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121 related items for PubMed ID: 24132895

  • 21. [Schizophrenia and/or bipolar disorder: neurobiological endophenotypes].
    Adida M, Azorin JM, Fakra E, Belzeaux R, Kaladjian A, Pomietto P, Corréard N.
    Encephale; 2012 Dec; 38 Suppl 3():S98-102. PubMed ID: 23279996
    [Abstract] [Full Text] [Related]

  • 22. [Neurological soft signs as a candidate for endophenotype of schizophrenia].
    Kałuzyńska O, Rabe-Jabłońska J.
    Psychiatr Pol; 2014 Dec; 48(1):5-18. PubMed ID: 24946431
    [Abstract] [Full Text] [Related]

  • 23. 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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  • 24. Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder.
    Lee IH, Koelliker E, Kong SW.
    Transl Psychiatry; 2022 Sep 24; 12(1):407. PubMed ID: 36153334
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  • 25. 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 24; 8(5):511-23. PubMed ID: 12808431
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  • 26. Consortium on the Genetics of Schizophrenia (COGS) assessment of endophenotypes for schizophrenia: an introduction to this Special Issue of Schizophrenia Research.
    Swerdlow NR, Gur RE, Braff DL.
    Schizophr Res; 2015 Apr 24; 163(1-3):9-16. PubMed ID: 25454799
    [Abstract] [Full Text] [Related]

  • 27. 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
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  • 28. The Maximum-Likelihood-Binomial method revisited: a robust approach for model-free linkage analysis of quantitative traits in large sibships.
    Cobat A, Abel L, Alcaïs A.
    Genet Epidemiol; 2011 Jan 05; 35(1):46-56. PubMed ID: 21181896
    [Abstract] [Full Text] [Related]

  • 29. 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]

  • 30. Increased efficiency of case-control association analysis by using allele-sharing and covariate information.
    Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER.
    Hum Hered; 2008 May 05; 65(3):154-65. PubMed ID: 17934318
    [Abstract] [Full Text] [Related]

  • 31. 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]

  • 32. 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
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  • 36. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
    Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA.
    BMC Genet; 2004 Jul 06; 5():18. PubMed ID: 15238159
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  • 37. Developments in schizophrenia genetics: from linkage to microchips, deletions and duplications.
    Haraldsson HM, Ettinger U, Sigurdsson E.
    Nord J Psychiatry; 2011 Apr 06; 65(2):82-8. PubMed ID: 21271949
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  • 38. The multidimensionality of schizotypy in nonpsychotic relatives of patients with schizophrenia and its applications in ordered subsets linkage analysis of schizophrenia.
    Lien YJ, Tsuang HC, Chiang A, Liu CM, Hsieh MH, Hwang TJ, Liu SK, Hsiao PC, Faraone SV, Tsuang MT, Hwu HG, Chen WJ.
    Am J Med Genet B Neuropsychiatr Genet; 2010 Jan 05; 153B(1):1-9. PubMed ID: 19326390
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  • 40. Prioritizing schizophrenia endophenotypes for future genetic studies: An example using data from the COGS-1 family study.
    Millard SP, Shofer J, Braff D, Calkins M, Cadenhead K, Freedman R, Green MF, Greenwood TA, Gur R, Gur R, Lazzeroni LC, Light GA, Olincy A, Nuechterlein K, Seidman L, Siever L, Silverman J, Stone WS, Sprock J, Sugar CA, Swerdlow NR, Tsuang M, Turetsky B, Radant A, Tsuang DW.
    Schizophr Res; 2016 Jul 05; 174(1-3):1-9. PubMed ID: 27132484
    [Abstract] [Full Text] [Related]

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