eline and Tortorella, Alfonso and Maj, Mario and Dedoussis, George and Dikeos, Dimitris and Gonidakis, Fragiskos and Tziouvas, Konstantinos and Tsitsika, Artemis and Papezova, Hana and Slachtova, Lenka and Martaskova, Debora and Kennedy, James L. and Levitan, Robert D. and Yilmaz, Zeynep and Huemer, Julia and Koubek, Doris and Merler, Elisabeth and Wagner, Gudrun and Lichtenstein, Paul and Breen, Gerome and Cohen-Woods, Sarah and Farmer, Ann and McGuffin, Peter and Cichon, Sven and Giegling, Ina and Herms, Stefan and Rujescu, Dan and Schreiber, Stefan and Wichmann, H-Erich and Dina, Christian and Sladek, Rob and Gambaro, Giovanni and Soranzo, Nicole and Julia, Antonio and Marsal, Sara and Rabionet, Raquel and Gaborieau, Valerie and Dick, Danielle M. and Palotie, Aarno and Ripatti, Samuli and Widen, Elisabeth and Andreassen, Ole A. and Espeseth, Thomas and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Le Hellard, Stephanie and Mattingsdal, Morten and Ntalla, Ioanna and Bencko, Vladimir and Foretova, Lenka and Janout, Vladimir and Navratilova, Marie and Gallinger, Steven and Pinto, Dalila and Scherer, Stephen W. and Aschauer, Harald and Carlberg, Laura and Schosser, Alexandra and Alfredsson, Lars and Ding, Bo and Klareskog, Lars and Padyukov, Leonid and Finan, Chris and Guillaume, Phillippe and Kalsi, Gursharan and Roberts, Marion and Logan, Darren W. and Peltonen, Leena and Ritchie, Graham R. S. and Barrett, Jeffrey C. and Wellcome Trust Case Control Consortium, and Estivill, Xavier and Hinney, Anke and Sullivan, Patrik F. and Collier, David A. and Zeggini, Eleftheria and Bulik, Cynthia M.. (2014) A genome-wide association study of anorexia nervosa. Molecular Psychiatry, 19 (10). pp. 1085-1094.

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.

Elia, Josephine and Glessner, Joseph T. and Wang, Kai and Takahashi, Nagahide and Shtir, Corina J. and Hadley, Dexter and Sleiman, Patrick M. A. and Zhang, Haitao and Kim, Cecilia E. and Robison, Reid and Lyon, Gholson J. and Flory, James H. and Bradfield, Jonathan P. and Imielinski, Marcin and Hou, Cuiping and Frackelton, Edward C. and Chiavacci, Rosetta M. and Sakurai, Takeshi and Rabin, Cara and Middleton, Frank A. and Thomas, Kelly A. and Garris, Maria and Mentch, Frank and Freitag, Christine M. and Steinhausen, Hans-Christoph and Todorov, Alexandre A. and Reif, Andreas and Rothenberger, Aribert and Franke, Barbara and Mick, Eric O. and Roeyers, Herbert and Buitelaar, Jan and Lesch, Klaus-Peter and Banaschewski, Tobias and Ebstein, Richard P. and Mulas, Fernando and Oades, Robert D. and Sergeant, Joseph and Sonuga-Barke, Edmund and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Warnke, Andreas and Walitza, Susanne and Meyer, Jobst and Pálmason, Haukur and Seitz, Christiane and Loo, Sandra K. and Smalley, Susan L. and Biederman, Joseph and Kent, Lindsey and Asherson, Philip and Anney, Richard J. L. and Gaynor, J. William and Shaw, Philip and Devoto, Marcella and White, Peter S. and Grant, Struan F. A. and Buxbaum, Joseph D. and Rapoport, Judith L. and Williams, Nigel M. and Nelson, Stanley F. and Faraone, Stephen V. and Hakonarson, Hakon. (2012) Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature genetics, Vol. 44, H. 1. pp. 78-84.

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.