User profiles for Keeley Brookes
Keeley J BrookesNottingham 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 …
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 …
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
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, …
disease, by its enrichment in transcriptional networks expressed by microglia. However, …
Association of fatty acid desaturase genes with attention-deficit/hyperactivity disorder
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-…
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
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 …
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
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 …
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
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 …
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 …
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
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 …
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
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), …
haplotype of the dopamine transporter gene and attention deficit hyperactivity disorder (ADHD), …