‘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 pandemic in the UK

Autor: Diana Baralle, Susan Walker, Ramya Srinivasan, Sarah Davies, Shelagh Joss, Jonathan Berg, Miranda Splitt, Usha Kini, Pradeep Vasudevan, John Dean, William Newman, Yanick Crow, Beverly Searle, Julian Barwell, Lyn Chitty, Peter Holmans, Sarah Law, Virginia Clowes, Rachel Harrison, Muriel Holder, Sahar Mansour, Spiros Denaxas, Ellie Kerry, Frances Flinter, Zheng Ye, Julia Rankin, Oliver Quarrell, Nicola Lewis, Anne Lampe, Astrid Weber, David Skuse, Kate Baker, Annie Procter, Jeremy Hall, Alison Kraus, Neil Walker, Jeanne Wolstencroft, Laura Hull, Lauren Warner, Tooba Nadeem Akhtar, William Mandy, Eleanor Dewhurst, Amy Lafont, F Lucy Raymond, Terry Shirley, Hayley Tilley, Husne Timur, Catherine Titterton, Sarah Wallwork, Francesca Wicks, Marie Erwood, Sophie Andrews, Philippa Birch, Samantha Bowen, Karen Bradley, Aimee Challenger, Samuel Chawner, Andrew Cuthbert, Sinead Morrison, Hayley Moss, Michael Owen, Sinead Ray, Matthew Sopp, Molly Tong, Marianne van den Bree, Nadia Coscini, Hayley Denyer, Nasrtullah Fatih, Manoj Juj, Anna Lucock, Frida Printzlau, Alice Watkins, Anna Pelling, Lisa Robertson, Denise Williams Alan, Donaldson Lucy, Fleur van Dijk

Publikováno v: BMJ Open, Vol 11, Iss 9 (2021)

Objectives This study aimed to explore the experiences of parents caring for children with intellectual and developmental disabilities (IDD) during the UK national lockdown in spring 2020, resulting from the COVID-19 pandemic.Design Participants were

Externí odkaz: https://doaj.org/article/6e3c9d93947f4c879e95fa8e598ed6e2

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology

Autor: Claudia Vingerhoets, Elfi Vergaelen, Michael John Owen, Therese van Amelsvoort, Ann Swillen, Marianne Bernadette van den Bree, Samuel J.R.A. Chawner, Stefanie C. Linden, Sinead Morrison, David Edmund Johannes Linden

Publikováno v: Translational Psychiatry, Vol 10, Iss 1, Pp 1-11 (2020)
Translational Psychiatry, 10(1):53. Nature Publishing Group
Translational psychiatry, 10(1):53. Nature Publishing Group
Translational Psychiatry

22q11.2 Deletion Syndrome (22q11.2DS) is associated with high risk of psychiatric disorders and cognitive impairment. It remains unclear to what extent key cognitive skills are associated with psychopathology, and whether cognition is stable over tim

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4887bf3e844d956c7c46caedfe366cfe
https://doi.org/10.1038/s41398-020-0736-7

Stopping to food can reduce intake. Effects of stimulus-specificity and individual differences in dietary restraint☆

Autor: Sinead Morrison, Rachel Adams, Christopher D. Chambers, Fredrick Verbruggen, Natalia Lawrence

Publikováno v: Appetite

Highlights • We examine whether cognitive training (response inhibition) modifies food intake. • Food stimulus-specific training can influence food intake. • These effects are more pronounced in restrained eaters. • General training to non-fo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de0a30cc158191dcdf40cae22a6e3045
http://europepmc.org/articles/PMC4286116

SA118LONGITUDINAL COGNITIVE DEVELOPMENT AND ASSOCIATION WITH PRODROMAL PSYCHOTIC SYMPTOMS IN ADOLESCENTS WITH 22Q11.2 DELETION SYNDROME

Autor: Marianne Bernadette van den Bree, Sinead Morrison, Michael John Owen, Samuel J.R.A. Chawner

Publikováno v: European Neuropsychopharmacology. 29:S1253

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9c8f55cc0bc05b71a34714bb07f680e0
https://doi.org/10.1016/j.euroneuro.2018.08.340

O4.8. VULNERABLE PERIODS FOR COGNITIVE DEVELOPMENT IN INDIVIDUALS AT HIGH GENOMIC RISK OF SCHIZOPHRENIA

Autor: Sinead Morrison, Michael John Owen, Therese van Amelsvoort, Ann Swillen, Elfi Vergaelen, Samuel J.R.A. Chawner, Marianne Bernadette van den Bree

Publikováno v: Schizophrenia Bulletin

22q11.2 Deletion Syndrome (22q11.2DS) is caused by the deletion of approximately 60 genes on chromosome 22 and represents one of the strongest known genetic risk factors for schizophrenia. Approximately 1 in 4 adults with 22q11.2DS are diagnosed with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2869121dacb4bc0c4647d41647548eef
https://doi.org/10.1093/schbul/sby015.214