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Journal Abstract Search


99 related items for PubMed ID: 17262803

  • 1. A genome-wide scan for modifier loci in schizophrenia.
    Fanous AH, Neale MC, Webb BT, Straub RE, Amdur RL, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jul 05; 144B(5):589-95. PubMed ID: 17262803
    [Abstract] [Full Text] [Related]

  • 2. Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy.
    Fanous AH, Neale MC, Gardner CO, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Mol Psychiatry; 2007 Oct 05; 12(10):958-65. PubMed ID: 17440434
    [Abstract] [Full Text] [Related]

  • 3. Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.
    Ryu S, Won HH, Oh S, Kim JW, Park T, Cho EY, Cho Y, Park DY, Lee YS, Kwon JS, Hong KS.
    Psychiatry Res; 2013 Dec 30; 210(3):756-60. PubMed ID: 24035701
    [Abstract] [Full Text] [Related]

  • 4. Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33.
    Goes FS, Zandi PP, Miao K, McMahon FJ, Steele J, Willour VL, Mackinnon DF, Mondimore FM, Schweizer B, Nurnberger JI, Rice JP, Scheftner W, Coryell W, Berrettini WH, Kelsoe JR, Byerley W, Murphy DL, Gershon ES, Bipolar Disorder Phenome Group, Depaulo JR, McInnis MG, Potash JB.
    Am J Psychiatry; 2007 Feb 30; 164(2):236-47. PubMed ID: 17267786
    [Abstract] [Full Text] [Related]

  • 5. Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia.
    Fanous AH, van den Oord EJ, Riley BP, Aggen SH, Neale MC, O'Neill FA, Walsh D, Kendler KS.
    Am J Psychiatry; 2005 Oct 30; 162(10):1824-32. PubMed ID: 16199828
    [Abstract] [Full Text] [Related]

  • 6. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.
    Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N, Yakir A, Kerem B, Macciardi F.
    Mol Psychiatry; 2003 May 30; 8(5):488-98. PubMed ID: 12808429
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 9(7):695-702. PubMed ID: 20528959
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. A genome-wide scan for schizophrenia and psychosis susceptibility loci in families of Mexican and Central American ancestry.
    Escamilla MA, Ontiveros A, Nicolini H, Raventos H, Mendoza R, Medina R, Munoz R, Levinson D, Peralta JM, Dassori A, Almasy L.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Mar 05; 144B(2):193-9. PubMed ID: 17044102
    [Abstract] [Full Text] [Related]

  • 11. Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.
    Park N, Juo SH, Cheng R, Liu J, Loth JE, Lilliston B, Nee J, Grunn A, Kanyas K, Lerer B, Endicott J, Gilliam TC, Baron M.
    Mol Psychiatry; 2004 Dec 05; 9(12):1091-9. PubMed ID: 15241432
    [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 05; 66(10):1058-67. PubMed ID: 19805696
    [Abstract] [Full Text] [Related]

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  • 14. Clinical phenotype of schizophrenia in a Finnish isolate.
    Arajärvi R, Haukka J, Varilo T, Suokas J, Juvonen H, Suvisaari J, Muhonen M, Suominen K, Tuulio-Henriksson A, Schreck M, Hovatta I, Partonen T, Lönnqvist J.
    Schizophr Res; 2004 Apr 01; 67(2-3):195-205. PubMed ID: 14984878
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. A genome-wide quantitative linkage scan of niacin skin flush response in families with schizophrenia.
    Lien YJ, Huang SS, Liu CM, Hwu HG, Faraone SV, Tsuang MT, Chen WJ.
    Schizophr Bull; 2013 Jan 01; 39(1):68-76. PubMed ID: 21653277
    [Abstract] [Full Text] [Related]

  • 17. Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.
    Straub RE, MacLean CJ, Ma Y, Webb BT, Myakishev MV, Harris-Kerr C, Wormley B, Sadek H, Kadambi B, O'Neill FA, Walsh D, Kendler KS.
    Mol Psychiatry; 2002 Jan 01; 7(6):542-59. PubMed ID: 12140777
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  • 19. Irish study on high-density schizophrenia families: field methods and power to detect linkage.
    Kendler KS, O'Neill FA, Burke J, Murphy B, Duke F, Straub RE, Shinkwin R, Ni Nuallain M, MacLean CJ, Walsh D.
    Am J Med Genet; 1996 Apr 09; 67(2):179-90. PubMed ID: 8723045
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  • 20. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
    Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B.
    Eur J Hum Genet; 2005 Jun 09; 13(6):763-71. PubMed ID: 15812564
    [Abstract] [Full Text] [Related]


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