Dopamine, cocaine and the development of cerebral cortical cytoarchitecture: A review of current concepts

Excitatory actions of gaba during development: the nature of the nurture

Ben-Ari, Y. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn920 · Cited by 2,448 · see citing works

Cocaine Receptors on Dopamine Transporters Are Related to Self-Administration of Cocaine

Ritz, M. C., Lamb, R. J., Goldberg, S. R., & Kuhar, M. J. (1987) · Science · doi:10.1126/science.2820058 · Cited by 2,180 · see citing works

Molecular biology of dopamine receptors

Sibley, D. R., & Monsma, F. J. (1992) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(92)90025-2 · Cited by 993 · see citing works

The origin and specification of cortical interneurons

Wonders, C. P., & Anderson, S. A. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1954 · Cited by 980 · see citing works

Beyond the Dopamine Receptor

Greengard, P., Allen, P. B., & Nairn, A. C. (1999) · Neuron · doi:10.1016/s0896-6273(00)80798-9 · Cited by 743 · see citing works

Developing networks play a similar melody

Ben-Ari, Y. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01813-0 · Cited by 614 · see citing works

Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model

Caviness, V. S., Takahashi, T., & Nowakowski, R. S. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93933-o · Cited by 566 · see citing works

D1–D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of G q /11 in the striatum

Rashid, A. J., So, C. H., Kong, M. M. C., Furtak, T., El-Ghundi, M., Cheng, R., O’Dowd, B. F., & George, S. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604049104 · Cited by 492 · see citing works

Cocaine inhibition of ligand binding at dopamine, norepinephrine and serotonin transporters: A structure-activity study

Ritz, M. C., Cone, E. J., & Kuhar, M. J. (1990) · Life Sciences · doi:10.1016/0024-3205(90)90132-b · Cited by 469 · see citing works

Molecular cloning and expression of a D1 dopamine receptor linked to adenylyl cyclase activation.

Monsma, F. J., Mahan, L. C., McVittie, L. D., Gerfen, C. R., & Sibley, D. R. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.17.6723 · Cited by 456 · see citing works

Temporal Patterns of Cocaine Use in Pregnancy

Chasnoff, I. J. (1989) · JAMA · doi:10.1001/jama.1989.03420120079030 · Cited by 452 · see citing works

Human brain dopamine receptors in children and aging adults

Seeman, P., Bzowej, N. H., Guan, H. ‐., Bergeron, C., Becker, L. E., Reynolds, G. P., Bird, E. D., Riederer, P., Jellinger, K., Watanabe, S., et al. (1987) · Synapse · doi:10.1002/syn.890010503 · Cited by 404 · see citing works

Dynamics of Cell Migration from the Lateral Ganglionic Eminence in the Rat

Carlos, J., López‐Mascaraque, L., & Valverde, F. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-19-06146.1996 · Cited by 403 · see citing works

New evidence for neurotransmitter influences on brain development

Levitt, P., Harvey, J. A., Friedman, E., Simansky, K., & Murphy, E. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)01028-4 · Cited by 362 · see citing works

moody Encodes Two GPCRs that Regulate Cocaine Behaviors and Blood-Brain Barrier Permeability in Drosophila

Bainton, R. J., Tsai, L. T.-Y., Schwabe, T., DeSalvo, M. K., Gaul, U., & Heberlein, U. (2005) · Cell · doi:10.1016/j.cell.2005.07.029 · Cited by 228 · see citing works

Ontogeny of D1a and D2 dopamine receptor subtypes in rat brain using in situ hybridization and receptor binding

Schambra, U. B., Duncan, G. E., Breese, G. R., Fornaretto, M. G., Caron, M. G., & Fremeau, R. T. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90315-8 · Cited by 209 · see citing works

Dopamine Modulates Cell Cycle in the Lateral Ganglionic Eminence

Ohtani, N., Goto, T., Waeber, C., & Bhide, P. G. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02840.2003 · Cited by 193 · see citing works

