ORCA
Online Research @ Cardiff

Clear Cookie - decide language by browser settings

Browse by Current Cardiff authors

Number of items: 17.

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., Moss, Hayley, Owen, Michael and Van den Bree, Marianne 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 10.1093/cercor/bhab008

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, 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, 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, 2021. 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 10.1002/hbm.25354

Cunningham, Adam, Hall, Jeremy, Owen, Michael and Van den Bree, Marianne 2021. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 51 (2) , pp. 290-299. 10.1017/S0033291719003210

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, Linden, David, Owen, Michael, 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

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., Linden, David E. J., Moss, Hayley, Owen, Michael J., 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

Cunningham, Adam, Fung, Wilson, Massey, Thomas, Hall, Jeremy, Owen, Michael, Van Den Bree, Marianne and Peall, Kathryn 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078

Cunningham, Adam C., Hall, Jeremy, Owen, Michael and van den Bree, Marianne B. M. 2020. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. Psychological Medicine 10.1017/S0033291720002330

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., van den Bree, Marianne, 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., Thomas, Rhys H., Hamandi, Khalid, Payne, Gareth C., Kerr, Michael P., Linden, David E. J., Owen, Michael J., Cunningham, Adam C., Bartsch, Ullrich, Struik, Siske S. and van den Bree, Marianne B. M. 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, Genc, Sila, Raven, Erika P., Parker, Greg D., Cunningham, Adam, Doherty, Joanne, van den Bree, Marianne, Tax, Chantal M. W. and Jones, Derek K. 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.

Eaton, C. B., Thomas, R. H., Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J., Owen, M. J., Cunningham, A. C., Bartsch, U. B., Struik, S. S. and van den Bree, M. B. M. 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. , vol. 9. Wiley, p. 1080. 10.1111/jir.12676

Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn, Linden, David, Hall, Jeremy, Owen, Michael and van den Bree, Marianne 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

Eaton, Christopher, Thomas, Rhys, Hamandi, Khalid, Payne, Gareth, Kerr, Michael, Linden, David, Owen, Michael, Cunningham, Adam, Bartsch, Ullrich, Struik, Siske and van den Bree, Marianne 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

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, Linden, David E., Van Den Bree, Marianne, 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 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Cunningham, Adam C., Delport, Sue, Cumines, Wendy, Busse, Monica, Linden, David E. J., Hall, Jeremy, Owen, Michael J. and van den Bree, Marianne 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

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.

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

This list was generated on Tue Apr 20 04:17:43 2021 BST.

Export as	Atom RSS 1.0 RSS 2.0