User profiles for Keeley Brookes

Keeley J Brookes

Nottingham Trent
Verified email at ntu.ac.uk
Cited by 5846

[HTML][HTML] New insights into the genetic etiology of Alzheimer's disease and related dementias

…, J Bressler, C Bresner, H Brodaty, KJ Brookes… - Nature …, 2022 - nature.com
Abstract Characterization of the genetic landscape of Alzheimer’s disease (AD) and related
dementias (ADD) provides a unique opportunity for a better understanding of the associated …

A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during …

KJ Brookes, J Mill, C Guindalini, S Curran… - Archives of general …, 2006 - jamanetwork.com
Context Attention-deficit/hyperactivity disorder (ADHD) is a common heritable childhood
behavioral disorder. Identifying risk factors for ADHD may lead to improved intervention and …

A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene

…, M Shoai, RH Reynolds, JA Botia, KJ Brookes… - Brain, 2021 - academic.oup.com
Recently, we reported oligoadenylate synthetase 1 (OAS1) contributed to the risk of Alzheimer’s
disease, by its enrichment in transcriptional networks expressed by microglia. However, …

Association of fatty acid desaturase genes with attention-deficit/hyperactivity disorder

KJ Brookes, W Chen, X Xu, E Taylor, P Asherson - Biological psychiatry, 2006 - Elsevier
BACKGROUND: Fatty acids, in particular omega-3 fatty acids, have been found to affect
behavior and cognition both directly and indirectly. Evidence to suggest a link with attention-…

Recalibrating the epigenetic clock: implications for assessing biological age in the human cortex

…, M Kumari, LC Schalkwyk, K Morgan, K Brookes… - Brain, 2020 - academic.oup.com
Human DNA methylation data have been used to develop biomarkers of ageing, referred to
as ‘epigenetic clocks’, which have been widely used to identify differences between …

[HTML][HTML] DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types

…, S Love, A Thomas, K Brookes… - Nature …, 2022 - nature.com
Alzheimer’s disease (AD) is a chronic neurodegenerative disease characterized by the
progressive accumulation of amyloid-beta and neurofibrillary tangles of tau in the neocortex. We …

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies

KE Tansey, KJ Brookes, MJ Hill, LE Cochrane, M Gill… - Neuroscience …, 2010 - Elsevier
Oxytocin (OXT) has been hypothesized to play a role in aetiology of autism based on a
demonstrated involvement in the regulation of social behaviours. It is postulated that OXT …

New insights on the genetic etiology of Alzheimer's and related dementia

…, S Boschi, P Bossù, G Bråthen, C Bresner, KJ Brookes… - MedRxiv, 2020 - medrxiv.org
Deciphering the genetic landscape of Alzheimer’s disease (AD) is essential to define the
pathophysiological pathways involved and to successfully translate genomics to potential …

[HTML][HTML] Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment

S Chaudhury, KJ Brookes, T Patel, A Fallows… - Translational …, 2019 - nature.com
Mild-cognitive impairment (MCI) occurs in up to one-fifth of individuals over the age of 65,
with approximately a third of MCI individuals converting to dementia in later life. There is a …

Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD

P Asherson, K Brookes, B Franke… - American Journal of …, 2007 - Am Psychiatric Assoc
Objective: The primary purpose of this study was to confirm the association of a specific
haplotype of the dopamine transporter gene and attention deficit hyperactivity disorder (ADHD), …