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David Skuse
David Skuse
Professor of Behavioural and Brain Sciences, University College London
Bestätigte E-Mail-Adresse bei ucl.ac.uk
Titel
Zitiert von
Zitiert von
Jahr
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
35252007
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
29512014
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
DH Skuse, RS James, DVM Bishop, B Coppin, P Dalton, ...
Nature 387 (6634), 705-708, 1997
9701997
Sex differences in autism spectrum disorder: evidence from a large sample of children and adolescents
W Mandy, R Chilvers, U Chowdhury, G Salter, A Seigal, D Skuse
Journal of autism and developmental disorders 42, 1304-1313, 2012
9522012
Microduplications of 16p11. 2 are associated with schizophrenia
SE McCarthy, V Makarov, G Kirov, AM Addington, J McClellan, S Yoon, ...
Nature genetics 41 (11), 1223-1227, 2009
8432009
Prevalence of feeding problems and oral motor dysfunction in children with cerebral palsy: a community survey
S Reilly, D Skuse, X Poblete
The Journal of pediatrics 129 (6), 877-882, 1996
6431996
Development of sexually abusive behaviour in sexually victimised males: A longitudinal study
D Salter, D McMillan, M Richards, T Talbot, J Hodges, A Bentovim, ...
The Lancet 361 (9356), 471-476, 2003
5222003
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
5062017
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ...
PLoS genetics 8 (2), e1002521, 2012
4952012
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ...
Nature genetics 48 (5), 552-555, 2016
4532016
Dopaminergic-neuropeptide interactions in the social brain
DH Skuse, L Gallagher
Trends in cognitive sciences 13 (1), 27-35, 2009
4472009
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 8111, 2015
4462015
Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism
DH Skuse
Pediatric research 47 (1), 9-9, 2000
4282000
The developmental, dimensional and diagnostic interview (3di): a novel computerized assessment for autism spectrum disorders
D Skuse, R Warrington, D Bishop, U Chowdhury, J Lau, W Mandy, ...
Journal of the American Academy of Child & Adolescent Psychiatry 43 (5), 548-558, 2004
4252004
Avoidance of emotionally arousing stimuli predicts social–perceptual impairment in Asperger's syndrome
B Corden, R Chilvers, D Skuse
Neuropsychologia 46 (1), 137-147, 2008
4222008
Age, gender, and puberty influence the development of facial emotion recognition
K Lawrence, R Campbell, D Skuse
Frontiers in psychology 6, 761, 2015
4072015
Measuring autistic traits: heritability, reliability and validity of the Social and Communication Disorders Checklist
DH Skuse, WPL Mandy, J Scourfield
The British Journal of Psychiatry 187 (6), 568-572, 2005
3872005
Turner syndrome: a cytogenetic and molecular study
P Jacobs, P Dalton, R James, K Mosse, M Power, D Robinson, D Skuse
Annals of human genetics 61 (6), 471-483, 1997
3451997
Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations
V Ricotti, WPL Mandy, M Scoto, M Pane, N Deconinck, S Messina, ...
Developmental Medicine & Child Neurology 58 (1), 77-84, 2016
3372016
X-linked genes and mental functioning
DH Skuse
Human molecular genetics 14 (suppl_1), R27-R32, 2005
2882005
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