Development of the prefrontal cortex during adolescence: Insights into vulnerable neural circuits in schizophrenia

Implications of Normal Brain Development for the Pathogenesis of Schizophrenia

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

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685 · see citing works

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

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

The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe

Fuster, J. M. (1980) · Cited by 2,367 · see citing works

Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia

Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,019 · see citing works

Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory

Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960 · see citing works

Modulation of memory fields by dopamine Dl receptors in prefrontal cortex

Williams, G. V., & Goldman-Rakic, P. S. (1995) · Nature · doi:10.1038/376572a0 · Cited by 1,593 · see citing works

Positron emission tomography study of human brain functional development

Chugani, H. T., Phelps, M. E., & Mazziotta, J. C. (1987) · Annals of Neurology · doi:10.1002/ana.410220408 · Cited by 1,548 · see citing works

Cognitive Deficit Caused by Regional Depletion of Dopamine in Prefrontal Cortex of Rhesus Monkey

Brozoski, T. J., Brown, R. M., Rosvold, H. E., & Goldman, P. S. (1979) · Science · doi:10.1126/science.112679 · Cited by 1,500 · see citing works

Context, cortex, and dopamine: A connectionist approach to behavior and biology in schizophrenia.

Cohen, J. D., & Servan‐Schreiber, D. (1992) · Psychological Review · doi:10.1037/0033-295x.99.1.45 · Cited by 1,494 · see citing works

Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks

Changeux, J.-P., & Danchin, A. (1976) · Nature · doi:10.1038/264705a0 · Cited by 1,448 · see citing works

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

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

D1 Dopamine Receptors in Prefrontal Cortex: Involvement in Working Memory

Sawaguchi, T., & Goldman-Rakic, P. S. (1991) · Science · doi:10.1126/science.1825731 · Cited by 1,364 · see citing works

The prefrontal cortex: Anatomy, physiology, and neuropsychology of the frontal lobe

Holmes, G. L. (1989) · Journal of Epilepsy · doi:10.1016/0896-6974(89)90035-2 · Cited by 1,210 · see citing works

Concurrent overproduction of synapses in diverse regions of the primate cerebral cortex

Rakic, P., Bourgeois, J.-P., Eckenhoff, M. F., Zecevic, N., & Goldman-Rakic, P. S. (1986) · Science · doi:10.1126/science.3952506 · Cited by 1,133 · see citing works

Gene expression for glutamic acid decarboxylase is reduced without loss of neurons in prefrontal cortex of schizophrenics.

Akbarian, S. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160008002 · Cited by 1,002 · see citing works

Schizophrenics Show Spatial Working Memory Deficits

Park, S. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820120063009 · Cited by 946 · see citing works

Synaptic patterns on different cell types in the different laminae of the cat visual cortex. An electron microscope study

Colonnier, M. (1968) · Brain Research · doi:10.1016/0006-8993(68)90234-5 · Cited by 946 · see citing works

Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey

Barbas, H., & Pandya, D. Ν. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902860306 · Cited by 937 · see citing works

Deficits in Small Interneurons in Prefrontal and Cingulate Cortices of Schizophrenic and Schizoaffective Patients

Benes, F. M. (1991) · Archives of General Psychiatry · doi:10.1001/archpsyc.1991.01810350036005 · Cited by 894 · see citing works

Abnormally High Neuronal Density in the Schizophrenic Cortex

Selemon, L. D. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950220015005 · Cited by 876 · see citing works

Development of Cortical Circuitry and Cognitive Function

Goldman‐Rakic, P. S. (1987) · Child Development · doi:10.2307/1130201 · Cited by 817 · see citing works

Elimination of synapses in the developing nervous system

Purves, D., & Lichtman, J. W. (1980) · Science · doi:10.1126/science.7414326 · Cited by 808 · see citing works

Parvalbumin in Most γ-Aminobutyric Acid-Containing Neurons of the Rat Cerebral Cortex

Celio, M. R. (1986) · Science · doi:10.1126/science.3945815 · Cited by 740 · see citing works

Thalamic Abnormalities in Schizophrenia Visualized Through Magnetic Resonance Image Averaging

Andreasen, N. C., Arndt, S. V., Swayze, V. W., Cizadlo, T., Flaum, M. A., OʼLeary, D. S., Ehrhardt, J. C., & Yuh, W. T. C. (1994) · Science · doi:10.1126/science.7939669 · Cited by 694 · see citing works

Synaptogenesis in the Prefrontal Cortex of Rhesus Monkeys

Bourgeois, J.-P., Goldman-Rakic, P. S., & Rakic, P. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.1.78 · Cited by 687 · 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

Varieties and distribution of non‐pyramidal cells in the somatic sensory cortex of the squirrel monkey

Jones, E. G. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600204 · Cited by 593 · see citing works

Increased dopamine turnover in the prefrontal cortex impairs spatial working memory performance in rats and monkeys

Murphy, B. L., Arnsten, A. F., Goldman-Rakic, P. S., & Roth, R. H. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.3.1325 · Cited by 590 · see citing works

Developmental changes in performance on tests of purported frontal lobe functioning

Levin, H. S., Culhane, K. A., Hartmann, J., Evankovich, K. D., Mattson, A. J., Harward, H. N., Ringholz, G. M., Ewing‐Cobbs, L., & Fletcher, J. M. (1991) · Developmental Neuropsychology · doi:10.1080/87565649109540499 · Cited by 581 · see citing works

