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    Results: 1 to 20 of 89

    1.

    Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data.

    Waaijenborg S, Zwinderman AH.

    Algorithms Mol Biol. 2010 Feb 11;5:17.PMID: 20205905 [PubMed]Free PMC ArticleFree textRelated citations

    2.

    Decision forest analysis of 61 single nucleotide polymorphisms in a case-control study of esophageal cancer; a novel method.

    Xie Q, Ratnasinghe LD, Hong H, Perkins R, Tang ZZ, Hu N, Taylor PR, Tong W.

    BMC Bioinformatics. 2005 Jul 15;6 Suppl 2:S4.PMID: 16026601 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    3.

    Associating multiple longitudinal traits with high-dimensional single-nucleotide polymorphism data: application to the Framingham Heart Study.

    Waaijenborg S, Zwinderman AH.

    BMC Proc. 2009 Dec 15;3 Suppl 7:S47.PMID: 20018039 [PubMed - in process]Free PMC ArticleFree textRelated citations

    4.

    Correlating multiple SNPs and multiple disease phenotypes: penalized non-linear canonical correlation analysis.

    Waaijenborg S, Zwinderman AH.

    Bioinformatics. 2009 Nov 1;25(21):2764-71. Epub 2009 Aug 17.PMID: 19689958 [PubMed - indexed for MEDLINE]Related citations

    5.

    [DNA diagnosis in the age of individual made-to-order medications]

    Mashima Y.

    Nippon Ganka Gakkai Zasshi. 2004 Dec;108(12):863-85; discussion 886. Review. Japanese. PMID: 15656090 [PubMed - indexed for MEDLINE]Related citations

    6.

    GLOSSI: a method to assess the association of genetic loci-sets with complex diseases.

    Chai HS, Sicotte H, Bailey KR, Turner ST, Asmann YW, Kocher JP.

    BMC Bioinformatics. 2009 Apr 3;10:102.PMID: 19344520 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    7.

    Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen.

    Adams GT, Snieder H, McKie VC, Clair B, Brambilla D, Adams RJ, Kutlar F, Kutlar A.

    BMC Med Genet. 2003 Jul 18;4:6.PMID: 12871600 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    8.

    Construction of the model for the Genetic Analysis Workshop 14 simulated data: genotype-phenotype relationships, gene interaction, linkage, association, disequilibrium, and ascertainment effects for a complex phenotype.

    Greenberg DA, Zhang J, Shmulewitz D, Strug LJ, Zimmerman R, Singh V, Marathe S.

    BMC Genet. 2005 Dec 30;6 Suppl 1:S3.PMID: 16451639 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    9.

    The adiponectin gene SNP+276G>T associates with early-onset coronary artery disease and with lower levels of adiponectin in younger coronary artery disease patients (age <or=50 years).

    Filippi E, Sentinelli F, Romeo S, Arca M, Berni A, Tiberti C, Verrienti A, Fanelli M, Fallarino M, Sorropago G, Baroni MG.

    J Mol Med. 2005 Sep;83(9):711-9. Epub 2005 May 5.PMID: 15877215 [PubMed - indexed for MEDLINE]Related citations

    10.

    Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs.

    Benusiglio PR, Lesueur F, Luccarini C, McIntosh J, Luben RN, Smith P, Dunning A, Easton DF, Ponder BA, Pharoah PD.

    BMC Cancer. 2005 Jul 19;5:81.PMID: 16029503 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    11.

    [Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers]

    Hengstenberg C, Bröckel U, Holmer S, Mayer B, Fischer M, Baessler A, Erdmann J, Lieb W, Löwel H, Riegger G, Schunkert H.

    Herz. 2002 Nov;27(7):649-61. German. Erratum in: Herz. 2003 May;28(3):266. PMID: 12439636 [PubMed - indexed for MEDLINE]Related citations

    12.

    Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

    Ban HJ, Heo JY, Oh KS, Park KJ.

    BMC Genet. 2010 Apr 23;11:26.PMID: 20416077 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    13.

    A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the multiethnic cohort.

    Lee SA, Haiman CA, Burtt NP, Pooler LC, Cheng I, Kolonel LN, Pike MC, Altshuler D, Hirschhorn JN, Henderson BE, Stram DO.

    BMC Med Genet. 2007 Dec 1;8:72.PMID: 18053149 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    14.

    A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.

    Coon KD, Myers AJ, Craig DW, Webster JA, Pearson JV, Lince DH, Zismann VL, Beach TG, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Walker DG, Ravid R, Heward CB, Rogers J, Papassotiropoulos A, Reiman EM, Hardy J, Stephan DA.

    J Clin Psychiatry. 2007 Apr;68(4):613-8.PMID: 17474819 [PubMed - indexed for MEDLINE]Related citations

    15.

    Exploiting interactions among polymorphisms contributing to complex disease traits with boosted generative modeling.

    Wang LY, Comaniciu D, Fasulo D.

    J Comput Biol. 2006 Dec;13(10):1673-84.PMID: 17238838 [PubMed - indexed for MEDLINE]Related citations

    16.

    Health-related disparities: influence of environmental factors.

    Olden K, White SL.

    Med Clin North Am. 2005 Jul;89(4):721-38. Review.PMID: 15925646 [PubMed - indexed for MEDLINE]Related citations

    17.

    Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions.

    Mechanic LE, Luke BT, Goodman JE, Chanock SJ, Harris CC.

    BMC Bioinformatics. 2008 Mar 6;9:146.PMID: 18325117 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    18.

    Fear of harm, a possible phenotype of pediatric bipolar disorder: a dimensional approach to diagnosis for genotyping psychiatric syndromes.

    Papolos D, Mattis S, Golshan S, Molay F.

    J Affect Disord. 2009 Nov;118(1-3):28-38. Epub 2009 Jul 23.PMID: 19631388 [PubMed - indexed for MEDLINE]Related citations

    19.

    Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population.

    Cheyssac C, Lecoeur C, Dechaume A, Bibi A, Charpentier G, Balkau B, Marre M, Froguel P, Gibson F, Vaxillaire M.

    BMC Med Genet. 2006 May 5;7:44.PMID: 16677372 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    20.

    A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis.

    Kurreeman FA, Padyukov L, Marques RB, Schrodi SJ, Seddighzadeh M, Stoeken-Rijsbergen G, van der Helm-van Mil AH, Allaart CF, Verduyn W, Houwing-Duistermaat J, Alfredsson L, Begovich AB, Klareskog L, Huizinga TW, Toes RE.

    PLoS Med. 2007 Sep;4(9):e278. Erratum in: PLoS Med. 2007 Dec;4(12):e358. PMID: 17880261 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

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