Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jessica H. Hall"'
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:
Charlotte E. Butter, Caitlin L. Goldie, Jessica H. Hall, Kathy Leadbitter, Emma M.M. Burkitt, Marianne B.M. van den Bree, Jonathan M. Green
Publikováno v:
BMC Psychology, Vol 12, Iss 1, Pp 1-11 (2024)
Abstract Background 16p11.2 proximal deletion and duplication syndromes (Break points 4–5) (593KB, Chr16; 29.6-30.2mb - HG38) are observed to have highly varied phenotypes, with a known propensity for lifelong psychiatric problems. This study aimed
Externí odkaz:
https://doaj.org/article/d05bc6fd32984de1bbdf8b04fb6592e2
Autor:
Nicholas A Donnelly, Ullrich Bartsch, Hayley A Moulding, Christopher Eaton, Hugh Marston, Jessica H Hall, Jeremy Hall, Michael J Owen, Marianne BM van den Bree, Matt W Jones
Publikováno v:
eLife, Vol 11 (2022)
Background: Young people living with 22q11.2 Deletion Syndrome (22q11.2DS) are at increased risk of schizophrenia, intellectual disability, attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). In common with these condi
Externí odkaz:
https://doaj.org/article/10e17dd171704029965f897bf2879c84
Autor:
Ullrich Bartsch, Nicholas A Donnelly, Hayley A Moulding, Christopher Eaton, Hugh Marston, Jessica H Hall, Jeremy Hall, Michael J Owen, Marianne BM van den Bree, Matt W Jones
Publikováno v:
Donnelly, N, Bartsch, U, Moulding, H, Marston, H M, Eaton, C B, Hall, J, Hall, J, Owen, M J, van den Bree, M B M & Jones, M W 2022, ' Sleep EEG in young people with 22q11.2 deletion syndrome : a cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms ', eLife, vol. 11, e75482 . https://doi.org/10.7554/eLife.75482
eLife
eLife
Background:Young people living with 22q11.2 Deletion Syndrome (22q11.2DS) are at increased risk of schizophrenia, intellectual disability, attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). In common with these condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35b391e8a390dda2c3a7050606373b2c
https://research-information.bris.ac.uk/en/publications/3ac831f4-5158-4e8e-a81a-f3ee5a6d4c49
https://research-information.bris.ac.uk/en/publications/3ac831f4-5158-4e8e-a81a-f3ee5a6d4c49
Autor:
Ullrich Bartsch, Nicholas A Donnelly, Hayley A Moulding, Christopher Eaton, Hugh Marston, Jessica H Hall, Jeremy Hall, Michael J Owen, Marianne BM van den Bree, Matt W Jones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e12fbfd6cf109e8a41a3a982cb8cc45f
https://doi.org/10.7554/elife.75482.sa2
https://doi.org/10.7554/elife.75482.sa2
Autor:
Jessica H. Hall, Elizabeth M. C. Fisher, Mark Andrew Good, Victor L. J. Tybulewicz, John L. Harwood, Frances K. Wiseman
Publikováno v:
Alzheimer's & Dementia. 12
Autor:
Jessica H, Hall, Frances K, Wiseman, Elizabeth M C, Fisher, Victor L J, Tybulewicz, John L, Harwood, Mark A, Good
Publikováno v:
Neurobiology of learning and memory
The present study examined memory function in Tc1 mice, a transchromosomic model of Down syndrome (DS). Tc1 mice demonstrated an unusual delay-dependent deficit in recognition memory. More specifically, Tc1 mice showed intact immediate (30 sec), impa