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Number of items: 21.

Silva, Ana ORCID: https://orcid.org/0000-0002-1184-4909, Sønderby, Ida, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Abdellaoui, Abdel, Agartz, Ingrid, Ames, David, Armstrong, Nicola, Artiges, Eric, Banaschewski, Tobias, Basset, Anne, Bearden, Carrie, Blangero, John, Boen, Rune, Boomsma, Dorret, Bulow, Robin, Butcher, Nancy, Calhoun, Vince, Campbell, Linda, Chow, Eva, Ciufolini, Simone, Craig, Michael, Crespo-farrocco, Benedicto, Cunningham, Adam, Dalvie, Shareefa, Daly, Eileen, Dazzan, Paola, de Geus, Eco, Zubicaray, Greig, Doherty, Joanne, Donohoe, Gary, Drakesmith, Mark, Espeseth, Thomas, Frouin, Vincent, Garavan, Hugh, Glahn, David, Goodrich-Hunsaker, Naomi, Gowland, Penny, Grabe, Hans, Grigis, Antonie, Gudbrandsen, Maria, Gutman, Boris, Haavik, Jan, Haberg, Asta, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Heinz, Andreas, Hoh mann, Sarah, Hottenga, Jouke-Jan, Jacquemont, Sebastien, Jahanshad, Neda, Jones, Rachel, Jones, Derek ORCID: https://orcid.org/0000-0003-4409-8049, Jonsson, Erik, Koops, Sanne, Kumar, Kuldeep, Le Hellard, Stephanie, Lemaitre, Herve, Liu, Jingyu, Lundervold, Astri, Martinot, Jean-Luc, Mather, Karen, McDonald-McGinn, Donna, McMahon, Katie, McRae, Allan, Medland, Sarah, Moreau, Clara, Murphy, Kieran, Murphy, Declan, Murray, Robin, Nees, Frauke, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Papadopoulos Orfanos, Diimitri, Paus, Tomas, Poustka, Luise, Reis Marques, Tiago, Roalf, David, Sachdev, Perminder, Scheffler, Freda, Schmitt, Eric, Schumann, Gunter, Steen, Vidar, Stein, Dan, Strike, Lachlan, Teumer, Alexander, Thalamuthu, Anbupalam, Thomopoulos, Sophia, Tordesillas-Gutierrez, Diana, Trolbr, Julian, Uhlmann, Anne, Vajdi, Ariana, Van't Ent, Dennis, Van Amelsvoort, Therese, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, van der Meer, Dennis, Vazquez-Bourgon, Javier, Villalon-Reina, Julio, Volker, Uwe, Volzke, Henry, Vorstman, Jacob, Westlye, Lars, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Wittfeld, Katharina, Wright, Margaret, Thompson, Paul, Andreassen, Ole and Linden, David ORCID: https://orcid.org/0000-0002-5638-9292 2025. Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology. Biological Psychiatry 10.1016/j.bpsc.2025.05.010
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Doherty, Joanne L., Cunningham, Adam C., Chawner, Samuel J. R. A., Moss, Hayley M., Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, 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 Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2024. Atypical cortical networks in children at high-genetic risk of psychiatric and eurodevelopmental disorders. Neuropsychopharmacology 49 , pp. 368-376. 10.1038/s41386-023-01628-x
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Niarchou, Maria, Cunningham, Adam, Chawner, Samuel, Moulding, Hayley, Sopp, Matthew, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2023. Psychopathology in mothers of children with pathogenic copy number variants. Journal of Medical Genetics 60 , pp. 706-711. 10.1136/jmg-2022-108752
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Donnelly, Nicholas, Cunningham, Adam, Salas, Sergio Marco, Bracher-Smith, Matthew, Chawner, Samuel, Stochl, Jan, Ford, Tamsin, Raymond, F. Lucy, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2023. Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach. Molecular Autism 14 (1) , 19. 10.1186/s13229-023-00549-2
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Cunningham, Adam C., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2022. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. Psychological Medicine 52 (3) , pp. 574-586. 10.1017/S0033291720002330
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Sønderby, Ida, Ching, Christopher, Thomopoulos, Sophia, van der Meer, Dennis, Sun, Daqiang, Villalon Reina, Julio, Agartz, Ingrid, Amunts, Katrin, Arango, Celso, Armstrong, Nicola, Ayesa-Arriola, Rosa, Bakker, Geor, Bassett, Anne, Boomsma, Dorret, Bülow, Robin, Butcher, Nancy, Calhoun, Vince, Caspers, Svenja, Chow, Eva, Cichon, Sven, Ciufolini, Simone, Craig, Michael, Crespo-Facorro, Benedicto, Cunningham, Adam, Dale, Anders, Dazzan, Paola, de Zubicaray, Greig, Djurovic, Srdjan, Doherty, Joanne, Donohoe, Gary, Draganski, Bogdan, Durdle, Courtney, Ehrlich, Stefan, Emanuel, Beverly, Espeseth, Thomas, Fisher, Simon, Ge, Tian, Glahn, David, Grabe, Hans, Gur, Raquel, Gutman, Boris, Haavik, Jan, Håberg, Asta, Hansen, Laura, Hashimoto, Ryota, Hibar, Derrek, Holmes, Avram, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke, Jalbrzikowski, Maria, Knowles, Emma, Kushan, Leila, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Liu, Jingyu, Lundervold, Astri, Martin-Brevet, Sandra, Martínez, Kenia, Mather, Karen, Mathias, Samuel, McDonald- McGinn, Donna, McRae, Allan, Medland, Sarah, Moberget, Torgeir, Modenato, Claudia, Monereo