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Journal Abstract Search

120 related items for PubMed ID: 12497606

  • 1. Genetic linkage and association between chromosome 1q and working memory function in schizophrenia.
    Gasperoni TL, Ekelund J, Huttunen M, Palmer CG, Tuulio-Henriksson A, Lönnqvist J, Kaprio J, Peltonen L, Cannon TD.
    Am J Med Genet B Neuropsychiatr Genet; 2003 Jan 01; 116B(1):8-16. PubMed ID: 12497606
    [Abstract] [Full Text] [Related]

  • 2. The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia.
    Cannon TD, Huttunen MO, Lonnqvist J, Tuulio-Henriksson A, Pirkola T, Glahn D, Finkelstein J, Hietanen M, Kaprio J, Koskenvuo M.
    Am J Hum Genet; 2000 Aug 01; 67(2):369-82. PubMed ID: 10880296
    [Abstract] [Full Text] [Related]

  • 3. Spatial working memory as an endophenotype for schizophrenia.
    Glahn DC, Therman S, Manninen M, Huttunen M, Kaprio J, Lönnqvist J, Cannon TD.
    Biol Psychiatry; 2003 Apr 01; 53(7):624-6. PubMed ID: 12679242
    [Abstract] [Full Text] [Related]

  • 4. Genetic overlap between episodic memory deficits and schizophrenia: results from the Maudsley Twin Study.
    Owens SF, Picchioni MM, Rijsdijk FV, Stahl D, Vassos E, Rodger AK, Collier DA, Murray RM, Toulopoulou T.
    Psychol Med; 2011 Mar 01; 41(3):521-32. PubMed ID: 20459888
    [Abstract] [Full Text] [Related]

  • 5. Substantial genetic overlap between neurocognition and schizophrenia: genetic modeling in twin samples.
    Toulopoulou T, Picchioni M, Rijsdijk F, Hua-Hall M, Ettinger U, Sham P, Murray R.
    Arch Gen Psychiatry; 2007 Dec 01; 64(12):1348-55. PubMed ID: 18056542
    [Abstract] [Full Text] [Related]

  • 6. A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.
    Hennah W, Tuulio-Henriksson A, Paunio T, Ekelund J, Varilo T, Partonen T, Cannon TD, Lönnqvist J, Peltonen L.
    Mol Psychiatry; 2005 Dec 01; 10(12):1097-103. PubMed ID: 16103888
    [Abstract] [Full Text] [Related]

  • 7. Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families.
    Wedenoja J, Loukola A, Tuulio-Henriksson A, Paunio T, Ekelund J, Silander K, Varilo T, Heikkilä K, Suvisaari J, Partonen T, Lönnqvist J, Peltonen L.
    Mol Psychiatry; 2008 Jul 01; 13(7):673-84. PubMed ID: 17684500
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory.
    Cannon TD, Hennah W, van Erp TG, Thompson PM, Lonnqvist J, Huttunen M, Gasperoni T, Tuulio-Henriksson A, Pirkola T, Toga AW, Kaprio J, Mazziotta J, Peltonen L.
    Arch Gen Psychiatry; 2005 Nov 08; 62(11):1205-13. PubMed ID: 16275808
    [Abstract] [Full Text] [Related]

  • 10. Heritability of specific cognitive functions and associations with schizophrenia spectrum disorders using CANTAB: a nation-wide twin study.
    Lemvigh CK, Brouwer RM, Pantelis C, Jensen MH, Hilker RW, Legind CS, Anhøj SJ, Robbins TW, Sahakian BJ, Glenthøj BY, Fagerlund B.
    Psychol Med; 2022 Apr 08; 52(6):1101-1114. PubMed ID: 32779562
    [Abstract] [Full Text] [Related]

  • 11. Spatial working memory function in twins with schizophrenia and bipolar disorder.
    Pirkola T, Tuulio-Henriksson A, Glahn D, Kieseppä T, Haukka J, Kaprio J, Lönnqvist J, Cannon TD.
    Biol Psychiatry; 2005 Dec 15; 58(12):930-6. PubMed ID: 16112657
    [Abstract] [Full Text] [Related]

  • 12. Genetic risk of neuropsychological impairment in schizophrenia: a study of monozygotic twins discordant and concordant for the disorder.
    Goldberg TE, Torrey EF, Gold JM, Bigelow LB, Ragland RD, Taylor E, Weinberger DR.
    Schizophr Res; 1995 Sep 15; 17(1):77-84. PubMed ID: 8541253
    [Abstract] [Full Text] [Related]

  • 13. Is there change in intelligence quotient in chronically ill schizophrenia patients? A longitudinal study in twins discordant for schizophrenia.
    Hedman AM, van Haren NE, van Baal GC, Brans RG, Hijman R, Kahn RS, Hulshoff Pol HE.
    Psychol Med; 2012 Dec 15; 42(12):2535-41. PubMed ID: 22717138
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 165(9):1185-92. PubMed ID: 18628350
    [Abstract] [Full Text] [Related]

  • 15. Structural Brain Connectivity as a Genetic Marker for Schizophrenia.
    Bohlken MM, Brouwer RM, Mandl RC, Van den Heuvel MP, Hedman AM, De Hert M, Cahn W, Kahn RS, Hulshoff Pol HE.
    JAMA Psychiatry; 2016 Jan 15; 73(1):11-9. PubMed ID: 26606729
    [Abstract] [Full Text] [Related]

  • 16. Parental representation in twins discordant for schizophrenia.
    Onstad S, Skre I, Torgersen S, Kringlen E.
    Psychol Med; 1993 May 15; 23(2):335-40. PubMed ID: 8332650
    [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 15; 19(4):281-4. PubMed ID: 12170462
    [Abstract] [Full Text] [Related]

  • 18. Genetic and developmental factors in spontaneous selective attention: a study of normal twins.
    Myles-Worsley M, Coon H.
    Psychiatry Res; 1997 Aug 08; 71(3):163-74. PubMed ID: 9271789
    [Abstract] [Full Text] [Related]

  • 19. Chromosome 1 loci in Finnish schizophrenia families.
    Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajärvi R, Partonen T, Suvisaari J, Lönnqvist J, Meyer J, Peltonen L.
    Hum Mol Genet; 2001 Jul 15; 10(15):1611-7. PubMed ID: 11468279
    [Abstract] [Full Text] [Related]

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