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dc.contributor.authorZhou, Kaixin-
dc.contributor.authorDempfle, Astrid-
dc.contributor.authorArcos Burgos, Oscar Mauricio-
dc.contributor.authorBakker, Steven-
dc.contributor.authorBanaschewski, Tobias-
dc.contributor.authorBiederman, Joseph-
dc.contributor.authorBuitelaar, Jan-
dc.contributor.authorCastellanos, Francisco Xavier-
dc.contributor.authorDoyle, Alysa-
dc.contributor.authorEbstein, Richard-
dc.contributor.authorEkholm, Jenny-
dc.contributor.authorForabosco, Paola-
dc.contributor.authorFranke, Barbara-
dc.contributor.authorFreitag, Christine-
dc.contributor.authorFriedel, Susann-
dc.contributor.authorGill, Michael-
dc.contributor.authorHebebrand, Johannes-
dc.contributor.authorHinney, Anke-
dc.contributor.authorJacob, Christian-
dc.contributor.authorLesch, Klaus Peter-
dc.contributor.authorLoo, Sandra-
dc.contributor.authorLopera Restrepo, Francisco Javier-
dc.contributor.authorMcCracken, James-
dc.contributor.authorMcGough, James-
dc.contributor.authorMeyer, Jobst-
dc.contributor.authorMick, Eric-
dc.contributor.authorMiranda Casas, Ana-
dc.contributor.authorMuenke, Maximilian-
dc.contributor.authorMulas Delgado, Fernando-
dc.contributor.authorNelson, Stanley F.-
dc.contributor.authorNguyen, Trang-
dc.contributor.authorOades, Robert-
dc.contributor.authorOgdie, Matthew-
dc.contributor.authorPalacio Ortiz, Juan David-
dc.contributor.authorPineda Álvarez, Daniel-
dc.contributor.authorReif, Andreas-
dc.contributor.authorRenner, Tobias-
dc.contributor.authorRoeyers, Herbert-
dc.contributor.authorRomanos, Marcel-
dc.contributor.authorRothenberger, Aribert-
dc.contributor.authorSchäfer, Helmut-
dc.contributor.authorSergeant, Joseph-
dc.contributor.authorSinke, Richard-
dc.contributor.authorSmalley, Susan-
dc.contributor.authorSonugac Barke, Edmund-
dc.contributor.authorSteinhausen, Hans Christoph-
dc.contributor.authorVan der Meulen, Emma-
dc.contributor.authorWalitza, Susanne-
dc.contributor.authorWarnke, Andreas-
dc.contributor.authorLewis, Cathryn-
dc.contributor.authorFaraone, Stephen-
dc.contributor.authorAsherson, Philip-
dc.date.accessioned2022-03-21T15:47:41Z-
dc.date.available2022-03-21T15:47:41Z-
dc.date.issued2008-
dc.identifier.citationZhou, K., Dempfle, A., Arcos, M., Bakker, S., Banaschewski, T., Biederman, J., Buitelaar, J., Castellanos, F. X., Doyle, A., Ebstein, R. P., Ekholm, J., Forabosco, P., Franke, B., Freitag, C., Friedel, S., Gill, M., Hebebrand, J., Hinney, A., Jacob, C., Lesch, K. P., … Asherson, P. (2008). Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 147B(8), 1392–1398. https://doi.org/10.1002/ajmg.b.30878spa
dc.identifier.issn1552-4841-
dc.identifier.urihttp://hdl.handle.net/10495/26760-
dc.description.abstractABSTRACT: Genetic contribution to the development of attention deficit hyperactivity disorder (ADHD) is well established. Seven independent genome-widelinkage scans have been performed to map loci that increase the risk for ADHD. Although sig-nificant linkage signals were identified in some ofthe studies, there has been limited replications between the various independent datasets. The current study gathered the results from all sevenof the ADHD linkage scans and performed a Genome Scan Meta Analysis (GSMA) to identify the genomic region with most consistent linkage evidence across the studies. Genome-wide signifi-cant linkage (PSR¼0.00034,POR¼0.04) was identi-fied on chromosome 16 between 64 and 83 Mb. In addition there are nine other genomic regions from the GSMA showing nominal or suggestive evidence of linkage. All these linkage results maybe informative and focus the search for novel ADHD susceptibility genes.spa
dc.format.extent7spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherWiley-Blackwellspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleMeta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorderspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGenética Regeneración y Cáncerspa
dc.publisher.groupGrupo de Neurociencias de Antioquiaspa
dc.publisher.groupGrupo de Investigación en Psiquiatría GIPSIspa
dc.publisher.groupGrupo Neuropsicología y Conductaspa
dc.identifier.doi10.1002/ajmg.b.30878-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1552-485X-
oaire.citationtitleAmerican Journal of Medical Genetics, Part B, Neuropsychiatric Geneticsspa
oaire.citationstartpage392spa
oaire.citationendpage398spa
oaire.citationvolume147Bspa
oaire.citationissue8spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeHoboken, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_dcae04bcspa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTREVspa
dc.type.localArtículo de revisiónspa
dc.subject.decsAttention Deficit Disorder with Hyperactivity-
dc.subject.decsTrastorno por Déficit de Atención con Hiperactividad-
dc.subject.decsGenetic Linkage-
dc.subject.decsLigamiento Genético-
dc.subject.decsChromosome Mapping-
dc.subject.decsMapeo Cromosómico-
dc.subject.decsChromosomes, Human, Pair 16-
dc.subject.decsCromosomas Humanos Par 16-
dc.subject.decsGenome, Human-
dc.subject.decsGenoma Humano-
dc.subject.decsEuropean Continental Ancestry Group-
dc.subject.decsGrupo de Ascendencia Continental Europea-
dc.description.researchgroupidCOL0006769spa
dc.description.researchgroupidCOL0010744spa
dc.description.researchgroupidCOL0029147spa
dc.description.researchgroupidCOL0007551spa
dc.relation.ispartofjournalabbrevAm. J. Med. Genet. B. Neuropsychiatr. Genet.spa
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