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7. Copy number variation in schizophrenia in the Japanese population. Ikeda M; Aleksic B; Kirov G; Kinoshita Y; Yamanouchi Y; Kitajima T; Kawashima K; Okochi T; Kishi T; Zaharieva I; Owen MJ; O'Donovan MC; Ozaki N; Iwata N Biol Psychiatry; 2010 Feb; 67(3):283-6. PubMed ID: 19880096 [TBL] [Abstract][Full Text] [Related]
8. Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes. Luo X; Huang L; Han L; Luo Z; Hu F; Tieu R; Gan L Schizophr Bull; 2014 Nov; 40(6):1285-99. PubMed ID: 24664977 [TBL] [Abstract][Full Text] [Related]
9. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia. Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412 [TBL] [Abstract][Full Text] [Related]
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11. [Genetic variation with increased risk of schizophrenia]. Bakker SC; Kahn RS; Ophoff RA Ned Tijdschr Geneeskd; 2010; 154():A1909. PubMed ID: 20977796 [TBL] [Abstract][Full Text] [Related]
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13. Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity. Khan FF; Melton PE; McCarthy NS; Morar B; Blangero J; Moses EK; Jablensky A Schizophr Res; 2018 Jul; 197():337-345. PubMed ID: 29486958 [TBL] [Abstract][Full Text] [Related]
14. Identification of rare copy number variants in high burden schizophrenia families. Van Den Bossche MJ; Strazisar M; Cammaerts S; Liekens AM; Vandeweyer G; Depreeuw V; Mattheijssens M; Lenaerts AS; De Zutter S; De Rijk P; Sabbe B; Del-Favero J Am J Med Genet B Neuropsychiatr Genet; 2013 Apr; 162B(3):273-82. PubMed ID: 23505263 [TBL] [Abstract][Full Text] [Related]
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18. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259 [TBL] [Abstract][Full Text] [Related]
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