Cell Output, Cell Cycle Duration and Neuronal Specification: a Model of Integrated Mechanisms of the Neocortical Proliferative Process

Caviness, V. S. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.6.592 · Cited by 188 · see citing works

Ontogeny of dopamine D1 and D2 receptor subtypes in rat basal ganglia: a quantitative autoradiographic study

Rao, P. A., Molinoff, P. B., & Joyce, J. N. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90045-k · Cited by 165 · see citing works

Birth and fate of proliferative cells in the inner nuclear layer of the mature fish retina

Julian, D. A., Ennis, K., & Korenbrot, J. I. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980511)394:3 · Cited by 154 · see citing works

Interneurons set the tune of developing networks

Ben‐Ari, Y., Khalilov, I., Represa, A., & GOZLAN, H. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.05.002 · Cited by 149 · see citing works

The time of genesis, embryonic origin and differentiation of the brain stem monoamine neurons in the rhesus monkey

Levitt, P. R., & RAKIC, P. T. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90095-5 · Cited by 145 · see citing works

Scheduling of Monoaminergic Neurotransmitter Receptor Expression in the Primate Neocortex during Postnatal Development

Lidow, M. S., & Rakic, P. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.5.401 · Cited by 141 · see citing works

SKF83959 selectively regulates phosphatidylinositol‐linked D1 dopamine receptors in rat brain

Jin, L., Goswami, S. K., Cai, G., Zhen, X., & Friedman, E. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01698.x · Cited by 140 · see citing works

Prenatal cocaine exposure disrupts the development of the serotonergic system

Akbari, H. M., Kramer, H. K., Whitaker‐Azmitia, P. M., SPEAR, L. P., & Azmitia, E. C. (1992) · Brain Research · doi:10.1016/0006-8993(92)90450-n · Cited by 140 · see citing works

Excess of serotonin affects embryonic interneuron migration through activation of the serotonin receptor 6

Riccio, O., Potter, G., Walzer, C., Vallet, P., Szabó, G., Vutskits, L., Kiss, J. Z., & Dayer, A. G. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.89 · Cited by 138 · see citing works

Prenatal Cocaine and Neonatal Outcome: Evaluation of Dose-Response Relationship

Delaney‐Black, V., Covington, C. Y., Ostrea, E. M., et al. (1996) · PEDIATRICS · doi:10.1542/peds.98.4.735 · Cited by 137 · see citing works

Developing brain and in utero cocaine exposure: Effects on neural ontogeny

Mayes, L. C. (1999) · Development and Psychopathology · doi:10.1017/s0954579499002278 · Cited by 136 · see citing works

Dopamine Receptor Activation Modulates GABA Neuron Migration from the Basal Forebrain to the Cerebral Cortex

Crandall, J. E., McCarthy, D. M., Araki, K. Y., Sims, J. R., Ren, J.-Q., & Bhide, P. G. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5124-06.2007 · Cited by 134 · see citing works

Dopamine receptor mRNA and protein expression in the mouse corpus striatum and cerebral cortex during pre- and postnatal development

Araki, K. Y., Sims, J. R., & Bhide, P. G. (2007) · Brain Research · doi:10.1016/j.brainres.2007.04.043 · Cited by 131 · see citing works

Specification of Distinct Dopaminergic Neural Pathways: Roles of the Eph Family Receptor EphB1 and Ligand Ephrin-B2

Yue, Y., Widmer, D. A. J., Halladay, A. K., Cerretti, D. P., Wagner, G. C., Dreyer, J., & Zhou, R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02090.1999 · Cited by 130 · see citing works

Prenatal development of the biogenic amine systems of the mouse brain

Golden, G. S. (1973) · Developmental Biology · doi:10.1016/0012-1606(73)90139-5 · Cited by 127 · see citing works

