Glucocorticoid Hormones and Early Brain Development in Schizophrenia

Dopamine in schizophrenia: a review and reconceptualization

Davis, K. L., Kahn, R. S., Ko, G., & Davidson, M. (1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.11.1474 · Cited by 2,051

Stress and glucocorticoids affect the expression of brain-derived neurotrophic factor and neurotrophin-3 mRNAs in the hippocampus

Smith, M., Makino, S., Květňanský, R., & Post, R. M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01768.1995 · Cited by 1,449

Regulation of the Hypothalamic-Pituitary-Adrenal Axis by Cytokines: Actions and Mechanisms of Action

TURNBULL, A. V., & RIVIER, C. L. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.1.1 · Cited by 1,297

Single photon emission computerized tomography imaging of amphetamine-induced dopamine release in drug-free schizophrenic subjects

Laruelle, M., Abi-Dargham, A., van Dyck, C. H., Gil, R., D'Souza, C. D., Erdos, J., McCance, E., Rosenblatt, W., Fingado, C., Zoghbi, S. S., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.9235 · Cited by 1,291

Adult Schizophrenia Following Prenatal Exposure to an Influenza Epidemic

Mednick, S. A. (1988) · Archives of General Psychiatry · doi:10.1001/archpsyc.1988.01800260109013 · Cited by 1,203

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

Freedman, R., Coon, H., Myles-Worsley, M., Orr-Urtreger, A., Olincy, A., Davis, A., Polymeropoulos, M., Holik, J., Hopkins, J., Hoff, M., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.2.587 · Cited by 1,141

Prenatal stress produces learning deficits associated with an inhibition of neurogenesis in the hippocampus

Lemaire, V., Koehl, M., Le Moal, M., & Abrous, D. N. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.20.11032 · Cited by 1,044 · cited 2×

Timetables of neurogenesis in the human brain based on experimentally determined patterns in the rat.

Bayer, S. A., Altman, J., Russo, R. J., & Zhang, X. (1993) · PubMed · Cited by 912

The reduced neuropil hypothesis: a circuit based model of schizophrenia

Selemon, L. D., & Goldman-Rakic, P. S. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00281-9 · Cited by 909

Schizophrenia After Prenatal Famine

Susser, E. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830010027005 · Cited by 741

Effect of socioeconomic status and parents’ education at birth on risk of schizophrenia in offspring

Corcoran, C. M., Perrin, M. C., Harlap, S., Deutsch, L., Fennig, S., Manor, O., Nahon, D., Kimhy, D., Malaspina, D., & Susser, E. (2008) · Social Psychiatry and Psychiatric Epidemiology · doi:10.1007/s00127-008-0439-5 · Cited by 51

Glutamate receptors in domestication and modern human evolution

O’Rourke, T., & Boeckx, C. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.10.004 · Cited by 50

Genetically Induced Retrograde Amnesia of Associative Memories After Neuroplastin Ablation

Bhattacharya, S., Herrera‐Molina, R., Sabanov, V., Ahmed, T., Iscru, E., Stöber, F., Richter, K., Fischer, K.-D., Angenstein, F., Goldschmidt, J., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.2107 · Cited by 51

Pre-attentive processing and schizophrenia: animal studies

Ellenbroek, B. A. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1684-7 · Cited by 50

Reduced anterior hippocampal formation volume in hyponatremic schizophrenic patients

Goldman, M. B., Torres, I. J., Keedy, S., Marlow-O’Connor, M., Beenken, B., & Pilla, R. S. (2007) · Hippocampus · doi:10.1002/hipo.20292 · Cited by 45

Hyperthermia in utero due to maternal influenza is an environmental risk factor for schizophrenia

Edwards, M. J. (2007) · Congenital Anomalies · doi:10.1111/j.1741-4520.2007.00151.x · Cited by 44

Preterm Birth and Corticotrophin-Releasing Hormone as a Placental Clock

Herrera, C. L., Maiti, K., & Smith, R. (2022) · Endocrinology · doi:10.1210/endocr/bqac206 · Cited by 50

Sensorimotor gating deficits in “two-hit” models of schizophrenia risk factors

Khan, A., & Powell, S. B. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.10.009 · Cited by 47

Glucocorticoid receptor beta splice variant expression in patients with high and low activity of systemic lupus erythematosus.

