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Journal Abstract Search

114 related items for PubMed ID: 15685625

  • 1. Taiwan schizophrenia linkage study: the field study.
    Hwu HG, Faraone SV, Liu CM, Chen WJ, Liu SK, Shieh MH, Hwang TJ, Tsuang MM, OuYang WC, Chen CY, Chen CC, Lin JJ, Chou FH, Chueh CM, Liu WM, Hall MH, Tsuang MT.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Apr 05; 134B(1):30-6. PubMed ID: 15685625
    [Abstract] [Full Text] [Related]

  • 2. Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective.
    Chen WJ.
    Am J Med Genet B Neuropsychiatr Genet; 2013 Oct 05; 162B(7):636-47. PubMed ID: 24132895
    [Abstract] [Full Text] [Related]

  • 3. 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 05; 9(7):695-702. PubMed ID: 20528959
    [Abstract] [Full Text] [Related]

  • 4. Sustained attention deficits in nonpsychotic relatives of schizophrenic patients: a recurrence risk ratio analysis.
    Chen WJ, Chang CH, Liu SK, Hwang TJ, Hwu HG, Multidimensional Psychopathology Group Research Project.
    Biol Psychiatry; 2004 May 15; 55(10):995-1000. PubMed ID: 15121483
    [Abstract] [Full Text] [Related]

  • 5. Sustained attention deficit and schizotypal personality features in nonpsychotic relatives of schizophrenic patients.
    Chen WJ, Liu SK, Chang CJ, Lien YJ, Chang YH, Hwu HG.
    Am J Psychiatry; 1998 Sep 15; 155(9):1214-20. PubMed ID: 9734545
    [Abstract] [Full Text] [Related]

  • 6. Department of Veterans Affairs Cooperative Studies Program genetic linkage study of schizophrenia: ascertainment methods and sample description.
    Tsuang MT, Faraone SV, Bingham S, Young K, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Pepple J, Johnson J, Baldwin C, Weiss D, Collins J.
    Am J Med Genet; 2000 Jun 12; 96(3):342-7. PubMed ID: 10898912
    [Abstract] [Full Text] [Related]

  • 7. A genome-wide linkage scan for distinct subsets of schizophrenia characterized by age at onset and neurocognitive deficits.
    Lien YJ, Hsiao PC, Liu CM, Faraone SV, Tsuang MT, Hwu HG, Chen WJ.
    PLoS One; 2011 Jun 12; 6(8):e24103. PubMed ID: 21897869
    [Abstract] [Full Text] [Related]

  • 8. Psychosis among "healthy" siblings of schizophrenia patients.
    Arajärvi R, Ukkola J, Haukka J, Suvisaari J, Hintikka J, Partonen T, Lönnqvist J.
    BMC Psychiatry; 2006 Jan 31; 6():6. PubMed ID: 16448569
    [Abstract] [Full Text] [Related]

  • 9. More severe sustained attention deficits in nonpsychotic siblings of multiplex schizophrenia families than in those of simplex ones.
    Tsuang HC, Lin SH, Liu SK, Hsieh MH, Hwang TJ, Liu CM, Hwu HG, Chen WJ.
    Schizophr Res; 2006 Oct 31; 87(1-3):172-80. PubMed ID: 16737801
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. [Wiscosin card sorting task in patients with schizophrenia and thier siblings].
    El Hamaoui Y, Elyazaji M, Yaalaoui S, Rachidi L, Saoud M, d'Amato T, Moussaoui D, Dalery J, Battas O.
    Can J Psychiatry; 2006 Jan 09; 51(1):48-54. PubMed ID: 16491984
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Impaired executive performance in healthy siblings of schizophrenia patients in a population-based study.
    Kuha A, Tuulio-Henriksson A, Eerola M, Perälä J, Suvisaari J, Partonen T, Lönnqvist J.
    Schizophr Res; 2007 May 01; 92(1-3):142-50. PubMed ID: 17344027
    [Abstract] [Full Text] [Related]

  • 14. Positive and negative symptoms in affected sib pairs with schizophrenia: implications for genetic studies in an African Xhosa sample.
    Niehaus DJ, Koen L, Laurent C, Muller J, Deleuze JF, Mallet J, Seller C, Jordaan E, Emsley R.
    Schizophr Res; 2005 Nov 15; 79(2-3):239-49. PubMed ID: 15993564
    [Abstract] [Full Text] [Related]

  • 15. Association of older paternal age with earlier onset among co-affected schizophrenia sib-pairs.
    Wang SH, Liu CM, Hwu HG, Hsiao CK, Chen WJ.
    Psychol Med; 2015 Jul 15; 45(10):2205-13. PubMed ID: 25746410
    [Abstract] [Full Text] [Related]

  • 16. Availability of schizophrenic patients and their families for genetic linkage studies: findings from the Maryland epidemiology sample.
    Pulver AE, Bale SJ.
    Genet Epidemiol; 1989 Jul 15; 6(6):671-80. PubMed ID: 2606340
    [Abstract] [Full Text] [Related]

  • 17. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families.
    Liu CM, Hwu HG, Fann CS, Lin CY, Liu YL, Ou-Yang WC, Lee SF.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Apr 05; 134B(1):79-83. PubMed ID: 15704228
    [Abstract] [Full Text] [Related]

  • 18. Genetically predisposed offspring with schizotypal features: an ultra high-risk group for schizophrenia?
    Diwadkar VA, Montrose DM, Dworakowski D, Sweeney JA, Keshavan MS.
    Prog Neuropsychopharmacol Biol Psychiatry; 2006 Mar 05; 30(2):230-8. PubMed ID: 16318899
    [Abstract] [Full Text] [Related]

  • 19. Relative risk of attention deficits in siblings of patients with schizophrenia.
    Egan MF, Goldberg TE, Gscheidle T, Weirich M, Bigelow LB, Weinberger DR.
    Am J Psychiatry; 2000 Aug 05; 157(8):1309-16. PubMed ID: 10910796
    [Abstract] [Full Text] [Related]

  • 20. [Cannabis and schizophrenia: demographic and clinical correlates].
    Dervaux A, Laqueille X, Bourdel MC, Leborgne MH, Olié JP, Lôo H, Krebs MO.
    Encephale; 2003 Aug 05; 29(1):11-7. PubMed ID: 12640322
    [Abstract] [Full Text] [Related]

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