Cocaine-induced disturbances of corticogenesis in the developing murine brain

Gressèns, P., Kosofsky, B. E., & Evrard, P. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90694-3 · Cited by 125 · see citing works

Ontogeny of dopaminergic D-2 receptors in the rat nervous system: Characterization and detailed autoradiographic mapping with [125I]iodosulpride

Salès, N., Martres, M., Bouthenet, M.-L., & Schwartz, J. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90014-6 · Cited by 124 · see citing works

PATTERNING AND SPECIFICATION OF THE CEREBRAL CORTEX

Levitt, P. R., Barbe, M. F., & Eagleson, K. L. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.1 · Cited by 123 · see citing works

Cocaine and pregnancy: clinical and toxicological implications for the neonate.

Chasnoff, I. J., Lewis, D., Griffith, D. R., et al. (1989) · Clinical Chemistry · doi:10.1093/clinchem/35.7.1276 · Cited by 115 · see citing works

Influence of Dopamine on Precursor Cell Proliferation and Differentiation in the Embryonic Mouse Telencephalon

Popolo, M., McCarthy, D. M., & Bhide, P. G. (2004) · Developmental Neuroscience · doi:10.1159/000082140 · Cited by 113 · see citing works

Primates exposed to cocaine in utero display reduced density and number of cerebral cortical neurons

Lidow, M. S., & Song, Z. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1028 · Cited by 106 · see citing works

In UteroCocaine-Induced Dysfunction of Dopamine D1Receptor Signaling And Abnormal Differentiation of Cerebral Cortical Neurons

Jones, L. B., Stanwood, G. D., Reinoso, B. S., Washington, R. A., Wang, H.-Y., Friedman, E., & Levitt, P. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04606.2000 · Cited by 106 · see citing works

Prenatal exposure to cocaine selectively reduces D1 dopamine receptor-mediated activation of striatal Gs proteins.

Wang, H. Y., Runyan, S., Yadin, E., & Friedman, E. (1995) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)09613-2 · Cited by 105 · see citing works

Prenatal cocaine exposure adversely affects development of the primate cerebral cortex

Lidow, M. S. (1995) · Synapse · doi:10.1002/syn.890210408 · Cited by 100 · see citing works

Transplacental Cocaine Exposure: A Mouse Model Demonstrating Neuroanatomic and Behavioral Abnormalities

Kosofsky, B. E., Wilkins, A. S., Gressèns, P., & Evrard, P. (1994) · Journal of Child Neurology · doi:10.1177/088307389400900303 · Cited by 98 · see citing works

Temporal patterns of cocaine use in pregnancy. Perinatal outcome

Chasnoff, I. J. (1989) · JAMA · doi:10.1001/jama.261.12.1741 · Cited by 95 · see citing works

Development of striatal dopaminergic function. I. Pre- and postnatal development of mRNAs and binding sites for striatal D1 (D1a) and D2 (D2a) receptors

Jung, A. B., & Bennett, J. P. (1996) · Developmental Brain Research · doi:10.1016/0165-3806(96)00033-8 · Cited by 94 · see citing works

Prenatal cocaine exposure produces consistent developmental alterations in dopamine-rich regions of the cerebral cortex

Stanwood, G. D., Washington, R. A., Shumsky, J. S., & Levitt, P. R. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00256-1 · Cited by 94 · see citing works

Effect of prenatal cocaine on dopamine receptor-G protein coupling in mesocortical regions of the rabbit brain

Friedman, E., Yadin, E., & Wang, H. Y. (1996) · Neuroscience · doi:10.1016/s0306-4522(96)83011-9 · Cited by 84 · see citing works

Cocaine Exposure Decreases GABA Neuron Migration from the Ganglionic Eminence to the Cerebral Cortex in Embryonic Mice

Crandall, J. E. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh027 · Cited by 80 · see citing works

Identification of a Sensitive Period of Prenatal Cocaine Exposure that Alters the Development of the Anterior Cingulate Cortex

Stanwood, G. D. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.5.430 · Cited by 75 · see citing works

