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dc.contributor.authorGILL, MICHAELen
dc.contributor.authorGALLAGHER, LOUISEen
dc.date.accessioned2015-12-11T12:37:03Z
dc.date.available2015-12-11T12:37:03Z
dc.date.issued2011en
dc.date.submitted2011en
dc.identifier.citationCasey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI Jr, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S, A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder., Human Genetics, 131, 4, 2011, 565-579en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/75289
dc.descriptionPUBLISHEDen
dc.descriptionPMID21996756en
dc.format.extent565-579en
dc.language.isoenen
dc.relation.ispartofseriesHuman Geneticsen
dc.relation.ispartofseries131en
dc.relation.ispartofseries4en
dc.rightsYen
dc.titleA novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.en
dc.typeJournal Articleen
dc.contributor.sponsorNational Institutes of Health (NIH)en
dc.contributor.sponsorIrish Research Council for Science and Engineering Technology (IRCSET)en
dc.contributor.sponsorHealth Research Board (HRB)en
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mgillen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lgallaghen
dc.identifier.rssinternalid76096en
dc.identifier.doihttp://dx.doi.org/10.1007/s00439-011-1094-6en
dc.rights.ecaccessrightsopenAccess
dc.contributor.sponsorGrantNumberHD055751, HD055782, HD055784,en
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDThemeNeuroscienceen


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