Changes of synaptic density in the primary visual cortex of the macaque monkey from fetal to adult stage

Bourgeois, J., & Rakic, P. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-07-02801.1993 · Cited by 567 · see citing works

Pronounced Reduction of Total Neuron Number in Mediodorsal Thalamic Nucleus and Nucleus Accumbens in Schizophrenics

Pakkenberg, B. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810230039007 · Cited by 566 · see citing works

Dopamine D1 receptor mechanisms in the cognitive performance of young adult and aged monkeys

Arnsten, A. F. T., Cai, J. X., Murphy, B. L., & Goldman-Rakic, P. S. (1994) · Psychopharmacology · doi:10.1007/bf02245056 · Cited by 566 · see citing works

Requirement for subplate neurons in the formation of thalamocortical connections

Ghosh, A., Antonini, A., McConnell, S. K., & Shatz, C. J. (1990) · Nature · doi:10.1038/347179a0 · Cited by 563 · see citing works

Development of the ability to use recall to guide action, as indicated by infants’ performance on AB.

Diamond, A. (1985) · Child Development · doi:10.2307/1130099 · Cited by 555 · see citing works

Developmental Time Course in Human Infants and Infant Monkeys, and the Neural Bases of, Inhibitory Control in Reachinga

Diamond, A. D. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb48913.x · Cited by 541 · see citing works

Physiological subgroups of nonpyramidal cells with specific morphological characteristics in layer II/III of rat frontal cortex

Kawaguchi, Y. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-04-02638.1995 · Cited by 533 · see citing works

A specific ‘axo-axonal’ interneuron in the visual cortex of the rat

Somogyi, P. (1977) · Brain Research · doi:10.1016/0006-8993(77)90808-3 · Cited by 530 · see citing works

Mediodorsal nucleus: Areal, laminar, and tangential distribution of afferents and efferents in the frontal lobe of rhesus monkeys

Giguere, M., & Goldman-Rakic, P. S. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902770204 · Cited by 529 · see citing works

The development of synapses in striate cortex of man.

Huttenlocher, P. R., & de Courten, C. (1987) · PubMed · Cited by 526 · see citing works

A Neurodevelopmental Approach to the Classification of Schizophrenia

Murray, R. M., O’Callaghan, E., Castle, D. J., & Lewis, S. W. (1992) · Schizophrenia Bulletin · doi:10.1093/schbul/18.2.319 · Cited by 516 · see citing works

Conceptual Models of Neural Organization.

Pritchard, J. J. (1976) · Europe PMC (PubMed Central) · Cited by 514 · see citing works

Brain Morphology and Schizophrenia: A Magnetic Resonance Imaging Study of Limbic, Prefrontal Cortex, and Caudate Structures

Breier, A. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820120009003 · Cited by 513 · see citing works

Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey

LaMantia, A., & RAKIC, P. T. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-07-02156.1990 · Cited by 511 · see citing works

Local circuit neurons immunoreactive for calretinin, calbindin D‐28k or parvalbumin in monkey prefronatal cortex: Distribution and morphology

Condé, F., Lund, J. S., Jacobowitz, D. M., Baimbridge, K. G., & Lewis, D. A. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410109 · Cited by 500 · see citing works

Alterations in Brain High-Energy Phosphate and Membrane Phospholipid Metabolism in First-Episode, Drug-Naive Schizophrenics

Pettegrew, J. W. (1991) · Archives of General Psychiatry · doi:10.1001/archpsyc.1991.01810300075011 · Cited by 482 · see citing works

The neurodevelopmental basis of sex differences in schizophrenia

Castle, D. J., & Murray, R. M. (1991) · Psychological Medicine · doi:10.1017/s0033291700022194 · Cited by 437 · see citing works

Dopamine synaptic complex with pyramidal neurons in primate cerebral cortex.

Goldman-Rakic, P. S., Leranth, C., Williams, S. M., Mons, N. E., & Geffard, M. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.22.9015 · Cited by 433 · see citing works

Widespread Cerebral Gray Matter Volume Deficits in Schizophrenia

Zipursky, R. B. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820030027004 · Cited by 425 · see citing works

6-Hydroxydopamine lesions of the prefrontal cortex in monkeys enhance performance on an analog of the Wisconsin Card Sort Test: possible interactions with subcortical dopamine

Roberts, A., De Salvia, M., Wilkinson, L., Collins, P., Muir, J., Everitt, B., & Robbins, T. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-05-02531.1994 · Cited by 415 · see citing works

Changes in regional cerebral blood flow during brain maturation in children and adolescents.

