Schizophrenia as a Disorder of Neurodevelopment

Implications of Normal Brain Development for the Pathogenesis of Schizophrenia

Weinberger, D. R. (1987) · Archives of General Psychiatry · doi:10.1001/archpsyc.1987.01800190080012 · Cited by 3,724

The Molecular Biology of Axon Guidance

Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311

Synaptic density in human frontal cortex —Developmental changes and effects of aging

Peter R., H. (1979) · Brain Research · doi:10.1016/0006-8993(79)90349-4 · Cited by 2,645

A review of MRI findings in schizophrenia

Shenton, M. E., Dickey, C. C., Frumin, M., & McCarley, R. W. (2001) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00163-3 · Cited by 2,346

Neuronal specification in the spinal cord: inductive signals and transcriptional codes

Jessell, T. M. (2000) · Nature Reviews Genetics · doi:10.1038/35049541 · Cited by 2,089

Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice

Kuida, K., Zheng, T. S., Na, S., Kuan, C.-Y., Yang, D., Karasuyama, H., RAKIC, P. T., & Flavell, R. A. (1996) · Nature · doi:10.1038/384368a0 · Cited by 1,881

Searching for genetic determinants in the new millennium

Risch, N. J. (2000) · Nature · doi:10.1038/35015718 · Cited by 1,839

Schizophrenia: Caused by a fault in programmed synaptic elimination during adolescence?

Feinberg, I. (1982) · Journal of Psychiatric Research · doi:10.1016/0022-3956(82)90038-3 · Cited by 1,395

Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies

Crawley, J. N., Belknap, J. K., Collins, A. C., Crabbe, J. C., Frankel, W. N., Henderson, N. D., HITZEMANN, R. J., Maxson, S. C., Miner, L. L., Silva, A. J., et al. (1997) · Psychopharmacology · doi:10.1007/s002130050327 · Cited by 1,389

Child developmental risk factors for adult schizophrenia in the British 1946 birth cohort

JONES, P. (1994) · The Lancet · doi:10.1016/s0140-6736(94)90569-x · Cited by 1,353

Electrophysiological correlates of visual backward masking in patients with first episode psychosis

Favrod, O., Roinishvili, M., da Cruz, J. N., Brand, A., Okruashvili, M., Gamkrelidze, T., Figueiredo, P., Herzog, M. H., Chkonia, E. D., & Shaqiri, A. (2018) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2018.10.008 · Cited by 14

Neuronal glucose metabolism and schizophrenia: therapeutic prospects?

Dwyer, D. S., Lu, X., & Freeman, A. M. (2003) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.3.1.29 · Cited by 14

Work-Related Abilities in Schizophrenia and HIV Infection

Twamley, E. W., Narvaez, J. M., Sadek, J. R., Jeste, D. V., Grant, I., & Heaton, R. K. (2006) · The Journal of Nervous and Mental Disease · doi:10.1097/01.nmd.0000207362.84045.1b · Cited by 14

Meta-analyses of the association between genetic polymorphisms of neurotrophic factors and schizophrenia

Lin, P., & Tsai, G. E. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.03.018 · Cited by 14

In Pursuit of the Pathogenesis and Pathophysiology of Schizophrenia: Where Do We Stand?

Lewis, D. A. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.9.1467 · Cited by 14

The multi-faceted, “global” cognitive impairment profile in schizophrenia

Dickinson, D., Schaefer, J. D., & Weinberger, D. R. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139003872.003 · Cited by 13

Mitochondrial regulation of adult hippocampal neurogenesis: Insights into neurological function and neurodevelopmental disorders

Bonzano, S., Dallorto, E., Bovetti, S., Studer, M., & Marchis, S. D. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106604 · Cited by 16

Pathways to Psychosis in Cannabis Abuse

Shrivastava, A., Johnston, M., Terpstra, K. J., & Bureau, Y. (2013) · Clinical Schizophrenia & Related Psychoses · doi:10.3371/csrp.shjo.030813 · Cited by 13

Enduring, Sexually Dimorphic Impact of In Utero Exposure to Elevated Levels of Glucocorticoids on Midbrain Dopaminergic Populations