Sánchez, Jennifer, Moreau, Clara, Mühleisen, Thomas, Paus, Tomas, Pausova, Zdenka, Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline, Reis Marques, Tiago, Repetto, Gabriela, Reymond, Alexandre, Roalf, David, Rodriguez-Herreros, Borja, Rucker, James, Sachdev, Perminder, Schmitt, James, Schofield, Peter, Silva, Ana, Stefansson, Hreinn, Stein, Dan, Tamnes, Christian, Tordesillas-Gutiérrez, Diana, Ulfarsson, Magnus, Vajdi, Ariana, van 't Ent, Dennis, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vassos, Evangelos, Vázquez- Bourgon, Javier, Vila-Rodriguez, Fidel, Walters, G Bragi, Wen, Wei, Westlye, Lars, Wittfeld, Katharina, Zackai, Elaine, Stefánsson, Kári, Jacquemont, Sebastien, Thompson, Paul, Bearden, Carrie, Andreassen, Ole, ENIGMA-CNV Working Group and ENIGMA 22q11.2 Deletion Syndrome Working Group 2022. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA Working Groups on CNVs. Human Brain Mapping 43 (1) , pp. 300-328. 10.1002/hbm.25354
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Forsyth, Jennifer K., Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R. K., Villalon-Reina, Julio E., Thompson, Paul M., Bearden, Carrie E., Cunningham, Adam, Doherty, Joanne L., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7) , pp. 3285-3298. 10.1093/cercor/bhab008
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Cunningham, Adam, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 51 (2) , pp. 290-299. 10.1017/S0033291719003210
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Villalon-Reina, Julio, Martinez, Kenia, Qu, Xiaoping, Ching, Christopher, Nir, Talia, Kothapalli, Deydeep, Corbin, Conor, Dagiang, Sun, Lin, Amy, Forsyth, Jennifer, Kushan, Lelia, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy, Antshel, Kevin, Fremont, Wanda, Campbell, Linda, McCable, Kathryn, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh, Murphy, Declan, Craig, Michael, Emanual, Beverly, McDonna-McGinn, Donna, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David, Raquel, Gur, Eric, Schmitt, Simon, Tony, Goodrich-Hunsaker, Naomi, Durdle, Courtney, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran, Arango, Celso, Jahanshad, Neda, Thompson, Paul and Bearden, Carrie 2020. Altered white matter microstructure in 22q11.2 deletion syndrome: a multi-site diffusion tensor imaging study. Molecular Psychiatry 25 , pp. 2818-2831. 10.1038/s41380-019-0450-0
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Sun, Daqiang, Ching, Christopher R. K., Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E., Qu, Xiaoping, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan, Craig, Michael, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David R., Gur, Raquel E., Schmitt, J. Eric, Simon, Tony J., Goodrich-Hunsaker, Naomi J., Durdle, Courtney A., Bassett, Anne S., Chow, Eva W. C., Butcher, Nancy J., Vila-Rodriguez, Fidel, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne B M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., McDonald-McGinn, Donna M., Emanuel, Beverly, van Erp, Theo G. M., Turner, Jessica A., Thompson, Paul M. and Bearden, Carrie E. 2020. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry 25 , pp. 1822-1834. 10.1038/s41380-018-0078-5
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Cunningham, Adam, Fung, Wilson, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078
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Ching, Christopher R.K., Gutman, Boris A., Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K., Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K., Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Campbell, Linda E., McCabe, Kathryn L., Craig, Michael C., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Murphy, Kieran C., Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T. Blaine, Emanuel, Beverly S., Gur, Raquel E., McDonald-McGinn, Donna M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Zackai, Elaine H., Durdle, Courtney A., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Bassett, Anne S., Butcher, Nancy J., Chow, Eva W.C., Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E., Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Crossley, Nicolas A., Repetto, Gabriela M., Thompson, Paul M. and Bearden, Carrie E. 2020. Mapping subcortical brain alterations in 22q11.2 deletion syndrome: effects of seletion size and convergence with idiopathic neuropsychiatric illness. American Journal of Psychiatry 177 (7) , pp. 589-600. 10.1176/appi.ajp.2019.19060583

