Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions

Simple item page
dc.contributor.authorAcosta, M. T.
dc.contributor.authorCastellanos, F. X.
dc.contributor.authorBolton, Kelly L.
dc.contributor.authorBalog, J.
dc.contributor.authorEagen, P.
dc.contributor.authorNee, L.
dc.contributor.authorJanet, Jones
dc.contributor.authorLuis Guillermo, Palacio
dc.contributor.authorSarampote, C.
dc.contributor.authorRussell, H. F.
dc.contributor.authorBerg, kate
dc.contributor.authorArcos-Burgos, Mauricio
dc.contributor.authorMuenke, Maximilian
dc.date.accessioned2015-12-13T22:54:48Z
dc.date.available2015-12-13T22:54:48Z
dc.date.issued2008
dc.date.updated2015-12-11T11:06:06Z
dc.description.abstractObjective: Genetic studies of attention-deficit/hyperactivity disorder (ADHD) generally use discrete DSM-IV subtypes to define diagnostic status. To improve correspondence between phenotypic variance and putative susceptibility genes, multivariate classif
dc.identifier.issn0890-8567
dc.identifier.urihttp://hdl.handle.net/1885/82253
dc.publisherLippincott Williams & Wilkins
dc.sourceAmerican Academy of Child and Adolescent Psychiatry, Journal
dc.subjectKeywords: adolescent; adult; anxiety; article; attention deficit disorder; child; comorbidity; conduct disorder; depression; female; genetic model; genetic susceptibility; genetic variability; human; major clinical study; male; phenotype; preschool child; priority Attention-deficit/hyperactivity disorder; Comorbidity; Genetics; Latent class analysis
dc.titleLatent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage807
local.bibliographicCitation.startpage797
local.contributor.affiliationAcosta, MT, National Institutes of Health
local.contributor.affiliationCastellanos, F.X., New York University Child Study Center
local.contributor.affiliationBolton, Kelly L., National Human Genome Research Institute
local.contributor.affiliationBalog, J., National Institutes of Health
local.contributor.affiliationEagen, P., National Institute of Health
local.contributor.affiliationNee, L., National Insititue of Health
local.contributor.affiliationJanet, Jones, National Insitute of Health
local.contributor.affiliationLuis Guillermo, Palacio, Universidad de Antioquia
local.contributor.affiliationSarampote, C., National Institute of Health
local.contributor.affiliationRussell, H.F., National Institute of Health
local.contributor.affiliationBerg, kate, National Institutes of Health
local.contributor.affiliationArcos-Burgos, Mauricio (Oscar), College of Medicine, Biology and Environment, ANU
local.contributor.affiliationMuenke, Maximilian, National Human Genome Research Institute
local.contributor.authoremailu5088570@anu.edu.au
local.contributor.authoruidArcos-Burgos, Mauricio (Oscar), u5088570
local.description.notesImported from ARIES
local.identifier.absfor060408 - Genomics
local.identifier.ariespublicationf5625xPUB10526
local.identifier.citationvolume47
local.identifier.doi10.1097/CHI.0b013e318173f70b
local.identifier.scopusID2-s2.0-50549091936
local.identifier.uidSubmittedByf5625
local.type.statusMetadata only

Downloads

Collections

ANU Research Publications

DSpace software copyright © 2002-2024 LYRASIS