These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 18628350

  • 1. 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; 165(9):1185-92. PubMed ID: 18628350
    [Abstract] [Full Text] [Related]

  • 2. Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia.
    Gur RE, Nimgaonkar VL, Almasy L, Calkins ME, Ragland JD, Pogue-Geile MF, Kanes S, Blangero J, Gur RC.
    Am J Psychiatry; 2007 May; 164(5):813-9. PubMed ID: 17475741
    [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; 9(7):695-702. PubMed ID: 20528959
    [Abstract] [Full Text] [Related]

  • 4. 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; 36(5):983-90. PubMed ID: 19282471
    [Abstract] [Full Text] [Related]

  • 5. Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients.
    Calkins ME, Tepper P, Gur RC, Ragland JD, Klei L, Wiener HW, Richard J, Savage RM, Allen TB, O'Jile J, Devlin B, Kwentus J, Aliyu MH, Bradford LD, Edwards N, Lyons PD, Nimgaonkar VL, Santos AB, Go RC, Gur RE.
    Am J Psychiatry; 2010 Apr; 167(4):459-72. PubMed ID: 20194479
    [Abstract] [Full Text] [Related]

  • 6. Identification of Genetic Loci Jointly Influencing Schizophrenia Risk and the Cognitive Traits of Verbal-Numerical Reasoning, Reaction Time, and General Cognitive Function.
    Smeland OB, Frei O, Kauppi K, Hill WD, Li W, Wang Y, Krull F, Bettella F, Eriksen JA, Witoelar A, Davies G, Fan CC, Thompson WK, Lam M, Lencz T, Chen CH, Ueland T, Jönsson EG, Djurovic S, Deary IJ, Dale AM, Andreassen OA, NeuroCHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) Cognitive Working Group.
    JAMA Psychiatry; 2017 Oct 01; 74(10):1065-1075. PubMed ID: 28746715
    [Abstract] [Full Text] [Related]

  • 7. Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis.
    Goldenberg PC, Calkins ME, Richard J, McDonald-McGinn D, Zackai E, Mitra N, Emanuel B, Devoto M, Borgmann-Winter K, Kohler C, Conroy CG, Gur RC, Gur RE.
    Am J Med Genet B Neuropsychiatr Genet; 2012 Jan 01; 159B(1):87-93. PubMed ID: 22170773
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Linkage analysis of candidate regions using a composite neurocognitive phenotype correlated with schizophrenia.
    Hallmayer JF, Jablensky A, Michie P, Woodbury M, Salmon B, Combrinck J, Wichmann H, Rock D, D'Ercole M, Howell S, Dragović M, Kent A.
    Mol Psychiatry; 2003 May 30; 8(5):511-23. PubMed ID: 12808431
    [Abstract] [Full Text] [Related]

  • 10. Heritability of neurocognitive traits in familial schizophrenia.
    Husted JA, Lim S, Chow EW, Greenwood C, Bassett AS.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Sep 05; 150B(6):845-53. PubMed ID: 19180565
    [Abstract] [Full Text] [Related]

  • 11. Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.
    Kos MZ, Carless MA, Peralta J, Blackburn A, Almeida M, Roalf D, Pogue-Geile MF, Prasad K, Gur RC, Nimgaonkar V, Curran JE, Duggirala R, Glahn DC, Blangero J, Gur RE, Almasy L.
    Schizophr Bull; 2016 Mar 05; 42(2):288-300. PubMed ID: 26405221
    [Abstract] [Full Text] [Related]

  • 12. 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 05; 8(8):785-94. PubMed ID: 19694819
    [Abstract] [Full Text] [Related]

  • 13. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.
    SLI Consortium (SLIC).
    Am J Hum Genet; 2004 Jun 05; 74(6):1225-38. PubMed ID: 15133743
    [Abstract] [Full Text] [Related]

  • 14. Neurocognitive performance stability in a multiplex multigenerational study of schizophrenia.
    Roalf DR, Gur RC, Almasy L, Richard J, Gallagher RS, Prasad K, Wood J, Pogue-Geile MF, Nimgaonkar VL, Gur RE.
    Schizophr Bull; 2013 Sep 05; 39(5):1008-17. PubMed ID: 22927671
    [Abstract] [Full Text] [Related]

  • 15. Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.
    Tuulio-Henriksson A, Haukka J, Partonen T, Varilo T, Paunio T, Ekelund J, Cannon TD, Meyer JM, Lönnqvist J.
    Am J Med Genet; 2002 Jul 08; 114(5):483-90. PubMed ID: 12116181
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. [A linkage analysis of quantitative trait loci for familial schizophrenia on chromosome 1].
    Cai G, Wu X, Li T, Collier DA, Liu X, Feng B, Deng H, Tong D, Li J, Ou J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug 08; 19(4):281-4. PubMed ID: 12170462
    [Abstract] [Full Text] [Related]

  • 18. Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational families.
    Glahn DC, Almasy L, Barguil M, Hare E, Peralta JM, Kent JW, Dassori A, Contreras J, Pacheco A, Lanzagorta N, Nicolini H, Raventós H, Escamilla MA.
    Arch Gen Psychiatry; 2010 Feb 08; 67(2):168-77. PubMed ID: 20124116
    [Abstract] [Full Text] [Related]

  • 19. Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.
    Greenwood TA, Swerdlow NR, Gur RE, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RC, Lazzeroni LC, Nuechterlein KH, Olincy A, Radant AD, Ray A, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Light GA, Braff DL.
    Am J Psychiatry; 2013 May 08; 170(5):521-32. PubMed ID: 23511790
    [Abstract] [Full Text] [Related]

  • 20. 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 08; 77(3):468-76. PubMed ID: 16080121
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.