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Schizophrenia Research, ISSN 0920-9964, 2014, Volume 160, Issue 1, pp. e1 - e2
Journal Article
Schizophrenia Research, ISSN 0920-9964, 2014, Volume 153, pp. S72 - S72
Journal Article
Journal Article
BMC Biology, ISSN 1741-7007, 11/2011, Volume 9, Issue 1, pp. 77 - 77
Progress is being made in schizophrenia genomics, suggesting that this complex brain disorder involves rare, moderate to high-risk mutations and the cumulative... 
Genome-Wide Association Study | Schizophrenia - genetics | Base Sequence | Humans | Genomics - methods | Mutation - genetics | Schizophrenia - epidemiology | Genome, Human - genetics | Schizophrenia | Development and progression | Genetic aspects | Research | Single nucleotide polymorphisms | Genomics | Studies | Autism | Social research | Illnesses | Disease | Genetics | Mutation | Behavior | Risk factors
Journal Article
by Savage, Jeanne E and Jansen, Philip R and Stringer, Sven and Watanabe, Kyoko and Bryois, Julien and de Leeuw, Christiaan A and Nagel, Mats and Awasthi, Swapnil and Barr, Peter B and Coleman, Jonathan R. I and Grasby, Katrina L and Hammerschlag, Anke R and Kaminski, Jakob A and Karlsson, Robert and Krapohl, Eva and Lam, Max and Nygaard, Marianne and Reynolds, Chandra A and Trampush, Joey W and Young, Hannah and Zabaneh, Delilah and Hägg, Sara and Hansell, Narelle K and Karlsson, Ida K and Linnarsson, Sten and Montgomery, Grant W and Muñoz-Manchado, Ana B and Quinlan, Erin B and Schumann, Gunter and Skene, Nathan G and Webb, Bradley T and White, Tonya and Arking, Dan E and Avramopoulos, Dimitrios and Bilder, Robert M and Bitsios, Panos and Burdick, Katherine E and Cannon, Tyrone D and Chiba-Falek, Ornit and Christoforou, Andrea and Cirulli, Elizabeth T and Congdon, Eliza and Corvin, Aiden and Davies, Gail and Deary, Ian J and DeRosse, Pamela and Dickinson, Dwight and Djurovic, Srdjan and Donohoe, Gary and Conley, Emily Drabant and Eriksson, Johan G and Espeseth, Thomas and Freimer, Nelson A and Giakoumaki, Stella and Giegling, Ina and Gill, Michael and Glahn, David C and Hariri, Ahmad R and Hatzimanolis, Alex and Keller, Matthew C and Knowles, Emma and Koltai, Deborah and Konte, Bettina and Lahti, Jari and Le Hellard, Stephanie and Lencz, Todd and Liewald, David C and London, Edythe and Lundervold, Astri J and Malhotra, Anil K and Melle, Ingrid and Morris, Derek and Need, Anna C and Ollier, William and Palotie, Aarno and Payton, Antony and Pendleton, Neil and Poldrack, Russell A and Räikkönen, Katri and Reinvang, Ivar and Roussos, Panos and Rujescu, Dan and Sabb, Fred W and Scult, Matthew A and Smeland, Olav B and Smyrnis, Nikolaos and Starr, John M and Steen, Vidar M and Stefanis, Nikos C and Straub, Richard E and Sundet, Kjetil and Tiemeier, Henning and Voineskos, Aristotle N and Weinberger, Daniel R and Widen, Elisabeth and Yu, Jin and Abecasis, Goncalo and Andreassen, Ole A and Breen, Gerome and Christiansen, Lene and ...
Nature genetics, ISSN 1546-1718, 2018, Volume 50, Issue 7, pp. 912 - 919
Journal Article
Nature (London), ISSN 1476-4687, 2011, Volume 471, Issue 7339, pp. 499 - 503
Journal Article
Nature genetics, ISSN 1546-1718, 2008, Volume 40, Issue 9, pp. 1056 - 1058
Journal Article
Schizophrenia Research, ISSN 0920-9964, 2008, Volume 102, Issue 1, pp. 184 - 184
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2011, Volume 6, Issue 11, p. e26488
...Author(s): Annette E. Runker 1 , Colm O'Tuathaigh 2 , Mark Dunleavy 3 , Derek W. Morris 4 , Graham E. Little 1 , Aiden P. Corvin 4 , Michael Gill 4 , David C... 
MOLECULAR CHARACTERIZATION | PLXNA2 GENE | MENTAL-RETARDATION | LAMINA-RESTRICTED PROJECTION | RECEPTOR HYPOFUNCTION | MULTIDISCIPLINARY SCIENCES | SCHIZOPHRENIA-SUSCEPTIBILITY LOCUS | WHITE-MATTER ABNORMALITIES | BIPOLAR DISORDER | D-AMPHETAMINE | INTERSTITIAL DELETION | Limbic System - pathology | Humans | Memory | Prefrontal Cortex - physiopathology | Male | Mental Disorders - complications | Gait - physiology | Mice, Neurologic Mutants | Prefrontal Cortex - pathology | Mental Disorders - genetics | Anxiety - complications | Limbic System - physiopathology | Female | Nerve Net - physiopathology | Semaphorins - genetics | Disease Models, Animal | Limbic System - growth & development | Mice, Inbred C57BL | Anxiety - psychology | Anxiety - physiopathology | Behavior, Animal - physiology | Mutation - genetics | Mental Disorders - physiopathology | Mental Disorders - psychology | Phenotype | Animals | Mice | Locomotion - physiology | Psychological aspects | Autism | Brain | Neurons | Analysis | Physiological aspects | Schizophrenia | Genetic aspects | Clozapine | Neurosciences | Animal models | Neuroleptics | Mental disorders | Genes | Disorders | Nervous system | Genomes | Health physics | Neurodevelopmental disorders | Defects | Proteins | Psychosis | Rodents | Genetics | Physiology | Psychopathology | Narcotics | EEG | Exploratory behavior | Cortex | Behavior disorders | Pattern recognition | Object recognition | Mutants | Brain research | Lamination | Anxieties | Neural networks | Psychopharmacology | Mutation | Short term memory | Psychiatry | Organizational aspects
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2019, Volume 116, Issue 19, pp. 9604 - 9609
Journal Article