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281 related items for PubMed ID: 18449910

  • 1. Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.
    IrmansyahDepartment of Psychiatry, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia., Schwab SG, Heriani, Handoko HY, Kusumawardhani A, Widyawati I, Amir N, Nasrun MW, Holmans P, Knapp M, Wildenauer DB.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1245-52. PubMed ID: 18449910
    [Abstract] [Full Text] [Related]

  • 2. Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica.
    DeLisi LE, Mesen A, Rodriguez C, Bertheau A, LaPrade B, Llach M, Riondet S, Razi K, Relja M, Byerley W, Sherrington R.
    Am J Med Genet; 2002 Jul 08; 114(5):497-508. PubMed ID: 12116183
    [Abstract] [Full Text] [Related]

  • 3. Initial genome-wide scan for linkage with schizophrenia in the Japanese Schizophrenia Sib-Pair Linkage Group (JSSLG) families.
    Japanese Schizophrenia Sib-Pair Linkage Group.
    Am J Med Genet B Neuropsychiatr Genet; 2003 Jul 01; 120B(1):22-8. PubMed ID: 12815734
    [Abstract] [Full Text] [Related]

  • 4. Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.
    Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D.
    Am J Hum Genet; 2001 Mar 01; 68(3):661-73. PubMed ID: 11179014
    [Abstract] [Full Text] [Related]

  • 5. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs.
    Williams NM, Rees MI, Holmans P, Norton N, Cardno AG, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Fenton I, McGuffin P, Owen MJ.
    Hum Mol Genet; 1999 Sep 01; 8(9):1729-39. PubMed ID: 10441337
    [Abstract] [Full Text] [Related]

  • 6. Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.
    Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P.
    Am J Hum Genet; 2000 Dec 01; 67(6):1470-80. PubMed ID: 11067779
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 66(10):1058-67. PubMed ID: 19805696
    [Abstract] [Full Text] [Related]

  • 8. A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
    Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.
    Hum Mol Genet; 2001 Nov 15; 10(24):2751-65. PubMed ID: 11734540
    [Abstract] [Full Text] [Related]

  • 9. Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.
    Arinami T, Ohtsuki T, Ishiguro H, Ujike H, Tanaka Y, Morita Y, Mineta M, Takeichi M, Yamada S, Imamura A, Ohara K, Shibuya H, Ohara K, Suzuki Y, Muratake T, Kaneko N, Someya T, Inada T, Yoshikawa T, Toyota T, Yamada K, Kojima T, Takahashi S, Osamu O, Shinkai T, Nakamura M, Fukuzako H, Hashiguchi T, Niwa SI, Ueno T, Tachikawa H, Hori T, Asada T, Nanko S, Kunugi H, Hashimoto R, Ozaki N, Iwata N, Harano M, Arai H, Ohnuma T, Kusumi I, Koyama T, Yoneda H, Fukumaki Y, Shibata H, Kaneko S, Higuchi H, Yasui-Furukori N, Numachi Y, Itokawa M, Okazaki Y, Japanese Schizophrenia Sib-Pair Linkage Group.
    Am J Hum Genet; 2005 Dec 15; 77(6):937-44. PubMed ID: 16380906
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 5(6):638-49. PubMed ID: 11126394
    [Abstract] [Full Text] [Related]

  • 11. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
    Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.
    Am J Med Genet; 2001 Aug 08; 105(6):548-57. PubMed ID: 11496373
    [Abstract] [Full Text] [Related]

  • 12. Identification of susceptibility loci for autoimmune thyroid disease to 5q31-q33 and Hashimoto's thyroiditis to 8q23-q24 by multipoint affected sib-pair linkage analysis in Japanese.
    Sakai K, Shirasawa S, Ishikawa N, Ito K, Tamai H, Kuma K, Akamizu T, Tanimura M, Furugaki K, Yamamoto K, Sasazuki T.
    Hum Mol Genet; 2001 Jun 15; 10(13):1379-86. PubMed ID: 11440990
    [Abstract] [Full Text] [Related]

  • 13. Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis.
    Schwab SG, Eckstein GN, Hallmayer J, Lerer B, Albus M, Borrmann M, Lichtermann D, Ertl MA, Maier W, Wildenauer DB.
    Mol Psychiatry; 1997 Mar 15; 2(2):156-60. PubMed ID: 9106241
    [Abstract] [Full Text] [Related]

  • 14. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.
    Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M, Craddock N.
    Mol Psychiatry; 2005 Sep 15; 10(9):831-41. PubMed ID: 15940300
    [Abstract] [Full Text] [Related]

  • 15. Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.
    Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin ML, Lönnqvist J, Peltonen L.
    Hum Mol Genet; 2000 Apr 12; 9(7):1049-57. PubMed ID: 10767329
    [Abstract] [Full Text] [Related]

  • 16. 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 12; 8(5):488-98. PubMed ID: 12808429
    [Abstract] [Full Text] [Related]

  • 17. A genomewide screen for autism susceptibility loci.
    Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC, Autism Genetic Resource Exchange Consortium.
    Am J Hum Genet; 2001 Aug 12; 69(2):327-40. PubMed ID: 11452361
    [Abstract] [Full Text] [Related]

  • 18. A genomewide linkage study of age at onset in schizophrenia.
    Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ.
    Am J Med Genet; 2001 Jul 08; 105(5):439-45. PubMed ID: 11449396
    [Abstract] [Full Text] [Related]

  • 19. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.
    Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrièze F, Go R, Fallin D, Lovestone S, Hardy J, Goate A, O'Donovan M, Williams J, Owen MJ.
    Hum Mol Genet; 2007 Nov 15; 16(22):2703-12. PubMed ID: 17725986
    [Abstract] [Full Text] [Related]

  • 20. Evidence for the multigenic inheritance of schizophrenia.
    Freedman R, Leonard S, Olincy A, Kaufmann CA, Malaspina D, Cloninger CR, Svrakic D, Faraone SV, Tsuang MT.
    Am J Med Genet; 2001 Dec 08; 105(8):794-800. PubMed ID: 11803533
    [Abstract] [Full Text] [Related]

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