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    Results: 1 to 20 of 151

    1.

    Genetic copy number variants in sib pairs both affected with schizophrenia.

    Lee CH, Liu CM, Wen CC, Chang SM, Hwu HG.

    J Biomed Sci. 2010 Jan 11;17:2.

    PMID:
    20064257
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

    Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N; Wellcome Trust Case Control Consortium.

    Arch Gen Psychiatry. 2010 Apr;67(4):318-27.

    PMID:
    20368508
    [PubMed - indexed for MEDLINE]
    Free Article
    3.

    Copy number variation in schizophrenia in the Japanese population.

    Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N.

    Biol Psychiatry. 2010 Feb 1;67(3):283-6. Epub 2009 Oct 31.

    PMID:
    19880096
    [PubMed - indexed for MEDLINE]
    4.

    Final Report on Carcinogens Background Document for Formaldehyde.

    National Toxicology Program.

    Rep Carcinog Backgr Doc. 2010 Jan;(10-5981):i-512.

    PMID:
    20737003
    [PubMed - as supplied by publisher]
    5.

    Strong synaptic transmission impact by copy number variations in schizophrenia.

    Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PM, Flory JH, Imielinski M, Frackelton EC, Chiavacci R, Thomas KA, Garris M, Otieno FG, Davidson M, Weiser M, Reichenberg A, Davis KL, Friedman JI, Cappola TP, Margulies KB, Rader DJ, Grant SF, Buxbaum JD, Gur RE, Hakonarson H.

    Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10584-9. Epub 2010 May 20.

    PMID:
    20489179
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

    Wain LV, Pedroso I, Landers JE, Breen G, Shaw CE, Leigh PN, Brown RH, Tobin MD, Al-Chalabi A.

    PLoS One. 2009 Dec 4;4(12):e8175.

    PMID:
    19997636
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.

    Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti-Hümmer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schäfer H, Warnke A, Reif A, Ropers HH, Ullmann R.

    Mol Psychiatry. 2011 May;16(5):491-503. Epub 2010 Mar 23.

    PMID:
    20308990
    [PubMed - indexed for MEDLINE]
    8.

    Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

    Bae JS, Cheong HS, Park BL, Kim LH, Park TJ, Kim JY, Pasaje CF, Lee JS, Cui T, Inoue I, Shin HD.

    J Hum Genet. 2010 Nov;55(11):726-30. Epub 2010 Aug 12.

    PMID:
    20703242
    [PubMed - indexed for MEDLINE]
    9.

    De novo rates and selection of large copy number variation.

    Itsara A, Wu H, Smith JD, Nickerson DA, Romieu I, London SJ, Eichler EE.

    Genome Res. 2010 Nov;20(11):1469-81. Epub 2010 Sep 14.

    PMID:
    20841430
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    10.

    Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

    Buizer-Voskamp JE, Muntjewerff JW; Genetic Risk and Outcome in Psychosis (GROUP) Consortium Members, Strengman E, Sabatti C, Stefansson H, Vorstman JA, Ophoff RA.

    Biol Psychiatry. 2011 Oct 1;70(7):655-62. Epub 2011 Apr 13.

    PMID:
    21489405
    [PubMed - indexed for MEDLINE]
    11.

    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]
    12.

    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]
    13.

    Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.

    Raychaudhuri S, Korn JM, McCarroll SA; International Schizophrenia Consortium, Altshuler D, Sklar P, Purcell S, Daly MJ.

    PLoS Genet. 2010 Sep 9;6(9). pii: e1001097.

    PMID:
    20838587
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia.

    Maiti S, Kumar KH, Castellani CA, O'Reilly R, Singh SM.

    PLoS One. 2011 Mar 2;6(3):e17125.

    PMID:
    21399695
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

    Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

    BMC Genomics. 2007 Feb 20;8:53.

    PMID:
    17311676
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    16.

    The role of DNA copy number variation in schizophrenia.

    Tam GW, Redon R, Carter NP, Grant SG.

    Biol Psychiatry. 2009 Dec 1;66(11):1005-12. Epub 2009 Sep 12. Review.

    PMID:
    19748074
    [PubMed - indexed for MEDLINE]
    17.

    Failure to confirm CNVs as of aetiological significance in twin pairs discordant for schizophrenia.

    Ono S, Imamura A, Tasaki S, Kurotaki N, Ozawa H, Yoshiura K, Okazaki Y.

    Twin Res Hum Genet. 2010 Oct;13(5):455-60.

    PMID:
    20874467
    [PubMed - indexed for MEDLINE]
    18.

    Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.

    Bae JS, Cheong HS, Chun JY, Park TJ, Kim JO, Kim EM, Park M, Kim DJ, Lee EJ, Kim EK, Lee JY, Shin HD.

    Ophthalmology. 2010 Jul;117(7):1306-12.e4. Epub 2010 Mar 3.

    PMID:
    20202685
    [PubMed - indexed for MEDLINE]
    19.

    A genome wide association study between copy number variation (CNV) and human height in Chinese population.

    Li X, Tan L, Liu X, Lei S, Yang T, Chen X, Zhang F, Fang Y, Guo Y, Zhang L, Yan H, Pan F, Zhang Z, Peng Y, Zhou Q, He L, Zhu X, Cheng J, Zhang L, Liu Y, Tian Q, Deng H.

    J Genet Genomics. 2010 Dec;37(12):779-85.

    PMID:
    21193156
    [PubMed - indexed for MEDLINE]
    20.

    Origins and functional impact of copy number variation in the human genome.

    Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J; Wellcome Trust Case Control Consortium, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME.

    Nature. 2010 Apr 1;464(7289):704-12. Epub 2009 Oct 7.

    PMID:
    19812545
    [PubMed - indexed for MEDLINE]

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