Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Browse by Current Cardiff authors

[up] Up a level
Number of items: 29.

Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Duffin, Donna, Doherty, Joanne, Irving, Rachel, Procter, Annie and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2024. The translation of psychiatric genetics findings to the clinic. Schizophrenia Research 267 , pp. 470-472. 10.1016/j.schres.2023.10.024
file

Boen, Rune, Kaufmann, Tobias, van der Meer, Dennis, Frei, Oleksandr, Agartz, Ingrid, Ames, David, Andersson, Micael, Armstrong, Nicola J., Artiges, Eric, Atkins, Joshua R., Bauer, Jochen, Benedetti, Francesco, Boomsma, Dorret I., Brodaty, Henry, Brosch, Katharina, Buckner, Randy L., Cairns, Murray J., Calhoun, Vince, Caspers, Svenja, Cichon, Sven, Corvin, Aiden P., Facorro, Benedicto Crespo, Dannlowski, Udo, David, Friederike S., de Geus, Eco J.C., de Zubicaray, Greig I., Desrivières, Sylvane, Doherty, Joanne L., Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fisher, Simon E., Forstner, Andreas J., Uyà, Lidia Fortaner, Frouin, Vincent, Fukunaga, Masaki, Ge, Tian, Glahn, David C., Goltermann, Janik, Grabe, Hans J., Green, Melissa J., Groenewold, Nynke A., Grotegerd, Dominik, Hahn, Tim, Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Henskens, Frans A., Holmes, Avram J., Haberg, Asta K., Haavik, Jan, Jacquemont, Sebastien, Jansen, Andreas, Jockwitz, Christiane, Jonsson, Erik G., Kikuchi, Masataka, Kircher, Tilo, Kumar, Kuldeep, Le Hellard, Stephanie, Leu, Costin, Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Liu, Jingyu, Loughnan, Robert, Mather, Karen A., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Meinert, Susanne, Moreau, Clara A., Morris, Derek W., Mowry, Bryan J., Muhleisen, Thomas W., Nenadi?, Igor, Nöthen, Markus M., Nyberg, Lars, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paolini, Marco, Paus, Tomas, Pausova, Zdenka, Persson, Karin, Quidé, Yann, Marques, Tiago Reis, Sachdev, Perminder S., Sando, Sigrid B., Schall, Ulrich, Scott, Rodney J., Selbæk, Geir, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Stein, Frederike, Stein, Dan J., Straube, Benjamin, Streit, Fabian, Strike, Lachlan T., Teumer, Alexander, Teutenberg, Lea, Thalamuthu, Anbupalam, Tooney, Paul A., Tordesillas-Gutierrez, Diana, Trollor, Julian N., Ent, Dennis van 't, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254, van Haren, Neeltje E.M., Vazquez-Bourgon, Javier, Volzke, Henry, Wen, Wei, Wittfeld, Katharina, Ching, Christopher R.K., Westlye, Lars T., Thompson, Paul M., Bearden, Carrie E., Selmer, Kaja K., Alnæs, Dag, Andreassen, Ole A. and Sonderby, Ida E. 2024. Beyond the global brain differences: Intra-individual variability differences in 1q21.1 distal and 15q11.2 BP1-BP2 deletion carriers. Biological Psychiatry 95 (2) , pp. 147-160. 10.1016/j.biopsych.2023.08.018
file

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
file

Ge, Ruiyang, Ching, Christopher R. K., Bassett, Anne S., Kushan, Leila, Antshel, Kevin M., van Amelsvoort, Therese, Bakker, Geor, Butcher, Nancy J., Campbell, Linda E., Chow, Eva W. C., Craig, Michael, Crossley, Nicolas A., Cunningham, Adam, Daly, Eileen, Doherty, Joanne L., Durdle, Courtney A., Emanuel, Beverly S., Fiksinski, Ania, Forsyth, Jennifer K., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Gur, Raquel E., Jalbrzikowski, Maria, Kates, Wendy R., Lin, Amy, Linden, David E. J., McCabe, Kathryn L., McDonald‐McGinn, Donna, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Villalon‐Reina, Julio E., Repetto, Gabriela M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Schuite‐Koops, Sanne, Angkustsiri, Kathleen, Sun, Daqiang, Vajdi, Ariana, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vorstman, Jacob, Thompson, Paul M., Vila‐Rodriguez, Fidel and Bearden, Carrie E. 2024. Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping 45 (1) , e26553. 10.1002/hbm.26553
file

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
file

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
file

Chamberland, Maxime ORCID: https://orcid.org/0000-0001-7064-0984, Genc, Sila, Tax, Chantal M.W. ORCID: https://orcid.org/0000-0002-7480-8817, Shastin, Dmitri, Koller, Kristin ORCID: https://orcid.org/0000-0001-6676-7106, Raven, Erika P., Cunningham, Adam, Doherty, Joanne, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Parker, Greg D., Hamandi, Khalid, Gray, William ORCID: https://orcid.org/0000-0001-7595-8887 and Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 2021. Detecting microstructural deviations in individuals with deep diffusion MRI tractometry. Nature Computational Science 1 , pp. 598-606. 10.1038/s43588-021-00126-8
file