Numbers of Meynert and layer IVB cells in area V1: A stereologic analysis in young and aged macaque monkeys

Hof, P. R., Nimchinsky, E. A., Young, W. G., & Morrison, J. H. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000424)420:1 · Cited by 71 · see citing works

Consequences of prenatal cocaine exposure in nonhuman primates

Lidow, M. S. (2003) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.09.001 · Cited by 70 · see citing works

Prenatal Exposure to Cocaine Disrupts D1ADopamine Receptor Function Via Selective Inhibition of Protein Phosphatase 1 Pathway in Rabbit Frontal Cortex

Zhen, X., Torres, C. A., Wang, H.-Y., & Friedman, E. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-23-09160.2001 · Cited by 67 · see citing works

Increased tyrosine hydroxylase immunoreactivity in the rat cortex following prenatal cocaine exposure

Akbari, H. M., & Azmitia, E. C. (1992) · Developmental Brain Research · doi:10.1016/0165-3806(92)90093-c · Cited by 64 · see citing works

Anatomical abnormalities in dopaminoceptive regions of the cerebral cortex of dopamine D1 receptor mutant mice

Stanwood, G. D., Parlaman, J. P., & Levitt, P. R. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20548 · Cited by 62 · see citing works

Intrauterine cocaine exposure of rabbits: persistent elevation of GABA-immunoreactive neurons in anterior cingulate cortex but not visual cortex

Wang, X.-H., Levitt, P. R., Grayson, D. R., & Murphy, E. H. (1995) · Brain Research · doi:10.1016/0006-8993(95)00528-x · Cited by 60 · see citing works

Prenatal Exposure to Cocaine Produces Unique Developmental and Long-Term Adaptive Changes in Dopamine D1Receptor Activity and Subcellular Distribution

Stanwood, G. D., & Levitt, P. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4591-06.2007 · Cited by 60 · see citing works

D2 dopamine receptor gene expression in the rat striatum during ontogeny: an in situ hybridization study

Guennoun, R., & Bloch, B. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90157-e · Cited by 55 · see citing works

Different mechanisms of glutamate-induced neuronal death between dopaminergic and non-dopaminergic neurons in rat mesencephalic culture

Sawada, H., Kawamura, T., Shimohama, S., AKAIKE, A., & Kimura, J. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960215)43:4 · Cited by 52 · see citing works

Nonhuman Primate Model of the Effect of Prenatal Cocaine Exposure on Cerebral Cortical Development

Lidow, M. S. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09736.x · Cited by 52 · see citing works

Cocaine inhibits NGF-induced PC12 cells differentiation through D1-type dopamine receptors

Zachor, D. A., Moore, J. F., Brezausek, C. M., et al. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02355-6 · Cited by 50 · see citing works

Opposing Actions of D1and D2‐Dopamine Receptors on Arachidonic Acid Release and Cyclic AMP Production in Striatal Neurons

Schinelli, S., Paolillo, M., & Corona, G. L. (1994) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1994.62030944.x · Cited by 49 · see citing works

Prenatal exposure to cocaine selectively disrupts motor responding to d-Amphetamine in young and mature rabbits

Simansky, K. J., & Kachelries, W. J. (1996) · Neuropharmacology · doi:10.1016/0028-3908(95)00151-4 · Cited by 47 · see citing works

Chronic cocaine exposure in the fetal rhesus monkey: consequences for early development of dopamine neurons

Rönnekleiv, O., & Naylor, B. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07330.1995 · Cited by 47 · see citing works

Prenatal Cocaine Exposure Alters Signal Transduction in the Brain D1 Dopamine Receptor Systema

Friedman, E., & Wang, H. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09741.x · Cited by 46 · see citing works

Cocaine affects cerebral neocortical cytoarchitecture in primates only if administered during neocortical neuronogenesis

