Ontogeny of altered dendritic morphology in the rat prefrontal cortex, hippocampus, and nucleus accumbens following Cesarean delivery and birth anoxia

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Unresponsiveness to Cannabinoids and Reduced Addictive Effects of Opiates in CB 1 Receptor Knockout Mice

Ledent, C. A., Valverde, O., Cossu, G., Petitet, F., Aubert, J.-F., Beslot, F., Böhme, G. A., Impérato, A., Pedrazzini, T., Roques, B. P., et al. (1999) · Science · doi:10.1126/science.283.5400.401 · Cited by 3,612 · see citing works

Maternal Care, Hippocampal Glucocorticoid Receptors, and Hypothalamic-Pituitary-Adrenal Responses to Stress

Liu, D., Diorio, J., Tannenbaum, B., Caldji, C., Francis, D., Freedman, A., Sharma, S., Pearson, D., Plotsky, P. M., & Meaney, M. J. (1997) · Science · doi:10.1126/science.277.5332.1659 · Cited by 3,170 · see citing works

Dendritic organization in the neurons of the visual and motor cortices of the cat.

Sholl, D. A. (1953) · Europe PMC (PubMed Central) · Cited by 2,204 · see citing works

Decreased Dendritic Spine Density on Prefrontal Cortical Pyramidal Neurons in Schizophrenia

Glantz, L. A., & Lewis, D. A. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.1.65 · Cited by 1,636 · see citing works

Obstetric Complications and Schizophrenia: Historical and Meta-Analytic Review

Cannon, M. D., Jones, P. B., & Murray, R. M. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.7.1080 · Cited by 1,138 · see citing works

Dendritic spines of CA 1 pyramidal cells in the rat hippocampus: serial electron microscopy with reference to their biophysical characteristics

Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073 · see citing works

Dendritic spines: cellular specializations imparting both stability and flexibility to synaptic function.

Harris, K., & Kater, S. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,032 · see citing works

Anatomical Abnormalities in the Brains of Monozygotic Twins Discordant for Schizophrenia

Suddath, R. L., Christison, G. W., Torrey, E. F., Casanova, M. F., & Weinberger, D. R. (1990) · New England Journal of Medicine · doi:10.1056/nejm199003223221201 · Cited by 1,007 · see citing works

Projections from the Rat Prefrontal Cortex to the Ventral Tegmental Area: Target Specificity in the Synaptic Associations with Mesoaccumbens and Mesocortical Neurons

Carr, D. B., & Sesack, S. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03864.2000 · Cited by 880 · see citing works

Distribution of hippocampal CA1 and subicular efferents in the prefrontal cortex of the rat studied by means of anterograde transport of Phaseolus vulgaris ‐leucoagglutinin

Jay, T. M., & Witter, M. P. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130404 · Cited by 841 · see citing works

Repeated Stress Induces Dendritic Spine Loss in the Rat Medial Prefrontal Cortex

Radley, J. J., Rocher, A. B., Miller, M., Janssen, W. G. M., Liston, C., Hof, P. R., McEwen, B. S., & Morrison, J. H. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhi104 · Cited by 820 · see citing works

Prefrontal cortical efferents in the rat synapse on unlabeled neuronal targets of catecholamine terminals in the nucleus accumbens septi and on dopamine neurons in the ventral tegmental area

Sesack, S. R., & Pickel, V. M. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903200202 · Cited by 820 · see citing works

Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?

Fiala, J. C., Spacek, J., & Harris, K. M. (2002) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00158-3 · Cited by 811 · see citing works

Reorganization of the morphology of hippocampal neurites and synapses after stress-induced damage correlates with behavioral improvement

Sousa, N., Lukoyanov, N. V., Madeira, M. D., Almeida, O. F. X., & Paula-Barbosa, M. M. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00050-6 · Cited by 758 · see citing works

Persistent structural modifications in nucleus accumbens and prefrontal cortex neurons produced by previous experience with amphetamine

Robinson, T. E., & Kolb, B. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08491.1997 · Cited by 704 · see citing works

Altered Distribution of Nicotinamide-Adenine Dinucleotide Phosphate—Diaphorase Cells in Frontal Lobe of Schizophrenics Implies Disturbances of Cortical Development

Akbarian, S. (1993) · Archives of General Psychiatry · doi:10.1001/archpsyc.1993.01820150007001 · Cited by 679 · see citing works

Two types of neurone in the rat ventral tegmental area and their synaptic inputs.

Johnson, S. W., & NORTH, R. A. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019136 · Cited by 672 · see citing works

A method for vibratome sectioning of Golgi–Cox stained whole rat brain

Gibb, R. L., & Kolb, B. E. (1998) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(97)00163-5 · Cited by 618 · see citing works

Pattern Discrimination and the Visual Cortex

Sholl, D. A., & Uttley, A. M. (1953) · Nature · doi:10.1038/171387a0 · Cited by 605 · see citing works

At what age is the developing cerebral cortex of the rat comparable to that of the full-term newborn human baby?

Romijn, H. J., Hofman, M. A., & Gramsbergen, A. (1991) · Early Human Development · doi:10.1016/0378-3782(91)90044-4 · Cited by 553 · see citing works

Development of the dopaminergic innervation in the prefrontal cortex of the rat

Kalsbeek, A., Voorn, P., Buijs, R. M., Pool, C. W., & Uylings, H. B. M. (1988) · Journal of Comparative Neurology · doi:10.1002/cne.902690105 · Cited by 545 · see citing works

In the rat medial nucleus accumbens, hippocampal and catecholaminergic terminals converge on spiny neurons and are in apposition to each other

Sesack, S. R., & Pickel, V. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)91146-8 · Cited by 439 · see citing works

Synaptic Activity Mediates Death of Hypoxic Neurons

Rothman, S. M. (1983) · Science · doi:10.1126/science.6836300 · Cited by 438 · see citing works

Dopamine–Glutamate Interactions Controlling Prefrontal Cortical Pyramidal Cell Excitability Involve Multiple Signaling Mechanisms

Tseng, K. Y., & O'Donnell, P. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1021-04.2004 · Cited by 402 · see citing works

Stress activation of glutamate neurotransmission in the prefrontal cortex: implications for dopamine-associated psychiatric disorders

Moghaddam, B. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01362-2 · Cited by 392 · see citing works

The pharmacology of mesolimbic dopamine neurons: a dual-probe microdialysis study in the ventral tegmental area and nucleus accumbens of the rat brain

Westerink, B. H. C., Kwint, H., & Devries, J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02605.1996 · Cited by 372 · see citing works

GABA and enkephalin projection from the nucleus accumbens and ventral pallidum to the ventral tegmental area

