{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T16:40:16Z","timestamp":1791304816631,"version":"4.3.1"},"reference-count":49,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2011,11,15]],"date-time":"2011-11-15T00:00:00Z","timestamp":1321315200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Mol Psychiatry"],"published-print":{"date-parts":[[2012,2]]},"DOI":"10.1038\/mp.2011.154","type":"journal-article","created":{"date-parts":[[2011,11,15]],"date-time":"2011-11-15T09:28:12Z","timestamp":1321349292000},"page":"142-153","source":"Crossref","is-referenced-by-count":796,"title":["De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia"],"prefix":"10.1038","volume":"17","author":[{"given":"G","family":"Kirov","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A J","family":"Pocklington","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Holmans","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Ivanov","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Ikeda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Ruderfer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J","family":"Moran","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K","family":"Chambert","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Toncheva","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L","family":"Georgieva","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Grozeva","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Fjodorova","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R","family":"Wollerton","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"Rees","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"I","family":"Nikolov","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L N","family":"van de Lagemaat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u00c0","family":"Bay\u00e9s","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"Fernandez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P I","family":"Olason","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y","family":"B\u00f6ttcher","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N H","family":"Komiyama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M O","family":"Collins","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J","family":"Choudhary","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K","family":"Stefansson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Stefansson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S G N","family":"Grant","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Purcell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Sklar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M C","family":"O'Donovan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M J","family":"Owen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2011,11,15]]},"reference":[{"key":"BFmp2011154_CR1","doi-asserted-by":"publisher","first-page":"667","DOI":"10.1001\/archgenpsychiatry.2010.69","volume":"67","author":"MJ Owen","year":"2010","unstructured":"Owen MJ, Craddock N, O'Donovan MC . Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. Arch Gen Psychiatry 2010; 67: 667\u2013673.","journal-title":"Arch Gen Psychiatry"},{"key":"BFmp2011154_CR2","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1038\/nature07239","volume":"455","author":"International Schizophrenia Consortium (ISC)","year":"2008","unstructured":"International Schizophrenia Consortium (ISC). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237\u2013241.","journal-title":"Nature"},{"key":"BFmp2011154_CR3","doi-asserted-by":"publisher","first-page":"1497","DOI":"10.1093\/hmg\/ddp043","volume":"18","author":"G Kirov","year":"2009","unstructured":"Kirov G, Grozeva D, Norton N, Ivanov D, Mantripragada KK, Holmans P et al. Support for the involvement of large CNVs in the pathogenesis of schizophrenia. Hum Mol Genet 2009; 18: 1497\u20131503.","journal-title":"Hum Mol Genet"},{"key":"BFmp2011154_CR4","doi-asserted-by":"publisher","first-page":"302","DOI":"10.1176\/appi.ajp.2010.10060876","volume":"168","author":"DF Levinson","year":"2011","unstructured":"Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J et al. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry 2011; 168: 302\u2013316.","journal-title":"Am J Psychiatry"},{"key":"BFmp2011154_CR5","doi-asserted-by":"publisher","first-page":"618","DOI":"10.1016\/j.ajhg.2010.10.004","volume":"87","author":"D Moreno-De-Luca","year":"2010","unstructured":"Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP et al. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet 2010; 87: 618\u2013630.","journal-title":"Am J Hum Genet"},{"key":"BFmp2011154_CR6","doi-asserted-by":"publisher","first-page":"229","DOI":"10.1016\/j.ajhg.2010.07.013","volume":"87","author":"JG Mulle","year":"2010","unstructured":"Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC et al. Microdeletions of 3q29 confer high risk for schizophrenia. Am J Hum Genet 2010; 87: 229\u2013236.","journal-title":"Am J Hum Genet"},{"key":"BFmp2011154_CR7","doi-asserted-by":"publisher","first-page":"232","DOI":"10.1038\/nature07229","volume":"455","author":"H Stefansson","year":"2008","unstructured":"Stefansson H, Rujescu D, Cichon S, Pietilainen OPH, Ingason A, Steinberg S et al. Large recurrent microdeletions associated with schizophrenia. Nature 2008; 455: 232\u2013236.","journal-title":"Nature"},{"key":"BFmp2011154_CR8","doi-asserted-by":"publisher","first-page":"499","DOI":"10.1038\/nature09884","volume":"471","author":"V Vacic","year":"2011","unstructured":"Vacic V, McCarthy S, Malhotra D, Murray F, Chou H-H, Peoples A et al. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. Nature 2011; 471: 499\u2013503.","journal-title":"Nature"},{"key":"BFmp2011154_CR9","doi-asserted-by":"publisher","first-page":"408","DOI":"10.1176\/appi.ajp.2010.09111660","volume":"168","author":"A Ingason","year":"2011","unstructured":"Ingason A, Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD et al. Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry 2011; 168: 408\u2013417.","journal-title":"Am J Psychiatry"},{"key":"BFmp2011154_CR10","doi-asserted-by":"publisher","first-page":"17","DOI":"10.1038\/mp.2009.101","volume":"16","author":"Ingason A","year":"2011","unstructured":"Ingason A, Rujescu D, Cichon S, Sigurdsson E, Sigmundsson T, Pietilainen OPH et al. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Mol Psychiatry 2011; 16: 17\u201325.","journal-title":"Mol Psychiatry"},{"key":"BFmp2011154_CR11","doi-asserted-by":"publisher","first-page":"851","DOI":"10.1093\/schbul\/sbp079","volume":"35","author":"G Kirov","year":"2009","unstructured":"Kirov G, Rujescu D, Ingason A, Collier DA, O'Donovan MC, Owen MJ . Neurexin 1 (NRXN1) deletions in schizophrenia. Schizophr Bull 2009; 35: 851\u2013854.","journal-title":"Schizophr Bull"},{"key":"BFmp2011154_CR12","doi-asserted-by":"publisher","first-page":"1223","DOI":"10.1038\/ng.474","volume":"41","author":"SE McCarthy","year":"2009","unstructured":"McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S et al. Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009; 41: 1223\u20131227.","journal-title":"Nat Genet"},{"key":"BFmp2011154_CR13","doi-asserted-by":"publisher","first-page":"528","DOI":"10.1016\/j.tig.2009.10.004","volume":"25","author":"J Sebat","year":"2009","unstructured":"Sebat J, Levy DL, McCarthy SE . Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders. Trends Genet 2009; 25: 528\u2013535.","journal-title":"Trends Genet"},{"key":"BFmp2011154_CR14","doi-asserted-by":"publisher","first-page":"318","DOI":"10.1001\/archgenpsychiatry.2010.25","volume":"67","author":"D Grozeva","year":"2010","unstructured":"Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK et al. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. Arch Gen Psychiatry 2010; 67: 318\u2013327.","journal-title":"Arch Gen Psychiatry"},{"key":"BFmp2011154_CR15","doi-asserted-by":"publisher","first-page":"458","DOI":"10.1093\/hmg\/ddm323","volume":"17","author":"G Kirov","year":"2008","unstructured":"Kirov G, Gumus D, Chen W, Norton N, Georgieva L, Sari M et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum Mol Genet 2008; 17: 458\u2013465.","journal-title":"Hum Mol Genet"},{"key":"BFmp2011154_CR16","doi-asserted-by":"publisher","first-page":"1005","DOI":"10.1016\/j.biopsych.2009.07.027","volume":"66","author":"GWC Tam","year":"2009","unstructured":"Tam GWC, Redon R, Carter NP, Grant SGN . The role of DNA copy number variation in schizophrenia. Biol Psychiatry 2009; 66: 1005\u20131012.","journal-title":"Biol Psychiatry"},{"key":"BFmp2011154_CR17","doi-asserted-by":"publisher","first-page":"539","DOI":"10.1126\/science.1155174","volume":"320","author":"T Walsh","year":"2008","unstructured":"Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM et al. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 2008; 320: 539\u2013543.","journal-title":"Science"},{"key":"BFmp2011154_CR18","doi-asserted-by":"publisher","first-page":"10584","DOI":"10.1073\/pnas.1000274107","volume":"107","author":"JT Glessner","year":"2010","unstructured":"Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C et al. Strong synaptic transmission impact by copy number variations in schizophrenia. Proc Natl Acad Sci USA 2010; 107: 10584\u201310589.","journal-title":"Proc Natl Acad Sci USA"},{"key":"BFmp2011154_CR19","doi-asserted-by":"publisher","first-page":"e1001097","DOI":"10.1371\/journal.pgen.1001097","volume":"6","author":"S Raychaudhuri","year":"2010","unstructured":"Raychaudhuri S, Korn JM, McCarroll SA, Consortium TIS, Altshuler D, Sklar P et al. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genet 2010; 6: pii: e1001097.","journal-title":"PLoS Genet"},{"key":"BFmp2011154_CR20","doi-asserted-by":"publisher","first-page":"98","DOI":"10.1111\/j.1600-0447.2010.01623.x","volume":"123","author":"H Bundy","year":"2010","unstructured":"Bundy H, Stahl D, MacCabe JH . A systematic review and meta-analysis of the fertility of patients with schizophrenia and their unaffected relatives. Acta Psychiat Scand 2010; 123: 98\u2013106.","journal-title":"Acta Psychiat Scand"},{"key":"BFmp2011154_CR21","doi-asserted-by":"publisher","first-page":"234","DOI":"10.1016\/j.schres.2010.05.018","volume":"121","author":"TM Laursen","year":"2010","unstructured":"Laursen TM, Munk-Olsen T . Reproductive patterns in psychotic patients. Schizophr Res 2010; 121: 234\u2013240.","journal-title":"Schizophr Res"},{"key":"BFmp2011154_CR22","doi-asserted-by":"crossref","unstructured":"Rees E, Moskvina V, Owen MJ, O'Donovan MC, Kirov G . De novo rates and selection of schizophrenia-associated copy number variants. Biol Psychiatry; advance online publication, 18 August 2011 [e-pub ahead of print].","DOI":"10.1016\/j.biopsych.2011.07.011"},{"key":"BFmp2011154_CR23","doi-asserted-by":"publisher","first-page":"445","DOI":"10.1126\/science.1138659","volume":"316","author":"J Sebat","year":"2007","unstructured":"Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T et al. Strong association of de novo copy number mutations with autism. Science 2007; 316: 445\u2013449.","journal-title":"Science"},{"key":"BFmp2011154_CR24","doi-asserted-by":"publisher","first-page":"880","DOI":"10.1038\/ng.162","volume":"40","author":"B Xu","year":"2008","unstructured":"Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M . Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet 2008; 40: 880\u2013885.","journal-title":"Nat Genet"},{"key":"BFmp2011154_CR25","doi-asserted-by":"publisher","first-page":"863","DOI":"10.1016\/j.neuron.2011.05.002","volume":"70","author":"J Sanders Stephan","year":"2011","unstructured":"Sanders Stephan J, Ercan-Sencicek AG, Hus V, Luo R, Murtha Michael T, Moreno-De-Luca D et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011; 70: 863\u2013885.","journal-title":"Neuron"},{"key":"BFmp2011154_CR26","doi-asserted-by":"publisher","first-page":"283","DOI":"10.1016\/j.biopsych.2009.08.034","volume":"67","author":"M Ikeda","year":"2010","unstructured":"Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T et al. Copy number variation in schizophrenia in the Japanese population. Biol Psychiatry 2010; 67: 283\u2013286.","journal-title":"Biol Psychiatry"},{"key":"BFmp2011154_CR27","doi-asserted-by":"publisher","first-page":"1665","DOI":"10.1101\/gr.6861907","volume":"17","author":"K Wang","year":"2007","unstructured":"Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA et al. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 2007; 17: 1665\u20131674.","journal-title":"Genome Res"},{"key":"BFmp2011154_CR28","doi-asserted-by":"publisher","first-page":"512","DOI":"10.1038\/nbt.1852","volume":"29","author":"D Pinto","year":"2011","unstructured":"Pinto D, Darvishi K, Shi X, Rajan D, Rigler D, Fitzgerald T et al. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat Biotech 2011; 29: 512\u2013520.","journal-title":"Nat Biotech"},{"key":"BFmp2011154_CR29","doi-asserted-by":"publisher","first-page":"988","DOI":"10.1093\/hmg\/ddn351","volume":"18","author":"D Rujescu","year":"2009","unstructured":"Rujescu D, Ingason A, Cichon S, Pietil\u00e4inen OP, Barnes MR, Toulopoulou T et al. Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet 2009; 18: 988\u2013996.","journal-title":"Hum Mol Genet"},{"key":"BFmp2011154_CR30","doi-asserted-by":"publisher","first-page":"368","DOI":"10.1038\/nature09146","volume":"466","author":"D Pinto","year":"2010","unstructured":"Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368\u2013372.","journal-title":"Nature"},{"key":"BFmp2011154_CR31","doi-asserted-by":"publisher","first-page":"598","DOI":"10.1136\/jmg.2008.062950","volume":"46","author":"T Kleefstra","year":"2009","unstructured":"Kleefstra T, van Zelst-Stams WA, Nillesen WM, Cormier-Daire V, Houge G, Foulds N et al. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. J Med Genet 2009; 46: 598\u2013606.","journal-title":"J Med Genet"},{"key":"BFmp2011154_CR32","doi-asserted-by":"publisher","first-page":"838","DOI":"10.1038\/ng.909","volume":"43","author":"GM Cooper","year":"2011","unstructured":"Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C et al. A copy number variation morbidity map of developmental delay. Nat Genet 2011; 43: 838\u2013846.","journal-title":"Nat Genet"},{"key":"BFmp2011154_CR33","doi-asserted-by":"publisher","first-page":"e1000569","DOI":"10.1371\/journal.pbio.1000569","volume":"9","author":"JM Kramer","year":"2011","unstructured":"Kramer JM, Kochinke K, Oortveld MAW, Marks H, Kramer D, de Jong EK et al. Epigenetic regulation of learning and memory by Drosophila EHMT\/G9a. PLoS Biol 2011; 9: e1000569.","journal-title":"PLoS Biol"},{"key":"BFmp2011154_CR34","doi-asserted-by":"publisher","first-page":"19","DOI":"10.1038\/nn.2719","volume":"14","author":"A Bay\u00e9s","year":"2011","unstructured":"Bay\u00e9s A, van de Lagemaat LN, Collins MO, Croning MDR, Whittle IR, Choudhary JS et al. Characterization of the proteome, diseases and evolution of the human postsynaptic density. Nat Neurosci 2011; 14: 19\u201321.","journal-title":"Nat Neurosci"},{"key":"BFmp2011154_CR35","doi-asserted-by":"publisher","first-page":"318","DOI":"10.1086\/422703","volume":"75","author":"P Tarpey","year":"2004","unstructured":"Tarpey P, Parnau J, Blow M, Woffendin H, Bignell G, Cox C et al. Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. Am J Hum Genet 2004; 75: 318\u2013324.","journal-title":"Am J Hum Genet"},{"key":"BFmp2011154_CR36","doi-asserted-by":"publisher","first-page":"947","DOI":"10.1001\/archgenpsychiatry.2009.80","volume":"66","author":"A Guilmatre","year":"2009","unstructured":"Guilmatre A, Dubourg C, Mosca A-L, Legallic S, Goldenberg A, Drouin-Garraud V et al. Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. Arch Gen Psychiatry 2009; 66: 947\u2013956.","journal-title":"Arch Gen Psychiatry"},{"key":"BFmp2011154_CR37","doi-asserted-by":"publisher","first-page":"232","DOI":"10.1086\/510919","volume":"80","author":"E Klopocki","year":"2007","unstructured":"Klopocki E, Schulze H, Strau G, Ott C-E, Hall J, Trotier F et al. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. Am J Hum Genet 2007; 80: 232\u2013240.","journal-title":"Am J Hum Genet"},{"key":"BFmp2011154_CR38","doi-asserted-by":"publisher","first-page":"94","DOI":"10.1016\/j.ejmg.2009.02.006","volume":"52","author":"N Van der Aa","year":"2009","unstructured":"Van der Aa N, Rooms L, Vandeweyer G, van den Ende J, Reyniers E, Fichera M et al. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome. Eur J Med Genet 2009; 52: 94\u2013100.","journal-title":"Eur J Med Genet"},{"key":"BFmp2011154_CR39","doi-asserted-by":"publisher","first-page":"1223","DOI":"10.1038\/ng.474","volume":"41","author":"SE McCarthy","year":"2009","unstructured":"McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S et al. Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009; 41: 1223\u20131227.","journal-title":"Nat Genet"},{"key":"BFmp2011154_CR40","doi-asserted-by":"publisher","first-page":"528","DOI":"10.1016\/j.tig.2009.10.004","volume":"25","author":"J Sebat","year":"2009","unstructured":"Sebat J, Levy DL, McCarthy SE . Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders. Trends Genet 2009; 25: 528\u2013535.","journal-title":"Trends Genet"},{"key":"BFmp2011154_CR41","doi-asserted-by":"publisher","first-page":"1401","DOI":"10.1016\/S0140-6736(10)61109-9","volume":"376","author":"NM Williams","year":"2010","unstructured":"Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R et al. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet 2010; 376: 1401\u20131408.","journal-title":"Lancet"},{"issue":"S 2","key":"BFmp2011154_CR42","doi-asserted-by":"publisher","first-page":"104","DOI":"10.1055\/s-2007-979354","volume":"31","author":"WM Abi-Saab","year":"1998","unstructured":"Abi-Saab WM, D'Souza DC, Moghaddam B, Krystal JH . The NMDA antagonist model for schizophrenia: promise and pitfalls. Pharmacopsychiatry 1998; 31 (S 2): 104\u2013109.","journal-title":"Pharmacopsychiatry"},{"key":"BFmp2011154_CR43","doi-asserted-by":"publisher","first-page":"661","DOI":"10.1038\/76615","volume":"3","author":"H Husi","year":"2000","unstructured":"Husi H, Ward MA, Choudhary JS, Blackstock WP, Grant SGN . Proteomic analysis of NMDA receptor-adhesion protein signaling complexes. Nat Neurosci 2000; 3: 661\u2013669.","journal-title":"Nat Neurosci"},{"key":"BFmp2011154_CR44","doi-asserted-by":"publisher","first-page":"R225","DOI":"10.1093\/hmg\/ddi330","volume":"14","author":"SG Grant","year":"2005","unstructured":"Grant SG, Marshall MC, Page KL, Cumiskey MA, Armstrong JD . Synapse proteomics of multiprotein complexes: en route from genes to nervous system diseases. Hum Mol Genet 2005; 14: R225\u2013R234.","journal-title":"Hum Mol Genet"},{"key":"BFmp2011154_CR45","doi-asserted-by":"publisher","first-page":"197","DOI":"10.1016\/j.conb.2010.08.009","volume":"21","author":"KJ Mitchell","year":"2011","unstructured":"Mitchell KJ . The genetics of neurodevelopmental disease. Cur Opin Neurobiol 2011; 21: 197\u2013203.","journal-title":"Cur Opin Neurobiol"},{"key":"BFmp2011154_CR46","doi-asserted-by":"publisher","first-page":"521","DOI":"10.1016\/0166-2236(93)90197-T","volume":"16","author":"RC Malenka","year":"1993","unstructured":"Malenka RC, Nicoll RA . NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms. Trends Neurosci 1993; 16: 521\u2013527.","journal-title":"Trends Neurosci"},{"key":"BFmp2011154_CR47","doi-asserted-by":"publisher","first-page":"125","DOI":"10.1007\/s00221-009-1959-2","volume":"200","author":"C Bramham","year":"2010","unstructured":"Bramham C, Alme M, Bittins M, Kuipers S, Nair R, Pai B et al. The Arc of synaptic memory. Exp Brain Res 2010; 200: 125\u2013140.","journal-title":"Exp Brain Res"},{"key":"BFmp2011154_CR48","doi-asserted-by":"publisher","first-page":"25","DOI":"10.1586\/ern.09.133","volume":"10","author":"G Kirov","year":"2010","unstructured":"Kirov G . The role of copy number variation in schizophrenia. Exp Rev Neurotherapeutics 2010; 10: 25\u201332.","journal-title":"Exp Rev Neurotherapeutics"},{"key":"BFmp2011154_CR49","doi-asserted-by":"publisher","first-page":"1042","DOI":"10.1016\/j.cell.2008.07.031","volume":"134","author":"I Napoli","year":"2008","unstructured":"Napoli I, Mercaldo V, Boyl PP, Eleuteri B, Zalfa F, De Rubeis S et al. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell 2008; 134: 1042\u20131054.","journal-title":"Cell"}],"container-title":["Molecular Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/mp2011154.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/mp2011154","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/mp2011154.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T18:14:02Z","timestamp":1684433642000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/mp2011154"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,11,15]]},"references-count":49,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2012,2]]}},"alternative-id":["BFmp2011154"],"URL":"https:\/\/doi.org\/10.1038\/mp.2011.154","relation":{},"ISSN":["1359-4184","1476-5578"],"issn-type":[{"value":"1359-4184","type":"print"},{"value":"1476-5578","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,11,15]]}}}