Piotrowski, P., Burzynski, M., Lianeri, M., Mostowska, M., Wudarski, M., Chwalinska-Sadowska, H., & Jagodziński, P. P. (2007) · PubMed · doi:10.5603/4505 · Cited by 41

Early adverse experience alters dendritic spine density and gene expression in prefrontal cortex and hippocampus in lambs

Coulon, M., Wellman, C. L., Marjara, I. S., Janczak, A. M., & Zanella, A. J. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.10.018 · Cited by 40

Does unwantedness of pregnancy predict schizophrenia in the offspring?

Herman, D. B., Brown, A. S., Opler, M. G. A., Desai, M., Malaspina, D., Bresnahan, M. A., Schaefer, C. A., & Susser, E. (2006) · Social Psychiatry and Psychiatric Epidemiology · doi:10.1007/s00127-006-0078-7 · Cited by 38

The prenatal methylazoxymethanol acetate treatment: a neurodevelopmental animal model for schizophrenia?

Jongen‐Rêlo, A. L., Leng, A., Lüber, M., Pothuizen, H. H. J., Weber, L., & Feldon, J. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00228-6 · Cited by 38

Changes Induced by Prenatal Stress in Behavior and Brain Morphology: Can They Be Prevented or Reversed?

Weinstock, M. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1372-5_1 · Cited by 36

Disruption of the neuregulin 1 gene in the rat alters HPA axis activity and behavioral responses to environmental stimuli

Taylor, S. B., Taylor, A. R., Markham, J. A., Geurts, A., Kanaskie, B. Z., & Koenig, J. I. (2010) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.11.015 · Cited by 37

Living in a dangerous world decreases maternal care: A study in serotonin transporter knockout mice

Heiming, R. S., Bodden, C., Jansen, F., Lewejohann, L., Kaiser, S., Lesch, K., Palme, R., & Sachser, N. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.07.006 · Cited by 36

Effects of psychologic stress on fetal development and pregnancy outcome

Koubovec, D., Geerts, L., Odendaal, H. J., Stein, D. J., & Vythilingum, B. (2005) · Current Psychiatry Reports · doi:10.1007/s11920-005-0081-9 · Cited by 33

Prenatal restraint stress decreases the expression of alpha-7 nicotinic receptor in the brain of adult rat offspring

Baier, C. J., Pallarés, M. E., Adrover, E., Monteleone, M., Brocco, M., Barrantes, F., & Antonelli, M. (2015) · Stress · doi:10.3109/10253890.2015.1022148 · Cited by 32

Immunocytochemical expression of dopamine‐related transcription factors Pitx3 and Nurr1 in prenatally stressed adult rats

Katunar, M. R., Saez, T. M. M., Brusco, A., & Antonelli, M. C. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21911 · Cited by 28

Maternal restraint stress negatively influences growth capacity of preimplantation mouse embryos

Burkuš, J., Číkoš, Š., Fabián, D., Babeľová, J., Czikková, S., & Koppel, J. (2013) · General Physiology and Biophysics · doi:10.4149/gpb_2013010 · Cited by 28

Prenatal stress induces vulnerability to stress together with the disruption of central serotonin neurons in mice

Miyagawa, K., Tsuji, M., Ishii, D., Takeda, K., & Takeda, H. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.04.052 · Cited by 26

Antenatal maternal stress alters functional brain responses in adult offspring during conditioned fear

Sadler, T. R., Nguyen, P. T., Yang, J., Givrad, T. K., Mayer, E. A., Maarek, J. I., Hinton, D. R., & Holschneider, D. P. (2011) · Brain Research · doi:10.1016/j.brainres.2011.01.104 · Cited by 26

