Zobrazeno 1 - 10
of 291
pro vyhledávání: '"Imagine-Id"'
Autor:
Chawner, Samuel J R A, Owen, Michael J, Holmans, Peter, Raymond, F Lucy, Skuse, David, Hall, Jeremy, van den Bree, Marianne B M
Publikováno v:
In The Lancet Psychiatry June 2019 6(6):493-505
Akademický článek
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Autor:
Zhaotian Chi, Rory T. Devine, Jeanne Wolstencroft, David Skuse, Claire Hughes, Kate Baker, IMAGINE-ID consortium
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Parents of individuals with rare neurodevelopmental conditions and intellectual disabilities (ID) are vulnerable to mental health difficulties, which vary between parents and within parents over time. The underlying cause of a chi
Externí odkaz:
https://doaj.org/article/76edbd8d368747fd88ea5ee979eaa131
Autor:
Jessica H. Hall, Samuel J. R. A. Chawner, IMAGINE-ID consortium, Jeanne Wolstencroft, David Skuse, Jeremy Hall, Peter Holmans, Michael J. Owen, Marianne B. M. van den Bree
Publikováno v:
Translational Psychiatry, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract A range of rare mutations involving micro-deletion or -duplication of genetic material (copy number variants (CNVs)) have been associated with high neurodevelopmental and psychiatric risk (ND-CNVs). Irritability is frequently observed in chi
Externí odkaz:
https://doaj.org/article/81154eda50754e09b297917153b839e0
Autor:
Jeremy Hall, Marianne Bernadette van den Bree, Samuel J.R.A. Chawner, Michael J. Owen, Peter Holmans, David Skuse, Lucy Raymond
Summary Background Several copy number variants (CNVs) are associated with a high risk of neurodevelopmental and psychiatric disorders (referred to as ND-CNVs). We aimed to characterise the effect of ND-CNVs on childhood development and investigate w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15fe5c9c3a670f1bf51949ac646ebec2
Autor:
Lucy Raymond, David Skuse, Michael John Owen, Peter Holmans, Marianne Bernadette van den Bree, Samuel J.R.A. Chawner, Jeremy Hall
BackgroundA variety of copy number variants are associated with a high risk of neurodevelopmental and psychiatric disorders (ND-CNVs). Different ND-CNVs could lead to distinct and specific patterns of cognitive and behavioural outcomes, but supportin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::876a93e428f430976e5da69ff587cc9d
https://doi.org/10.1101/535708
https://doi.org/10.1101/535708
Autor:
Samuel J. R. A. Chawner, Alexandra Evans, IMAGINE-ID consortium, Nigel Williams, Michael J. Owen, Jeremy Hall, Marianne B. M. van den Bree
Publikováno v:
Translational Psychiatry, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Children with rare neurodevelopmental genetic conditions (ND-GCs) are at high risk for a range of neuropsychiatric conditions. Sleep symptomatology may represent a transdiagnostic risk indicator within this patient group. Here we present dat
Externí odkaz:
https://doaj.org/article/22ab6f6cc0c7413ea74ce08703ef8cd7
Autor:
Samuel J. R. A. Chawner, Amy L. Paine, Matt J. Dunn, Alice Walsh, Poppy Sloane, Megan Thomas, Alexandra Evans, Lucinda Hopkins‐Jones, Siske Struik, IMAGINE‐ID consortium, Jeremy Hall, Jonathan T. Erichsen, Susan R. Leekam, Michael J. Owen, Dale Hay, Marianne B. M. van denBree
Publikováno v:
JCPP Advances, Vol 3, Iss 2, Pp n/a-n/a (2023)
Abstract Background Individuals with 22q11.2 deletion are at considerably increased risk of neurodevelopmental and psychiatric conditions. There have been very few studies investigating how this risk manifests in early childhood and what factors may
Externí odkaz:
https://doaj.org/article/482cdaea28664d24988dbbfae66564be
Akademický článek
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Akademický článek
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