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Number of items: 20.

Cleynen, Isabelle, International q.DS Brain and Behavior Consortium, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A.S., Bearden, Carrie E., Chow, Eva W. C., Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Emanuel, Beverley S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Chopra, Pankaj, Cutler, David J., Duncan, Richard, Kotlar, Alex V., Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Demaeral, Wolfman, Boot, Erik, Butcher, Nancy J., Costain, Gregory A., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koren, Vergaelen, Elfi, Vogels, Annick, Crowley, Blaine, McGinn, Daniel E., Moss, Edward M., Sharkus, Robert J., Unolt, Marta, Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Moss, Hayley, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan C., Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stephan, Sandini, Corrado, Schneider, Maude, Bena, Frederique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, McCabe, Kathryn L., Philip, Nicole, Campbell, Linda E., Shashi, Vandana, Hooper, Stephen R., Schoch, Kelly, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, Garcia-Miñaur, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suner, Damia H., Raventos-Simic, Jasna, Epstein, Michael, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Bassett, Anne S. 2021. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry , pp. 4496-4510. 10.1038/s41380-020-0654-3
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Chawner, Samuel, Fiksinski, Ania, Vorstman, Jacob A.S., Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M., Emanuel, Beverly, Zackai, Elaine, Bearden, Carrie E., Shashi, Vandana, Hooper, Stephen R., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Gur, Raquel A., Wray, Naomi R., van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2019. Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome. Schizophrenia Research 204 , pp. 320-325. 10.1016/j.schres.2018.07.044
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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
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Byrne, Enda, Trzaskowski, Maciej, Sidorenko, Julia, Kemper, Kathryn, McGrath, John J., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Wray, Naomi R. 2019. Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Translational Psychiatry 10 , 51. 10.1038/s41398-020-0688-y
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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
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Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald-McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, van Amelsvoort, Thérèse A., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Bearden, Carrie E., Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C., Murphy, Clodagh, Garcia-Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey-Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine-Suner, Damian, Shprintzen, Robert J., Gur, Raquel E., Zackai, Elaine, Emanuel, Beverly S., Wang, Tao, Kates, Wendy R., Bassett, Anne S., Vorstman, Jacob A. S., Morrow, Bernice E., International 22q11.2, Brain and Behavior Consortium and Chawner, Samuel 2018. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics Part A 176 (10) , pp. 2172-2181. 10.1002/ajmg.a.40359
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Calkins, Monica E., Moore, Tyler M., Tang, Sunny, X., McDonald-McGinn, Donna M., Zackai, Elaine H., Emanuel, Beverly S., Gur, Ruben C. and Gur, Raquel E. 2018. Attention deficit hyperactivity disorder symptoms and psychosis in 22q11.2 deletion syndrome. Schizophrenia Bulletin 44 (4) , pp. 824-833. 10.1093/schbul/sbx113
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Demaerel, Wolfram, Hestand, Matthew S., Vergaelen, Elfi, Swillen, Ann, López-Sánchez, Marcos, Pérez-Jurado, Luis A., McDonald-McGinn, Donna M., Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E., Breckpot, Jeroen, Devriendt, Koenraad, Vermeesch, Joris R., Antshel, Kevin, Arango, Celso, Armando, Marco, Bassett, Anne, Bearden, Carrie, Boot, Erik, Bravo-Sanchez, Marta, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Campbell, Linda, Carmel, Miri, Chow, Eva, Crowley, T. Blaine, Cubells, Joseph, Cutler, David, Demaerel, Wolfram, Digilio, Maria Cristina, Duijff, Sasja, Eliez, Stephan, Emanuel, Beverly, Epstein, Michael, Evers, Rens, Fernandez Garcia-Moya, Luis, Fiksinski, Ania, Fraguas, David, Fremont, Wanda, Fritsch, Rosemarie, Garcia-Minaur, Sixto, Golden, Aaron, Gothelf, Doron, Guo, Tingwei, Gur, Ruben, Gur, Raquel, Heine-Suner, Damian, Hestand, Matthew, Hooper, Stephen, Kates, Wendy, Kushan, Leila, Laorden-Nieto, Alejandra, Maeder, Johanna, Marino, Bruno, Marshall, Christian, McCabe, Kathryn, McDonald-McGinn, Donna, Michaelovosky, Elena, Morrow, Bernice, Moss, Edward, Mulle, Jennifer, Murphy, Declan, Murphy, Kieran, Murphy, Clodagh, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Ornstein, Claudia, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Philip, Nicole, Repetto, Gabriela, Schneider, Maude, Shashi, Vandana, Simon, Tony, Swillen, Ann, Tassone, Flora, Unolt, Marta, van Amelsvoort, Therese, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Van Duin, Esther, Vergaelen, Elfi, Vermeesch, Joris, Vicari, Stefano, Vingerhoets, Claudia, Vorstman, Jacob, Warren, Steve, Weinberger, Ronnie, Weisman, Omri, Weizman, Abraham, Zackai, Elaine, Zhang, Zhengdong and Zwick, Michael 2017. Nested inversion polymorphisms predispose chromosome 22q11.2 to meiotic rearrangements [RETRACTED]. American Journal of Human Genetics 101 (4) , pp. 616-622. 10.1016/j.ajhg.2017.09.002
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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
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Gur, RE, Bassett, AS, McDonald-McGinn, DM, Bearden, CE, Chow, E, Emanuel, BS, Owen, M, Swillen, A, Van Den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Vermeesch, J, Vorstman, JAS, Warren, S, Lehner, T, Morrow, B and Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393 2017. A neurogenetic model for the study of schizophrenia spectrum disorders: The International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry 22 , pp. 1664-1672.
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Moore, Tyler M., Tang, Sunny X., Calkins, Monica E., McDonald-McGuinn, Donna M., Zackai, Elaine H., Emanuel, Beverly S., Gur, Ruben C. and Gur, Raquel E. 2017. The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 92 , pp. 124-131. 10.1016/j.jpsychires.2017.04.006
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2015. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 (8) , pp. 730-738. 10.1002/ajmg.b.32378
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Lewis, Glyn 2015. The Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort as a resource for studying psychopathology in childhood and adolescence: a summary of findings for depression and psychosis. Social Psychiatry and Psychiatric Epidemiology 50 (7) , pp. 1017-1027. 10.1007/s00127-015-1072-8