Sex-specific neuroendocrine and behavioral phenotypes in hypomorphic Type II Neuregulin 1 rats

Taylor, S. B., Markham, J. A., Taylor, A. R., Kanaskie, B. Z., & Koenig, J. I. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.05.008 · Cited by 25

Structural pathology underlying neuroendocrine dysfunction in schizophrenia

Goldman, M. B., Wang, L., Wachi, C., Daudi, S., Csernansky, J. G., Marlow-O’Connor, M., Keedy, S., & Torres, I. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.025 · Cited by 24

Altered prepulse inhibition in rats treated prenatally with the antimitotic Ara-C: an animal model for sensorimotor gating deficits in schizophrenia

Elmer, G. I., Sydnor, J., GUARD, H. L., Hercher, E., & Vogel, M. W. (2004) · Psychopharmacology · doi:10.1007/s00213-003-1757-7 · Cited by 23

Predicting Risk and the Emergence of Schizophrenia

Clarke, M. C., Kelleher, I., Clancy, M., & Cannon, M. D. (2012) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2012.06.003 · Cited by 22

Prenatal stress increases the striatal and hippocampal expression of correlating c‐FOS and serotonin transporters in murine offspring

Bielas, H., Arck, P., Bruenahl, C. A., Walitza, S., & Grünblatt, E. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.07.006 · Cited by 21

Do genes and environment meet to regulate cerebrospinal fluid dynamics? Relevance for schizophrenia

Palha, J. A., Santos, N. C., Marques, F., Sousa, J. C., Bessa, J. M., Miguelote, R. F. O., Sousa, N., & Belmonte-de-Abreu, P. S. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00031 · Cited by 21

Limbic system activation is affected by prenatal predator exposure and postnatal environmental enrichment and further moderated by dam and sex

Korgan, A. C., Green, A. D., Perrot, T. S., & Esser, M. J. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.10.037 · Cited by 22

Effects of prenatal exposure to antipsychotic risperidone on developmental neurotoxicity, apoptotic neurodegeneration and neurobehavioral sequelae in rat offspring

Singh, K. P., Singh, M. K., & Singh, M. P. (2016) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2016.05.006 · Cited by 20

Influence of aripiprazole and olanzapine on behavioral dysfunctions of adolescent rats exposed to stress in perinatal period

Ratajczak, P., Kus, K., Jarmuszkiewicz, Z., Woźniak, A., Cichocki, M., & Nowakowska, E. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)70961-7 · Cited by 20

Challenges of Introducing New Biomarker Products for Neuropsychiatric Disorders into the Market

Bahn, S., Noll, R., Barnes, A., Schwarz, E., & Guest, P. C. (2011) · International review of neurobiology · doi:10.1016/b978-0-12-387718-5.00012-2 · Cited by 20

Functional connectivity in prenatally stressed rats with and without maternal treatment with ladostigil, a brain‐selective monoamine oxidase inhibitor

Goelman, G., Ilinca, R., Zohar, I., & Weinstock, M. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12621 · Cited by 18

Is the glucocorticoid receptor a key player in prostate cancer?: A literature review

Sakellakis, M., & Flores, L. J. (2022) · Medicine · doi:10.1097/md.0000000000029716 · Cited by 17

Prenatal Stress and Adult Drug-Seeking Behavior: Interactions with Genes and Relation to Nondrug-Related Behavior

Kippin, T. E., Campbell, J. C., Ploense, K. L., Knight, C. P., & Bagley, J. R. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1372-5_5 · Cited by 18

Glucocorticoid Regulates Parkin Expression in Mouse Frontal Cortex: Implications in Schizophrenia

Pandya, C. D., Crider, A., & Pillai, A. (2014) · Current Neuropharmacology · doi:10.2174/1570159x11666131120224950 · Cited by 16

Antiinflammatory Treatment Ameliorates HPA Stress Axis Dysfunction in a Mouse Model of Stress Sensitivity

