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    Results: 1 to 20 of 104

    1.

    Copy number variations and cancer.

    Shlien A, Malkin D.

    Genome Med. 2009 Jun 16;1(6):62.

    PMID:
    19566914
    [PubMed]
    Free PMC Article
    2.

    Copy number variations and cancer susceptibility.

    Shlien A, Malkin D.

    Curr Opin Oncol. 2010 Jan;22(1):55-63. Review.

    PMID:
    19952747
    [PubMed - indexed for MEDLINE]
    3.

    Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.

    Komura D, Shen F, Ishikawa S, Fitch KR, Chen W, Zhang J, Liu G, Ihara S, Nakamura H, Hurles ME, Lee C, Scherer SW, Jones KW, Shapero MH, Huang J, Aburatani H.

    Genome Res. 2006 Dec;16(12):1575-84. Epub 2006 Nov 22.

    PMID:
    17122084
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    A gender-specific association of CNV at 6p21.3 with NPC susceptibility.

    Tse KP, Su WH, Yang ML, Cheng HY, Tsang NM, Chang KP, Hao SP, Yao Shugart Y, Chang YS.

    Hum Mol Genet. 2011 Jul 15;20(14):2889-96. Epub 2011 May 2.

    PMID:
    21536588
    [PubMed - indexed for MEDLINE]
    5.

    Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.

    Estivill X, Armengol L.

    PLoS Genet. 2007 Oct;3(10):1787-99.

    PMID:
    17953491
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.

    Shlien A, Tabori U, Marshall CR, Pienkowska M, Feuk L, Novokmet A, Nanda S, Druker H, Scherer SW, Malkin D.

    Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11264-9. Epub 2008 Aug 6.

    PMID:
    18685109
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    SNP and gene networks construction and analysis from classification of copy number variations data.

    Liu Y, Lee YF, Ng MK.

    BMC Bioinformatics. 2011;12 Suppl 5:S4. Epub 2011 Jul 27.

    PMID:
    21989070
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencing.

    Arlt MF, Ozdemir AC, Birkeland SR, Lyons RH Jr, Glover TW, Wilson TE.

    Genetics. 2011 Mar;187(3):675-83. Epub 2011 Jan 6.

    PMID:
    21212237
    [PubMed - indexed for MEDLINE]
    Free Article
    9.

    CONAN: copy number variation analysis software for genome-wide association studies.

    Forer L, Schönherr S, Weissensteiner H, Haider F, Kluckner T, Gieger C, Wichmann HE, Specht G, Kronenberg F, Kloss-Brandstätter A.

    BMC Bioinformatics. 2010 Jun 14;11:318.

    PMID:
    20546565
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    10.

    Implications of gene copy-number variation in health and diseases.

    Almal SH, Padh H.

    J Hum Genet. 2012 Jan;57(1):6-13. doi: 10.1038/jhg.2011.108. Epub 2011 Sep 29.

    PMID:
    21956041
    [PubMed - in process]
    11.

    Copy number polymorphisms and anticancer pharmacogenomics.

    Gamazon ER, Huang RS, Dolan ME, Cox NJ.

    Genome Biol. 2011;12(5):R46. Epub 2011 May 25.

    PMID:
    21609475
    [PubMed - in process]
    Free PMC Article
    12.

    Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity.

    Waszak SM, Hasin Y, Zichner T, Olender T, Keydar I, Khen M, Stütz AM, Schlattl A, Lancet D, Korbel JO.

    PLoS Comput Biol. 2010 Nov 11;6(11):e1000988.

    PMID:
    21085617
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.

    Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, Franke L, Burbach JP, Wokke JH, Ophoff RA, van den Berg LH.

    Lancet Neurol. 2008 Apr;7(4):319-26. Epub 2008 Mar 3.

    PMID:
    18313986
    [PubMed - indexed for MEDLINE]
    14.

    Copy number alterations and copy number variation in cancer: close encounters of the bad kind.

    Speleman F, Kumps C, Buysse K, Poppe B, Menten B, De Preter K.

    Cytogenet Genome Res. 2008;123(1-4):176-82. Epub 2009 Mar 11. Review.

    PMID:
    19287153
    [PubMed - indexed for MEDLINE]
    15.

    Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

    Bassett AS, Scherer SW, Brzustowicz LM.

    Am J Psychiatry. 2010 Aug;167(8):899-914. Epub 2010 May 3. Review.

    PMID:
    20439386
    [PubMed - indexed for MEDLINE]
    16.

    Structural variation in the human genome and its role in disease.

    Stankiewicz P, Lupski JR.

    Annu Rev Med. 2010;61:437-55. Review.

    PMID:
    20059347
    [PubMed - indexed for MEDLINE]
    17.

    A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.

    Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS.

    Genomics. 2009 Oct;94(4):241-6. Epub 2009 Jun 25.

    PMID:
    19559783
    [PubMed - indexed for MEDLINE]
    18.

    Structural genomic variation in ischemic stroke.

    Matarin M, Simon-Sanchez J, Fung HC, Scholz S, Gibbs JR, Hernandez DG, Crews C, Britton A, De Vrieze FW, Brott TG, Brown RD Jr, Worrall BB, Silliman S, Case LD, Hardy JA, Rich SS, Meschia JF, Singleton AB.

    Neurogenetics. 2008 May;9(2):101-8. Epub 2008 Feb 21.

    PMID:
    18288507
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    19.

    A genome-wide investigation of SNPs and CNVs in schizophrenia.

    Need AC, Ge D, Weale ME, Maia J, Feng S, Heinzen EL, Shianna KV, Yoon W, Kasperaviciūte D, Gennarelli M, Strittmatter WJ, Bonvicini C, Rossi G, Jayathilake K, Cola PA, McEvoy JP, Keefe RS, Fisher EM, St Jean PL, Giegling I, Hartmann AM, Möller HJ, Ruppert A, Fraser G, Crombie C, Middleton LT, St Clair D, Roses AD, Muglia P, Francks C, Rujescu D, Meltzer HY, Goldstein DB.

    PLoS Genet. 2009 Feb;5(2):e1000373. Epub 2009 Feb 6. Erratum in: PLoS Genet. 2009 Mar;5(3). doi: 10.1371/annotation/e0196ebb-de40-453f-8f8c-791b126618da.

    PMID:
    19197363
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    20.

    Copy number variation.

    Wain LV, Tobin MD.

    Methods Mol Biol. 2011;713:167-83.

    PMID:
    21153619
    [PubMed - indexed for MEDLINE]

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