Gillies, G. E., Virdee, K., Pienaar, I. S., Al-Zaid, F. S., & Dalley, J. W. (2016) · Brain Sciences · doi:10.3390/brainsci7010005 · Cited by 13

Environmental exposure to 17β-trenbolone during adolescence inhibits social interaction in male mice

Zhang, S., Jiao, Z., Zhao, X. J., Sun, M., & Feng, X. (2021) · Environmental Pollution · doi:10.1016/j.envpol.2021.117710 · Cited by 13

Toxoplasma gondii seropositivity and cognitive function in adults with schizophrenia

VELEVA, I. I., Stoychev, K., Stoimenova-Popova, M. Y., STOYANOV, L. S., Mineva-Dimitrova, E., & Angelov, I. (2022) · Schizophrenia Research Cognition · doi:10.1016/j.scog.2022.100269 · Cited by 13

Primate models of schizophrenia: future possibilities

Simen, A. A., Dileone, R., & Arnsten, A. F. T. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17913-x · Cited by 13

Association of theNOTCH4Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population

Zhang, B., Fan, Q., Li, W. H., Lu, N., Fu, D., Kang, Y. J., Wang, N., Li, T., Wen, X. P., & Li, D. X. (2015) · BioMed Research International · doi:10.1155/2015/408096 · Cited by 13

PD_NGSAtlas: a reference database combining next-generation sequencing epigenomic and transcriptomic data for psychiatric disorders

Zhao, Z., Li, Y., Chen, H., Lu, J., Thompson, P. M., Chen, J., Wang, Z., Xu, J., Xu, C. D., & Li, X. (2014) · BMC Medical Genomics · doi:10.1186/s12920-014-0071-z · Cited by 13

Finding a druggable target for schizophrenia

Rico, B. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209389109 · Cited by 12

Male increase in brain gene expression variability is linked to genetic risk for schizophrenia

Chen, J., Cao, H., Meyer‐Lindenberg, A., & Schwarz, E. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0200-0 · Cited by 13

Mechanistic insights into autocrine and paracrine roles of endothelial GABA signaling in the embryonic forebrain

Choi, Y. K., & Vasudevan, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-52729-x · Cited by 14

Conceptual Foundations of Biological Psychiatry

Murphy, D. (2011) · Elsevier eBooks · doi:10.1016/b978-0-444-51787-6.50013-1 · Cited by 13

No association between the genetic polymorphisms within RTN4 and schizophrenia in the Chinese population

Chen, W., Gu, N., Duan, S., Sun, Y. W., Zheng, Y., Li, C., Pan, Y., Xu, Y., Feng, G., & He, L. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.04.021 · Cited by 13

A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population

Ito, Y., Nakamura, Y., Takahashi, N., Saito, S., Aleksić, B., Iwata, N., Inada, T., & Ozaki, N. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.04.010 · Cited by 13

Redox Dysregulation and Oxidative Stress in Schizophrenia: Nutrigenetics as a Challenge in Psychiatric Disease Prevention

Kim, Q., Conus, P., & Cuénod, M. (2010) · Lifestyle Genomics · doi:10.1159/000324366 · Cited by 13

Pre-clinical models of cognitive dysfunction in schizophrenia: new avenues to addressing unmet needs

Jentsch, J. D. (2003) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2003.10.011 · Cited by 13

Bases neurobiológicas de la Esquizofrenia

Jerónimo, S. R., de la Vega Sanchez Diego, C., & Patricia, S. P. (2010) · Clínica y Salud · doi:10.5093/cl2010v21n3a3 · Cited by 20

Examining the impact of neuroimmune dysregulation on social behavior of male and female juvenile rats

Turano, A., McAuley, E. M., Muench, M. C., & Schwarz, J. M. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113449 · Cited by 11

EEG microstate D as psychosis-specific correlate in adolescents and young adults with clinical high risk for psychosis and first-episode psychosis

Liebrand, M., Katsarakis, A., Josi, J., Diezig, S., Michel, C., Schultze‐Lutter, F., Rochas, V., Mancini, V., Kaess, M., Hubl, D., et al. (2023) · Schizophrenia Research · doi:10.1016/j.schres.2023.11.014 · Cited by 13

