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by Michailidou, Kyriaki and Lindström, Sara and Dennis, Joe and Beesley, Jonathan and Hui, Shirley and Kar, Siddhartha and Lemaçon, Auey and Soucy, Penny and Glubb, Dylan and Rostamianfar, Asha and Bolla, Manjeet K and Wang, Qin and Tyrer, Jonathan and Dicks, Ed and Lee, Anew and Wang, Zhaoming and Allen, Jamie and Keeman, Renske and Eilber, Ursula and French, Juliet D and Qing Chen, Xiao and Fachal, Laura and McCue, Karen and McCart Reed, Amy E and Ghoussaini, Maya and Carroll, Jason S and Jiang, Xia and Finucane, Hilary and Adams, Marcia and Adank, Muriel A and Ahsan, Habibul and Aittomäki, Kristiina and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Aronson, Kristan J and Arun, Banu and Auer, Paul L and Bacot, François and Barrdahl, Myrto and Baynes, Caroline and Beckmann, Matthias W and Behrens, Sabine and Benitez, Javier and Bermisheva, Marina and Bernstein, Leslie and Blomqvist, Carl and Bogdanova, Natalia V and Bojesen, Stig E and Bonanni, Bernardo and Børresen-Dale, Anne-Lise and Brand, Judith S and Brauch, Hiltrud and Brennan, Paul and Brenner, Hermann and Brinton, Louise and Broberg, Per and Brock, Ian W and Broeks, Annegien and Brooks-Wilson, Angela and Brucker, Sara Y and Brüning, Thomas and Burwinkel, Barbara and Butterbach, Katja and Cai, Qiuyin and Cai, Hui and Caldés, Trinidad and Canzian, Federico and Carracedo, Angel and Carter, Brian D and Castelao, Jose E and Chan, Tsun L and David Cheng, Ting-Yuan and Seng Chia, Kee and Choi, Ji-Yeob and Christiansen, Hans and Clarke, Christine L and Collée, Margriet and Conroy, Don M and Cordina-Duverger, Emilie and Cornelissen, Sten and Cox, David G and Cox, Angela and Cross, Simon S and Cunningham, Julie M and Czene, Kamila and Daly, Mary B and Devilee, Peter and Doheny, Kimberly F and Dörk, Thilo and Dos-Santos-Silva, Isabel and Dumont, Martine and Durcan, Lorraine and Dwek, Miriam and Eccles, Diana M and Ekici, Arif B and Eliassen, A. Heather and Ellberg, Carolina and Elvira, Mingajeva and Engel, Christoph and ... and KConFab AOCS Investigators and ABCTB Investigators and NBCS Collaborators and ConFab/AOCS Investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature, ISSN 0028-0836, 2017, Volume 551, Issue 7678, pp. 92 - 94
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1371 - 1379
Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present... 
Internal Medicine | POPULATION | DEPRESSION | MEDICINE, GENERAL & INTERNAL | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | METAANALYSIS | GENE-EXPRESSION | SCHIZOPHRENIA | CACNA1C | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | Child Development Disorders, Pervasive - epidemiology | Genome-Wide Association Study | Humans | Genetic Loci - genetics | Logistic Models | Bipolar Disorder - genetics | Depressive Disorder, Major - epidemiology | Schizophrenia - epidemiology | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Depressive Disorder, Major - genetics | Age of Onset | Polymorphism, Single Nucleotide - genetics | Adult | Child | Bipolar Disorder - epidemiology | Attention Deficit Disorder with Hyperactivity - epidemiology | Physiological aspects | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Medical research | Calcium channels | Genes | Depression, Mental | Genomics | Schizophrenia | Bipolar disorder | Child psychopathology | Quantitative genetics | Autism | Medicine, Experimental | Genetic research | Single nucleotide polymorphisms | Studies | Genetics | Children & youth | Attention deficit disorder | Enrichment | Brain | Calcium | Disease | Mental disorders | Hyperactivity | Mental