Lidow, M. S., Bozian, D., & Song, Z. (2001) · Developmental Brain Research · doi:10.1016/s0165-3806(01)00139-0 · Cited by 45 · see citing works

Elevated dopamine levels during gestation produce region-specific decreases in neurogenesis and subtle deficits in neuronal numbers

McCarthy, D. M., Lueras, P., & Bhide, P. G. (2007) · Brain Research · doi:10.1016/j.brainres.2007.08.088 · Cited by 44 · see citing works

Effect of Cocaine on Cell Proliferation in the Cerebral Wall of Monkey Fetuses

Lidow, M. S. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.6.545 · Cited by 44 · see citing works

Cocaine binding sites in fetal rat brain: implications for prenatal cocaine action

Meyer, J. S., Shearman, L. P., Collins, L. M., et al. (1993) · Psychopharmacology · doi:10.1007/bf02244892 · Cited by 43 · see citing works

Chimeric D2/D3 Dopamine Receptors Efficiently Inhibit Adenylyl Cyclase in HEK 293 Cells

Robinson, S. W., & Caron, M. G. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.67010212.x · Cited by 43 · see citing works

A Mouse Model of Transplacental Cocaine Exposure: Clinical Implications for Exposed Infants and Childrena

Kosofsky, B. E., & Wilkins, A. S. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09742.x · Cited by 39 · see citing works

Cocaine differentially inhibits neuronal differentiation and proliferation in vitro.

Zachor, D. A., Cherkes, J. K., Fay, C. T., et al. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117071 · Cited by 38 · see citing works

Widespread expression of functional D1-dopamine receptors in fetal rat brain

Shearman, L. P., Zeitzer, J., & Weaver, D. R. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00091-6 · Cited by 35 · see citing works

Neuropathological consequences of prenatal cocaine exposure in the mouse

Ren, J., Malanga, C. J., Tabit, E., & Kosofsky, B. E. (2004) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.05.003 · Cited by 32 · see citing works

D1 Dopamine Receptor Regulation of the Levels of the Cell-cycle-controlling Proteins, Cyclin D, P27 and Raf-1, in Cerebral Cortical Precursor Cells is Mediated Through cAMP-independent Pathways

Zhang, L. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh110 · Cited by 30 · see citing works

Changes in the Midbrain‐Rostral Forebrain Dopamine Circuitry in the Cocaine‐Exposed Primate Fetal Braina

Rønnekleiv, O. K., Fang, Y., Choi, W. S., et al. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09735.x · Cited by 29 · see citing works

Axo-Axonic Structures in the Medial Prefrontal Cortex of the Rat: Reduction by Prenatal Exposure to Cocaine

Morrow, B. A., Elsworth, J. D., & Roth, R. H. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05227.2003 · Cited by 27 · see citing works

MK-801 interaction with the 5-HT transporter: a real-time study in brain slices using fast cyclic voltammetry

Iravani, M. M., Muscat, R., & Kruk, Z. L. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990601)32:3 · Cited by 27 · see citing works

Neuropathology of the cerebral cortex observed in a range of animal models of prenatal cocaine exposure may reflect alterations in genes involved in the Wnt and cadherin systems

Novikova, S. I., He, F., Bai, J., & Lidow, M. S. (2005) · Synapse · doi:10.1002/syn.20134 · Cited by 24 · see citing works

Hippocampal dysplasia in rats exposed to cocaine in utero

Baraban, S. C., Wenzel, H. J., Castro, P. A., et al. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00106-6 · Cited by 23 · see citing works

Regional differences in cortical dendrite morphology following in utero exposure to cocaine

Lloyd, S. A., Wensley, B. G., Faherty, C. J., & Smeyne, R. J. (2003) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.09.008 · Cited by 23 · see citing works

D1 dopamine receptor regulation of cell cycle in FGF‐ and EGF‐supported primary cultures of embryonic cerebral cortical precursor cells

Zhang, L., & Lidow, M. S. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00104-1 · Cited by 22 · see citing works

