Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment
dc.contributor.author | Nudel, R. | |
dc.contributor.author | Simpson, N. H. | |
dc.contributor.author | Baird, G. | |
dc.contributor.author | O'Hare, A. | |
dc.contributor.author | Conti-Ramsden, G. | |
dc.contributor.author | Bolton, P. F. | |
dc.contributor.author | Hennessy, E. R. | |
dc.contributor.author | Ring, S. M. | |
dc.contributor.author | Smith, G. Davey | |
dc.contributor.author | Francks, C. | |
dc.contributor.author | Paracchini, S. | |
dc.contributor.author | Monaco, A. P. | |
dc.contributor.author | Fisher, S. E. | |
dc.contributor.author | Newbury, D. F. | |
dc.contributor.author | SLI Consortium | |
dc.date.accessioned | 2015-02-06T16:37:01Z | |
dc.date.available | 2015-02-06T16:37:01Z | |
dc.date.issued | 2014-04 | |
dc.identifier | 45922067 | |
dc.identifier | 559ea20a-5ae0-4cdc-9d25-618f47c94ee1 | |
dc.identifier | 000333887500007 | |
dc.identifier | 84897958382 | |
dc.identifier.citation | Nudel , R , Simpson , N H , Baird , G , O'Hare , A , Conti-Ramsden , G , Bolton , P F , Hennessy , E R , Ring , S M , Smith , G D , Francks , C , Paracchini , S , Monaco , A P , Fisher , S E , Newbury , D F & SLI Consortium 2014 , ' Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment ' , Genes, Brain, and Behavior , vol. 13 , no. 4 , pp. 418-429 . https://doi.org/10.1111/gbb.12127 | en |
dc.identifier.issn | 1601-1848 | |
dc.identifier.uri | http://hdl.handle.net/2164/4249 | |
dc.description | Funded by •Medical Research Council. Grant Numbers: G1000569/1, MR/J003719/1, G0800523/86473 •University of Oxford Nuffield Department of Medicine Prize Studentship •Max Planck Society •Wellcome Trust. Grant Numbers: 060774, 076566, 090532/Z/09/Z, 092731 •National Institute of Health Research (UK) Senior Investigator award •Biomedical Research Centre in Mental Health | en |
dc.format.extent | 12 | |
dc.format.extent | 1025630 | |
dc.language.iso | eng | |
dc.relation.ispartof | Genes, Brain, and Behavior | en |
dc.subject | ALSPAC | en |
dc.subject | GWAS | en |
dc.subject | imprinting | en |
dc.subject | neurodevelopmental disorder | en |
dc.subject | specific language impairment | en |
dc.subject | attention-deficit/hyperactivity disorder | en |
dc.subject | nucleotide exchange factor | en |
dc.subject | RHO-GTPASES | en |
dc.subject | communication checklist | en |
dc.subject | hyperactivity disorder | en |
dc.subject | developmental dyslexia | en |
dc.subject | susceptibility locus | en |
dc.subject | suggestive linkage | en |
dc.subject | mental-retardation | en |
dc.subject | reading-disability | en |
dc.subject | R Medicine | en |
dc.subject | Medical Research Council (MRC) | en |
dc.subject | G1000569/1 | en |
dc.subject | G0800523/86473 | en |
dc.subject | MR/J003719/1 | en |
dc.subject | Wellcome Trust | en |
dc.subject | 060774 | en |
dc.subject | 076566 | en |
dc.subject | 090532/Z/09/Z | en |
dc.subject | 092731 | en |
dc.subject.lcc | R | en |
dc.title | Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment | en |
dc.type | Journal article | en |
dc.contributor.institution | University of Aberdeen.Medical Education | en |
dc.description.status | Peer reviewed | en |
dc.identifier.doi | 10.1111/gbb.12127 |