Chiron, C., Raynaud, C., Maziere, B., Zilbovicius, M., Laflamme, L., Masure, M. C., Dulac, O., Bourguignon, M., & Syrota, A. (1992) · PubMed · Cited by 405 · see citing works

Maldistribution of Interstitial Neurons in Prefrontal White Matter of the Brains of Schizophrenic Patients

Akbarian, S. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830050061010 · Cited by 398 · see citing works

Comparison of Intrinsic Connectivity in Different Areas of Macaque Monkey Cerebral Cortex

Lund, J. S., Yoshioka, T., & Levitt, J. B. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.2.148 · Cited by 379 · see citing works

Parvalbumin, and intracellular calcium-binding protein; distribution, properties and possible roles in mammalian cells

Heizmann, C. W. (1984) · Cellular and Molecular Life Sciences · doi:10.1007/bf01946439 · Cited by 365 · see citing works

Cellular discharge in the dorsolateral prefrontal cortex of the monkey in cognitive tasks

Fuster, J. M., Bauer, R. H., & Jervey, J. P. (1982) · Experimental Neurology · doi:10.1016/0014-4886(82)90238-2 · Cited by 357 · see citing works

Decreased regional cortical gray matter volume in schizophrenia

Schlaepfer, T. E., Harris, G. J., Tien, A. Y., Peng, L. W., Lee, S., Federman, E. B., Chase, G. A., Barta, P. E., & Pearlson, G. D. (1994) · American Journal of Psychiatry · doi:10.1176/ajp.151.6.842 · Cited by 354 · see citing works

Synaptic patterns in the visual cortex of the cat and monkey. Electron microscopy of Golgi Preparations

LeVay, S. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901500104 · Cited by 341 · see citing works

Visualization of chandelier cell axons by parvalbumin immunoreactivity in monkey cerebral cortex.

DeFelipe, J., Hendry, S. H. C., & Jones, E. G. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.6.2093 · Cited by 338 · see citing works

Conceptual models of neural organization.

Szentágothai, J., & Arbib, M. A. (1974) · PubMed · Cited by 329 · see citing works

PET and MRI of the thalamus in never-medicated patients with schizophrenia

Buchsbaum, M. S., Someya, T., Teng, C. Y., Abel, L., Chin, S., Najafi, A., Haier, R., Wu, J. C., & Bunney, W. E. (1996) · American Journal of Psychiatry · doi:10.1176/ajp.153.2.191 · Cited by 324 · see citing works

Postnatal maturation of the dopaminergic innervation of monkey prefrontal and motor cortices: A tyrosine hydroxylase immunohistochemical analysis

Rosenberg, D. R., & Lewis, D. A. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903580306 · Cited by 319 · see citing works

Gender differences in onset of illness, treatment response, course, and biologic indexes in first-episode schizophrenic patients

Szymanski, S., Lieberman, J. A., Alvir, J. M., Mayerhoff, D. I., Loebel, A., Geisler, S., Chakos, M., Koreen, A., Jody, D. N., & Kane, J. M. (1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.5.698 · Cited by 319 · see citing works

Regional Brain Abnormalities in Schizophrenia Measured With Magnetic Resonance Imaging

Andreasen, N. C. (1994) · JAMA · doi:10.1001/jama.1994.03520220057031 · Cited by 315 · see citing works

Coactivation of prefrontal cortex and inferior parietal cortex in working memory tasks revealed by 2DG functional mapping in the rhesus monkey

Friedman, H., & Goldman-Rakic, P. S. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-05-02775.1994 · Cited by 311 · see citing works

Intrinsic circuit organization of the major layers and sublayers of the dorsolateral prefrontal cortex in the rhesus monkey

Kritzer, M. F., & Goldman‐Rakic, P. S. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590109 · Cited by 300 · see citing works

Postnatal development of monoamine content and synthesis in the cerebral cortex of rhesus monkeys

Goldman‐Rakic, P. S., & Brown, R. M. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90146-8 · Cited by 283 · see citing works

Delayed-matching and delayed-response deficit from cooling dorsolateral prefrontal cortex in monkeys.

Bauer, R. H., & Fuster, J. M. (1976) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0087996 · Cited by 277 · see citing works

Functional development of the prefrontal cortex in early life and the problem of neuronal plasticity

Goldman, P. S. (1971) · Experimental Neurology · doi:10.1016/0014-4886(71)90005-7 · Cited by 271 · see citing works

Cortical Pruning and the Development of Schizophrenia: A Computer Model

Hoffman, R. E., & Dobscha, S. K. (1989) · Schizophrenia Bulletin · doi:10.1093/schbul/15.3.477 · Cited by 268 · see citing works

Topography of pyramidal neuron intrinsic connections in macaque monkey prefrontal cortex (areas 9 and 46)

Levitt, J. B., Lewis, D. A., Yoshioka, T., & Lund, J. S. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903380304 · Cited by 260 · see citing works

Callosal and intrahemispheric connectivity of the prefrontal association cortex in rhesus monkey: Relation between intraparietal and principal sulcal cortex

Schwartz, M. L., & Goldman, P. S. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902260309 · Cited by 257 · see citing works

Synchronous development of pyramidal neuron dendritic spines and parvalbumin-immunoreactive chandelier neuron axon terminals in layer III of monkey prefrontal cortex

Anderson, S. A., Classey, J. D., Condé, F., Lund, J. S., & Lewis, D. A. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00051-j · Cited by 245 · see citing works

Schizophrenia: A disease of heteromodal association cortex?