First Rank Symptoms and Neurological Soft Signs in Schizophrenia

Hembram, M., Simlai, J., Chaudhury, S., & Biswas, P. (2014) · Psychiatry Journal · doi:10.1155/2014/931014 · Cited by 13

Synaptotagmin I Regulates Patterned Spontaneous Activity in the Developing Rat Retina via Calcium Binding to the C2AB Domains

Chiang, C.-W., Chen, Y., Lu, J., Hsiao, Y., Chang, C.-W., Huang, P.-C., Chang, Y., Chang, P. Y., & Wang, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047465 · Cited by 12

Consequences at adulthood of transient inactivation of the parahippocampal and prefrontal regions during early development: new insights from a disconnection animal model for schizophrenia

Meyer, F. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00118 · Cited by 12

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study

John, J., Kukshal, P., Sharma, A. K., Triptish Bhatia, A., Nimgaonkar, V. L., Deshpande, S. N., & Thelma, B. K. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.12.012 · Cited by 12

Nicotinic modulation of auditory evoked potential electroencephalography in a rodent neurodevelopmental model of schizophrenia

Kohlhaas, K. L., Robb, H. M., Roderwald, V. A., & Rueter, L. E. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.05.011 · Cited by 12

Late gestation immune activation increases IBA1-positive immunoreactivity levels in the corpus callosum of adult rat offspring

Duchatel, R. J., Meehan, C. L., Harms, L. R., Michie, P. T., Bigland, M. J., Smith, D. W., Walker, F. R., Jobling, P., Hodgson, D. M., & Tooney, P. A. (2018) · Psychiatry Research · doi:10.1016/j.psychres.2018.05.063 · Cited by 12

Discriminative Analysis of Symptom Severity and Ultra-High Risk of Schizophrenia Using Intrinsic Functional Connectivity

Wang, L., Li, X., Zhu, Y., Lin, B., Bo, Q., Li, F., & Wang, C. (2020) · International Journal of Neural Systems · doi:10.1142/s0129065720500471 · Cited by 12

The Antipsychotic Effects of Omega-3 Fatty Acids in Rats

Kokaçya, M. H., Çöpoğlu, Ü. S., Dokuyucu, R., İnanır, S., & Erbaş, O. (2015) · The American Journal of the Medical Sciences · doi:10.1097/maj.0000000000000531 · Cited by 13

Frontal lobe syndrome or adolescent‐onset schizophrenia? A case report

Ferrara, M., Freda, F., Massa, R., & Carratelli, T. J. (2006) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2006.00808.x · Cited by 12

Interaction between DISC1 and CHL1 in regulation of neurite outgrowth

Ren, J., Zhao, T., Xu, Y., & Ye, H. (2016) · Brain Research · doi:10.1016/j.brainres.2016.06.033 · Cited by 12

Regionally Distinct Alterations in Membrane Phospholipid Metabolism in Schizophrenia: A Meta-analysis of Phosphorus Magnetic Resonance Spectroscopy Studies

Haszto, C. S., Stanley, J. A., Iyengar, S., & Prasad, K. M. R. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.09.008 · Cited by 12

To die or to sleep, perhaps to dream

Gasic, G. P. (2003) · Toxicology Letters · doi:10.1016/s0378-4274(02)00487-3 · Cited by 12

Can the neurodevelopmental theory account for sex differences in schizophrenia across the life span?

Baldwin, C. H., & Srivastava, L. K. (2015) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.150014 · Cited by 12

Sexual dimorphic abnormalities in white matter geometry common to schizophrenia and non-psychotic high-risk subjects: Evidence for a neurodevelopmental risk marker?

