Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways von Cappi, C, Brentani, H, Lima, L, Sanders, S J, Zai, G, Diniz, B J, Reis, V N S, Hounie, A G, Conceição do Rosário, M, Mariani, D, Requena, G L, Puga, R, Souza-Duran, F L, Shavitt, R G, Pauls, D L, Miguel, E C, Fernandez, T V

Volltext

P.1.a.018 Personalised medicine in psychiatry – pharmacogenetics of antidepressant response in obsessive-compulsive disorder von Zai, G, Cappi, C, Gonçalves, V, Zai, C, Shavitt, R, Miguel, E, Richter, M, Kennedy, J

Volltext

Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder von Yilmaz, Zeynep, Halvorsen, Matthew, Bryois, Julien, Yu, Dongmei, Thornton, Laura M., Zerwas, Stephanie, Micali, Nadia, Moessner, Rainald, Burton, Christie L., Zai, Gwyneth, Erdman, Lauren, Kas, Martien J., Arnold, Paul D., Davis, Lea K., Knowles, James A., Breen, Gerome, Scharf, Jeremiah M., Nestadt, Gerald, Mathews, Carol A., Bulik, Cynthia M., Mattheisen, Manuel, Crowley, James J.

Volltext

5HT1Dβ receptor gene implicated in the pathogenesis of Obsessive-Compulsive Disorder: further evidence from a family-based association study von MUNDO, E, RICHTER, M. A, ZAI, G, SAM, F, MCBRIDE, J, MACCIARDI, F, KENNEDY, J. L

Volltext

Identification of VRK1 as a Novel Potential Biomarker for Prognosis and Immunotherapy in Hepatocellular Carcinoma von He, Xiaoyan, Zai, Guozhen, Zhou, Lidan, Chen, Shengyang, Wang, Guizhi

Volltext

Genetics for mental health clinicians: a call for a globally accessible and equitable psychiatric genetics education von Alnor, A., Besterman, A.D., Castaño, M., DeLisi, L., Grice, D.E., Lohof, F.W., Middeldorp, C., Moreno‐De‐Luca, D., Quattrone, D., Nurnberger, J.I., Nurmi, E., Ross, D.A., Soda, T., Schulze, T.G., Trost, B., Vilella, E., Yap, C., Zai, G.

Volltext

Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor von BARR, C. L, WIGG, K. G, FENG, Y, ZAI, G, MALONE, M, ROBERTS, W, SCHACHAR, R, TANNOCK, R, KENNEDY, J. L

Volltext

Attention Deficit Hyperactivity Disorder and the Gene for Dopamine Beta-Hydroxylase von Wigg, Karen, Zai, Gwyneth, Schachar, Russell, Tannock, Rosemary, Roberts, Wendy, Malone, Molly, Kennedy, James L., Barr, Cathy L.

Volltext

Attention-deficit hyperactivity disorder and the adrenergic receptors α1C and α2C von BARR, C. L, WIGG, K, ZAI, G, ROBERTS, W, MALONE, M, SCHACHAR, R, TANNOCK, R, KENNEDY, J. L

Volltext

Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia von Zai, G., King, N., Wigg, K., Couto, J., Wong, G. W. H., Honer, W. G., Barr, C. L., Kennedy, J. L.

Volltext

Genetic study of eight AKT1 gene polymorphisms and their interaction with DRD2 gene polymorphisms in tardive dyskinesia von Zai, Clement C, Romano-Silva, Marco A, Hwang, Rudi, Zai, Gwyneth C, DeLuca, Vincenzo, Müller, Daniel J, King, Nicole, Voineskos, Aristotle N, Meltzer, Herbert Y, Lieberman, Jeffrey A, Potkin, Steven G, Remington, Gary, Kennedy, James L

Volltext

Trichotillomania: the impact of treatment history on the outcome of an Internet-based intervention von Weidt, Steffi, Bruehl, Annette Beatrix, Delsignore, Aba, Zai, Gwyneth, Kuenburg, Alexa, Klaghofer, Richard, Rufer, Michael

Volltext

Unravelling the GSK3 beta-related genotypic interaction network influencing hippocampal volume in recurrent major depressive disorder von Inkster, B, Simmons, A, Cole, JH, Schoof, E, Linding, R, Nichols, T, Muglia, P, Holsboer, F, Saemann, PG, McGuffin, P, Fu, CHY, Miskowiak, K, Matthews, PM, Zai, G, Nicodemus, K

Volltext

Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015 von Zai, Gwyneth, Alberry, Bonnie, Arloth, Janine, Bánlaki, Zsófia, Bares, Cristina, Boot, Erik, Camilo, Caroline, Chadha, Kartikay, Chen, Qi, Cole, Christopher B, Cost, Katherine T, Crow, Megan, Ekpor, Ibene, Fischer, Sascha B, Flatau, Laura, Gagliano, Sarah, Kirli, Umut, Kukshal, Prachi, Labrie, Viviane, Lang, Maren, Lett, Tristram A, Maffioletti, Elisabetta, Maier, Robert, Mihaljevic, Marina, Mittal, Kirti, Monson, Eric T, O’Brien, Niamh L, Østergaard, Søren D, Ovenden, Ellen, Patel, Sejal, Peterson, Roseann E, Pouget, Jennie G, Rovaris, Diego L, Seaman, Lauren, Shankarappa, Bhagya, Tsetsos, Fotis, Vereczkei, Andrea, Wang, Chenyao, Xulu, Khethelo, Yuen, Ryan K.C, Zhao, Jingjing, Zai, Clement C, Kennedy, James L

Volltext

Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder von Barr, Cathy L, Xu, Chun, Kroft, Jamie, Feng, Yu, Wigg, Karen, Zai, Gwyneth, Tannock, Rosemary, Schachar, Russell, Malone, Molly, Roberts, Wendy, Nöthen, Markus M, Grünhage, Frank, Vandenbergh, David J, Uhl, George, Sunohara, Glen, King, Nicole, Kennedy, James L

Volltext

Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways von Cappi, C, Brentani, H, Lima, L, Sanders, S J, Zai, G, Diniz, B J, Reis, V N S, Hounie, A G, Conceição do Rosário, M, Mariani, D, Requena, G L, Puga, R, Souza-Duran, F L, Shavitt, R G, Pauls, D L, Miguel, E C, Fernandez, T V

Volltext

Myelin oligodendrocyte glycoprotein (MOG) gene is associated with obsessive-compulsive disorder von Zai, Gwyneth, Bezchlibnyk, Yarema B., Richter, Margaret A., Arnold, Paul, Burroughs, Eliza, Barr, Cathy L., Kennedy, James L.

Volltext

Association study between the novel functional polymorphism of the serotonin transporter gene and suicidal behaviour in schizophrenia von De Luca, Vincenzo, Zai, Gwyneth, Tharmalingam, Subi, de Bartolomeis, Andrea, Wong, Greg, Kennedy, James L.

Volltext

Malignant Mesothelioma of the Pleura. The Reproducibility of the Immunohistological Diagnosis von Betta, P.-G., Andrion, A., Donna, A., Mollo, F., Scelsi, M., Zai, G., Terracini, B., Magnani, C.

Volltext

Possible association between the gamma-aminobutyric acid type B receptor 1 (GABBR1) gene and schizophrenia von Zai, Gwyneth, King, Nicole, Wong, Gregory W.H., Barr, Cathy L., Kennedy, James L.

Volltext