Kalivas, P. W., Churchill, L., & Klitenick, M. A. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90048-k · Cited by 353 · see citing works

Decreased dendritic spine density on prefrontal cortical and hippocampal pyramidal neurons in postweaning social isolation rats

Silva-Gómez, A. B., Rojas, D., Juárez, I., & Flores, G. (2003) · Brain Research · doi:10.1016/s0006-8993(03)03042-7 · Cited by 336 · see citing works

Early Environmental Regulation of Hippocampal Glucocorticoid Receptor Gene Expression: Characterization of Intracellular Mediators and Potential Genomic Target Sites

Weaver, I. C. G., Diorio, J. C., Seckl, J. R., Moshe Szyf, A., & Meaney, M. J. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1321.099 · Cited by 330 · see citing works

Stressful Life Events and Schizophrenia

Norman, R. M. G., & MALLA, A. K. (1993) · The British Journal of Psychiatry · doi:10.1192/bjp.162.2.161 · Cited by 328 · see citing works

Reversibility of apical dendritic retraction in the rat medial prefrontal cortex following repeated stress

RADLEY, J., ROCHER, A., JANSSEN, W., HOF, P., MCEWEN, B., & MORRISON, J. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.07.008 · Cited by 323 · see citing works

CARBOHYDRATE AND ENERGY METABOLISM IN PERINATAL RAT BRAIN: RELATION TO SURVIVAL IN ANOXIA

Duffy, T. E., Kohle, S. J., & Vannucci, R. C. (1975) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1975.tb11875.x · Cited by 312 · see citing works

Regulation of somatodendritic dopamine release in the ventral tegmental area by opioids and GABA: an in vivo microdialysis study

Klitenick, M., DeWitte, P., & Kalivas, P. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02623.1992 · Cited by 309 · see citing works

Relationship between dopamine release in the rat nucleus accumbens and the discharge activity of dopaminergic neurons during local in vivo application of amino acids in the ventral tegmental area

Suaud-Chagny, M. F., Chergui, K., Chouvet, G., & Gonon, F. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90076-e · Cited by 307 · see citing works

Age, Experience and the Changing Brain

Kolb, B. E. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00008-0 · Cited by 302 · see citing works

Convergence and Plasticity of Monoaminergic Systems in the Medial Prefrontal Cortex during the Postnatal Period: Implications for the Development of Psychopathology

Benes, F. M. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.1014 · Cited by 268 · see citing works

Three-Dimensional analysis of dendritic spines

Špaček, J., & Hartmann, M. (1983) · Anatomy and Embryology · doi:10.1007/bf00298517 · Cited by 267 · see citing works

Modulation of A10 dopamine neurons by gamma-aminobutyric acid agonists.

Kalivas, P. W., Duffy, P., & Eberhardt, H. (1990) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)13057-7 · Cited by 267 · see citing works

Postnatal Handling Increases the Expression of cAMP-Inducible Transcription Factors in the Rat Hippocampus: The Effects of Thyroid Hormones and Serotonin

Meaney, M. J., Diorio, J., Francis, D., Weaver, S., Yau, J., Chapman, K., & Seckl, J. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03926.2000 · Cited by 266 · see citing works

Abnormal expression of two microtubule-associated proteins (MAP2 and MAP5) in specific subfields of the hippocampal formation in schizophrenia.

Arnold, S. E., Lee, V. M., Gur, R. E., & Trojanowski, J. Q. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.23.10850 · Cited by 236 · see citing works

Biochemical evidence for γ-aminobutyrate containing fibres from the nucleus accumbens to the substantia nigra and ventral tegmental area in the rat

Walaas, I., & Fonnum, F. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90071-8 · Cited by 235 · see citing works

Alterations in dendritic morphology of prefrontal cortical and nucleus accumbens neurons in post-pubertal rats after neonatal excitotoxic lesions of the ventral hippocampus

Flores, G., Alquicer, G., Gómez, A. B. S., Zaldivar, G. A., Stewart, J., Quirion, R., & Srivastava, L. K. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.02.021 · Cited by 220 · see citing works

Organization of pyramidal neurons in area 17 of monkey visual cortex

Peters, A., & Sethares, C. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903060102 · Cited by 212 · see citing works

Spine Loss and Other Persistent Alterations of Hippocampal Pyramidal Cell Dendrites in a Model of Early-Onset Epilepsy

Jiang, M., Lee, C. L., Smith, K. L., & Swann, J. W. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08356.1998 · Cited by 207 · see citing works

Pregnancy, delivery and infancy complications and attention deficit hyperactivity disorder: Issues of gene-environment interaction

Milberger, S., Biederman, J., Faraone, S. V., Guite, J., & Tsuang, M. T. (1997) · Biological Psychiatry · doi:10.1016/0006-3223(95)00653-2 · Cited by 200 · see citing works

Birth insult interacts with stress at adulthood to alter dopaminergic function in animal models: possible implications for schizophrenia and other disorders.

Boksa, P., & El-Khodor, B. (2003) · Neuroscience and Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00012-5 · Cited by 197 · see citing works

Rapid reversal of stress induced loss of synapses in CA3 of rat hippocampus following water maze training

Sandi, C., Davies, H. A., Cordero, M. I., Rodriguez, J. J., Popov, V. I., & Stewart, M. G. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02675.x · Cited by 194 · see citing works

A technique for estimating total spine numbers on golgi‐impregnated dendrites

Feldman, M. L., & Peters, A. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901880403 · Cited by 194 · see citing works

Influence of the hippocampus on interneurons of the rat prefrontal cortex

Tierney, P. L., Dégenètais, E., Thierry, A., Glowinski, J., & Gioanni, Y. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03501.x · Cited by 192 · see citing works

Decreased binding of dopamine D3 receptors in limbic subregions after neonatal bilateral lesion of rat hippocampus

Flores, G., Barbeau, D., Quirion, R., & Srivastava, L. K. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-06-02020.1996 · Cited by 187 · see citing works

Microanatomy of dendritic spines: emerging principles of synaptic pathology in psychiatric and neurological disease

Blanpied, T. A., & Ehlers, M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.10.006 · Cited by 179 · see citing works

Asphyctic lesion: proliferation of tyrosine hydroxylase-immunoreactive nerve cell bodies in the rat substantia nigra and functional changes in dopamine neurotransmission

Bjelke, B., Andersson, K., Ögren, S. O., & Bolme, P. (1991) · Brain Research · doi:10.1016/0006-8993(91)91041-x · Cited by 179 · see citing works

Dopamine Enhances EPSCs in Layer II–III Pyramidal Neurons in Rat Prefrontal Cortex

Gonzalez-Islas, C. E., & Hablitz, J. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-03-00867.2003 · Cited by 173 · see citing works

Distinct muscarinic receptors inhibit release of gamma-aminobutyric acid and excitatory amino acids in mammalian brain.