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
file

Chawner, Samuel, Doherty, Joanne L., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Antshel, Kevin M., Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Koche, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., MihaljevicMihaljevic, Marina Mihaljevic, Miller, Judith S., Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., 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 B.M. ORCID: https://orcid.org/0000-0002-4426-3254 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178 (1) , pp. 77-86. 10.1176/appi.ajp.2020.20010015
filefilefile

Sønderby, Ida E., 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, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Silva, Ana ORCID: https://orcid.org/0000-0002-1184-4909 and Doherty, Joanne 2021. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry 11 , 182. 10.1038/s41398-021-01213-0
file

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
file

Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Adams, Rachael, Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Baird, Alister, Smith, Jacqueline, Foley, Sonya ORCID: https://orcid.org/0000-0002-8390-2709, Perry, Gavin ORCID: https://orcid.org/0000-0003-0468-0421, Routley, Bethany C., Magazzini, Lorenzo ORCID: https://orcid.org/0000-0002-8934-8374, Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Doherty, Joanne, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292 and Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2020. Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk. Translational Psychiatry 10 , 324. 10.1038/s41398-020-00998-w
file

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
file

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

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.
file

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Chawner, Samuel J.R.A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sbastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Raymond, F. Lucy, Skuse, David, 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 B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry 10.1038/s41398-018-0339-8
file

Doherty, Joanne Louise 2019. Excitatory-inhibitory balance in children with 22q11.2 deletion syndrome. PhD Thesis, Cardiff University.
Item availability restricted.
filefile

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

Chawner, Samuel J.R.A., Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Doherty, Joanne L., Moss, Hayley, 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. The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 109 , pp. 10-17. 10.1016/j.jpsychires.2018.11.002
file

Doherty, Joanne, Cooper, Miriam ORCID: https://orcid.org/0000-0002-4695-5481 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2018. Advances in our understanding of the genetics of childhood neurodevelopmental disorders. Evidence-Based Mental Health 21 (4) , pp. 171-172. 10.1136/ebmental-2018-300067
file

Reddaway, Jack, Doherty, Joanne L., Lancaster, Thomas ORCID: https://orcid.org/0000-0003-1322-2449, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Walters, James T. ORCID: https://orcid.org/0000-0002-6980-4053 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2018. Genomic and imaging biomarkers in schizophrenia. Current Topics in Behavioral Neurosciences, Berlin and Heidelberg: Springer, pp. 325-352. (10.1007/7854_2018_52)

Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2017. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study. British Journal of Psychiatry 211 (4) , pp. 223-230. 10.1192/bjp.bp.116.195651
file

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Doherty, Joanne L 2016. What can we learn from the high rates of schizophrenia in people with 22q11.2 deletion syndrome? World Psychiatry 15 (1) , pp. 23-25. 10.1002/wps.20274

Cooper, Miriam ORCID: https://orcid.org/0000-0002-4695-5481, Eyre, Olga, Doherty, Joanne L. and Bevan-Jones, Rhys ORCID: https://orcid.org/0000-0001-8976-9825 2016. Gaining approvals for mental health research in the NHS. BJPscyh Advances 22 (1) , pp. 64-72. 10.1192/apt.bp.114.014035
file

Doherty, Joanne and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2014. Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. Genome Medicine 6 (4) , 29. 10.1186/gm546

Doherty, Joanne L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2014. The Research Domain Criteria: moving the goalposts to change the game. British Journal of Psychiatry 204 (3) , pp. 171-173. 10.1192/bjp.bp.113.133330

Yip, Sarah W, Doherty, Joanne L., Wakeley, Judi, Saunders, Kate, Tzagarakis, Charidimos, de Wit, Harriet, Goodwin, Guy M and Rogers, Robert D 2012. Reduced subjective response to acute ethanol administration among young men with a broad bipolar phenotype. Neuropsychopharmacology 37 (8) , pp. 1808-1815. 10.1038/npp.2012.45

Doherty, Joanne L., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. Recent genomic advances in schizophrenia. Clinical Genetics 81 (2) , pp. 103-109. 10.1111/j.1399-0004.2011.01773.x

Zarei, Mojtaba, Mataix-Cols, David, Heyman, Isobel, Hough, Morgan, Doherty, Joanne L., Burge, Linda, Winmill, Louise, Nijhawan, Sunita, Matthews, Paul M. and James, Anthony 2011. Changes in gray matter volume and white matter microstructure in adolescents with obsessive-compulsive disorder. Biological psychiatry 70 (11) , pp. 1083-1090. 10.1016/j.biopsych.2011.06.032

This list was generated on Thu May 1 06:15:54 2025 BST.


Maintained by Cardiff University Information Services