Howerton, A. R., & Bale, T. L. (2012) · Endocrinology · doi:10.1210/en.2012-1601 · Cited by 17

Stress during pregnancy affected neonatal outcomes and changed cortisol and leptin levels both in mothers and newborns

Rabiepoor, S., Abedi, M., Saboory, E., & Khalkhali, H. R. (2019) · Journal of Neonatal-Perinatal Medicine · doi:10.3233/npm-1818 · Cited by 15

Testes sanguíneos de biomarcadores para diagnóstico e tratamento de desordens mentais: foco em esquizofrenia

Bahn, S., Schwarz, E., Harris, L. W., Martins‐de‐Souza, D., Rahmoune, H., & Guest, P. C. (2012) · Archives of Clinical Psychiatry (São Paulo) · doi:10.1590/s0101-60832012005000005 · Cited by 15

Intrauterine Programmierung von Störungen der Hirnfunktion im späteren Leben

Schwab, M. (2009) · Gyn�kologisch-geburtshilfliche Rundschau · doi:10.1159/000184442 · Cited by 14

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

The Application of Multiplex Biomarker Techniques for Improved Stratification and Treatment of Schizophrenia Patients

Steiner, J. H., Guest, P. C., Rahmoune, H., & Martins‐de‐Souza, D. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6730-8_2 · Cited by 11

Effects of Neonatal Dexamethasone Exposure on Adult Neuropsychiatric Traits in Rats

Yates, N. J., Robertson, D., Rodger, J., & Martin-Iverson, M. T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0167220 · Cited by 12

Prenatal stress alters sensitivity to benzodiazepines in adult rats

Lakehayli, S., Said, N., Battas, O., Hakkou, F., & Tazi, A. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.02.015 · Cited by 10

Effects of prenatal chronic mild stress exposure on hippocampal cell proliferation, expression of GSK‐3α, β and NR2B in adult offspring during fear extinction in rats

Li, M., Li, X., Zhang, X., Ren, J., Jiang, H., Wang, Y., Ma, Y., & Cheng, W. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.02.004 · Cited by 10

Early Life Stress Causes Refractoriness to Haloperidol-Induced Catalepsy

Marrocco, J., Mairesse, J., Bucci, D., Lionetto, L., Battaglia, G., Consolazione, M., Ravasi, L., Simmaco, M., Morley‐Fletcher, S., Maccari, S., et al. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.085530 · Cited by 10

Application of Proteomic Techniques for Improved Stratification and Treatment of Schizophrenia Patients

Steiner, J. H., Guest, P. C., & Martins‐de‐Souza, D. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-52479-5_1 · Cited by 10

Gene Expression Profiling in Rodent Models for Schizophrenia

van Schijndel, J. E., & Martens, G. J. M. (2010) · Current Neuropharmacology · doi:10.2174/157015910793358132 · Cited by 10

Prenatal stress alters diazepam withdrawal syndrome and 5HT1A receptor expression in the raphe nuclei of adult rats

Lakehayli, S., Said, N., Khachibi, M. E., Ouahli, M. E., Nadifi, S., Hakkou, F., & Tazi, A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.035 · Cited by 9

Early environmental risk factors for schizophrenia

Cannon, M. D., Dean, K., & Jones, P. B. (2004) · Cambridge University Press eBooks · doi:10.1017/cbo9780511735103.013 · Cited by 9

Network analysis of positional candidate genes of schizophrenia highlights…more than… myelin-related pathways

Guilloux, J., Gaiteri, C., & Sibille, E. L. (2010) · Molecular Psychiatry · doi:10.1038/mp.2009.68 · Cited by 9

Gestational stress induced differential expression of HDAC2 in male rat offspring hippocampus during development

Liao, L., Wang, X., Yao, X., Zhang, B., Zhou, L., & Huang, J. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.11.006 · Cited by 8

Hormones and Steroids as Neurotransmitters

Marwein, S., Biswal, S., & Acharya, P. C. (2020) · Springer eBooks · doi:10.1007/978-981-15-3556-7_14 · Cited by 8