Sugita, S., Uchimura, N., Jiang, Z. G., & North, R. A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.6.2608 · Cited by 171 · see citing works

The Location of Persistent Amphetamine-Induced Changes in the Density of Dendritic Spines on Medium Spiny Neurons in the Nucleus Accumbens and Caudate-Putamen

Li, Y., Kolb, B. E., & Robinson, T. E. (2002) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300115 · Cited by 164 · see citing works

Fetal and maternal plasma catecholamine levels at elective cesarean section under general or epidural anesthesia versus vaginal delivery

Irestedt, L., Lagercrantz, H., Hjemdahl, P., Hägnevik, K., & Belfrage, P. (1982) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(82)90783-9 · Cited by 160 · see citing works

Dopamine Terminals in the Rat Prefrontal Cortex Synapse on Pyramidal Cells that Project to the Nucleus Accumbens

Carr, D. B., O’Donnell, P., Card, J. P., & Sesack, S. R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-24-11049.1999 · Cited by 160 · see citing works

Medical factors in hyperactive and normal children: Prenatal, developmental, and health history findings.

Hartsough, C. S., & Lambert, N. M. (1985) · American Journal of Orthopsychiatry · doi:10.1111/j.1939-0025.1985.tb03433.x · Cited by 150 · see citing works

Obstetric complications and congenital malformation in schizophrenia

McNeil, T. F. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00034-x · Cited by 133 · see citing works

Pyramidal neurones of the dorsal cochlear nucleus: A golgi and computer reconstruction study in cat

Blackstad, T. W., Osen, K. K., & Mugnaini, E. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90099-x · Cited by 132 · see citing works

Perinatal Distress Leads to Lateralized Medial Prefrontal Cortical Dopamine Hypofunction in Adult Rats

Brake, W. G., Sullivan, R. M., & Gratton, A. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05538.2000 · Cited by 131 · see citing works

Catecholamine Surge and Metabolic Adaptation in the Newborn after Vaginal Delivery and Caesarean Section

Hägnevik, K., Faxelius, G., Irestedt, L., Lagercrantz, H., Lundell, B. P. W., & Persson, B. (1984) · Acta Paediatrica · doi:10.1111/j.1651-2227.1984.tb09982.x · Cited by 128 · see citing works

Synaptic Influence of Hippocampus on Pyramidal Cells of the Rat Prefrontal Cortex: An In Vivo Intracellular Recording Study

Dégenètais, E. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.7.782 · Cited by 127 · see citing works

What the rodent prefrontal cortex can teach us about attention-deficit/hyperactivity disorder: the critical role of early developmental events on prefrontal function

Sullivan, R. M., & Brake, W. G. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.015 · Cited by 126 · see citing works

Alteration in dendritic morphology of cortical neurons in rats with diabetes mellitus induced by streptozotocin

Martínez‐Téllez, R. I., Gómez-Villalobos, M. D. J., & Flores, G. (2005) · Brain Research · doi:10.1016/j.brainres.2005.04.048 · Cited by 121 · see citing works

Medial prefrontal cortical D1 receptor modulation of the meso-accumbens dopamine response to stress: an electrochemical study in freely-behaving rats

Doherty, M. D., & Gratton, A. P. (1996) · Brain Research · doi:10.1016/0006-8993(95)01557-4 · Cited by 120 · see citing works

Altered Cortical Glutamate Neurotransmission in Schizophrenia

Lewis, D. A., Glantz, L. A., Pierri, J. N., & Sweet, R. A. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.007 · Cited by 113 · see citing works

A comparative study of obstetric history in schizophrenics, bipolar patients and normal subjects

Verdoux, H., & Bourgeois, M. L. (1993) · Schizophrenia Research · doi:10.1016/0920-9964(93)90011-7 · Cited by 112 · see citing works

Post-mortem Interval Effects on the Phosphorylation of Signaling Proteins

Li, J., Gould, T. D., Yuan, P., Manji, H. K., & Chen, G. (2002) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300112 · Cited by 105 · see citing works

Autoradiographic localization of ?-aminobutyric acidA receptors within the ventral tegmental area

Churchill, L., Dilts, R. P., & Kalivas, P. W. (1992) · Neurochemical Research · doi:10.1007/bf00966870 · Cited by 105 · see citing works

Long-Term Reciprocal Changes in Dopamine Levels in Prefrontal Cortex versus Nucleus Accumbens in Rats Born by Caesarean Section Compared to Vaginal Birth

El‐Khodor, B. F., & Boksa, P. (1997) · Experimental Neurology · doi:10.1006/exnr.1997.6437 · Cited by 104 · see citing works

Multiple Effects of Dopamine on Layer V Pyramidal Cell Excitability in Rat Prefrontal Cortex

Gulledge, A. T., & Jaffe, D. B. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.2.586 · Cited by 96 · see citing works

Alterations in dendritic morphology of the prefrontal cortical and striatum neurons in the unilateral 6‐OHDA‐rat model of Parkinson's disease

Solís, Ó., Limón, I. D., Flores‐Hernández, J., & Flores, G. (2007) · Synapse · doi:10.1002/syn.20381 · Cited by 94 · see citing works

Methods of estimation of spine density--are spines evenly distributed throughout the dendritic field?

Horner, C. H., & Arbuthnott, E. R. (1991) · Europe PMC (PubMed Central) · Cited by 90 · see citing works

Influence of labor and route of delivery on the frequency of respiratory morbidity in term neonates

Hales, K. A., Morgan, M. A., & Thurnau, G. R. (1993) · International Journal of Gynecology & Obstetrics · doi:10.1016/0020-7292(93)90271-w · Cited by 86 · see citing works

Differences in the laminar origin of projections from the medial prefrontal cortex to the nucleus accumbens shell and core regions in the rat

Ding, D. C. D., Gabbott, P. L. A., & Totterdell, S. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02912-2 · Cited by 76 · see citing works

Prolonged Episodes of Hypoxemia in Preterm Infants Undetectable by Cardiorespiratory Monitors

Poets, C. F., Stebbens, V. A., Richard, D., & Southall, D. P. (1995) · PEDIATRICS · doi:10.1542/peds.95.6.860 · Cited by 76 · see citing works

Influence of perinatal factors on the nucleus accumbens dopamine response to repeated stress during adulthood: an electrochemical study in the rat

