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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 |
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 |
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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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, 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 |
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 |
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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.
Item availability restricted. |