Long-term low level glucocorticoid exposure induces persistent repression in chromatin

Burkhart, B. A., Ivey, M. L., & Archer, T. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2008.10.011 · Cited by 8

Caldesmon, an actin-linked regulatory protein, comes across glucocorticoids

Sobue, K., & Fukumoto, K. (2010) · Cell Adhesion & Migration · doi:10.4161/cam.4.2.10886 · Cited by 8

Maternally Mediated Effects on Development

Miller, D., & Hood, R. D. (2005) · Informa Healthcare eBooks · doi:10.1201/9781420040548.ch4 · Cited by 7

The influence of aripiprazole and olanzapine on the anxiolytic-like effect observed in prenatally stressed rats (animal model of schizophrenia) exposed to the ethyl alcohol

Ratajczak, P., Kus, K., Giermaziak, W., & Nowakowska, E. (2015) · Pharmacological Reports · doi:10.1016/j.pharep.2015.10.010 · Cited by 5

Patients' perception of family involvement and its relationship to medication adherence for persons with schizophrenia and schizoaffective disorders

Edelman, E. M. (2010) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3df6r88 · Cited by 5

Prenatal glucocorticoid exposure and physiological programming of adult disease

Nyirenda, M. (2006) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.1.3.391 · Cited by 4

Fetal Growth and Development in the First Two Trimesters

Aikat, A., Roy, T. K., & Bhattacharya, N. (2016) · Springer eBooks · doi:10.1007/978-3-319-14874-8_5 · Cited by 4

Explanations for Elevated Psychiatric Vulnerability in Nonheterosexuals: Environmental Stressors, Genetics, and the HPA and HPG Axes

Brendan, P. (2011) · InTech eBooks · doi:10.5772/26216 · Cited by 4

Counteractive effects of antenatal glucocorticoid treatment on D1 receptor modulation of spatial working memory

Virdee, K., Kentrop, J., Jupp, B., Venus, B., Hensman, D., McArthur, S., Wilkinson, J., Robbins, T. W., Gillies, G. E., & Dalley, J. W. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4405-8 · Cited by 4

Advances in Neurobiology

Schmidt, B. L., Santos, M. J., Cariaga-Martínez, A. E., Hill, L., Barloese, M. C. J., & Hall, Z. J. (2017) · Cited by 4

Latent inhibition of a conditioned taste aversion in fetal rats

Mickley, G. A., Hoxha, Z., DiSorbo, A., Wilson, G. N., Remus, J. L., Biesan, O. R., Ketchesin, K. D., Ramos, L., Luchsinger, J. R., Prodan, S., et al. (2013) · Developmental Psychobiology · doi:10.1002/dev.21110 · Cited by 3

Toward a Diathesis-Stress Model of Schizophrenia in a Neurodevelopmental Perspective

Berry, A., & Cirulli, F. (2015) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-800981-9.00013-4 · Cited by 2

Early Life Experience, Maternal Separation, and Involvement of GABA and Glutamate Transporters

Acosta, G. B. (2018) · InTech eBooks · doi:10.5772/intechopen.70868 · Cited by 2

The Role of Environmental Factors in the Pathogenesis of Obsessive-Compulsive and Related Disorders

Raposo-Lima, C., & Morgado, P. F. (2018) · Cambridge University Press eBooks · doi:10.1017/9781108164313.006 · Cited by 3

Novel Targets for Drug Treatment in Psychiatry

Kurita, M., García‐Bea, A., & González‐Maeso, J. (2016) · Springer eBooks · doi:10.1007/978-1-4939-2528-5_30 · Cited by 1

Neurodevelopmental Impact of Prenatal Stress: A Proteomic Analysis of Myelination Disruptions in the Avian Embryo

Gaertner, B., Moroşan‐Puopolo, G., Brand‐Saberi, B., Schücke, C., Saberi, D., Klöster, K., Faissner, S., Marcus, K., Gellisch, M., & Eggers, B. (2025) · Developmental Neurobiology · doi:10.1002/dneu.23003 · Cited by 1

SCHIZOPHRENIA: Interaction between factors

Voichcoski, B. M., & Machado, V. (2015) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-3-319-19387-8_303 · Cited by 1

Stereological analysis of cornu ammonis in prenatally stressed rats: a heuristic neurodevelopmental model of schizophrenia.

