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David Skuse
David Skuse
Professor of Behavioural and Brain Sciences, University College London
在 ucl.ac.uk 的电子邮件经过验证
标题
引用次数
年份
‘We have been in lockdown since he was born’: a mixed methods exploration of the experiences of families caring for children with intellectual disability during the COVID-19 …
J Wolstencroft, L Hull, L Warner, TN Akhtar, W Mandy, D Skuse
BMJ open 11 (9), e049386, 2021
182021
" Cortical anatomy in human X monosomy": Erratum.
A Raznahan, W Cutter, F Lalonde, D Robertson, E Daly, GS Conway, ...
Elsevier Science, 2010
2010
" Mother-child interaction and the cognitive and behavioural development of four-year-old children with poor growth': Erratum.
C Puckering, A Pickles, D Skuse, E Heptinstall, L Dowdney, S Zur-Szpiro
Elsevier Science, 1995
1995
“We’ve been in lockdown since he was born”: Experiences of families caring for children with intellectual disability during the Covid-19 pandemic
J Wolstencroft, L Hull, L Warner, T Akhtar, W Mandy, D Skuse, ...
PsyArXiv, 2021
32021
040 Autism spectrum disorders in girls and women with turner syndrome
J Wolstencroft, W Mandy, D Skuse
Archives of Disease in Childhood 103 (Suppl 2), A16-A16, 2018
42018
076 Increased physiological responses to threat in Duchenne muscular dystrophy: a potential CNS outcome measure
KE Maresh, A Papageorgiou, D Ridout, NA Harrison, W Mandy, D Skuse, ...
Journal of Neurology, Neurosurgery and Psychiatry 93 (6), A36-A36, 2022
2022
2. Extreme Deprivation in Early Childhood—I. Diverse Outcomes for Three Siblings from an Extraordinary Family
D Skuse
An Introductory Reader in Developmental Psychology, 19, 1995
11995
22q11 deletion syndrome-understanding neurodevelopmental disorders in a common CNV
K Baker, T Baldeweg, C Chaddock, D Skuse
Journal of Medical Genetics 48, S19-S19, 2011
2011
22Q11 deletion syndrome: a search for clues to the origins of schizophrenia.(BNPA Abstracts: Members' Papers).
KD Baker, T Baldeweg, P Scambler, DH Skuse
Journal of Neurology, Neurosurgery and Psychiatry 74 (6), 834-835, 2003
2003
249th ENMC International Workshop: The role of brain dystrophin in muscular dystrophy: Implications for clinical care and translational research, Hoofddorp, The Netherlands …
JGM Hendriksen, M Thangarajh, HE Kan, F Muntoni, Y Aoki, P Collin, ...
Neuromuscular Disorders 30 (9), 782-794, 2020
152020
382 Towards in vitro genetics
CS Haley, DJ de Koning, DH Skuse, S Ahmed, JH Brickner, CS Kwon, ...
Genetics 23 (8), 365-418, 2007
2007
48 PHYSIOLOGICAL GH SECRETION DURING THE RECOVERY FROM PSYCHOSOCIAL DWARFISM: THE PATTERN OF GH PULSATILITY IS REPRODUCIBLE
R Stanhope, P Adlard, G Hamill, J Jones, D Skuse, MA Preece
Pediatric Research 24 (4), 525-525, 1988
1988
A call for more evidence-based practice
D Skuse
BJPsych International 15 (3), 54-55, 2018
2018
A Case‐comparison Study of the Characteristics of Children with a Short Stature Syndrome Induced by Stress (Hyperphagic Short Stature) and a Consecutive Series of Unaffected …
J Gilmour, D Skuse
Journal of Child Psychology and Psychiatry 40 (6), 969-978, 1999
321999
A clinical, cytogenetic and molecular study of 47 females with r (X) chromosomes
N Dennis, B Coppin, C Turner, D Skuse, P Jacobs
Annals of human genetics 64 (4), 277-293, 2000
292000
A combined VBM and DTI investigation of brain structure and connectivity in 22q11 Deletion Syndrome
C Chaddock, L Lee, J Newton, T Baldeweg, R Frackwoiak, D Skuse
Proceedings of the International Society for Magnetic Resonance in Medicine …, 2006
12006
A combined VBM and DTI investigation of brain structure in 22Q11 deletion syndrome: Investigations of structure-function relationships
C Chaddock, L Lee, J Newton, T Baldeweg, R Frackowiak, D Skuse
SCHIZOPHRENIA RESEARCH 81, 155-156, 2006
2006
A framework for an evidence-based gene list relevant to autism spectrum disorder
CP Schaaf, C Betancur, RKC Yuen, JR Parr, DH Skuse, L Gallagher, ...
Nature Reviews Genetics 21 (6), 367-376, 2020
982020
A longitudinal study of general practitioner consultations for psychiatric disorders in adolescence
N Smeeton, G Wilkinson, D Skuse, J Fry
Psychological medicine 22 (3), 709-715, 1992
121992
A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome
DO Robinson, P Dalton, PA Jacobs, K Mosse, MM Power, DH Skuse, ...
Journal of medical genetics 36 (4), 279-284, 1999
821999
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