Eaton, Christopher B. ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, Rhys H., Hamandi, Khalid, Payne, Gareth C., Kerr, Michael P., Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, Adam C., Bartsch, Ullrich, Struik, Siske S. and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2020. Response to letter to editor: 'Knowing when and how to use epilepsy screening questionnaires'. Epilepsia 61 (4) , pp. 826-827. 10.1111/epi.16463

Chamberland, Maxime ORCID: https://orcid.org/0000-0001-7064-0984, Genc, Sila, Raven, Erika P., Parker, Greg D., Cunningham, Adam, Doherty, Joanne, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Tax, Chantal M. W. ORCID: https://orcid.org/0000-0002-7480-8817 and Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 2020. Tractometry-based anomaly detection for single-subject white matter analysis. Presented at: Medical Imaging with Deep Learning (MIDL 2020), Montréal, Canada, 6-9 July 2020.
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Eaton, C. B. ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, R. H. ORCID: https://orcid.org/0000-0003-2062-8623, Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, A. C., Bartsch, U. B., Struik, S. S. and van den Bree, M. B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Prevalence and aetiology of epileptic seizures in young people with 22Q11.2 Deletion syndrome and relationships with other neurodevelopmental disorders. Presented at: SSBP 22nd Educational Day and Research Symposium 2019, Birmingham, England, 4-6 September 2019. Journal of Intellectual Disability Research. , vol.63 (9) Wiley, p. 1080. 10.1111/jir.12676

Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944, Linden, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 , 8. 10.1186/s11689-019-9271-3
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Eaton, Christopher ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, Rhys ORCID: https://orcid.org/0000-0003-2062-8623, Hamandi, Khalid, Payne, Gareth, Kerr, Michael, Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, Adam, Bartsch, Ullrich, Struik, Siske and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2019. Epilepsy and seizures in young people with 22q11.2 deletion syndrome: prevalence and links with other neurodevelopmental disorders. Epilepsia 60 (5) , pp. 818-829. 10.1111/epi.14722
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Brieva, Jorge, Lepore, Natasha, Romero, Eduardo, Cunningham, Adam C., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Schmitt, Eric, Gur, Raquel E., Roalf, David, Ruparel, Kosha, McDonald-McGinn, Donna, Emanuel, Beverly, Craig, Michael, Murphy, Declan, Murphy, Clodaph, Gudbrandsen, Maria, Daly, Eileen, Kates, Wendy R., Bakker, Geor, van Amelsvoort, Therese, Jonas, Rachel, Hansen, Laura, Lin, Amy, Nir, Talia, Sun, Daqiang V., Kothapalli, Deydeep, Ching, Christopher R., Thompson, Paul M., Bearden, Carrie E., Jahanshad, Neda, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Doherty, Joanne, Durdle, Courtney A., McCabe, Kathryn L., Campbell, Linda E., Fremont, Wanda, Antshel, Kevin M., Jalbrzikowski, Maria, Vajdi, Ariana V., Kushan, Leila V., Forsyth, Jennifer K. and Villalón-Reina, Julio 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome. Presented at: 14th International Symposium on Medical Information Processing and Analysis,, Mazatlán, Mexico, 24-26 October 2018. Published in: Romero, Eduardo, Lepore, Natasha and Brieva, Jorge eds. 14th International Symposium on Medical Information Processing and Analysis. Proceedings of SPIE , vol.10975 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Cunningham, Adam C., Delport, Sue ORCID: https://orcid.org/0000-0001-8065-5493, Cumines, Wendy, Busse, Monica, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2018. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome. British Journal of Psychiatry 212 (1) , pp. 27-33. 10.1192/bjp.2017.6
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Cunningham, Adam 2017. Coordination and sensorimotor difficulties in children with 22q11.2 deletion syndrome: relationships with cognition and psychopathology. PhD Thesis, Cardiff University.
Item availability restricted.
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Wright, Josephine A., McHugh, Patrick C., Pan, Siyi, Cunningham, Adam and Brown, David R. 2013. Counter-regulation of alpha- and beta-synuclein expression at the transcriptional level. Molecular and Cellular Neuroscience 57 , pp. 33-41. 10.1016/j.mcn.2013.09.002

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