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Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 329 - 332
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2010, Volume 42, Issue 9, pp. 739 - 741
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2009, Volume 41, Issue 3, pp. 283 - 285
Journal Article
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
Journal Article
by Williams, Frances M K and Carter, Angela M and Hysi, Pirro G and Surdulescu, Gabriela and Hodgkiss, Dylan and Soranzo, Nicole and Traylor, Matthew and Bevan, Steve and Dichgans, Martin and Rothwell, Peter M W and Sudlow, Cathie and Farrall, Martin and Silander, Kaisa and Kaunisto, Mari and Wagner, Peter and Saarela, Olli and Kuulasmaa, Kari and Virtamo, Jarmo and Salomaa, Veikko and Amouyel, Philippe and Arveiler, Dominique and Ferrieres, Jean and Wiklund, Per-Gunnar and Ikram, M Arfan and Hofman, Albert and Boncoraglio, Giorgio B and Parati, Eugenio A and Helgadottir, Anna and Gretarsdottir, Solveig and Thorsteinsdottir, Unnur and Thorleifsson, Gudmar and Stefansson, Kari and Seshadri, Sudha and DeStefano, Anita and Gschwendtner, Andreas and Psaty, Bruce and Longstreth, Will and Mitchell, Braxton D and Cheng, Yu-Ching and Clarke, Robert and Ferrario, Marco and Bis, Joshua C and Levi, Christopher and Attia, John and Holliday, Elizabeth G and Scott, Rodney J and Fornage, Myriam and Sharma, Pankaj and Furie, Karen L and Rosand, Jonathan and Nalls, Mike and Meschia, James and Mosely, Thomas H and Evans, Alun and Palotie, Aarno and Markus, Hugh S and Grant, Peter J and Spector, Tim D and EuroCLOT Investigators, Investigators and Wellcome Trust Case Control Consortium 2, Trust Case Control Consortium 2 and MOnica Risk, Genetics, Archiving and Monograph, Risk, Genetics, Archiving and Monograph and MetaStroke, MetaStroke and International Stroke Genetics Consortium, Stroke Genetics Consortium and EuroCLOT Investigators and Wellcome Trust Case Control Consor and Int Stroke Genetics Consortium and MOnica Risk, Genetics, Archiving and Monograph and MetaStroke and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
Annals of neurology, ISSN 0364-5134, 2013, Volume 73, Issue 1, pp. 16 - 31
Journal Article
by Perret, Claire and Blankenberg, Stefan and Stark, Klaus and Braund, Peter S and Rubin, Diana and Deloukas, Panos and Ball, Stephen G and Schäfer, Arne and Thompson, John R and Voight, Benjamin F and Zeller, Tanja and Schunkert, Heribert and Ouwehand, Willem H and Merlini, Piera Angelica and Schrezenmeir, Jürgen and Linsel-Nitschke, Patrick and Bernardinelli, Luisa and Elosua, Roberto and Wright, Ben and Peyvandi, Flora and Schillert, Arne and Meisinger, Christa and Hengstenberg, Christian and Samani, Nilesh J and Salomaa, Veikko and Peltonen, Leena and Melander, Olle and Schreiber, Stefan and Trégouët, David-Alexandre and Mokhtari, Nour Eddine El and Schwarz, Daniel F and Balmforth, Anthony J and Kathiresan, Sekar and Wagner, Arnika K and Siscovick, David S and Schwartz, Stephen M and Bugert, Peter and Ardissino, Diego and König, Inke R and Aherrahrou, Zouhair and Wild, Philipp and Erdmann, Jeanette and Baumert, Jens and Renner, Wilfried and Bruse, Petra and Klüter, Harald and Altshuler, David and März, Winfried and Wichmann, H-Erich and Ziegler, Andreas and Fischer, Marcus and Hall, Alistair S and Cambien, Francois and Meitinger, Thomas and Großhennig, Anika and Tiret, Laurence and O'Donnell, Christopher J and Peters, Annette and Italian Atherosclerosis Thrombosis and Cardiogenics Consortium and Myocardial Infarction Genetics Con and Wellcome Trust Case Control Consor and Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics Consortium and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and Lunds universitet
Nature Genetics, ISSN 1061-4036, 03/2009, Volume 41, Issue 3, pp. 280 - 282
Journal Article
by Narisu, Narisu and Hu, Tianle and Herder, Christian and Jackson, Anne U and Mohlke, Karen L and Weedon, Michael N and Isomaa, Bo and Ardlie, Kristin and Illig, Thomas and Elliott, Katherine S and Hansen, Torben and Zeggini, Eleftheria and Jørgensen, Torben and Thorsteinsdottir, Unnur and Watanabe, Richard M and Qi, Lu and Grallert, Harald and Barroso, Inês and Kong, Augustine and Hattersley, Andrew T and Kuruvilla, Finny G and Stefansson, Kari and Swift, Amy J and Sandbæk, Anelli and Sjögren, Marketa and Bergman, Richard N and Tuomilehto, Jaakko and Erdos, Michael R and Lango, Hana and Grarup, Niels and Kuusisto, Johanna and Morken, Mario A and de Bakker, Paul IW and Boehnke, Michael and Ding, Chia-Jen and Abecasis, Gonçalo R and Chines, Peter S and Roix, Jeffrey J and Lyssenko, Valeriya and Freathy, Rachel M and Langenberg, Claudia and Pedersen, Oluf and Kubalanza, Kari and Borch-Johnsen, Knut and Andersen, Gitte and Platou, Carl and Altshuler, David and Boström, Kristina Bengtsson and Walker, Mark and McCarthy, Mark I and Chen, Hong and Meisinger, Christa and Hughes, Thomas E and Owen, Katharine R and Stringham, Heather M and Gianniny, Lauren and Nilsson, Peter and Palmer, Colin NA and Morris, Andrew D and Collins, Francis S and Saxena, Richa and Prokopenko, Inga and Scott, Laura J and Voight, Benjamin F and Payne, Felicity and Doney, Alex S F and Duren, William L and Daly, Mark J and Thorleifsson, Gudmar and Pettersen, Elin and Timpson, Nicholas J and Deodhar, Parimal and Laakso, Markku and Lauritzen, Torsten and Shields, Beverley and Bonnycastle, Lori L and Perry, John R B and Midthjell, Kristian and Marvelle, Amanda F and Marchini, Jonathan L and Hveem, Kristian and Frayling, Timothy M and Qin, Li and Groves, Christopher J and Wareham, Nicholas J and Lindgren, Cecilia M and Li, Yun and Groop, Leif and Willer, Cristen J and Guiducci, Candace and Hu, Frank B and Tuomi, Tiinamaija and Burtt, Noël P and Steinthorsdottir, Valgerdur and Almgren, Peter and Hitman, Graham A and Rayner, Nigel W and Rees, Matthew and Wellcome Trust Case Control Consor and DIAGRAM Consortium and Wellcome Trust Case Control Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet
Nature Genetics, ISSN 1061-4036, 05/2008, Volume 40, Issue 5, pp. 638 - 645
Journal Article
Science, ISSN 0036-8075, 5/2007, Volume 316, Issue 5826, pp. 889 - 894
Journal Article