Sharifabad, M. H., & Sabahi, A. A. R. (2014) · Europe PMC (PubMed Central) · Cited by 1

HDAC2 Inhibits Hippocampal Neurogenesis and Impairs the Cognitive Function in Prenatally Stressed Adult Offspring

Liao, L., Chai, B., Zhao, T., Liu, W., Zhang, X., Xu, X., Tian, X., Lv, M., Yao, X., & Bai, S. (2023) · International Journal of Morphology · doi:10.4067/s0717-95022023000300811 · Cited by 1

Epidemiology Research and Epigenetics: Translational Epidemiology of Schizophrenia

Perrin, M. C., Kleinhaus, K., Opler, M. G., Walsh‐Messinger, J., & Malaspina, D. (2011) · Springer eBooks · doi:10.1007/978-3-642-17426-1_5 · Cited by 1

Maternal Stress During the Lactation Period Rather than the Gestation Period Strongly Influences the Amino Acid Composition in Milk and Affects Growth and Behaviour in Offspring

Nishigawa, T., NAGAMACHI, S., Takakura, M., Ikeda, H., Kodaira, M., Yamaguchi, T., Chowdhury, V. S., Yasuo, S., & Furuse, M. (2018) · Journal of the Faculty of Agriculture Kyushu University · doi:10.5109/1909903 · Cited by 1

Maternally-mediated effects on development

Hood, R. D., & Rogers, J. M. (2011) · Informa Healthcare eBooks · doi:10.3109/9781841848211.004 · Cited by 1

Participação do sistema opioidérgico e dos glicocorticóides nas alterações comportamentais e da imunidade inata induzidas na prole pelo estresse pré-natal

Fonseca, E. D. S. M. (2005) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2005.tde-21092006-144127 · Cited by 1

Reproduction, Effects of Social Stress On

Shively, C. A. (2007) · Elsevier eBooks · doi:10.1016/b978-012373947-6.00330-5 · Cited by 1

Schizophrenia: Causes, course, and neurodevelopment

Buckley, P., Mahadik, S., Evans, D., & Stirewalt, E. (2003) · Current Psychosis & Therapeutics Reports · doi:10.1007/bf02629438 · Cited by 2

Transcriptional Regulation in Schizophrenia

Hemby, S. E., & O’Connor, J. A. (2007) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195306255.003.0005 · Cited by 1

Glucocorticoids, Developmental “Programming,” and the Risk of Affective Dysfunction

Olabi, B., & Seckl, J. R. (2011) · Wiley eBooks · doi:10.1002/9783527633968.ch5 · Cited by 1

Biological treatments: general considerations

Tsapakis, E. M., & Aitchison, K. J. (2008) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544125.026

The Polycomb complex: a key regulator in altered neurogenesis resulting from early-life stress?

Willemse, E. A. J. (2012) · Utrecht University Repository (Utrecht University)

The Involvement of the Hypothalamic-pituitary-gonadal, Hypothalamic-pituitary-adrenal and Somatotrophic Axes in the Development and Treatment of Schizophrenia

Gleich, T. (2014) · International Neuropsychiatric Disease Journal · doi:10.9734/indj/2014/6842

Tissue Metabolism of Glucocorticoids: New Controls of Cognitive Function and the Stress Response

Seckl, J. R. (2007) · Springer eBooks · doi:10.1007/4-431-29567-4_11

Perinatal Nicotine Exposure and Programming of HIE Sensitive Phenotype in Neonatal Rat Brains

Li, Y. (2013) · The Scholars Repository - LLU (Loma Linda University)