Brake, W. G., Noel, M. B., Boksa, P., & Gratton, A. P. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00543-x · Cited by 74 · see citing works

Interhemispheric and subcortical collaterals of medial prefrontal cortical neurons in the rat

Ferino, F., Thierry, A. M., Saffroy, M., & Glowinski, J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90450-1 · Cited by 72 · see citing works

Obstetric Complications and Schizophrenia a Case-Control Study

Günther-Genta, F., Bovet, P., & Hohlfeld, P. (1994) · The British Journal of Psychiatry · doi:10.1192/bjp.164.2.165 · Cited by 72 · see citing works

Short- and long-term effects of perinatal asphyxia on monoamine, amino acid and glycolysis product levels measured in the basal ganglia of the rat

Chen, Y., Engidawork, E., Loidl, C. F., Dell’Anna, E., Goiny, M., Lübec, G., Andersson, K., & Herrera‐Marschitz, M. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00131-4 · Cited by 62 · see citing works

Neurons in the ventral subiculum, amygdala and entorhinal cortex which project to the nucleus accumbens: Their input from somatostatin-immunoreactive boutons

Aylward, R. L. M., & Totterdell, S. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90005-o · Cited by 53 · see citing works

Alteration in dendritic morphology of pyramidal neurons from the prefrontal cortex of rats with renovascular hypertension

de la Vega, E. G., Gómez‐Villalobos, M. D. J., & Flores, G. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.042 · Cited by 51 · see citing works

Are neurological abnormalities in schizophrenic patients and their siblingsthe result of perinatal trauma?

Cantor‐Graae, E., Ismail, B., & McNeil, T. F. (2000) · Acta Psychiatrica Scandinavica · doi:10.1034/j.1600-0447.2000.90054.x · Cited by 51 · see citing works

Effects of neonatal hypoxia on brain development in the rat: immediate and long-term biochemical alterations in discrete regions

Slotkin, T. A., Cowdery, T., Orband, L., Pachman, S., & Whitmore, W. L. (1986) · Brain Research · doi:10.1016/0006-8993(86)90395-1 · Cited by 46 · see citing works

Differential involvement of ventral tegmental GABAA and GABAB receptors in the regulation of the nucleus accumbens dopamine response to stress

Doherty, M., & Gratton, A. P. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.081 · Cited by 44 · see citing works

Selective Dopamine Filter of Glutamate Striatal Afferents

Dani, J. A., & Zhou, F.-M. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.008 · Cited by 43 · see citing works

Dopamine D1 Receptor Changes Due to Caesarean Section Birth: Effects of Anesthesia, Developmental Time Course, and Functional Consequences

Boksa, P., Zhang, Y., & Bestawros, A. (2002) · Experimental Neurology · doi:10.1006/exnr.2002.7896 · Cited by 42 · see citing works

Effects of perinatal anoxia on the acute locomotor response to repeated amphetamine administration in adult rats

Brake, W. G., Boksa, P., & Gratton, A. P. (1997) · Psychopharmacology · doi:10.1007/s002130050419 · Cited by 41 · see citing works

The brain-islet axis: the nervous control of the endocrine pancreas.

Helman, A., Marre, M., Bobbioni, E., Poussier, P., Reach, G., & Assan, R. (1982) · PubMed · Cited by 38 · see citing works

Effects of glutamate, quisqualate, and N-methyl-d-aspartate in neonatal brain

Young, R. S. K., Petroff, O. A. C., Aquila, W. J., & Yates, J. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90104-k · Cited by 36 · see citing works

Anoxia at birth induced hyperresponsiveness to amphetamine and stress in postpubertal rats

Juárez, I., Gómez, A. B. S., Peralta, F., & Flores, G. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.060 · Cited by 35 · see citing works

Lower in vivo brain extracellular GABA concentration in diabetic rats during forced swimming

Gomez, R., Vargas, C. R., Wajner, M., & Barros, H. M. T. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02340-0 · Cited by 35 · see citing works

Effects of Vaginal Birth versus Caesarean Section Birth with General Anesthesia on Blood Gases and Brain Energy Metabolism in Neonatal Rats

Vaillancourt, C., Berger, N., & Boksa, P. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7201 · Cited by 27 · see citing works

Interactive effects of anoxia and general anesthesia during birth on the degree of CNS and systemic hypoxia produced in neonatal rats

Berger, N., Vaillancourt, C., & Boksa, P. (2000) · Experimental Brain Research · doi:10.1007/s002210050107 · Cited by 26 · see citing works

Effects of birth insult and stress at adulthood on excitatory amino acid receptors in adult rat brain

El-Khodor, B., Flores, G., Srivastava, L. K., & Boksa, P. (2004) · Synapse · doi:10.1002/syn.20073 · Cited by 23 · see citing works

Neural activity and the development of the somatic sensory system

Purves, D., Riddle, D. R., WHITE, L. E., & Gutiérrez‐Ospina, G. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90041-8 · Cited by 22 · see citing works

Effect of transient hypoxia on oxygenation of the developing rat brain: relationships among haemoglobin saturation, autoregulation of blood flow and mitochondrial redox state.

Sylvia, A. L., Seidler, F. J., & Slotkin, T. A. (1989) · PubMed · Cited by 21 · see citing works

Pathway specificity of dendritic spine morphology in identified synapses onto rat hippocampal CA1 neurons in organotypic slices

Simoni, A. D., & Edwards, F. A. (2006) · Hippocampus · doi:10.1002/hipo.20236 · Cited by 13 · see citing works

Cesarean plus anoxia at birth induces hyperresponsiveness to locomotor activity by dopamine D2 agonist

Juárez, I., de la Cruz, F., Zamudio, S., & Flores, G. (2005) · Synapse · doi:10.1002/syn.20203 · Cited by 11 · see citing works

Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.

Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1 · see citing works

Untitled work

(1996) · doi:10.1002/(sici)1096-9861(19960520)369:1

Untitled work

(1997) · doi:10.1002/(sici)1098-2396(199707)26:3

The Microbiota-Gut-Brain Axis

Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works

Microbiota in health and diseases

Hou, K., Wu, Z.-X., Chen, X.-Y., Wang, J.-Q., Zhang, D., Xiao, C., Zhu, D., Koya, J. B., Wei, L., Li, J., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00974-4 · Cited by 3,171 · see citing works

The interplay between the intestinal microbiota and the brain

Collins, S. M., Surette, M., & Bercik, P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2876 · Cited by 1,611 · see citing works

Antibiotic-induced perturbations in gut microbial diversity influences neuro-inflammation and amyloidosis in a murine model of Alzheimer’s disease

Minter, M. R., Zhang, C., Leone, V., Ringus, D. L., Zhang, X., Oyler-Castrillo, P., Musch, M. W., Liao, F., Ward, J. F., Holtzman, D. M., et al. (2016) · Scientific Reports · doi:10.1038/srep30028 · Cited by 655 · see citing works

Epidemiology-driven neurodevelopmental animal models of schizophrenia

Meyer, U., & Feldon, J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.10.018 · Cited by 366 · see citing works

Research Review: Birth by caesarean section and development of autism spectrum disorder and attention‐deficit/hyperactivity disorder: a systematic review and meta‐analysis

Curran, E. A., O'Neill, S. M., Cryan, J. F., Kenny, L. C., Dinan, T. G., Khashan, A. S., & Kearney, P. M. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12351 · Cited by 250 · see citing works

Prenatal Cerebral Ischemia Disrupts MRI-Defined Cortical Microstructure Through Disturbances in Neuronal Arborization

Dean, J. M., McClendon, E., Hansen, K., Azimi-Zonooz, A., Chen, K. Y., Riddle, A., Gong, X., Sharifnia, E., Hagen, M. W., Ahmad, T., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3004669 · Cited by 188 · see citing works

Maternal separation disrupts dendritic morphology of neurons in prefrontal cortex, hippocampus, and nucleus accumbens in male rat offspring

Monroy, E., Hernández‐Torres, E., & Flores, G. (2010) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2010.05.005 · Cited by 182 · see citing works

Review of Pathological Hallmarks of Schizophrenia: Comparison of Genetic Models With Patients and Nongenetic Models

Jaaro-Peled, H., Ayhan, Y., Pletnikov, M. V., & Sawa, A. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp133 · Cited by 134 · see citing works

Metabolic tinkering by the gut microbiome

Selkrig, J., Wong, P., Zhang, X., & Pettersson, S. (2014) · Gut Microbes · doi:10.4161/gmic.28681 · Cited by 116 · see citing works

Rearrangement of the dendritic morphology in limbic regions and altered exploratory behavior in a rat model of autism spectrum disorder

Bringas, M. E., Carvajal-Flores, F. N., López-Ramírez, T. A., Atzori, M., & Flores, G. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.030 · Cited by 114 · see citing works

Prenatal immune challenge induces developmental changes in the morphology of pyramidal neurons of the prefrontal cortex and hippocampus in rats

Baharnoori, M., Brake, W. G., & Srivastava, L. K. (2008) · Schizophrenia Research · doi:10.1016/j.schres.2008.10.003 · Cited by 113 · see citing works

Obstetrical mode of delivery and childhood behavior and psychological development in a British cohort

Curran, E. A., Cryan, J. F., Kenny, L. C., Dinan, T. G., Kearney, P. M., & Khashan, A. S. (2016) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-015-2616-1 · Cited by 94 · see citing works

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., & Louilot, A. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00118 · Cited by 84 · see citing works

Neuronal and brain morphological changes in animal models of schizophrenia

Flores, G., Morales‐Medina, J. C., & Díaz, A. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.12.034 · Cited by 81 · see citing works

Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents

Manitt, C., Labelle‐Dumais, C., Eng, C., Grant, A., Mimee, A., Stroh, T., & Flores, C. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011463 · Cited by 72 · see citing works

Microbial Immuno-Communication in Neurodegenerative Diseases

Main, B. S., & Minter, M. R. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00151 · Cited by 68 · see citing works

Neurodevelopmental Animal Models of Schizophrenia: Role in Novel Drug Discovery and Development

Wilson, C., & Terry, A. V. (2010) · Clinical Schizophrenia & Related Psychoses · doi:10.3371/csrp.4.2.4 · Cited by 66 · see citing works

Impaired structural hippocampal plasticity is associated with emotional and memory deficits in the olfactory bulbectomized rat

Morales‐Medina, J. C., Juárez, I., Venancio-García, E., Cabrera, S. N., Ménard, C., Yu, W., Flores, G., Mechawar, N., & Quirion, R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.01.037 · Cited by 61 · see citing works

Chronic administration of the neurotrophic agent cerebrolysin ameliorates the behavioral and morphological changes induced by neonatal ventral hippocampus lesion in a rat model of schizophrenia

Vázquez‐Roque, R. A., Ramos, B., Tecuatl, C., Juárez, I., Adame, A., de la Cruz, F., Zamudio, S., Mena, R., Rockenstein, E. M., Masliah, E., et al. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22753 · Cited by 61 · see citing works

Exploring the microbiota-gut-brain axis: impact on brain structure and function

Yassin, L. K., Nakhal, M. M., Alderei, A., Almehairbi, A., Mydeen, A. B., Akour, A. A., & Hamad, M. I. K. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1504065 · Cited by 60 · see citing works

Cesarean Section or Natural Childbirth? Cesarean Birth May Damage Your Health

Chen, H., & Tan, D. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00351 · Cited by 57 · see citing works

Combined administration of cerebrolysin and donepezil induces plastic changes in prefrontal cortex in aged mice

Alcántara-González, F., Mendoza-Perez, C. R., Zaragoza, N., Juárez, I., Arroyo‐García, L. E., Gamboa, C., de la Cruz, F., Zamudio, S., García‐Dolores, F., & Flores, G. (2012) · Synapse · doi:10.1002/syn.21588 · Cited by 56 · see citing works

Associations of caesarean delivery and the occurrence of neurodevelopmental disorders, asthma or obesity in childhood based on Taiwan birth cohort study

Chen, G., Chiang, W., Shu, B., Guo, Y. L., Chiou, S.-T., & Chiang, T. (2017) · BMJ Open · doi:10.1136/bmjopen-2017-017086 · Cited by 55 · see citing works

Clozapine administration reverses behavioral, neuronal, and nitric oxide disturbances in the neonatal ventral hippocampus rat

Bringas, M. E., Morales‐Medina, J. C., Flores-Vivaldo, Y., Negrete‐Díaz, J. V., Aguilar‐Alonso, P., León‐Chávez, B. A., Lazcano-Ortiz, Z., Monroy, E., Moreno, A. R., Quirion, R., et al. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.12.008 · Cited by 54 · see citing works

Involvement of CX3CL1/CX3CR1 in depression and cognitive impairment induced by chronic unpredictable stress and relevant underlying mechanism

Liu, Y., Zhang, T., Meng, D., Sun, L., Yang, G., He, Y., & Zhang, C. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112371 · Cited by 50 · see citing works

Enhanced dendritic spine number of neurons of the prefrontal cortex, hippocampus, and nucleus accumbens in old rats after chronic donepezil administration