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2014. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (5) , pp. 410-420. 10.1002/ajmg.b.32245

Schneider, Maude, Debbané, Martin, Bassett, Anne S., Chow, Eva W.C., Fung, Wai Lun Alan, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W.J., Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J. and Eliez, Stephan 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: Results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171 (6) , pp. 627-639. 10.1176/appi.ajp.2013.13070864

Monks, Stephen, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Davies, Aimee, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 and Murphy, Kieran 2014. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Schizophrenia Research 153 (1-3) , pp. 231-236. 10.1016/j.schres.2014.01.020

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, van Goozen, Stephanie H. M. ORCID: https://orcid.org/0000-0002-5983-4734, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Tierling, Hayley M., 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 2014. Psychopathology and cognition in children with 22q11.2 deletion syndrome. British Journal of Psychiatry 204 (1) , pp. 46-54. 10.1192/bjp.bp.113.132324
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Lewis, Glyn, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2013. Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort. American Journal of Psychiatry 170 (5) , pp. 550-557. 10.1176/appi.ajp.2012.12060792
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Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S. and Morrow, Bernice E. 2013. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics 92 (3) , pp. 439-447. 10.1016/j.ajhg.2013.01.018

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393 2013. Cognition, psychopathology and the role of genetic variation in Catechol-O-Methyltransferase in children at increased risk of schizophrenia. PhD Thesis, Cardiff University.
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