A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
| dc.contributor.author | GILL, MICHAEL | en |
| dc.contributor.author | GALLAGHER, LOUISE | en |
| dc.date.accessioned | 2015-12-11T12:37:03Z | |
| dc.date.available | 2015-12-11T12:37:03Z | |
| dc.date.issued | 2011 | en |
| dc.date.submitted | 2011 | en |
| dc.identifier.citation | Casey 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, 565-579 | en |
| dc.identifier.other | Y | en |
| dc.description | PUBLISHED | en |
| dc.description | PMID21996756 | en |
| dc.format.extent | 565-579 | en |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | Human Genetics | en |
| dc.relation.ispartofseries | 131 | en |
| dc.relation.ispartofseries | 4 | en |
| dc.rights | Y | en |
| dc.title | A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. | en |
| dc.type | Journal Article | en |
| dc.type.supercollection | scholarly_publications | en |
| dc.type.supercollection | refereed_publications | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/mgill | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/lgallagh | en |
| dc.identifier.rssinternalid | 76096 | en |
| dc.identifier.doi | http://dx.doi.org/10.1007/s00439-011-1094-6 | en |
| dc.rights.ecaccessrights | openAccess | |
| dc.subject.TCDTheme | Genes & Society | en |
| dc.subject.TCDTheme | Neuroscience | en |
| dc.contributor.sponsor | National Institutes of Health (NIH) | en |
| dc.contributor.sponsorGrantNumber | HD055751, HD055782, HD055784, | en |
| dc.contributor.sponsor | Irish Research Council for Science and Engineering Technology (IRCSET) | en |
| dc.contributor.sponsor | Health Research Board (HRB) | en |
| dc.identifier.uri | http://hdl.handle.net/2262/75289 |
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