‘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 | 18 | 2021 |
" 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 | 3 | 2021 |
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 | 4 | 2018 |
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 | 1 | 1995 |
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 | 15 | 2020 |
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 | 32 | 1999 |
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 | 29 | 2000 |
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 | 1 | 2006 |
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 | 98 | 2020 |
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 | 12 | 1992 |
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 | 82 | 1999 |