Savadjiev, P., Seidman, L. J., Thermenos, H. W., Keshavan, M. S., Whitfield, S., Crow, T. J., & Kubicki, M. R. (2015) · Human Brain Mapping · doi:10.1002/hbm.23026 · Cited by 11

Altered hippocampal-prefrontal functional network integrity in adult macaque monkeys with neonatal hippocampal lesions

Li, C., Li, Z., Hu, X., Zhang, X., & Bachevalier, J. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117645 · Cited by 12

Brave New World: Harnessing the promise of biomarkers to help solve the epigenetic puzzle

Gooding, D. C. (2022) · Schizophrenia Research · doi:10.1016/j.schres.2022.01.020 · Cited by 12

Evidence of Glutamatergic Dysfunction in the Pathophysiology of Schizophrenia

Hammond, J. C., Shan, D., Meador‐Woodruff, J. H., & McCullumsmith, R. E. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_15 · Cited by 12

Abnormal grooming activity in Dab1 (scrambler) mutant mice

Strazielle, C., Lefèvre, A., Jacquelin, C., & Lalonde, R. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.038 · Cited by 12

Association between the variability of theABCA13gene and the risk of major depressive disorder and schizophrenia in the Han Chinese population

Chen, J., Khan, R. A. W., Wang, M., He, K., Wang, Q., Li, Z., Li, W., Wen, Z., Song, Z., Shen, J., et al. (2016) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2016.1245442 · Cited by 11

Comprehensive association analysis of 27 genes from the GABAergic system in Japanese individuals affected with schizophrenia

Balan, S., Yamada, K., Iwayama, Y., Hashimoto, T., Toyota, T., Shimamoto, C., Maekawa, M., Takagai, S., Wakuda, T., Kameno, Y., et al. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.01.003 · Cited by 11

Hippocampal Dysfunction in Schizophrenia and Aberrant Hippocampal Synaptic Plasticity in Rodent Model Psychosis: a Selective Review

Bartsch, J., Schott, B. H., & Behr, J. (2019) · Pharmacopsychiatry · doi:10.1055/a-0960-9846 · Cited by 10

Effects of Cannabis Use on the Protein and Lipid Profile of Olfactory Neuroepithelium Cells from Schizophrenia Patients Studied by Synchrotron-Based FTIR Spectroscopy

Saladrigas-Manjón, S., Dučić, T., Galindo, L., Fernández-Avilés, C., Pérez, V., de la Torre, R., & Robledo, P. (2020) · Biomolecules · doi:10.3390/biom10020329 · Cited by 11

Animal models for schizophrenia via in utero gene transfer: understanding roles for genetic susceptibility factors in brain development

Kamiya, A. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17902-5 · Cited by 12

Psychiatric heredity and posttraumatic stress disorder: survey study of war veterans.

Plašć, I. D., Peraica, T., Grubišić-Ilić, M., Rak, D., Sakoman, A. J., & Kozarić‐Kovačić, D. (2007) · PubMed Central · Cited by 11

Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families

Liu, C., Liu, Y. ‐., Fann, C. S. J., Chen, W. J., Yang, W. ‐., Ouyang, W. ‐., Chen, C., Jou, Y., Hsieh, M. H., Liu, S.-K., et al. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00276.x · Cited by 11

Effects of withdrawal from repeated amphetamine exposure in peri-puberty on neuroplasticity-related genes in mice

Calabrese, F., Richetto, J., Racagni, G., Feldon, J., Meyer, U., & Riva, M. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.018 · Cited by 11

Neonatal immune activation by lipopolysaccharide causes inadequate emotional responses to novel situations but no changes in anxiety or cognitive behavior in Wistar rats

Vojtěchová, I., Petrásek, T., Malenínská, K., Brožka, H., Tejkalová, H., Horáček, J., Stuchlı́k, A., & Valeš, K. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.05.001 · Cited by 13

Activation of the Maternal Immune System as a Risk Factor for Neuropsychiatric Disorders

Smith, S. E. P., Hsiao, E. Y., & Patterson, P. H. (2010) · Springer eBooks · doi:10.1007/978-1-60327-921-5_7 · Cited by 12

On the use of animal modeling to study maternal infection during pregnancy and prenatal cytokine exposure as risk factors for schizophrenia

Boksa, P., & Luheshi, G. N. (2003) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2003.10.018 · Cited by 11

Ancestral, Pregnancy, and Negative Early-Life Risks Shape Children’s Brain (Dis)similarity to Schizophrenia

Kochunov, P., Ma, Y., Hatch, K. S., Gao, S., Acheson, A., Jahanshad, N., Thompson, P. M., Adhikari, B. M., Bruce, H. A., van der Vaart, A. D., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.03.009 · Cited by 14

