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Journal Abstract Search


174 related items for PubMed ID: 12815734

  • 1. 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]

  • 2. 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]

  • 3. 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 05; 77(6):937-44. PubMed ID: 16380906
    [Abstract] [Full Text] [Related]

  • 4. 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 05; 8(9):1729-39. PubMed ID: 10441337
    [Abstract] [Full Text] [Related]

  • 5. 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 05; 5(6):638-49. PubMed ID: 11126394
    [Abstract] [Full Text] [Related]

  • 6. Two-stage genome-wide linkage scan in keratoconus sib pair families.
    Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, Yang H.
    Invest Ophthalmol Vis Sci; 2006 Sep 05; 47(9):3791-5. PubMed ID: 16936089
    [Abstract] [Full Text] [Related]

  • 7. High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12.
    Duerr RH, Barmada MM, Zhang L, Pfützer R, Weeks DE.
    Am J Hum Genet; 2000 Jun 05; 66(6):1857-62. PubMed ID: 10747815
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.
    Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, Vanden Eng JL, Boehnke M, Tsuang MT, Schellenberg GD.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Nov 05; 139B(1):91-100. PubMed ID: 16152571
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Linkage of hypertension to chromosome 2q14-q23 in Chinese families.
    Zhu DL, Wang HY, Xiong MM, He X, Chu SL, Jin L, Wang GL, Yuan WT, Zhao GS, Boerwinkle E, Huang W.
    J Hypertens; 2001 Jan 05; 19(1):55-61. PubMed ID: 11204305
    [Abstract] [Full Text] [Related]

  • 12. Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.
    Faraone SV, Hwu HG, Liu CM, Chen WJ, Tsuang MM, Liu SK, Shieh MH, Hwang TJ, Ou-Yang WC, Chen CY, Chen CC, Lin JJ, Chou FH, Chueh CM, Liu WM, Hall MH, Su J, Van Eerdewegh P, Tsuang MT.
    Am J Psychiatry; 2006 Oct 05; 163(10):1760-6. PubMed ID: 17012687
    [Abstract] [Full Text] [Related]

  • 13. Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p.
    Mori Y, Otabe S, Dina C, Yasuda K, Populaire C, Lecoeur C, Vatin V, Durand E, Hara K, Okada T, Tobe K, Boutin P, Kadowaki T, Froguel P.
    Diabetes; 2002 Apr 05; 51(4):1247-55. PubMed ID: 11916952
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.
    Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Hardy J, De Michele G, Bonifati V, Oostra B, Gasser T, Wood NW, Dürr A, French Parkinson's Disease Genetics Study Group, European Consortium on Genetic Susceptibility in Parkinson's Disease.
    J Med Genet; 2004 Dec 08; 41(12):900-7. PubMed ID: 15591275
    [Abstract] [Full Text] [Related]

  • 16. A genome wide scan for early onset primary hypertension in Scandinavians.
    von Wowern F, Bengtsson K, Lindgren CM, Orho-Melander M, Fyhrquist F, Lindblad U, Råstam L, Forsblom C, Kanninen T, Almgren P, Burri P, Katzman P, Groop L, Hulthén UL, Melander O.
    Hum Mol Genet; 2003 Aug 15; 12(16):2077-81. PubMed ID: 12913078
    [Abstract] [Full Text] [Related]

  • 17. NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees.
    Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto CT, Schmitt K, Matise TC, Harkavy Friedman JM, Hampe C, Lee H, Shore D, Wynne D, Faraone SV, Tsuang MT, Cloninger CR.
    Am J Med Genet; 1998 Jul 10; 81(4):282-9. PubMed ID: 9674972
    [Abstract] [Full Text] [Related]

  • 18. 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 10; 8(5):488-98. PubMed ID: 12808429
    [Abstract] [Full Text] [Related]

  • 19. Genome-wide search for strabismus susceptibility loci.
    Fujiwara H, Matsuo T, Sato M, Yamane T, Kitada M, Hasebe S, Ohtsuki H.
    Acta Med Okayama; 2003 Jun 10; 57(3):109-16. PubMed ID: 12908008
    [Abstract] [Full Text] [Related]

  • 20. 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]


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