Damien Wright

Dr. Damien Wright


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 October 2016 in Cerebral Cortex
Verified
Journal Article
Open access
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AMAlexis Makin
Alexis Makin
DWDamien Wright
Damien Wright
GRGiulia Rampone
Giulia Rampone
LPLetizia Palumbo
Letizia Palumbo
MGMartin Guest
Martin Guest
MBMarco Bertamini
Marco Bertamini
A traditional line of work starting with the Gestalt school has shown that patterns vary in strength and salience; a difference in “Perceptual goodness.” The Holographic weight of evidence model quantifies goodness of visual regularities. The key formula states that W = E/N, where E is number of holographic identities in a pattern and N is number of elements. We tested whether W predicts the amplitude of the neural response to regularity in an extrastriate symmetry-sensitive network. We recorded an Event Related Potential (ERP) generated by symmetry called the Sustained Posterior Negativity (SPN). First, we reanalyzed the published work and found that W explained most variance in SPN amplitude. Then in four new studies, we confirmed specific predictions of the holographic model regarding 1) the differential effects of numerosity on reflection and repetition, 2) the similarity between reflection and Glass patterns, 3) multiple symmetries, and 4) symmetry and anti-symmetry. In all cases, the holographic approach predicted SPN amplitude remarkably well; particularly in an early window around 300–400 ms post stimulus onset. Although the holographic model was not conceived as a model of neural processing, it captures many details of the brain response to symmetry.

17 September 2021 in Brain Sciences
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Journal Article
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CHConstance Hicks-Smith
Constance Hicks-Smith
DWDamien Wright
Damien Wright
AKAisling Kenny
Aisling Kenny
RSRobert C. Stowe
Robert C. Stowe
MMMaria McCormack
Maria McCormack
JHJimmy Holder
Jimmy Holder
Neurodevelopmental disorders are frequently associated with sleep disturbances. One class of neurodevelopmental disorders, the genetic synaptopathies, is caused by mutations in genes encoding proteins found at the synapse. Mutations in these genes cause derangement of synapse development and function. We utilized a validated sleep instrument, Children’s Sleep Habits Questionnaire (CSHQ) to examine the nature of sleep abnormalities occurring in individuals with two synaptopathies—Phelan–McDermid syndrome (PMD) (N = 47, male = 23, female = 24, age 1–46 years) and SYNGAP1-related intellectual disability (SYNGAP1-ID) (N = 64, male = 31, female = 33, age 1–64 years), when compared with unaffected siblings (N = 61, male = 25, female = 36, age 1–17 years). We found that both PMD and SYNGAP1-ID have significant sleep abnormalities with SYNGAP1-ID having greater severity of sleep disturbance than PMD. In addition, sleep disturbances were more severe for PMD in individuals 11 years and older compared with those less than 11 years old. Individuals with either disorder were more likely to use sleep aids than unaffected siblings. In conclusion, sleep disturbances are a significant phenotype in the synaptopathies PMD and SYNGAP1-ID. Improved sleep is a viable endpoint for future clinical trials for these neurodevelopmental disorders.

1 January 2017 in Cortex
Verified
Journal Article
Open access
DWDamien Wright
Damien Wright
AMAlexis Makin
Alexis Makin
Marco BertaminiMarco Bertamini
Marco Bertamini
Symmetry is a highly salient feature in the visual world, abundant in both man-made and natural objects. In particular, humans find reflectional symmetry most salient. Electrophysiological work on symmetry perception has identified a difference wave known as the Sustained Posterior Negativity (SPN) originating from extrastriate areas. Amplitude is more negative for symmetrical than random patterns, from around 200 msec after stimulus onset. For the first time, we report responses to patterns presented exclusively in one hemifield. Participants were presented with reflection or random dot patterns to the left and right of fixation (3.2°). They judged whether the patterns were light red or dark red in colour. In Experiment 1, the pair always included one symmetrical and one random pattern. In Experiments 2 and 3 we varied the information presented contralaterally. The SPN was generated separately in each hemisphere in response to what was presented in the contralateral visual hemifield (a lateralised SPN). We conclude that a symmetry-sensitive network of extrastriate areas can be activated independently in each cerebral hemisphere.

23 December 2014 in Psychophysiology
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Journal Article
Open access
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DWDamien Wright
Damien Wright
AMAlexis Makin
Alexis Makin
Marco BertaminiMarco Bertamini
Marco Bertamini
When actively classifying abstract patterns according to their regularity, alpha desynchronization (ERD) becomes right lateralized over posterior brain areas. This could reflect temporary enhancement of contralateral visual inputs and specifically a shift of attention to the left, or right hemisphere specialization for regularity discrimination. This study tested these competing hypotheses. Twenty‐four participants discriminated between dot patterns containing a reflection or a translation. The direction of the transformation, which matched one half onto the other half, was either vertical or horizontal. The strategy of shifting attention to one side of the patterns would not produce lateralized ERD in the horizontal condition. However, right‐lateralized ERD was found in all conditions, regardless of orientation. We conclude that right hemisphere networks that incorporate the early posterior regions are specialized for regularity discrimination.

2 June 2022 in Journal of Neurodevelopmental Disorders
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Journal Article
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DWDamien Wright
Damien Wright
AKAisling Kenny
Aisling Kenny
SESarah Eley
Sarah Eley
AMAndrew G. McKechanie
Andrew G. McKechanie
ASAndrew C. Stanfield
Andrew C. Stanfield
Background: SYNGAP1-related intellectual disability (ID) is a recently described neurodevelopmental disorder that is caused by pathogenic variation in the SYNGAP1 gene. To date, the behavioural characteristics of this disorder have mainly been highlighted via the prevalence of existing diagnoses in case series. We set out to detail the behavioural features of this disorder by undertaking interviews with those who have a child with SYNGAP1-related ID to allow them to describe their child’s behaviour. Methods: We conducted 27 semi-structured interviews with parents and caregivers which covered basic information (e.g., age, gender), family history, perinatal history, past medical history, developmental history, epilepsy, behavioural history, and a general description of their child’s behaviour. Results: Using a mixed quantitative and qualitative approach, the responses from the parents indicated that those with SYNGAP1-related ID showed high rates of autism spectrum disorder (52%), difficulties with fine and gross motor skills, delays in language development, and a high prevalence of epilepsy (70%). A qualitative analysis highlighted their general behaviour affected the themes of daily living skills, distress-related behaviours, emotional regulation, difficulties with change, a lack of danger awareness, and sensory differences. Sensory features described involved auditory, visual, tactile, gustatory, and proprioceptive themes. Conclusions: Our findings and behavioural descriptions provide important insights as well as implications for the diagnosis and care of those with SYNGAP1-related ID.

15 June 2022 in eLife
Verified
Journal Article
Open access
AMAlexis Makin
Alexis Makin
JTJohn Tyson-Carr
John Tyson-Carr
GRGiulia Rampone
Giulia Rampone
YDYiovanna Derpsch
Yiovanna Derpsch
DWDamien Wright
Damien Wright
Marco BertaminiMarco Bertamini
Marco Bertamini
It is now possible for scientists to publicly catalogue all the data they have ever collected on one phenomenon. For a decade, we have been measuring a brain response to visual symmetry called the sustained posterior negativity (SPN). Here we report how we have made a total of 6674 individual SPNs from 2215 participants publicly available, along with data extraction and visualization tools (https://osf.io/2sncj/). We also report how re-analysis of the SPN catalogue has shed light on aspects of the scientific process, such as statistical power and publication bias, and revealed new scientific insights.