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PUBMED FOR HANDHELDS

Journal Abstract Search


281 related items for PubMed ID: 18628273

  • 1. The genetics of symptom-based phenotypes: toward a molecular classification of schizophrenia.
    DeRosse P, Lencz T, Burdick KE, Siris SG, Kane JM, Malhotra AK.
    Schizophr Bull; 2008 Nov; 34(6):1047-53. PubMed ID: 18628273
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  • 2. Disrupted in schizophrenia 1 genotype and positive symptoms in schizophrenia.
    DeRosse P, Hodgkinson CA, Lencz T, Burdick KE, Kane JM, Goldman D, Malhotra AK.
    Biol Psychiatry; 2007 May 15; 61(10):1208-10. PubMed ID: 17054920
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  • 3. Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness.
    Bigdeli TB, Maher BS, Zhao Z, Oord EJ, Thiselton DL, Sun J, Webb BT, Amdur RL, Wormley B, O'Neill FA, Walsh D, Riley BP, Kendler KS, Fanous AH.
    PLoS One; 2011 May 15; 6(12):e21440. PubMed ID: 22220189
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  • 4. Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.
    Kim JW, Lee YS, Cho EY, Jang YL, Park DY, Choi KS, Jeun HO, Cho SH, Jang SY, Hong KS.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):281-6. PubMed ID: 16526041
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  • 5. A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE).
    Djurovic S, Kähler AK, Kulle B, Jönsson EG, Agartz I, Le Hellard S, Hall H, Jakobsen KD, Hansen T, Melle I, Werge T, Steen VM, Andreassen OA.
    Schizophr Res; 2009 Feb 05; 107(2-3):242-8. PubMed ID: 19022628
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  • 8. AKT1 is associated with schizophrenia across multiple symptom dimensions in the Irish study of high density schizophrenia families.
    Thiselton DL, Vladimirov VI, Kuo PH, McClay J, Wormley B, Fanous A, O'Neill FA, Walsh D, Van den Oord EJ, Kendler KS, Riley BP.
    Biol Psychiatry; 2008 Mar 01; 63(5):449-57. PubMed ID: 17825267
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  • 9. Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.
    Chen J, Calhoun VD, Lin D, Perrone-Bizzozero NI, Bustillo JR, Pearlson GD, Potkin SG, van Erp TGM, Macciardi F, Ehrlich S, Ho BC, Sponheim SR, Wang L, Stephen JM, Mayer AR, Hanlon FM, Jung RE, Clementz BA, Keshavan MS, Gershon ES, Sweeney JA, Tamminga CA, Andreassen OA, Agartz I, Westlye LT, Sui J, Du Y, Turner JA, Liu J.
    Schizophr Bull; 2019 Jan 01; 45(1):222-232. PubMed ID: 29474680
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  • 10. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
    Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ.
    Mol Psychiatry; 2010 Nov 01; 15(11):1101-11. PubMed ID: 19786960
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  • 11. Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.
    Fanous AH, Neale MC, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Biol Psychiatry; 2008 Jul 15; 64(2):121-7. PubMed ID: 18255048
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  • 12. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.
    Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, Cardno AG.
    Am J Med Genet B Neuropsychiatr Genet; 2011 Dec 15; 156B(8):929-40. PubMed ID: 21960518
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  • 13. Genome scan of three quantitative traits in schizophrenia pedigrees.
    Wilcox MA, Faraone SV, Su J, Van Eerdewegh P, Tsuang MT.
    Biol Psychiatry; 2002 Nov 01; 52(9):847-54. PubMed ID: 12399137
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  • 15. Evidence for the multigenic inheritance of schizophrenia.
    Freedman R, Leonard S, Olincy A, Kaufmann CA, Malaspina D, Cloninger CR, Svrakic D, Faraone SV, Tsuang MT.
    Am J Med Genet; 2001 Dec 08; 105(8):794-800. PubMed ID: 11803533
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  • 16. Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia.
    Wassink TH, Epping EA, Rudd D, Axelsen M, Ziebell S, Fleming FW, Monson E, Ho BC, Andreasen NC.
    Arch Gen Psychiatry; 2012 Sep 08; 69(9):885-92. PubMed ID: 22945618
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  • 17. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG, McLean DE, Nyholt DR, Mowry BJ.
    Arch Gen Psychiatry; 2009 Oct 08; 66(10):1058-67. PubMed ID: 19805696
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