15 Prenatal infections and long-term mental outcome: Modeling schizophrenia-related dysfunctions using the prenatal Polyl:C model in mice

Feldon, J., & Meyer, U. (2011) · De Gruyter eBooks · doi:10.1515/9783110249453.171

Infection and schizophrenia

Brown, A. S., & Susser, E. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511789977.023

Esquizofrenia, en pocas palabras

Pérez‐Neri, I. (2015) · Archivos de Neurociencias · doi:10.31157/an.v20i3.93

Classifying Schizophrenia Based on Response to Antipsychotic Medications

Shah, P. (2019) · TSpace (University of Toronto)

Chapter 12. Multisignaling Approach to the Study of Sexual Differentiation of Brain and Behavior in Mammals

Komisaruk, B. R., & González-Mariscal, G. (2017) · CRC Press eBooks · doi:10.1201/9781315388069-15

Exploring Links between Pineal Gland Calcification and Central Nervous System Disease

Liu, X., & Liu, H. (2023) · Human Brain · doi:10.37819/hb.4.1790

Claudicação em vacas prenhes - influências no desenvolvimento neonatal e na morfometria cerebral de bezerros após o nascimento

Reis, G. A. (2024) · doi:10.11606/t.10.2024.tde-13052024-161327

Effects of early developmental stress on adult physiology and behavior

Frederick, M. J. (2010) · doi:10.54014/yzrq-ew86

Manuel des psychotraumatismes

Ouss, L. (2012) · doi:10.3917/lps.mouch.2012.01.0212

The Impact of Hemichannel-Mediated Neuroinflammation at Early Stages of CNS Ontogeny in the Development of Adult Neuropsychiatric Diseases

Ocaranza, F. J., & Sáez, J. C. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1012583

Understanding preterm birth: The role of infection and inflammation

Waldorf, K. A., & Coler, C. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-21564-3.00007-6

Prenatal stress in rat, an animal model of depression : brain plasticity, circadian disorders and new antidepressants

Giovine, A. (2010) · theses.fr (ABES) · doi:10.70675/1c5b5c59z4dafz4a8fz82e0zafa22917303c

Validation d'un modèle murin de schizophrénie pour améliorer la recherche de nouveaux traitements : approche psychopharmacologique, en imagerie et en électrophysiologie

Percelay, S. (2021) · theses.fr (ABES) · doi:10.70675/b6aa9b28z005fz4a8bz960dz3e55a52b2b59

Expression et fonctionnalité des récepteurs aux oestrogènes dans la gliomagenèse des astrocytomes et leur progression maligne

Hirtz, A. (2022) · doi:10.70675/5f182bb6z482bz4a55za94azde101cd29989

Nutrition and Stress and the Developing Fetus

Armony-Sivan, R., & Eidelman, A. I. (2006) · Humana Press eBooks · doi:10.1385/1-59259-952-4:205

Prenatal exposure to maternal stress and subsequent schizophrenia

van Os, J., & Selten, J. (1998) · The British Journal of Psychiatry · doi:10.1192/bjp.172.4.324 · Cited by 481

Prenatal Stress and Risk for Schizophrenia

Kinney, D. K. (2000) · International Journal of Mental Health · doi:10.1080/00207411.2000.11449503 · Cited by 30

Schizophrenia: A unique translational opportunity in behavioral neuroendocrinology

Koenig, J. I. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.06.027 · Cited by 51

Prenatal exposure to a repeated variable stress paradigm elicits behavioral and neuroendocrinological changes in the adult offspring: potential relevance to schizophrenia

Koenig, J. I., Elmer, G. I., Shepard, P. D., Lee, P. R., Mayo, C. L., Joy, B., Hercher, E., & Brady, D. L. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.05.030 · Cited by 297

Animal Models of the Maternal Stress Risk Factor for Schizophrenia

Patterson, P. H. (2011) · Columbia University Press eBooks · doi:10.7312/columbia/9780231151245.003.0013 · Cited by 1