Pearlson, G. D., Petty, R. G., ROSS, C., & Tien, A. Y. (1996) · Neuropsychopharmacology · doi:10.1016/s0893-133x(96)80054-6 · Cited by 235 · see citing works

Synchronized overproduction of neurotransmitter receptors in diverse regions of the primate cerebral cortex

Lidow, M. S., Goldman-Rakic, P. S., & Rakic, P. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.22.10218 · Cited by 232 · see citing works

Variability in the terminations of GABAergic chandelier cell axons on initial segments of pyramidal cell axons in the monkey sensory‐motor cortex

DeFelipe, J., Hendry, S. H. C., Jones, E. G., & Schmechel, D. E. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902310307 · Cited by 229 · see citing works

In vivo morphometry of the intrasulcal gray matter in the human cingulate, paracingulate, and superior-rostral sulci: Hemispheric asymmetries, gender differences and probability maps

Paus, T., Otaky, N., Caramanos, Z., MacDonald, D. J., Zijdenbos, A. P., d'Avirro, D., Gutmans, D. S., Holmes, C. J., Tomaiuolo, F., & Evans, A. C. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961223)376:4 · Cited by 228 · see citing works

Axon terminals immunolabeled for dopamine or tyrosine hydroxylase synapse on GABA‐immunoreactive dendrites in rat and monkey cortex

Sesack, S. R., Snyder, C. L., & Lewis, D. A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903630208 · Cited by 226 · see citing works

Implications of Normal Brain Development for the Pathogenesis of Schizophrenia

Siris, S. G. (1988) · Archives of General Psychiatry · doi:10.1001/archpsyc.1988.01800350089019 · Cited by 224 · see citing works

Heterogeneity of chandelier neurons in monkey neocortex: Corticotropin‐releasing factor‐and parvalbumin‐immunoreactive populations

Lewis, D. A., & Lund, J. S. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930406 · Cited by 220 · see citing works

Heterogeneous Targets of Dopamine Synapses in Monkey Prefrontal Cortex Demonstrated by Serial Section Electron Microscopy: A Laminar Analysis Using the Silver-enhanced Diaminobenzidine Sulfide (SEDS) Immunolabeling Technique

Smiley, J. F., & Goldman-Rakic, P. S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.3.223 · Cited by 211 · see citing works

Local circuit neurons of developing and mature macaque prefrontal cortex: Golgi and immunocytochemical characteristics

Lund, J. S., & Lewis, D. A. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903280209 · Cited by 207 · see citing works

Post-mortem Study of Chronic Schizophrenic Brains

Pakkenberg, B. (1987) · The British Journal of Psychiatry · doi:10.1192/bjp.151.6.744 · Cited by 205 · see citing works

Total nerve cell number in neocortex in chronic schizophrenics and controls estimated using optical disectors

Pakkenberg, B. (1993) · Biological Psychiatry · doi:10.1016/0006-3223(93)90065-l · Cited by 204 · see citing works

An In Vivo Study of the Prefrontal Cortex of Schizophrenic Patients at Different Stages of Illness via Phosphorus Magnetic Resonance Spectroscopy

Stanley, J. A. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950170073010 · Cited by 204 · see citing works

Frontal lobe dysfunctions in schizophrenia—II. impairments of psychological and brain functions

Levin, S. (1984) · Journal of Psychiatric Research · doi:10.1016/0022-3956(84)90047-5 · Cited by 199 · see citing works

Brain Anatomic Magnetic Resonance Imaging in Childhood-Onset Schizophrenia

Frazier, J. A. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830070065010 · Cited by 199 · see citing works

Premorbid and Onset Features of First-Episode Schizophrenia

Haas, G. L., & Sweeney, J. A. (1992) · Schizophrenia Bulletin · doi:10.1093/schbul/18.3.373 · Cited by 196 · see citing works

Schizophrenia: developmental neuroscience and pathobiology

Waddington, J. L. (1993) · The Lancet · doi:10.1016/0140-6736(93)90288-r · Cited by 194 · see citing works

Local circuit neurons of the prefrontal cortex in schizophrenia: selective increase in the density of calbindin-immunoreactive neurons

DAVISS, S. R., & Lewis, D. A. (1995) · Psychiatry Research · doi:10.1016/0165-1781(95)02720-3 · Cited by 187 · see citing works

Prefrontal Cortex and Schizophrenia

Wible, C. G. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160029007 · Cited by 167 · see citing works

Levels of the growth-associated protein GAP-43 are selectively increased in association cortices in schizophrenia

Perrone-Bizzozero, N. I., Sower, A. C., Bird, E. D., Benowitz, L. I., Ivins, K. J., & Neve, R. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.14182 · Cited by 162 · see citing works

Peripubertal refinement of the intrinsic and associational circuitry in monkey prefrontal cortex

Woo, T.-U., Pucak, M. L., Kye, C. H., Matus, C. V., & Lewis, D. A. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00059-6 · Cited by 157 · see citing works

Cerebral structural pathology in schizophrenia: evidence for a selective prefrontal cortical defect

Shelton, R. C., Karson, C. N., Doran, A. R., Pickar, D., Bigelow, L. B., & Weinberger, D. R. (1988) · American Journal of Psychiatry · doi:10.1176/ajp.145.2.154 · Cited by 155 · see citing works

Light and electron microscopic characterization of dopamine‐immunoreactive axons in human cerebral cortex

Smiley, J. F., Williams, S. M., Szigeti‐Buck, K., & Goldman‐Rakic, P. S. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903210302 · Cited by 154 · see citing works

