Research output per year
Research output per year
Personal profile
Research interests
Jennifer is interested in using brain markers to stratify hetergeneous clinical populations, such as neurodivergent populations and mental health conditions. The goal of her work is to refine diagnostics and improve the personalisation of interventions for those with complex presentations. She is also interested in promoting co-production within clinical and cognitive neuroscience research, particularly with neurodiverse populations. She has expertise in Electroencephalography (EEG) aquisition and analysis, as well as a working knowledge of MRI analysis and genomics. She specialises in the clinical and cognitive assessment of children, young people, and adults with complex needs.
External positions
Clinical Neurodevelopmental Specialist, COMPASS Psychology
1 Jan 2024 → …
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Collaborations and top research areas from the last five years
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Investigating social orienting in children with Phelan-McDermid syndrome and ‘idiopathic’ autism
San José Cáceres, A., Wilkinson, E., Cooke, J., Baskett, V., Blackmore, C., Crawley, D. V., Durkin, A., Halpern, D., Núñez, M., Siper, P., Murphy, D. G., Foss-Feig, J., Kolevzon, A. & Loth, E., 30 Dec 2024, In: Journal of Neurodevelopmental Disorders. 16, 1, p. 1-11 11 p., 64.Research output: Contribution to journal › Article › peer-review
Open AccessFile5 Downloads (Pure) -
Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey
European Phelan-McDermid syndrome consortium, Landlust, A. M., Koza, S. A., Carbin, M., Walinga, M., Robert, S., Cooke, J., Vyshka, K., van Balkom, I. D. C. & van Ravenswaaij-Arts, C., 30 Jul 2023, In: European journal of medical genetics (EJMG). 66, 7, 9 p., 104771.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Consensus recommendations on mental health issues in Phelan-McDermid syndrome
European Phelan-McDermid syndrome consortium, 30 Jun 2023, In: European journal of medical genetics (EJMG). 66, 6, 8 p., 104770.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Bridging the translational gap: what can synaptopathies tell us about autism?
Molloy, C. J., Cooke, J., Gatford, N. J. F., Rivera-Olvera, A., Avazzadeh, S., Homberg, J. R., Grandjean, J., Fernandes, C., Shen, S., Loth, E., Srivastava, D. P. & Gallagher, L., 27 Jun 2023, In: Frontiers in molecular neuroscience. 16, p. 1191323Research output: Contribution to journal › Review article › peer-review
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The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions.
Cooke, J., 18 Feb 2022, In: Frontiers in Neuroscience. 16Research output: Contribution to journal › Article › peer-review
Open Access