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Journal Abstract Search

137 related items for PubMed ID: 20528959

  • 21. 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]

  • 22. Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy.
    Fanous AH, Neale MC, Gardner CO, Webb BT, Straub RE, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Mol Psychiatry; 2007 Oct 08; 12(10):958-65. PubMed ID: 17440434
    [Abstract] [Full Text] [Related]

  • 23. 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 08; 77(6):937-44. PubMed ID: 16380906
    [Abstract] [Full Text] [Related]

  • 24. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.
    Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, Cardno AG.
    Am J Med Genet B Neuropsychiatr Genet; 2011 Dec 08; 156B(8):929-40. PubMed ID: 21960518
    [Abstract] [Full Text] [Related]

  • 25. Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.
    Hong KS, Won HH, Cho EY, Jeun HO, Cho SS, Lee YS, Park DY, Jang YL, Choi KS, Lee D, Kim MJ, Kim S, Han WS, Kim JW.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Jul 05; 150B(5):647-52. PubMed ID: 18980222
    [Abstract] [Full Text] [Related]

  • 26. Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.
    Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajärvi R, Suokas J, Partonen T, Lönnqvist J, Meyer J, Peltonen L.
    Hum Mol Genet; 2001 Dec 15; 10(26):3037-48. PubMed ID: 11751686
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
    Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B.
    Eur J Hum Genet; 2005 Jun 15; 13(6):763-71. PubMed ID: 15812564
    [Abstract] [Full Text] [Related]

  • 29. 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 15; 19(1):55-61. PubMed ID: 11204305
    [Abstract] [Full Text] [Related]

  • 30. A genome-wide scan for modifier loci in schizophrenia.
    Fanous AH, Neale MC, Webb BT, Straub RE, Amdur RL, O'Neill FA, Walsh D, Riley BP, Kendler KS.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jul 05; 144B(5):589-95. PubMed ID: 17262803
    [Abstract] [Full Text] [Related]

  • 31. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
    DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R.
    Am J Psychiatry; 2002 May 05; 159(5):803-12. PubMed ID: 11986135
    [Abstract] [Full Text] [Related]

  • 32. Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.
    Alkelai A, Kohn Y, Olender T, Sarner-Kanyas K, Rigbi A, Hamdan A, Ben-Asher E, Lancet D, Lerer B.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Oct 05; 150B(7):914-25. PubMed ID: 19152384
    [Abstract] [Full Text] [Related]

  • 33. 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 05; 8(5):488-98. PubMed ID: 12808429
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.
    Rommelse NN, Arias-Vásquez A, Altink ME, Buschgens CJ, Fliers E, Asherson P, Faraone SV, Buitelaar JK, Sergeant JA, Oosterlaan J, Franke B.
    Am J Hum Genet; 2008 Jul 05; 83(1):99-105. PubMed ID: 18599010
    [Abstract] [Full Text] [Related]

  • 36. 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 05; 8(5):511-23. PubMed ID: 12808431
    [Abstract] [Full Text] [Related]

  • 37. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
    EPICURE Consortium, Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T.
    Epilepsia; 2012 Feb 05; 53(2):308-18. PubMed ID: 22242659
    [Abstract] [Full Text] [Related]

  • 38. Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families.
    Liu CM, Hwu HG, Lin MW, Ou-Yang WC, Lee SF, Fann CS, Wong SH, Hsieh SH.
    Am J Med Genet; 2001 Dec 08; 105(8):658-61. PubMed ID: 11803511
    [Abstract] [Full Text] [Related]

  • 39. Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study.
    Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA, SAPPHIRe Study Group.
    Am J Hypertens; 2006 Dec 08; 19(12):1270-7. PubMed ID: 17161774
    [Abstract] [Full Text] [Related]

  • 40. 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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