Cocaine induces cell death within the primate fetal cerebral wall

He, Song, & Lidow (1999) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.1999.00211.x · Cited by 22 · see citing works

Inhalational model of cocaine exposure in mice: Neuroteratological effects

He, F., Lidow, I. A., & Lidow, M. S. (2006) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2005.12.001 · Cited by 16 · see citing works

Cerebral Cortical Abnormalities Seen in a Non-Human Primate Model of Prenatal Cocaine Exposure are not Related to Vasoconstriction

He, N. (2004) · NeuroToxicology · doi:10.1016/j.neuro.2003.10.002 · Cited by 15 · see citing works

Prenatal exposure to cocaine decreases adenylyl cyclase activity in embryonic mouse striatum

Unterwald, E. M., Ivković, S., Cuntapay, M., Stroppolo, A., Guinea, B., & Ehrlich, M. E. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00058-0 · Cited by 13 · see citing works

Characterization of Mouse Striatal Precursor Cell Lines Expressing Functional Dopamine Receptors

Araki, K. Y., Fujimura, S., MacDonald, M. E., & Bhide, P. G. (2006) · Developmental Neuroscience · doi:10.1159/000095114 · Cited by 9 · see citing works

Development of prefrontal cortex

Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378 · see citing works

Developmental origins of brain disorders: roles for dopamine

Money, K. M., & Stanwood, G. D. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00260 · Cited by 221 · see citing works

Prenatal Nicotine Exposure Mouse Model Showing Hyperactivity, Reduced Cingulate Cortex Volume, Reduced Dopamine Turnover, and Responsiveness to Oral Methylphenidate Treatment

Zhu, J., Zhang, X., Xu, Y., Spencer, T. J., Biederman, J., & Bhide, P. G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1041-12.2012 · Cited by 125 · see citing works

Prenatal stress and genetic risk: How prenatal stress interacts with genetics to alter risk for psychiatric illness

Abbott, P. W., Gumusoglu, S. B., Bittle, J., Beversdorf, D. Q., & Stevens, H. E. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.01.019 · Cited by 109 · see citing works

Cocaine exposure modulates dopamine and adenosine signaling in the fetal brain

Kubrusly, R. C. C., & Bhide, P. G. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.09.007 · Cited by 40 · see citing works

Perturbed Developmental Serotonin Signaling Affects Prefrontal Catecholaminergic Innervation and Cortical Integrity

Garcia, L. P., Witteveen, J. S., Middelman, A., van Hulten, J. A., Martens, G. J. M., Homberg, J. R., & Kolk, S. M. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1105-x · Cited by 28 · see citing works

The Concerted Modulation of Proliferation and Migration Contributes to the Specification of the Cytoarchitecture and Dimensions of Cortical Areas

Lukaszewicz, A. I., Cortay, V., Giroud, P., Berland, M., Smart, I. H. M., Kennedy, H., & Dehay, C. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk011 · Cited by 54 · see citing works

Patterning the cerebral cortex into distinct functional domains during development

Appan, D., Hsu, S.-M., Hsu, W.-H., & Chou, S. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102698 · Cited by 14 · see citing works

Cell Polarity in Cerebral Cortex Development—Cellular Architecture Shaped by Biochemical Networks

Hansen, A. H., Duellberg, C., Mieck, C., Loose, M., & Hippenmeyer, S. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00176 · Cited by 40 · see citing works

Cocaine affects cerebral neocortical cytoarchitecture in primates only if administered during neocortical neuronogenesis

Lidow, M. S., Bozian, D., & Song, Z. (2001) · Developmental Brain Research · doi:10.1016/s0165-3806(01)00139-0 · Cited by 45 · see citing works

Brodmann's localization in the cerebral cortex : the principles of comparative localisation in the cerebral cortex based on cytoarchitectonics

Brodmann, K., & Gary, L. J. (2006) · Springer eBooks · Cited by 48 · see citing works