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Number of items: 8.

Gur, Ruben C., Bearden, Carrie E., Jacquemont, Sebastien, Swillen, Ann, van Amelsvoort, Therese, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vorstman, Jacob, Sebat, Jonathan, Ruparel, Kosha, Gallagher, Robert Sean, McClellan, Emily, White, Lauren, Crowley, Terrence Blaine, Giunta, Victoria, Kushan, Leila, O'Hora, Kathleen, Verbesselt, Jente, Vandensande, Ans, Vingerhoets, Claudia, van Haelst, Mieke, Hall, Jessica, Harwood, Janet, Chawner, Samuel J. R. A., Patel, Nishi, Palad, Katrina, Hong, Oanh, Guevara, James, Martin, Charles Olivier, Jizi, Khadije, Bélanger, Anne-Marie, Scherer, Stephen W., Bassett, Anne S., McDonald-McGinn, Donna M. and Gur, Raquel E. 2025. Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular Psychiatry 30 , pp. 379-387. 10.1038/s41380-024-02661-y
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Hall, Jessica H., Chawner, Samuel J. R. A., Wolstencroft, Jeanne, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14 (1) , 259. 10.1038/s41398-024-02975-z
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Butter, Charlotte E., Goldie, Caitlin L., Hall, Jessica H., Leadbitter, Kathy, Burkitt, Emma M.M., van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254 and Green, Jonathan M. 2024. Experiences and concerns of parents of children with a 16p11.2 deletion or duplication diagnosis: a reflexive thematic analysis. BMC Psychology 12 , 137. 10.1186/s40359-024-01609-9
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Raven, Erika, Veraart, Jelle, Kievit, Rogier, Genc, Sila, Ward, Isobel, Hall, Jessica, Cunningham, Adam, Doherty, Joanne, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Jones, Derek ORCID: https://orcid.org/0000-0003-4409-8049 2023. In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome. Molecular Psychiatry 28 , pp. 4342-4352. 10.1038/s41380-023-02178-w
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Donnelly, Nicholas A., Bartsch, Ullrich, Moulding, Hayley A. ORCID: https://orcid.org/0000-0002-1277-4404, Eaton, Christopher ORCID: https://orcid.org/0000-0001-6739-1999, Marston, Hugh, Hall, Jessica H., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254 and Jones, Matt 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 11 , e75482. 10.7554/elife.75482
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Brydges, Nichola M., Hall, Jessica, Best, Caroline, Rule, Lowenna, Watkin, Holly, Drake, Amanda J., Lewis, Catrin ORCID: https://orcid.org/0000-0002-3818-9377, Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, Jeremy 2019. Childhood stress impairs social function through AVP-dependent mechanisms. Translational Psychiatry 9 (1) , 330. 10.1038/s41398-019-0678-0
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Hall, Jessica H. 2016. Dissociating aberrant properties of recognition memory in the TC1 mouse model of Trisomy-21. PhD Thesis, Cardiff University.
Item availability restricted.
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Hall, Jessica H., Wiseman, Frances K., Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Harwood, John L. ORCID: https://orcid.org/0000-0003-2377-2612 and Good, Mark A. ORCID: https://orcid.org/0000-0002-1824-1203 2016. Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory. Neurobiology of Learning and Memory 130 , pp. 118-128. 10.1016/j.nlm.2016.02.002
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