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Journal Abstract Search

153 related items for PubMed ID: 15704228

  • 1. 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
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  • 3. Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.
    Kim JW, Lee YS, Cho EY, Jang YL, Park DY, Choi KS, Jeun HO, Cho SH, Jang SY, Hong KS.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):281-6. PubMed ID: 16526041
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  • 7. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia.
    Gurling HM, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, Curtis D, Blackwood D, Muir W, Malhotra AK, Buchanan RW, Good CD, Frackowiak RS, Dolan RJ.
    Arch Gen Psychiatry; 2006 Aug 05; 63(8):844-54. PubMed ID: 16894060
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  • 8. Support for involvement of neuregulin 1 in schizophrenia pathophysiology.
    Petryshen TL, Middleton FA, Kirby A, Aldinger KA, Purcell S, Tahl AR, Morley CP, McGann L, Gentile KL, Rockwell GN, Medeiros HM, Carvalho C, Macedo A, Dourado A, Valente J, Ferreira CP, Patterson NJ, Azevedo MH, Daly MJ, Pato CN, Pato MT, Sklar P.
    Mol Psychiatry; 2005 Apr 05; 10(4):366-74, 328. PubMed ID: 15545978
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  • 9. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.
    Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Papadimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Housman DE, Kazazian HH, Antonarakis S, Pulver AE.
    Nat Genet; 1998 Sep 05; 20(1):70-3. PubMed ID: 9731535
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  • 16. No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).
    Thiselton DL, Webb BT, Neale BM, Ribble RC, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Mol Psychiatry; 2004 Aug 05; 9(8):777-83; image 729. PubMed ID: 15197397
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  • 17. 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
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  • 18. Support for schizophrenia susceptibility locus on chromosome 2q detected in a Swedish isolate using a dense map of microsatellites and SNPs.
    Aberg K, Axelsson E, Saetre P, Jiang L, Wetterberg L, Pettersson U, Lindholm E, Jazin E.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1238-44. PubMed ID: 18449909
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  • 19. Neuregulin-1 haplotype HAP(ICE) is associated with lower hippocampal volumes in schizophrenic patients and in non-affected family members.
    Gruber O, Falkai P, Schneider-Axmann T, Schwab SG, Wagner M, Maier W.
    J Psychiatr Res; 2008 Nov 05; 43(1):1-6. PubMed ID: 18291420
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  • 20. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13 in Caucasian but not Oriental populations.
    Lin MW, Sham P, Hwu HG, Collier D, Murray R, Powell JF.
    Hum Genet; 1997 Mar 05; 99(3):417-20. PubMed ID: 9050933
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