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Chawner, Samuel, Doherty, Joanne L., Anney, Richard, 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, Owen, Michael J. and van den Bree, Marianne B.M.
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
Item availability restricted. |
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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, 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
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Dima, Diana C., Adams, Rachael, Linden, Stefanie C., Baird, Alister, Smith, Jacqueline, Foley, Sonya, Perry, Gavin, Routley, Bethany C., Magazzini, Lorenzo, Drakesmith, Mark, Williams, Nigel, Doherty, Joanne, van den Bree, Marianne B. M., Owen, Michael J., Hall, Jeremy, Linden, David E. J. and Singh, Krish D.
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
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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., 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
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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., 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 |
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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. |
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Niarchou, Maria, 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., Linden, Stefanie C., Raymond, F. Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J. and Van Den Bree, Marianne B. M.
2019.
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Translational Psychiatry
10.1038/s41398-018-0339-8
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Doherty, Joanne Louise
2019.
Excitatory-inhibitory balance in children with 22q11.2 deletion syndrome.
PhD Thesis,
Cardiff University.
Item availability restricted. |
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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, 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 |
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Chawner, Samuel J.R.A., Niarchou, Maria, Doherty, Joanne L., Moss, Hayley, Owen, Michael J. and Van Den Bree, Marianne 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 |
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Doherty, Joanne, Cooper, Miriam and Thapar, Anita 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 |
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Reddaway, Jack, Doherty, Joanne L., Lancaster, Thomas, Linden, David, Walters, James T. and Hall, Jeremy 2018. Genomic and imaging biomarkers in schizophrenia. Current Topics in Behavioral Neurosciences, Berlin and Heidelberg: Springer, pp. 325-352. (10.1007/7854_2018_52) |
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Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria, Walters, James, Owen, Michael J. and Van Den Bree, Marianne Bernadette 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 |
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Owen, Michael John 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 |
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Cooper, Miriam, Eyre, Olga, Doherty, Joanne L. and Bevan-Jones, Rhys
2016.
Gaining approvals for mental health research in the NHS.
BJPscyh Advances
22
(1)
, pp. 64-72.
10.1192/apt.bp.114.014035
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Doherty, Joanne and Owen, Michael John 2014. Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. Genome Medicine 6 (4) , 29. 10.1186/gm546 |
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Doherty, Joanne L. and Owen, Michael John 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 |
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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 |
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Doherty, Joanne L., O'Donovan, Michael Conlon and Owen, Michael John 2012. Recent genomic advances in schizophrenia. Clinical Genetics 81 (2) , pp. 103-109. 10.1111/j.1399-0004.2011.01773.x |
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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 |
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