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by Power, Robert A and Tansey, Katherine E and Buttenschøn, Henriette Nørmølle and Cohen-Woods, Sarah and Bigdeli, Tim and Hall, Lynsey S and Kutalik, Zoltán and Lee, S. Hong and Ripke, Stephan and Steinberg, Stacy and Teumer, Alexander and Viktorin, Alexander and Wray, Naomi R and Arolt, Volker and Baune, Bernard T and Boomsma, Dorret I and Børglum, Anders D and Byrne, Enda M and Castelao, Enrique and Craddock, Nick and Craig, Ian W and Dannlowski, Udo and Deary, Ian J and Degenhardt, Franziska and Forstner, Andreas J and Gordon, Scott D and Grabe, Hans J and Grove, Jakob and Hamilton, Steven P and Hayward, Caroline and Heath, Andrew C and Hocking, Lynne J and Homuth, Georg and Hottenga, Jouke J and Kloiber, Stefan and Krogh, Jesper and Landén, Mikael and Lang, Maren and Levinson, Douglas F and Lichtenstein, Paul and Lucae, Susanne and MacIntyre, Donald J and Madden, Pamela and Magnusson, Patrik K.E and Martin, Nicholas G and McIntosh, Andrew M and Middeldorp, Christel M and Milaneschi, Yuri and Montgomery, Grant W and Mors, Ole and Müller-Myhsok, Bertram and Nyholt, Dale R and Oskarsson, Hogni and Owen, Michael J and Padmanabhan, Sandosh and Penninx, Brenda W.J.H and Pergadia, Michele L and Porteous, David J and Potash, James B and Preisig, Martin and Rivera, Margarita and Shi, Jianxin and Shyn, Stanley I and Sigurdsson, Engilbert and Smit, Johannes H and Smith, Blair H and Stefansson, Hreinn and Stefansson, Kari and Strohmaier, Jana and Sullivan, Patrick F and Thomson, Pippa and Thorgeirsson, Thorgeir E and Van der Auwera, Sandra and Weissman, Myrna M and Breen, Gerome and Lewis, Cathryn M and CONVERGE Consortium and CARDIoGRAM Consortium and GERAD1 Consortium and CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
Biological Psychiatry, ISSN 0006-3223, 02/2017, Volume 81, Issue 4, pp. 325 - 335
Journal Article
Journal Article
EUROPEAN NEUROPSYCHOPHARMACOLOGY, ISSN 0924-977X, 10/2017, Volume 27, pp. S119 - S119
Conference Proceeding
Journal Article
EUROPEAN NEUROPSYCHOPHARMACOLOGY, ISSN 0924-977X, 2019, Volume 29, pp. S816 - S816
Bipolar Disorder (BD) is a common, complex and severe mood disorder with high heritability. Genetic analyses of bipolar disorder continue to benefit from large... 
PHARMACOLOGY & PHARMACY | PSYCHIATRY | NEUROSCIENCES | CLINICAL NEUROLOGY | Genetic research | Schizophrenia | Bipolar disorder | Osteoarthritis | Analysis | Genomics
Conference Proceeding
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S816 - S816
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2018, Volume 13, Issue 10, pp. e0205895 - e0205895
Journal Article
Nature Genetics, ISSN 1061-4036, 2015, Volume 47, Issue 3, pp. 291 - 295
Both polygenicity (many small genetic effects) and confounding biases, such as cryptic relatedness and population stratification, can yield an inflated... 
Journal Article
by Arnau-Soler, Aleix and Arnau-Soler, Aleix and Adams, Mark J and Adams, Mark J and Hayward, Caroline and Thomson, Pippa A and Thomson, Pippa A and Porteous, David and Campbell, Archie and Smith, Blair H and Black, Corri and Padmanabhan, Sandosh and McIntosh, Andrew M and Wray, Naomi R and Ripke, Stephan and Mattheisen, Manuel and Trzaskowski, Maciej and Byrne, Enda M and Abdellaoui, Abdel and Agerbo, Esben and Air, Tracy M and Andlauer, Till F.M and Bacanu, Silviu-Alin and Bækvad-Hansen, Marie and Beekman, Aartjan T.F and Bigdeli, Tim B and Binder, Elisabeth B and Blackwood, Douglas H.R and Bryois, Julien and Buttenschøn, Henriette N and Bybjerg-Grauholm, Jonas and Cai, Na and Castelao, Enrique and Christensen, Jane Hvarregaard and Clarke, Toni-Kim and Coleman, Jonathan R.I and Colodro-Conde, Lucía and Couvy-Duchesne, Baptiste and Craddock, Nick and Crawford, Gregory E and Davies, Gail and Deary, Ian J and Degenhardt, Franziska and Derks, Eske M and Direk, Nese and Dolan, Conor V and Dunn, Erin C and Eley, Thalia C and Escott-Price, Valentina and Kiadeh, Farnush Farhadi Hassan and Finucane, Hilary K and Forstner, Andreas J and Frank, Josef and Gaspar, Héléna A and Gill, Michael and Goes, Fernando S and Gordon, Scott D and Grove, Jakob and Hall, Lynsey S and Hansen, Christine Søholm and Hansen, Thomas F and Herms, Stefan and Hickie, Ian B and Hoffmann, Per and Homuth, Georg and Horn, Carsten and Hottenga, Jouke-Jan and Hougaard, David M and