The effects of selective caudate lesions in infant and juvenile rhesus monkeys

Goldman, P. S., & Rosvold, H. E. (1972) · Brain Research · doi:10.1016/0006-8993(72)90274-0 · Cited by 154 · see citing works

The synaptology of parvalbumin‐immunoreactive neurons in the primate prefrontal cortex

Williams, S. M., Goldman, P. S., & Leranth, C. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903200307 · Cited by 139 · see citing works

First-episode Schizophrenia: II. Premorbid Patterns by Gender

Larsen, T. K., McGlashan, T. H., Johannessen, J. O., & Vibe-Hansen, L. (1996) · Schizophrenia Bulletin · doi:10.1093/schbul/22.2.257 · Cited by 137 · see citing works

Functional development of the dorsolateral prefrontal cortex: An analysis utilizing reversible cryogenic depression

Alexander, G. E., & Goldman, P. S. (1978) · Brain Research · doi:10.1016/0006-8993(78)90566-8 · Cited by 134 · see citing works

Schizophrenia: A Neurodevelopmental Perspective

Pilowsky, L. S., Kerwin, R. W., & Murray, R. M. (1993) · Neuropsychopharmacology · doi:10.1038/npp.1993.46 · Cited by 128 · see citing works

Increased density of microtubule associated protein 2-immunoreactive neurons in the prefrontal white matter of schizophrenic subjects

Anderson, S. A., Volk, D. W., & Lewis, D. A. (1996) · Schizophrenia Research · doi:10.1016/0920-9964(96)88521-5 · Cited by 123 · see citing works

Hypofrontality in schizophrenia: RIP

Gur, R., & Gur, R. (1995) · The Lancet · doi:10.1016/s0140-6736(95)92591-0 · Cited by 109 · see citing works

The hierarchical development of monkey visual cortical regions as revealed by the maturation of parvalbumin-immunoreactive neurons

Condé, F. (1996) · Developmental Brain Research · doi:10.1016/s0165-3806(96)00126-5 · Cited by 98 · see citing works

The morphology and synaptic connections of spiny stellate neurons in monkey visual cortex (area 17): A golgi‐electron microscopic study

Marie, R. L. S., & Peters, A. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902330205 · Cited by 81 · see citing works

Regional brain abnormalities in schizophrenia measured with magnetic resonance imaging

Andreasen, N. C. (1994) · JAMA · doi:10.1001/jama.272.22.1763 · Cited by 78 · see citing works

The functional architecture of the prefrontal cortex and schizophrenia

Lewis, D. A., & Anderson, S. A. (1995) · Psychological Medicine · doi:10.1017/s0033291700037375 · Cited by 76 · see citing works

Ultrastructural associations between dopamine terminals and local circuit neurons in the monkey prefrontal cortex: a study of calretinin-immunoreactive cells

Sesack, S. R., Bressler, C. N., & Lewis, D. A. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)12076-g · Cited by 70 · see citing works

Microglial response to N-methyl-D-aspartate-mediated excitotoxicity in the immature rat brain

Acarín, L., Gonz�lez, B., Castellano, B., & Castro, A. J. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960408)367:3 · Cited by 66 · see citing works

Differential distribution of parvalbumin-immunoreactive pericellular clusters of terminal boutons in developing and adult monkey neocortex

Akil, M., & Lewis, D. A. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90058-x · Cited by 58 · see citing works

Spine formation and maturation of type 1 synapses on spiny stellate neurons in primate visual cortex

Mates, S. L., & Lund, J. S. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902210107 · Cited by 58 · see citing works

Postnatal development of thalamic recipient neurons in the monkey striate cortex: Comparison of spine acquisition and dendritic growth of layer 4C alpha and beta spiny stellate neurons

Lund, J. S., & Holbach, S. M. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903090108 · Cited by 54 · see citing works

Delayed Recovery of Function following Orbital Prefrontal Lesions in Infant Monkeys

Miller, E. A., Goldman, P. S., & Rosvold, H. E. (1973) · Science · doi:10.1126/science.182.4109.304 · Cited by 44 · see citing works

Dopamine modulates neuronal activities related to motor performance in the monkey prefrontal cortex

Sawaguchi, T., Matsumura, M., & Kubota, K. (1986) · Brain Research · doi:10.1016/0006-8993(86)90385-9 · Cited by 37 · see citing works

Neural Circuitry of the Prefrontal Cortex in Schizophrenia

Lewis, D. A. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160019004 · Cited by 34 · see citing works

Postnatal development of the cholecystokinin innervation of monkey prefrontal cortex

Oeth, K. M., & Lewis, D. A. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903360307 · Cited by 33 · see citing works

Positron Emission Tomography Study of Human Brain Functional Development

Chugani, H. T., Phelps, M. E., & Mazziotta, J. C. (2008) · doi:10.1002/9780470753507.ch7 · Cited by 32 · see citing works

Functional development of frontal association cortex in monkeys: behavioural and electrophysiological studies.