Alcántara-González, F., Juárez, I., Solís, Ó., Martínez‐Téllez, R. I., Camacho‐Abrego, I., Masliah, E., Mena, R., & Flores, G. (2010) · Synapse · doi:10.1002/syn.20787 · Cited by 47 · see citing works

Dendritic morphology of neurons in medial prefrontal cortex, hippocampus, and nucleus accumbens in adult SH rats

Sánchez, F., Gómez‐Villalobos, M. D. J., Juárez, I., Quevedo, L., & Flores, G. (2010) · Synapse · doi:10.1002/syn.20837 · Cited by 46 · see citing works

25 years of research on global asphyxia in the immature rat brain

Barkhuizen, M., van den Hove, D., Vles, J. S. H., Steinbusch, H. W. M., Kramer, B. W. W., & Gavilanes, A. W. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.042 · Cited by 46 · see citing works

The chronic administration of cerebrolysin induces plastic changes in the prefrontal cortex and dentate gyrus in aged mice

Juárez, I., González, D. J., Mena, R., & Flores, G. (2011) · Synapse · doi:10.1002/syn.20950 · Cited by 46 · see citing works

Dendritic morphology changes in neurons from the prefrontal cortex, hippocampus and nucleus accumbens in rats after lesion of the thalamic reticular nucleus

García, M. E. T., Solís, Ó., Patricio-Martínez, A., Moreno, A. R., Camacho‐Abrego, I., Limón, I. D., & Flores, G. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.042 · Cited by 43 · see citing works

Dendritic development of hippocampal CA1 pyramidal cells in a neonatal hypoxia-ischemia injury model

Zhao, Y. D., Ou, S., Cheng, S. Y., Xiao, Z., He, W., Zhang, J. H., & Ruan, H. Z. (2013) · Journal of Neuroscience Research · doi:10.1002/jnr.23247 · Cited by 38 · see citing works

Cerebrolysin improves memory and ameliorates neuronal atrophy in spontaneously hypertensive, aged rats

Solis‐Gaspar, C., Vázquez‐Roque, R. A., Gómez-Villalobos, M. D. J., & Flores, G. (2016) · Synapse · doi:10.1002/syn.21912 · Cited by 36 · see citing works

Comprehensive Estimates of Potential Synaptic Connections in Local Circuits of the Rodent Hippocampal Formation by Axonal-Dendritic Overlap

Tecuatl, C., Wheeler, D. W., Sutton, N. M., & Ascoli, G. A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1193-20.2020 · Cited by 36 · see citing works

Hot executive function following moderate‐to‐late preterm birth: altered delay discounting at 4 years of age

Hodel, A. S., Brumbaugh, J. E., Morris, A. R., & Thomas, K. M. (2015) · Developmental Science · doi:10.1111/desc.12307 · Cited by 34 · see citing works

Microbes in Pharmaceutical Industry

Kapoor, D., Sharma, P., Sharma, M. M. M., Kumari, A., & Kumar, R. (2020) · Springer eBooks · doi:10.1007/978-981-15-4099-8_16 · Cited by 34 · see citing works

The change of spatial cognition ability in depression rat model and the possible association with down-regulated protein expression of TRPC6

Liu, Y., Liu, C., Qin, X., Zhu, M., & Yang, Z. R. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.07.062 · Cited by 32 · see citing works

Prefrontal cortex, hippocampus, and basolateral amygdala plasticity in a rat model of autism spectrum: Cortical Size in VPA Model

Sosa-Díaz, N., Bringas, M. E., Atzori, M., & Flores, G. (2014) · Synapse · doi:10.1002/syn.21759 · Cited by 31 · see citing works

Emotional and behavioural features of preschool children born by Caesarean deliveries at maternal request

Kelmanson, I. A. (2013) · European Journal of Developmental Psychology · doi:10.1080/17405629.2013.787024 · Cited by 32 · see citing works

Decreased dendritic spine density of neurons of the prefrontal cortex and nucleus accumbens and enhanced amphetamine sensitivity in postpubertal rats after a neonatal amygdala lesion

Solís, Ó., Vázquez‐Roque, R. A., Camacho‐Abrego, I., Gamboa, C., de la Cruz, F., Zamudio, S., & Flores, G. (2009) · Synapse · doi:10.1002/syn.20697 · Cited by 31 · see citing works

Effects of obstetric complications on volume and functional connectivity of striatum in anorexia nervosa patients

Favaro, A., Tenconi, E., Degortes, D., Manara, R., & Santonastaso, P. (2014) · International Journal of Eating Disorders · doi:10.1002/eat.22320 · Cited by 28 · see citing works

In vivo mitochondrial inhibition alters corticostriatal synaptic function and the modulatory effects of neurotrophins

Mendoza, E., Miranda-Barrientos, J. A., Vázquez‐Roque, R. A., Morales-Herrera, E., Ruelas, A., la Rosa, G. D., Flores, G., & Hernández, E. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.018 · Cited by 28 · see citing works

New insights on nitric oxide: Focus on animal models of schizophrenia

Morales‐Medina, J. C., Aguilar‐Alonso, P., Cerbo, A. D., Iannitti, T., & Flores, G. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113304 · Cited by 26 · see citing works

Elective caesarean section on maternal request prior to 39 gestational weeks and childhood psychopathology: a birth cohort study in China

Huang, K., Yan, S., Wu, X., Zhu, P., & Tao, F. (2019) · BMC Psychiatry · doi:10.1186/s12888-019-2012-z · Cited by 25 · see citing works

Unilateral injection of Aβ25–35in the hippocampus reduces the number of dendritic spines in hyperglycemic rats

Lazcano, Z., Solís, Ó., Bringas, M. E., Limón, I. D., Díaz, A., Espinosa, B., García‐Peláez, I., Flores, G., & Guevara, J. (2014) · Synapse · doi:10.1002/syn.21770 · Cited by 25 · see citing works

Long-term coordinated microstructural disruptions of the developing neocortex and subcortical white matter after early postnatal systemic inflammation

Prasad, J. D., van de Looij, Y., Gunn, K. C., Ranchhod, S. M., White, P. B., Berry, M. J., Bennet, L., Sizonenko, S. V., Gunn, A. J., & Dean, J. M. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.12.006 · Cited by 25 · see citing works

Cerebrolysin reverses hippocampal neural atrophy in a mice model of diabetes mellitus type 1

Sanchez‐Vega, L., Juárez, I., Gómez‐Villalobos, M. D. J., & Flores, G. (2015) · Synapse · doi:10.1002/syn.21819 · Cited by 23 · see citing works

