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210 related items for PubMed ID: 19694819

  • 1. Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.
    Lin SH, Liu CM, Liu YL, Shen-Jang Fann C, Hsiao PC, Wu JY, Hung SI, Chen CH, Wu HM, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG, Chen WJ.
    Genes Brain Behav; 2009 Nov; 8(8):785-94. PubMed ID: 19694819
    [Abstract] [Full Text] [Related]

  • 2. RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
    Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG.
    Biol Psychiatry; 2008 Nov 01; 64(9):789-96. PubMed ID: 18571626
    [Abstract] [Full Text] [Related]

  • 3. Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia.
    Liao SY, Lin SH, Liu CM, Hsieh MH, Hwang TJ, Liu SK, Guo SC, Hwu HG, Chen WJ.
    Genes Brain Behav; 2009 Mar 01; 8(2):228-37. PubMed ID: 19077118
    [Abstract] [Full Text] [Related]

  • 4. Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.
    Hallmayer JF, Kalaydjieva L, Badcock J, Dragovic M, Howell S, Michie PT, Rock D, Vile D, Williams R, Corder EH, Hollingsworth K, Jablensky A.
    Am J Hum Genet; 2005 Sep 01; 77(3):468-76. PubMed ID: 16080121
    [Abstract] [Full Text] [Related]

  • 5. A genome-wide quantitative trait loci scan of neurocognitive performances in families with schizophrenia.
    Lien YJ, Liu CM, Faraone SV, Tsuang MT, Hwu HG, Hsiao PC, Chen WJ.
    Genes Brain Behav; 2010 Oct 01; 9(7):695-702. PubMed ID: 20528959
    [Abstract] [Full Text] [Related]

  • 6. The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up.
    Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, Moskvina V, Fernández G, Gill M, Corvin A, O'Donovan MC, Donohoe G, Owen MJ.
    Am J Psychiatry; 2013 Aug 01; 170(8):877-85. PubMed ID: 23903335
    [Abstract] [Full Text] [Related]

  • 7. A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.
    Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Ouyang WC, Chan HY, Chen JJ, Yang WC, Lin CY, Lee SF, Hwu HG.
    Biol Psychiatry; 2006 Sep 15; 60(6):554-62. PubMed ID: 16997000
    [Abstract] [Full Text] [Related]

  • 8. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis.
    Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N.
    Nat Genet; 1995 Nov 15; 11(3):325-7. PubMed ID: 7581458
    [Abstract] [Full Text] [Related]

  • 9. ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function.
    Liu CM, Fann CS, Chen CY, Liu YL, Oyang YJ, Yang WC, Chang CC, Wen CC, Chen WJ, Hwang TJ, Hsieh MH, Liu CC, Faraone SV, Tsuang MT, Hwu HG.
    Biol Psychiatry; 2011 Jul 01; 70(1):51-8. PubMed ID: 21531385
    [Abstract] [Full Text] [Related]

  • 10. More evidence supports the association of PPP3CC with schizophrenia.
    Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Hung SI, Yu SL, Hwang TJ, Hsieh MH, Liu CC, Tsuang MM, Wu JY, Jou YS, Faraone SV, Tsuang MT, Chen WJ, Hwu HG.
    Mol Psychiatry; 2007 Oct 01; 12(10):966-74. PubMed ID: 17339875
    [Abstract] [Full Text] [Related]

  • 11. Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.
    Schwab SG, Knapp M, Mondabon S, Hallmayer J, Borrmann-Hassenbach M, Albus M, Lerer B, Rietschel M, Trixler M, Maier W, Wildenauer DB.
    Am J Hum Genet; 2003 Jan 01; 72(1):185-90. PubMed ID: 12474144
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 66(10):1058-67. PubMed ID: 19805696
    [Abstract] [Full Text] [Related]

  • 13. RGS4 polymorphisms associated with variability of cognitive performance in a family-based schizophrenia sample.
    Prasad KM, Almasy L, Gur RC, Gur RE, Pogue-Geile M, Chowdari KV, Talkowski ME, Nimgaonkar VL.
    Schizophr Bull; 2010 Sep 01; 36(5):983-90. PubMed ID: 19282471
    [Abstract] [Full Text] [Related]

  • 14. Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia.
    Bakken TE, Bloss CS, Roddey JC, Joyner AH, Rimol LM, Djurovic S, Melle I, Sundet K, Agartz I, Andreassen OA, Dale AM, Schork NJ.
    Arch Gen Psychiatry; 2011 Aug 01; 68(8):781-90. PubMed ID: 21810643
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 34(6):1047-53. PubMed ID: 18628273
    [Abstract] [Full Text] [Related]

  • 16. A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6.
    Schwab SG, Hallmayer J, Albus M, Lerer B, Eckstein GN, Borrmann M, Segman RH, Hanses C, Freymann J, Yakir A, Trixler M, Falkai P, Rietschel M, Maier W, Wildenauer DB.
    Mol Psychiatry; 2000 Nov 01; 5(6):638-49. PubMed ID: 11126394
    [Abstract] [Full Text] [Related]

  • 17. A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes.
    Almasy L, Gur RC, Haack K, Cole SA, Calkins ME, Peralta JM, Hare E, Prasad K, Pogue-Geile MF, Nimgaonkar V, Gur RE.
    Am J Psychiatry; 2008 Sep 01; 165(9):1185-92. PubMed ID: 18628350
    [Abstract] [Full Text] [Related]

  • 18. Neuropsychological deficit in siblings discordant for schizophrenia.
    Saoud M, d'Amato T, Gutknecht C, Triboulet P, Bertaud JP, Marie-Cardine M, Daléry J, Rochet T.
    Schizophr Bull; 2000 Sep 01; 26(4):893-902. PubMed ID: 11087021
    [Abstract] [Full Text] [Related]

  • 19. Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia.
    Hennah W, Varilo T, Paunio T, Peltonen L.
    Ann Med; 2004 Sep 01; 36(5):322-31. PubMed ID: 15478307
    [Abstract] [Full Text] [Related]

  • 20. Family-based clusters of cognitive test performance in familial schizophrenia.
    Hoti F, Tuulio-Henriksson A, Haukka J, Partonen T, Holmström L, Lönnqvist J.
    BMC Psychiatry; 2004 Jul 22; 4():20. PubMed ID: 15271222
    [Abstract] [Full Text] [Related]

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