Alexander, G. E. (1982) · PubMed · Cited by 29 · see citing works

Differential laminar distribution of tyrosine hydroxylase-immunoreactive axons in infant and adult monkey prefrontal cortex

Lewis, D. A., & Harris, H. W. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90014-k · Cited by 28 · see citing works

Cholecystokinin innervation of monkey prefrontal cortex:An immunohistochemical study

Oeth, K. M., & Lewis, D. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010112 · Cited by 23 · see citing works

Reduction in neuronal sizes in prefrontal cortex of schizophrenics and huntington patients

Rajkowska, G., Selemon, L. D., & Goldman‐Rakic, P. S. (1995) · Schizophrenia Research · doi:10.1016/0920-9964(95)95106-j · Cited by 16 · see citing works

Reduced levels of synaptic proteins in the prefrontal cortex in schizophrenia

Karson, C. N., Griffin, W. S. T., Mrak, R. E., Sturner, W. Q., SHILLCUTT, S. D., & Guggenheim, F. G. (1997) · Schizophrenia Research · doi:10.1016/s0920-9964(97)82094-4 · Cited by 6 · see citing works

The adolescent brain and age-related behavioral manifestations

Spear, L. P. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00014-2 · Cited by 5,433 · see citing works

Developmental neurocircuitry of motivation in adolescence: a critical period of addiction vulnerability

Chambers, R. A., Taylor, J. R., & Potenza, M. N. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.6.1041 · Cited by 1,719 · see citing works

The neuropathology of schizophrenia

Harrison, P. J. (1999) · Brain · doi:10.1093/brain/122.4.593 · Cited by 1,677 · 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

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

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

Decrease in Reelin and Glutamic Acid Decarboxylase67 (GAD67) Expression in Schizophrenia and Bipolar Disorder

Guidotti, A., Auta, J., Davis, J. M., Gerevini, V. D. G., Dwivedi, Y., Grayson, D. R., Impagnatiello, F., Pandey, G. N., Pesold, C., Sharma, R. P., et al. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.11.1061 · Cited by 1,203 · see citing works

Pubertal transitions in health

Patton, G. C., & Viner, R. (2007) · The Lancet · doi:10.1016/s0140-6736(07)60366-3 · Cited by 877 · see citing works

Explaining the Many Varieties of Working Memory Variation: Dual Mechanisms of Cognitive Control

Braver, T. S., Gray, J. R., & Burgess, G. C. (2008) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195168648.003.0004 · Cited by 859 · see citing works

A Susceptibility Gene for Affective Disorders and the Response of the Human Amygdala

Hariri, A. R., Drabant, E. M., Munoz, K. E., Kolachana, B. S., Mattay, V. S., Egan, M. F., & Weinberger, D. R. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.2.146 · Cited by 815 · see citing works

Catching up on schizophrenia: natural history and neurobiology.

Lewis, D. A., & Lieberman, J. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)00111-2 · Cited by 71 · see citing works

Physiological Dysfunction of the Dorsolateral Prefrontal Cortex in Schizophrenia Revisited

Callicott, J. H. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.11.1078 · Cited by 810 · see citing works

Prefrontal neurons and the genetics of schizophrenia

Weinberger, D. R., Egan, M. F., Bertolino, A., Callicott, J. H., Mattay, V. S., Lipska, B. K., Berman, K. F., & Goldberg, T. E. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01252-5 · Cited by 744 · see citing works

Triadic model of the neurobiology of motivated behavior in adolescence.

ERNST, M., PINE, D. S., & HARDIN, M. (2006) · Psychological Medicine · doi:10.1017/s0033291705005891 · Cited by 718 · see citing works

Neurobiological Mechanisms of the Onset of Puberty in Primates

Terasawa, E., & Fernandez, D. L. (2001) · Endocrine Reviews · doi:10.1210/edrv.22.1.0418 · Cited by 568 · see citing works

An Integrative Model of the Maturation of Cognitive Control

Luna, B., Marek, S., Larsen, B., Tervo-Clemmens, B., & Chahal, R. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034054 · Cited by 550 · see citing works

Psychopathology in Women and Men: Focus on Female Hormones

Seeman, M. V. (1997) · American Journal of Psychiatry · doi:10.1176/ajp.154.12.1641 · Cited by 542 · see citing works

The development of risk-taking: A multi-perspective review

Boyer, T. W. (2006) · Developmental Review · doi:10.1016/j.dr.2006.05.002 · Cited by 622 · see citing works

Is schizophrenia a neurodegenerative disorder? a clinical and neurobiological perspective

Lieberman, J. A. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00147-x · Cited by 486 · see citing works

Student factors: understanding individual variation in college drinking.

Baer, J. S. (2002) · Journal of Studies on Alcohol Supplement · doi:10.15288/jsas.2002.s14.40 · Cited by 426 · see citing works

Structural and functional maturation of the developing primate brain

Levitt, P. R. (2003) · The Journal of Pediatrics · doi:10.1067/s0022-3476(03)00400-1 · Cited by 409 · see citing works

Assessment of Neuropsychological Function Through Use of the Cambridge Neuropsychological Testing Automated Battery: Performance in 4- to 12-Year-Old Children

Luciana, M., & Nelson, C. A. (2002) · Developmental Neuropsychology · doi:10.1207/s15326942dn2203_3 · Cited by 400 · see citing works

The emergence of depression in adolescence: Development of the prefrontal cortex and the representation of reward

Davey, C. G., Yücel, M., & Allen, N. B. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.04.016 · Cited by 377 · see citing works

Neurobehavioral Changes in Adolescence

SPEAR, L. P. (2000) · Current Directions in Psychological Science · doi:10.1111/1467-8721.00072 · Cited by 377 · see citing works

