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PUBMED FOR HANDHELDS

Journal Abstract Search


212 related items for PubMed ID: 21795503

  • 21. Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.
    Lin SH, Liu CM, Liu YL, Shen-Jang Fann C, Hsiao PC, Wu JY, Hung SI, Chen CH, Wu HM, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG, Chen WJ.
    Genes Brain Behav; 2009 Nov; 8(8):785-94. PubMed ID: 19694819
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  • 22. Transmission disequilibrium and haplotype analyses of the G72/G30 locus: suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel.
    Korostishevsky M, Kremer I, Kaganovich M, Cholostoy A, Murad I, Muhaheed M, Bannoura I, Rietschel M, Dobrusin M, Bening-Abu-Shach U, Belmaker RH, Maier W, Ebstein RP, Navon R.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jan 05; 141B(1):91-5. PubMed ID: 16082701
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  • 23. Whole-genome association studies of alcoholism with loci linked to schizophrenia susceptibility.
    Namkung J, Kim Y, Park T.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S9. PubMed ID: 16451705
    [Abstract] [Full Text] [Related]

  • 24. Genome scan study of prostate cancer in Arabs: identification of three genomic regions with multiple prostate cancer susceptibility loci in Tunisians.
    Shan J, Al-Rumaihi K, Rabah D, Al-Bozom I, Kizhakayil D, Farhat K, Al-Said S, Kfoury H, Dsouza SP, Rowe J, Khalak HG, Jafri S, Aigha II, Chouchane L.
    J Transl Med; 2013 May 13; 11():121. PubMed ID: 23668334
    [Abstract] [Full Text] [Related]

  • 25. SNP-based pathway enrichment analysis for genome-wide association studies.
    Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.
    BMC Bioinformatics; 2011 Apr 15; 12():99. PubMed ID: 21496265
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  • 27. Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.
    Casselbrant ML, Mandel EM, Jung J, Ferrell RE, Tekely K, Szatkiewicz JP, Ray A, Weeks DE.
    BMC Med Genet; 2009 Sep 03; 10():85. PubMed ID: 19728873
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  • 31. A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE).
    Alblooshi H, Al Safar H, Fisher HF, Cordell HJ, El Kashef A, Al Ghaferi H, Shawky M, Reece S, Hulse GK, Tay GK.
    Am J Med Genet B Neuropsychiatr Genet; 2019 Jan 03; 180(1):68-79. PubMed ID: 30556296
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  • 33. Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.
    Yue WH, Wang HF, Sun LD, Tang FL, Liu ZH, Zhang HX, Li WQ, Zhang YL, Zhang Y, Ma CC, Du B, Wang LF, Ren YQ, Yang YF, Hu XF, Wang Y, Deng W, Tan LW, Tan YL, Chen Q, Xu GM, Yang GG, Zuo XB, Yan H, Ruan YY, Lu TL, Han X, Ma XH, Wang Y, Cai LW, Jin C, Zhang HY, Yan J, Mi WF, Yin XY, Ma WB, Liu Q, Kang L, Sun W, Pan CY, Shuang M, Yang FD, Wang CY, Yang JL, Li KQ, Ma X, Li LJ, Yu X, Li QZ, Huang X, Lv LX, Li T, Zhao GP, Huang W, Zhang XJ, Zhang D.
    Nat Genet; 2011 Oct 30; 43(12):1228-31. PubMed ID: 22037552
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  • 34. 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 30; 53(2):308-18. PubMed ID: 22242659
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  • 36. A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.
    Al Safar HS, Cordell HJ, Jafer O, Anderson D, Jamieson SE, Fakiola M, Khazanehdari K, Tay GK, Blackwell JM.
    Ann Hum Genet; 2013 Nov 30; 77(6):488-503. PubMed ID: 23937595
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  • 37. Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.
    Kondo K, Ikeda M, Kajio Y, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, Iwata N.
    PLoS One; 2013 Nov 30; 8(8):e70964. PubMed ID: 23967141
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  • 38. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
    Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl PO, Gillanders EM, Agnarsson BA, Jönsson G, Pylkäs K, Mustonen A, Heikkinen T, Aittomäki K, Blomqvist C, Melin B, Johannsson OT, Møller P, Winqvist R, Nevanlinna H, Borg A, Barkardottir RB.
    Breast Cancer Res; 2010 Nov 30; 12(4):R50. PubMed ID: 20637093
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  • 39. Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.
    Gonzalez S, Gupta J, Villa E, Mallawaarachchi I, Rodriguez M, Ramirez M, Zavala J, Armas R, Dassori A, Contreras J, Flores D, Jerez A, Ontiveros A, Nicolini H, Escamilla M.
    Bipolar Disord; 2016 Sep 30; 18(6):520-527. PubMed ID: 27759212
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  • 40. Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain.
    Ivorra JL, Rivero O, Costas J, Iniesta R, Arrojo M, Ramos-Ríos R, Carracedo A, Palomo T, Rodriguez-Jimenez R, Cervilla J, Gutiérrez B, Molina E, Arango C, Alvarez M, Pascual JC, Pérez V, Saiz PA, García-Portilla MP, Bobes J, González-Pinto A, Zorrilla I, Haro JM, Bernardo M, Baca-García E, González JC, Hoenicka J, Moltó MD, Sanjuán J.
    Schizophr Res; 2014 Oct 30; 159(1):107-13. PubMed ID: 25124521
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