Ising, Marcus and Jansen, Rick and Jorgenson, Eric and Knowles, James A and Kohane, Isaac S and Kraft, Julia and Kretzschmar, Warren W and Krogh, Jesper and Kutalik, Zoltán and Li, Yihan and Lind, Penelope A and MacIntyre, Donald J and MacKinnon, Dean F and Maier, Robert M and Maier, Wolfgang and Marchini, Jonathan and Mbarek, Hamdi and McGrath, Patrick and McGuffin, Peter and Medland, Sarah E and Mehta, Divya and Middeldorp, Christel M and Mihailov, Evelin and Milaneschi, Yuri and Milani, Lili and Mondimore, Francis M and Montgomery, Grant W and Mostafavi, Sara and Mullins, Niamh and Nauck, Matthias and Ng, Bernard and Nivard, Michel G and ... and Generation Scotland and Psychiat Genomics Consortium and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
PLoS ONE, ISSN 1932-6203, 12/2018, Volume 13, Issue 12, pp. e0209160 - e0209160
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S749 - S750
Development of post-traumatic stress disorder (PTSD) is influenced by both environmental and genetic factors. In the most current data (freeze 2), the... 
PHARMACOLOGY & PHARMACY | PSYCHIATRY | NEUROSCIENCES | CLINICAL NEUROLOGY | Medical research | Analysis | Genomics | Post-traumatic stress disorder | African Americans | Genetic research | Medicine, Experimental | Genetic aspects
Journal Article
by Anney, Richard J. L and Ripke, Stephan and Anttila, Verneri and Grove, Jakob and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Robinson, Elise and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A.Jeremy and Wijsman, Ellen M and Werge, Thomas and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Vanengeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Sanders, Stephan J and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne Giørtz and Pedersen, Carsten Bøcker and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Nordentoft, Merete and Murtha, Michael T and Mouga, Susana and Mortensen, Preben Bo and Mors, Ole and Morrow, Eric M and Moreno-De-Luca, Daniel and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and McGrew, Susan G and Mattheisen, Manuel and Martsenkovsky, Igor and Martin, Donna M and Mane, Shrikant M and Magnusson, Pall and Magalhaes, Tiago and Maestrini, Elena and Lowe, Jennifer K and Lord, Catherine and Levitt, Pat and Martin, Christa Lese and Ledbetter, David H and Leboyer, Marion and Lecouteur, Ann S and Ladd-Acosta, Christine and Kolevzon, Alexander and Klauck, Sabine M and Jacob, Suma and Iliadou, Bozenna and Hultman, Christina M and Hougaard, David M and Hertz-Picciotto, Irva and Hendren, Robert and Hansen, Christine Søholm and Haines, Jonathan L and Guter, Stephen J and ... and Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Molecular Autism, ISSN 2040-2392, 05/2017, Volume 8, Issue 1, pp. 21 - 21
Background: Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of... 
Gene-set analysis | Genome-wide association study | Genetic correlation | Neurodevelopment | Schizophrenia | Heritability | Autism spectrum disorder | Meta-analysis | MENTAL-RETARDATION | NEUROSCIENCES | FOXP1 | INTELLECTUAL DISABILITY | RISK LOCI | GENETICS & HEREDITY | COMMON | SCAN | COPY NUMBER VARIATION | LINKAGE | GENOME-WIDE ASSOCIATION | REVEALS | Autism Spectrum Disorder - genetics | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Plasma Membrane Calcium-Transporting ATPases - genetics | Membrane Proteins - genetics | Humans | Repressor Proteins - genetics | Male | Genetic Loci | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Carrier Proteins - genetics | Schizophrenia - genetics | Schizophrenia - diagnosis | Schizophrenia - physiopathology | Female | Autism Spectrum Disorder - diagnosis | Autism Spectrum Disorder - physiopathology | Genetic aspects | Research | Genetic susceptibility | Risk factors | Pervasive developmental disorders | Autism | Genomes | Gene expression | Index Medicus | Life Sciences | Genetics | Autism spectrum disorder, Genome-wide association study, Meta-analysis, Genetic correlation, Heritability, Gene-set analysis, Schizophrenia, Neurodevelopment | genetic | Neurologi | asperger-syndrome | resource exchange | Genetics & Heredity | Neurosciences & Neurology | pervasive developmental disorders | Neurology | copy number variation | neuronal migration | risk loci | de-novo mutations | genome-wide association | mental-retardation | intellectual disability
Journal Article