Neurodevelopment, Impulsivity, and Adolescent Gambling

Chambers, R., & Potenza, M. (2004) · Journal of Gambling Studies · doi:10.1023/a:1021275130071 · Cited by 375 · see citing works

Age of Onset of Schizophrenia: Perspectives From Structural Neuroimaging Studies

Gogtay, N., Vyas, N. S., Testa, R., Wood, S. J., & Pantelis, C. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr030 · Cited by 341 · see citing works

Developmental trajectories during adolescence in males and females: A cross-species understanding of underlying brain changes

Brenhouse, H. C., & Andersen, S. L. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.04.013 · Cited by 340 · see citing works

Impulsive and Self-Conscious: Adolescents' Vulnerability to Advertising and Promotion

Pechmann, C., Levine, L. J., Loughlin, S. E., & Leslie, F. M. (2005) · Journal of Public Policy & Marketing · doi:10.1509/jppm.2005.24.2.202 · Cited by 334 · see citing works

Development of response-monitoring ERPs in 7-to 25-year-olds

Davies, P. L., Segalowitz, S. J., & Gavin, W. J. (2004) · Developmental Neuropsychology · doi:10.1207/s15326942dn2503_6 · Cited by 339 · see citing works

Imaging Genetics: Perspectives from Studies of Genetically Driven Variation in Serotonin Function and Corticolimbic Affective Processing

Hariri, A. R., Drabant, E. M., & Weinberger, D. R. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.11.005 · Cited by 336 · see citing works

Cell biology of the hippocampal formation in schizophrenia

Weinberger, D. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00331-x · Cited by 321 · see citing works

Inhibition of Serotonin But Not Norepinephrine Transport during Development Produces Delayed, Persistent Perturbations of Emotional Behaviors in Mice

Ansorge, M. S., Morelli, E., & Gingrich, J. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3973-07.2008 · Cited by 296 · see citing works

Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications

Yan, Z., & Rein, B. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01092-3 · Cited by 300 · see citing works

Alterations in Chandelier Neuron Axon Terminals in the Prefrontal Cortex of Schizophrenic Subjects

Pierri, J. N., Chaudry, A. S., Woo, T.-U. W., & Lewis, D. A. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.11.1709 · Cited by 294 · see citing works

Brain manganese and the balance between essential roles and neurotoxicity

Balachandran, R. C., Mukhopadhyay, S., McBride, D. E., Veevers, J., Harrison, F. E., Aschner, M., Haynes, E. N., & Bowman, A. B. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.rev119.009453 · Cited by 288 · see citing works

Positive parenting predicts the development of adolescent brain structure: a longitudinal study

Whittle, S., Simmons, J. G., Dennison, M., Vijayakumar, N., Schwartz, O., Yap, M. B. H., Sheeber, L., & Allen, N. B. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2013.10.006 · Cited by 279 · see citing works

Modeling adolescent development and alcohol use in animals.

SPEAR, L. P. (2000) · PubMed Central · Cited by 258 · see citing works

Attention, researchers! It Is time to take a look at the real world

Kingstone, A., Smilek, D., Ristic, J., Kelland Friesen, C., & Eastwood, J. D. (2003) · Current Directions in Psychological Science · doi:10.1111/1467-8721.01255 · Cited by 236 · see citing works

Long-term behavioral and neurodegenerative effects of perinatal phencyclidine administration: implications for schizophrenia

Wang, C., McInnis, J., Ross-Sanchez, M., Shinnick‐Gallagher, P., Wiley, J. L., & Johnson, K. M. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00384-0 · Cited by 234 · see citing works

Neuron number decreases in the rat ventral, but not dorsal, medial prefrontal cortex between adolescence and adulthood

Markham, J. A., Morris, J. R., & Juraska, J. M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.015 · Cited by 230 · see citing works

Stress, the Hippocampus and the Hypothalamic-Pituitary-Adrenal Axis: Implications for the Development of Psychotic Disorders

Phillips, L., McGorry, P. D., Garner, B., Thompson, K. N., Pantelis, C., Wood, S. J., & Berger, G. E. (2006) · Australian & New Zealand Journal of Psychiatry · doi:10.1080/j.1440-1614.2006.01877.x · Cited by 230 · see citing works

The phenotypic characteristics of heterozygous reeler mouse

Tueting, P. A., Costa, E., Dwivedi, Y. K., Guidotti, A., Impagnatiello, F., Manev, R. M., & Pesold, C. (1999) · Neuroreport · doi:10.1097/00001756-199904260-00032 · Cited by 221 · see citing works

ADHD and the Prefrontal Cortex

Arnsten, A. F. T. (2009) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.01.018 · Cited by 220 · see citing works

Rethinking schizophrenia in the context of normal neurodevelopment

Catts, V. S., Fung, S. J., Long, L. E., Joshi, D., Vercammen, A., Allen, K. M., Fillman, S. G., Rothmond, D. A., Sinclair, D., Tiwari, Y., et al. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00060 · Cited by 206 · see citing works

Apoptotic Proteins in the Temporal Cortex in Schizophrenia: High Bax/Bcl-2 Ratio Without Caspase-3 Activation

Jarskog, L. F., Selinger, E. S., Lieberman, J. A., & Gilmore, J. H. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.1.109 · Cited by 205 · see citing works