Juvenile stress causes reduced locomotor behavior and dendritic spine density in the prefrontal cortex and basolateral amygdala in Sprague–Dawley rats

Pinzón-Parra, C. A., Vidal, B., Camacho‐Abrego, I., Flores‐Gómez, A. A., Moreno, A. R., & Flores, G. (2018) · Synapse · doi:10.1002/syn.22066 · Cited by 22 · see citing works

Birth by cesarean section and schizophrenia: results from the multicenter FACE-SZ data-set

Fond, G. B., Bulzacka, E., Boyer, L., Llorca, P., Godin, O., Brunel, L., Andrianarisoa, M., Aouizerate, B., Berna, F. S., Capdevielle, D., et al. (2016) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-016-0708-3 · Cited by 21 · see citing works

Effect of caesarean section on brain maturation

Kapellou, O. (2011) · Acta Paediatrica · doi:10.1111/j.1651-2227.2011.02427.x · Cited by 21 · see citing works

Effect of cesarean section on the risk of autism spectrum disorders/attention deficit hyperactivity disorder in offspring: a meta-analysis

Chen, M., Lin, Y., Yu, C., Fu, R., Shentu, H., Yao, J., Huang, J., He, Y., & Yu, M. (2023) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-023-07059-9 · Cited by 19 · see citing works

The effects of amphetamine exposure on juvenile rats on the neuronal morphology of the limbic system at prepubertal, pubertal and postpubertal ages

Tendilla‐Beltrán, H., Arroyo‐García, L. E., Díaz, A., Camacho‐Abrego, I., de la Cruz, F., Moreno, A. R., & Flores, G. (2016) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2016.05.004 · Cited by 20 · see citing works

Pregnancy improves cognitive deficit and neuronal morphology atrophy in the prefrontal cortex and hippocampus of aging spontaneously hypertensive rats

Cabrera-Pedraza, V. R., Gómez‐Villalobos, M. D. J., de la Cruz, F., Aguilar‐Alonso, P., Zamudio, S., & Flores, G. (2017) · Synapse · doi:10.1002/syn.21991 · Cited by 19 · see citing works

Attenuation of Piwil2 induced by hypoxic postconditioning prevents cerebral ischemic injury by inhibiting CREB2 promoter methylation

Zhan, L., Chen, M., Pang, T., Li, X., Long, L., Liang, D., Peng, L., Sun, W., & Xu, E. (2022) · Brain Pathology · doi:10.1111/bpa.13109 · Cited by 19 · see citing works

Animal models for assessing impact of C-section delivery on biological systems

Cabré, S., Ratsika, A., Rea, K., Stanton, C., & Cryan, J. F. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104555 · Cited by 18 · see citing works

Olfactory bulbectomy induces neuronal rearrangement in the entorhinal cortex in the rat

Morales‐Medina, J. C., Juárez, I., Iannitti, T., & Flores, G. (2013) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2013.07.001 · Cited by 18 · see citing works

Dexamethasone induces different morphological changes in the dorsal and ventral hippocampus of rats

Gómez, A. B. S., Aguilar-Salgado, Y., Reyes-Hernández, D. O., & Flores, G. (2012) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.12.004 · Cited by 17 · see citing works

Dendritic morphology changes in neurons from the ventral hippocampus, amygdala and nucleus accumbens in rats with neonatal lesions into the prefrontal cortex

Lazcano, Z., Solís, Ó., Díaz, A., Brambila, E., Aguilar‐Alonso, P., Guevara, J., & Flores, G. (2015) · Synapse · doi:10.1002/syn.21815 · Cited by 16 · see citing works

The effects of chronic restraint on the morphology of ventral CA1 neurons in female Long Evans rats

Rico, A. M., Mendoza, A. L., Durán, D. A. B., Torres, H., Mendoza, G. A., & Gómez, A. B. S. (2014) · Stress · doi:10.3109/10253890.2014.974029 · Cited by 16 · see citing works

Antibiotics-induced dysbiosis impacts dendritic morphology of adult mouse cortical interneurons

Nakhal, M. M., Mydeen, A. B., Yassin, L. K., Almazrouei, R., Alkamali, R., Alsulaimi, M., Elsaleh, R. I., BaniYas, S., Houqani, S. A., Al-Marzooq, F. I., et al. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1557961 · Cited by 12 · see citing works

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 · see citing works

Pregnancies alters spine number in cortical and subcortical limbic brain regions of old rats

Flores-Vivaldo, Y., Camacho‐Abrego, I., Picazo, O., & Flores, G. (2019) · Synapse · doi:10.1002/syn.22100 · Cited by 12 · see citing works

No effect of obstetric complications on basal ganglia volumes in schizophrenia

Haukvik, U. K., McNeil, T. F., Nesvåg, R., Söderman, E., Jönsson, E. G., & Agartz, I. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.02.024 · Cited by 11 · see citing works

Tooth pulp injury induces sex-dependent neuronal reshaping in the ventral posterolateral nucleus of the rat thalamus

Juárez, I., Morales‐Medina, J. C., Flores‐Tochihuitl, J., Juárez, G. S., Flores, G., & Oseki, H. C. (2018) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2018.10.007 · Cited by 11 · see citing works

Cognitive training increases dendritic arborization in the dorsal hippocampal CA1 and CA3 neurons of female and male Long–Evans rats

Espino, L. A. V., Gómez, A. B. S., & Durán, D. A. B. (2019) · Synapse · doi:10.1002/syn.22140 · Cited by 11 · see citing works

Expression of synaptophysin and BDNF in the medial prefrontal cortex following early life stress and neonatal hypoxia‐ischemia

Tata, D. Α., Dandi, Ε., & Spandou, E. (2020) · Developmental Psychobiology · doi:10.1002/dev.22011 · Cited by 11 · see citing works

Rearrangement of the dendritic morphology of the neurons from prefrontal cortex and hippocampus after subthalamic lesion in Sprague–Dawley rats

Camacho‐Abrego, I., Tellez‐Merlo, G., Melo, Á. I., Moreno, A. R., Garcés, L., de la Cruz, F., Zamudio, S., & Flores, G. (2013) · Synapse · doi:10.1002/syn.21722 · Cited by 10 · see citing works

Comparative utility of MRI and EEG for early detection of cortical dysmaturation after postnatal systemic inflammation in the neonatal rat

White, P. B., Ranasinghe, S., Chen, J., van de Looij, Y., Sizonenko, S. V., Prasad, J. D., Berry, M. J., Bennet, L., Gunn, A. J., & Dean, J. M. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.028 · Cited by 10 · see citing works