health | Disorders | Genomes | Single-nucleotide polymorphism | Mental depression | Consortia | Datasets | Calcium signalling | Genetic effects | Signal transduction | Regression models | Autopsy | Classification | Psychopathology | Children | Chromosomes | Genotypes | Phenotypes | Channel gating | Attention deficit hyperactivity disorder | Calcium channels (voltage-gated) | Behavior disorders | Regression analysis | Risk analysis | Loci | Quantitative trait loci | Government grants | Calcium channels (L-type) | Diagnostic systems | Polygenic inheritance | Psychiatry | Polymorphism | Index Medicus | Abridged Index Medicus | Neurosciences | Calcium Channels | Pervasive | Attention Deficit Disorder with Hyperactivity | L-Type | Child Development Disorders | Depressive Disorder | Genetic Loci | Single Nucleotide | epidemiology | genetics | Bipolar Disorder | Major | Neurovetenskaper
Journal Article
by Deloukas, Panos and Kanoni, Stavroula and Willenborg, Christina and Farrall, Martin and Assimes, Themistocles L and Thompson, John R and Ingelsson, Erik and Saleheen, Danish and Erdmann, Jeanette and Goldstein, Benjamin A and Stirrups, Kathleen and König, Inke R and Cazier, Jean-Baptiste and Johansson, Asa and Hall, Alistair S and Lee, Jong-Young and Willer, Cristen J and Chambers, John C and Esko, Tõnu and Folkersen, Lasse and Goel, Anuj and Grundberg, Elin and Havulinna, Aki S and Ho, Weang K and Hopewell, Jemma C and Eriksson, Niclas and Kleber, Marcus E and Kristiansson, Kati and Lundmark, Per and Lyytikäinen, Leo-Pekka and Rafelt, Suzanne and Shungin, Dmitry and Strawbridge, Rona J and Thorleifsson, Gudmar and Tikkanen, Emmi and van Zuydam, Natalie and Voight, Benjamin F and Waite, Lindsay L and Zhang, Weihua and Ziegler, Aneas and Absher, Devin and Altshuler, David and Balmforth, Anthony J and Barroso, Inês and Braund, Peter S and Burgdorf, Christof and Claudi-Boehm, Simone and Cox, David and Dimitriou, Maria and Do, Ron and Doney, Alex S. F and El Mokhtari, NourEddine and Eriksson, Per and Fischer, Krista and Fontanillas, Pierre and Franco-Cereceda, Anders and Gigante, Bruna and Groop, Leif and Gustafsson, Stefan and Hager, Jörg and Hallmans, Göran and Han, Bok-Ghee and Hunt, Sarah E and Kang, Hyun M and Illig, Thomas and Kessler, Thorsten and Knowles, Joshua W and Kolovou, Genovefa and Kuusisto, Johanna and Langenberg, Claudia and Langford, Cordelia and Leander, Karin and Lokki, Marja-Liisa and Lundmark, Anders and McCarthy, Mark I and Meisinger, Christa and Melander, Olle and Mihailov, Evelin and Maouche, Seraya and Morris, Anew D and Müller-Nurasyid, Martina and Nikus, Kjell and Peden, John F and Rayner, N. William and Rasheed, Asif and Rosinger, Silke and Rubin, Diana and Rumpf, Moritz P and Schäfer, Arne and Sivananthan, Mohan and Song, Ci and Stewart, Alexane F. R and Tan, Sian-Tsung and Thorgeirsson, Gudmundur and van der Schoot, C. Ellen and Wagner, Peter J and Wells, George A and Wild, Philipp S and Yang, Tsun-Po and Amouyel, Philippe and ... and CARDIOGENENICS Consortium and Wellcome Trust Case Control and DIAGRAM Consortium and CARDIoGRAMplusC4D Consortium and MuTHER Consortium and Wellcome Trust Case Control Consortium and CARDIOGENICS Consortium and The CARDIoGRAMplusC4D Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Näringsforskning and Umeå universitet and Medicin
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 1, pp. 25 - 33
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1355 - 1359
Journal Article
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article
Nature Genetics, ISSN 1061-4036, 10/2017, Volume 49, Issue 10, pp. 1511 - 1516
Journal Article