Attention-mediated genetic influences on psychotic symptomatology in adolescence

Chang, S. E., Hughes, D., Zhu, J., Hyat, M., Salone, S. D., Goodman, Z. T., Roffman, J. L., Karcher, N. R., Hernandez, L. M., Forsyth, J. K., et al. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00338-7 · Cited by 9

Cortical arealization of interneurons defines shared and distinct molecular programs in developing human and macaque brains

Feng, X., Gao, Y., Chu, F., Shan, Y., Liu, M., Wang, Y.-Y., Zhu, Y., Lu, Q. R., & Li, M. (2025) · Nature Communications · doi:10.1038/s41467-025-56058-8 · Cited by 10

Neural Substrates of Psychosis Revealed by Altered Dependencies between Brain Activity and White-Matter Architecture in Individuals with 22q11 Deletion Syndrome

Bortolin, K., Delavari, F., Preti, M. G., Sandini, C., Mancini, V., Mullier, E., Ville, D. V. D., & Eliez, S. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103075 · Cited by 13

Going beyond the DSM in predicting, diagnosing, and treating autism spectrum disorder with covarying alexithymia and OCD: A structural equation model and process-based predictive coding account

Edwards, D. J. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.993381 · Cited by 11

Characteristics of cognitive impairment in schizophrenia

Harvey, P. D. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139003872.002 · Cited by 10

Alterations in the hippocampal and striatal catecholaminergic fiber densities of heterozygous reeler mice

Nullmeier, S., Panther, P., Frotscher, M., Zhao, S., & Schwegler, H. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.027 · Cited by 10

Development of Depotentiation in Adult-Born Dentate Granule Cells

Tao, X., Sun, N., & Mu, Y. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00236 · Cited by 10

Altered netrin‐1 receptor expression in dopamine terminal regions following neonatal ventral hippocampal lesions in the rat

Flores, C., Bhardwaj, S. K., Labelle‐Dumais, C., & Srivastava, L. K. (2008) · Synapse · doi:10.1002/syn.20584 · Cited by 10

Etiología y Signos de Riesgo en la Esquizofrenia

Obiols, J. E., & Vicens-Vilanova, J. (2003) · Dialnet (Universidad de la Rioja) · Cited by 10

Diffusion magnetic resonance imaging study of schizophrenia in the context of abnormal neurodevelopment using multiple site data in a Chinese Han population

Li, Y., Xie, S., Liu, B., Song, M., Chen, Y., Li, P., Lü, L., Lv, L., Wang, H., Yan, H., et al. (2016) · Translational Psychiatry · doi:10.1038/tp.2015.202 · Cited by 10

Neurofunctional view of psychiatry: clinical brain imaging revisited

Hendler, T., Bleich‐Cohen, M., & Sharon, H. (2009) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32832a16f0 · Cited by 10

Drug discovery based on genetic and metabolic findings in schizophrenia

Dwyer, D. S., Weeks, K. R., & Aamodt, E. J. (2008) · Expert Review of Clinical Pharmacology · doi:10.1586/17512433.1.6.773 · Cited by 10

Differential regulation of polarized synaptic vesicle trafficking and synapse stability in neural circuit rewiring in Caenorhabditis elegans

Kurup, N. S., Yan, D., Kono, K., & Jin, Y. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006844 · Cited by 9

Presynaptic SNAP-25 regulates retinal waves and retinogeniculate projection via phosphorylation

Hsiao, Y., Shu, W., Chen, P., Yang, H.-J., Chen, H.-Y., Hsu, S.-P., Huang, Y., Yang, C., Chen, Y., Yu, N.-Y., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1812169116 · Cited by 9

DNA Methylation-Dependent Dysregulation of GABAergic Interneuron Functionality in Neuropsychiatric Diseases

Linde, J., & Zimmer‐Bensch, G. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.586133 · Cited by 11

The role of cell adhesion molecule IgSF9b at the inhibitory synapse and psychiatric disease

Clarin, J. D., Reddy, N., Alexandropoulos, C., & Gao, W. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105476 · Cited by 10

Development and Developmental Disorders of the Cerebral Cortex

ten Donkelaar, H. J., Lammens, M. M. Y., Aronica, E., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_10 · Cited by 9

