Schizophrenia: genes and environment

Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality.

Chae, T., Kwon, Y. T., Bronson, R., Dikkes, P., Li, E., & Tsai, L.-H. (1997) · Neuron · doi:10.1016/s0896-6273(01)80044-1 · Cited by 715

Trajectories of brain development: point of vulnerability or window of opportunity?

Andersen, S. L. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00005-8 · Cited by 1,503

Molecular Characterization of Schizophrenia Viewed by Microarray Analysis of Gene Expression in Prefrontal Cortex

Mirnics, K., Middleton, F. A., Marquez, A., Lewis, D. A., & Levitt, P. (2000) · Neuron · doi:10.1016/s0896-6273(00)00085-4 · Cited by 882

Alterations induced by gestational stress in brain morphology and behaviour of the offspring

Weinstock, M. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(01)00018-1 · Cited by 791

Towards an immuno-precipitated neurodevelopmental animal model of schizophrenia

Meyer, U., Feldon, J., Schedlowski, M., & Yee, B. K. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.10.012 · Cited by 494

Alterations in GABA-related transcriptome in the dorsolateral prefrontal cortex of subjects with schizophrenia

Hashimoto, T., Arion, D., Unger, T., Maldonado-Avilés, J. G., Morris, H. M., Volk, D. W., Mirnics, K., & Lewis, D. A. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002011 · Cited by 490

Experience-driven brain plasticity: Beyond the synapse

MARKHAM, J. A., & GREENOUGH, W. T. (2004) · Neuron Glia Biology · doi:10.1017/s1740925x05000219 · Cited by 437

Schizophrenia and Oxidative Stress: Glutamate Cysteine Ligase Modifier as a Susceptibility Gene

Tosic, M., Ott, J., Barral, S., Bovet, P., Deppen, P., Gheorghita, F., Matthey, M.-L., Parnas, J., Preisig, M., Saraga, M., et al. (2006) · The American Journal of Human Genetics · doi:10.1086/507566 · Cited by 234

Early developmental milestones in adult schizophrenia and other psychoses. A 31-year follow-up of the Northern Finland 1966 Birth Cohort

Isohanni, M., Jones, P. B., Moilanen, K., Rantakallio, P., Veijola, J., Oja, H., Koiranen, M., Jokelainen, J., Croudace, T., & Järvelin, M.-R. (2001) · Schizophrenia Research · doi:10.1016/s0920-9964(00)00179-1 · Cited by 184

Intestinal Microbiota Influences Non-intestinal Related Autoimmune Diseases

Opazo, M. C., Ortega-Rocha, E. M., Coronado-Arrázola, I., Bonifaz, L. C., Boudin, H., Neunlist, M., Bueno, S. M., Kalergis, A. M., & Riedel, C. A. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00432 · Cited by 179

The burden of complex genetics in brain disorders

Uhl, G. R., & Grow, R. W. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.3.223 · Cited by 176

Acute stress-induced impairment of spatial memory is associated with decreased expression of neural cell adhesion molecule in the hippocampus and prefrontal cortex

Sandi, C., Woodson, J. C., Haynes, V. F., Park, C. R., Touyarot, K., Lopez-Fernandez, M. A., Venero, C., & Diamond, D. M. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.12.034 · Cited by 122

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients

Buizer-Voskamp, J. E., Muntjewerff, J.-W., Strengman, E., Sabatti, C., Stefansson, H., Vorstman, J. A. S., & Ophoff, R. A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.015 · Cited by 68

Imprinting in the schizophrenia candidate gene GABRB2 encoding GABAA receptor β2 subunit

Pun, F. W., Zhao, C., Lo, W.-S., Ng, S.-K., Tsang, S.-Y., Nimgaonkar, V, Chung, W. S., Ungvari, G. S., & Xue, H. (2011) · Molecular Psychiatry · doi:10.1038/mp.2010.47 · Cited by 53

Convergent Evidence from Multimodal Imaging Reveals Amygdala Abnormalities in Schizophrenic Patients and Their First-Degree Relatives

Tian, L., Meng, C., Yan, H., Zhao, Q., Liu, Q., Yan, J., Han, Y., Yuan, H., Wang, L., Yue, W., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028794 · Cited by 44

Resting cortisol level, self-concept, and putative familial environment in adolescents at ultra high-risk for psychotic disorders

Carol, E. E., & Mittal, V. A. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.03.018 · Cited by 44

Reinforcement learning as an intermediate phenotype in psychosis? Deficits sensitive to illness stage but not associated with polygenic risk of schizophrenia in the general population

Montagnese, M., Knolle, F., Haarsma, J., Griffin, J. D., Richards, A., Vertes, P. E., Kiddle, B., Fletcher, P. C., Jones, P. B., Owen, M. J., et al. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.04.022 · Cited by 26

Stress Exposure in Dopamine D4 Receptor Knockout Mice Induces Schizophrenia-Like Behaviors via Disruption of GABAergic Transmission

Tan, T., Wang, W., Williams, J., Ma, K., Cao, Q., & Yan, Z. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sby163 · Cited by 29

Circular RNA: A novel and potential regulator in pathophysiology of schizophrenia

Singh, M., Dwibedy, S. L. L., Biswal, S. R., Muthuswamy, S., Kumar, A., & Kumar, S. (2022) · Metabolic Brain Disease · doi:10.1007/s11011-022-00978-7 · Cited by 15

Seeing Double: A Case Study Examining Systemic Supervision and Therapy Conceptualization of Identical Twins

Lowery, D. F., & Outler, C. (2026) · The Family Journal · doi:10.1177/10664807251384191