Riesgo neurológico en el niño de mediano riesgo neonatal

Vericat, A., & Orden, A. B. (2017) · Acta Pediátrica de México · doi:10.18233/apm38no4pp255-2661434 · Cited by 8 · see citing works

Cerebrolysin ameliorates prefrontal cortex and hippocampus neural atrophy of spontaneous hypertensive rats with hyperglycemia

Aguilar‐Hernández, L., Gómez‐Villalobos, M. D. J., & Flores, G. (2020) · Synapse · doi:10.1002/syn.22156 · Cited by 7 · see citing works

Maternal Exposure to Nano Titanium Dioxide Induces Neurotoxic Effects in Offspring Mice

Hong, F., Zhou, Y., Ji, J., & Wang, L. (2018) · Journal of Biomedical Sciencies · doi:10.4172/2254-609x.100086 · Cited by 7 · see citing works

Potential Biotics for Nutritional Improvement of Health via Microbiome-Gut-Brain Axis

Niazi, M. K., & Hassan, F. (2022) · Advanced Gut & Microbiome Research · doi:10.1155/2022/9976555 · Cited by 7 · see citing works

Increased dendritic length in CA1 and CA3 hippocampal neurons during the metestrus phase in Wistar rats

Mendoza, A. L., Durán, D. A. B., & Gómez, A. B. S. (2018) · Brain Research · doi:10.1016/j.brainres.2018.01.008 · Cited by 6 · see citing works

Probiotics as Curators of a Healthy Gut Microbiota

Murphy, A., Dinan, T. G., Cryan, J. F., Stanton, C., & Ross, R. P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802304-4.00005-0 · Cited by 6 · see citing works

Maternal oxytocin treatment at birth increases epigenetic age in male offspring

Danoff, J. S., Carter, C. S., Gordevičius, J., Milčiūtė, M., Brooke, R. T., Connelly, J. J., & Perkeybile, A. M. (2024) · Developmental Psychobiology · doi:10.1002/dev.22452 · Cited by 3 · see citing works

Hypoxic Postconditioning Offers Neuroprotection Against Transient Cerebral Ischemia via Down‐Regulation of rno_piR_011022

Chen, M., Duan, S., Chai, G., Zhan, L., Peng, L., Sun, W., & Xu, E. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70295 · Cited by 3 · see citing works

Obese female Zucker rats (fa/fa) exhibit dendritic retraction in neurons in the ventromedial hypothalamic nucleus

Durán, D. A. B., Guzmán, S. J. B., Trujillo, A., & Gómez, A. B. S. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.101919 · Cited by 3 · see citing works

Examination of the Relationship Between Caesarean Section Births and Attention Deficit Hyperactivity Disorder

Rosas, B. M. (2016) · ScholarWorks (Central Washington University) · Cited by 3 · see citing works

Birth by cesarean section and schizophrenia. Results from the multi-center FACE-SZ dataset

Fond, G. B., Boyer, L., Llorca, P., & Leboyer, M. (2016) · European Psychiatry · doi:10.1016/j.eurpsy.2016.01.073 · Cited by 3 · see citing works

Morphological Changes Induced by the Absence of Ovarian Hormones in Nucleus Accumbens of Ovariectomized Rats

Quinones, A. R., Camacho‐Abrego, I., Rivera, N. A., Flores, G., & Picazo, O. (2009) · The Open Neuroendocrinology Journal · doi:10.2174/1876528900902010031 · Cited by 2 · see citing works

Through Disturbances in Neuronal Arborization Prenatal Cerebral Ischemia Disrupts MRI-Defined Cortical Microstructure

Dean, J. M. (2013) · Cited by 2 · see citing works

Microbiome-based dietary supplements for better development and healthy brain

Upadhyay, R., Mani, S., & Sevanan, M. (2025) · International review of neurobiology · doi:10.1016/bs.irn.2025.03.009 · Cited by 1 · see citing works

EXAMINING THE INTERACTION OF NEONATAL ALCOHOL AND HYPOXIA IN VITRO

Carter, M. (2013) · UKnowledge (University of Kentucky) · Cited by 1 · see citing works

Neonatal olfactory bulbectomy causes dendritic spine retraction in dorsal hippocampal CA3 neurons in female rats and spatial learning deficits in male rats

Torres, H., Pérez, P. R., & Gómez, A. B. S. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02727-7 · Cited by 1 · see citing works

The effects of alcohol and hypoxia exposure in the developing brain

Carter, M. (2015) · UKnowledge (University of Kentucky)

Probiotics as Curators of a Healthy Gut Microbiota

Mills, S., Murphy, A., Dinan, T. G., Cryan, J. F., Stanton, C., & Ross, R. P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99971-7.00006-0

Impact of Cesarean Delivery on Reward Behavior and Tyrosine Hydroxylase in the Nucleus Accumbens of Adult Prairie Vole Offspring

Rogers, K., Kiernan, E., Partie, M. E., & Kenkel, W. M. (2025) · Developmental Psychobiology · doi:10.1002/dev.70109

Male Rats Carrying the Taiep Mutation Show Alterations in the Dendritic Arborization of CA1 and CA3 Neurons

Medina‐Flores, F., Durán, D. A. B., Robles‐Soto, R., & Gómez, A. B. S. (2026) · Hippocampus · doi:10.1002/hipo.70080

Term or preterm cesarean section delivery does not lead to long-term detrimental consequences in mice

Chiesa, M. (2018) · theses.fr (ABES) · doi:10.70675/6ef32b4fzb74az4b06zb8edz92268c28d542

Perinatal Distress Leads to Lateralized Medial Prefrontal Cortical Dopamine Hypofunction in Adult Rats

Brake, W. G., Sullivan, R. M., & Gratton, A. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05538.2000 · Cited by 131 · see citing works

S.19.03 Birth injury and the psychosis pathway: insights from animal models of obstetric complications

Boksa, P. (2006) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(06)70095-5

Análise estereológica de populações neuronais e astrocitárias do córtex pré-frontal de ratos submetidos a anóxia neonatal

Ribeiro, J. D. O. B. (2016) · UNESP Institutional Repository (São Paulo State University)

Prenatal stress alters spine density and dendritic length of nucleus accumbens and hippocampus neurons in rat offspring

Martínez‐Téllez, R. I., Hernández‐Torres, E., Gamboa, C., & Flores, G. (2009) · Synapse · doi:10.1002/syn.20664 · Cited by 174 · see citing works

Cesarean plus anoxia at birth induces hyperresponsiveness to locomotor activity by dopamine D2 agonist

Juárez, I., de la Cruz, F., Zamudio, S., & Flores, G. (2005) · Synapse · doi:10.1002/syn.20203 · Cited by 11 · see citing works