NGF polymorphisms and haplotypes are associated with schizophrenia in Korean population

Park, J. K., Lee, S. M., Kang, W. S., Kim, S. K., & Cho, A. R. (2011) · Molecular & Cellular Toxicology · doi:10.1007/s13273-011-0047-4 · Cited by 9

Role of Immune and Autoimmune Dysfunction in Schizophrenia

Severance, E. G., & Yolken, R. H. (2015) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-800981-9.00029-8 · Cited by 8

Comparison of prefrontal hemodynamic responses and cognitive deficits between adult patients with autism spectrum disorder and schizophrenia

Pu, S., Nakagome, K., Satake, T., Ohtachi, H., Itakura, M., Yamanashi, T., Miura, A., Yokoyama, K., Matsumura, H., Iwata, M., et al. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.10.007 · Cited by 9

Labeling and Stigma

Link, B. G., & Phelan, J. C. (2017) · Cambridge University Press eBooks · doi:10.1017/9781316471289.024 · Cited by 11

Hypothesized mechanisms and sites of action of electroconvulsive therapy

Michael, N. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511576393.005 · Cited by 9

Neuroprotection and Enhancement of Neurite Outgrowth With Small Molecular Weight Compounds From Screens of Chemical Libraries

Dwyer, D. S., & Dickson, A. (2006) · International review of neurobiology · doi:10.1016/s0074-7742(06)77008-8 · Cited by 9

Properties of spontaneous and miniature excitatory postsynaptic currents in neurons of the rat prefrontal cortex

Malkin, S. L., Kim, K. K., Tikhonov, D. B., & Zaitsev, A. V. (2014) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093014060052 · Cited by 10

Rheb1 mediates DISC1-dependent regulation of new neuron development in the adult hippocampus

Kang, E., Kim, J. Y., Liu, C. Y., Xiao, B., Chen, P., Christian, K. M., Worley, P. F., Song, H., & Ming, G. (2015) · Neurogenesis · doi:10.1080/23262133.2015.1081715 · Cited by 9

Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome

Kikinis, Z., Makris, N., Sydnor, V. J., Sylvain Bouix, A., Pasternak, O., Coman, I. L., Antshel, K. M., Fremont, W. P., Kubicki, M. R., Shenton, M. E., et al. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.101611 · Cited by 9

Identifying neurodevelopmental anomalies of white matter microstructure associated with high risk for psychosis in 22q11.2DS

Bagautdinova, J., Padula, M. C., Zöller, D., Sandini, C., Schneider, M., Schaer, M., & Eliez, S. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01090-z · Cited by 9

Gender and Mental Health

Rosenfield, S., Kato, K., & Smith, D. T. (2017) · Cambridge University Press eBooks · doi:10.1017/9781316471289.017 · Cited by 9

Effects ofSYN1Q555Xmutation on cortical gray matter microstructure

Cabana, J., Gilbert, G., Guillon, L. L., Safi, D., Rouleau, I., Cossette, P., & Nguyen, D. K. (2018) · Human Brain Mapping · doi:10.1002/hbm.24186 · Cited by 9

Comorbidity and Anticomorbidity: Autocognitive developmental disorders of structured psychosocial stressPreprint

Wallace, R. (2003) · arXiv (Cornell University) · doi:10.48550/arxiv.q-bio/0310001 · Cited by 9

Cognitive Neuroscience and the Prefrontal Cortex: Normative Development and Vulnerabilityto Psychopathology

Luciana, M. M. (2015) · Wiley eBooks · doi:10.1002/9780470939390.ch7 · Cited by 10

Brain Neuroplasticity Mechanisms in Psychiatric Illnesses and in the Development of Novel Treatments

O’Donnell, P., Etkin, A., & Manji, H. K. (2026) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20251212 · Cited by 8

Haloperidol rescues the schizophrenia-like phenotype in adulthood after rotenone administration in neonatal rats

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Robert, P. H. (1999) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(99)90100-1 · Cited by 8

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Pontén, H., Sönniksen, K., Abrahamsson, T., Waters, N., Gustafsson, B., Hanse, E., & Groc, L. (2005) · Developmental Brain Research · doi:10.1016/j.devbrainres.2004.12.006 · Cited by 8

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