Adolescents differ from adults in cocaine conditioned place preference and cocaine-induced dopamine in the nucleus accumbens septi

Badanich, K. A., Adler, K. J., & Kirstein, C. L. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.08.034 · Cited by 203 · see citing works

The Study of Developmental Psychopathology in Adolescence: Integrating Affective Neuroscience with the Study of Context

Steinberg, L., Dahl, R., Keating, D., Kupfer, D., Masten, A., & Pine, D. (2015) · Wiley eBooks · doi:10.1002/9780470939390.ch18 · Cited by 160 · see citing works

Catechol-o-Methyltransferase Enzyme Activity and Protein Expression in Human Prefrontal Cortex across the Postnatal Lifespan

Tunbridge, E., Weickert, C., Kleinman, J., Herman, M., Chen, J., Kolachana, B., Harrison, P., & Weinberger, D. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl032 · Cited by 197 · see citing works

Mitochondria, synaptic plasticity, and schizophrenia.

Ben-Shachar, D., & Laifenfeld, D. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59011-6 · Cited by 193 · see citing works

The adolescent brain and the college drinker: biological basis of propensity to use and misuse alcohol.

SPEAR, L. P. (2002) · Journal of Studies on Alcohol Supplement · doi:10.15288/jsas.2002.s14.71 · Cited by 193 · see citing works

Impacts of stress and sex hormones on dopamine neurotransmission in the adolescent brain

Sinclair, D., Purves-Tyson, T. D., Allen, K. M., & Weickert, C. S. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3415-z · Cited by 191 · see citing works

Experience effects on brain development: possible contributions to psychopathology

Grossman, A. W., Churchill, J. D., McKinney, B. C., Kodish, I. M., Otte, S. L., & Greenough, W. T. (2002) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.t01-1-00102 · Cited by 186 · see citing works

Childhood abuse and neglect and cognitive flexibility in adolescents

Spann, M. N., Mayes, L. C., Kalmar, J. H., Guiney, J., Womer, F. Y., Pittman, B. P., Mazure, C. M., Sinha, R., & Blumberg, H. P. (2011) · Child Neuropsychology · doi:10.1080/09297049.2011.595400 · Cited by 187 · see citing works

Developing a Neuronal Model for the Pathophysiology of Schizophrenia Based on the Nature of Electrophysiological Actions of Dopamine in the Prefrontal Cortex

Yang, C. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(98)00112-2 · Cited by 183 · see citing works

Glutamatergic Synaptic Dysregulation in Schizophrenia: Therapeutic Implications

Coyle, J. T., Basu, A., Benneyworth, M., Balu, D., & Konopaske, G. (2012) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-642-25758-2_10 · Cited by 180 · see citing works

Linking mPFC circuit maturation to the developmental regulation of emotional memory and cognitive flexibility

Klune, C. B., Jin, B., & DeNardo, L. A. (2021) · eLife · doi:10.7554/elife.64567 · Cited by 171 · see citing works

Age, Rapid-Cycling, and Pharmacotherapy Effects on Ventral Prefrontal Cortex in Bipolar Disorder: A Cross-Sectional Study

Blumberg, H. P., Krystal, J. H., Bansal, R., Martin, A., Dziura, J., Durkin, K., Martin, L., Gerard, E., Charney, D. S., & Peterson, B. S. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.08.031 · Cited by 171 · see citing works

Affect regulation, brain development, and behavioral/emotional health in adolescence

Dahl, R. E. (2001) · CNS Spectrums · doi:10.1017/s1092852900022884 · Cited by 168 · see citing works

Predicting female depression across puberty: A two-nation longitudinal study

Patton, G. C., Olsson, C., Bond, L., Toumbourou, J. W., Carlin, J. B., Hemphill, S. A., & Catalano, R. F. (2008) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/chi.0b013e3181886ebe · Cited by 159 · see citing works

Specific Relationship Between Prefrontal NeuronalN-Acetylaspartate and Activation of the Working Memory Cortical Network in Schizophrenia

Bertolino, A., Esposito, G., Callicott, J. H., Mattay, V. S., Horn, J. D. V., Frank, J. A., Berman, K. F., & Weinberger, D. R. (2000) · American Journal of Psychiatry · doi:10.1176/ajp.157.1.26 · Cited by 149 · see citing works

Abnormalities of SNARE Mechanism Proteins in Anterior Frontal Cortex in Severe Mental Illness

Honer, W. G. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.4.349 · Cited by 149 · see citing works

Pubertal stage and deliberate self-harm in adolescents

PATTON, G. C., HEMPHILL, S. A., BEYERS, J. M., BOND, L., TOUMBOUROU, J. W., McMORRIS, B. J., & CATALANO, R. F. (2007) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/chi.0b013e31803065c7 · Cited by 148 · see citing works

Neurocognitive Functioning in Subjects at Risk for a First Episode of Psychosis Compared with First- and Multiple-episode Schizophrenia

Pukrop, R., Schultze‐Lutter, F., Ruhrmann, S., Brockhaus‐Dumke, A., Tendolkar, I., Bechdolf, A., Matuschek, E., & Klosterkötter, J. (2006) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803390500434425 · Cited by 146 · see citing works

Functional Connectivity of Substantia Nigra and Ventral Tegmental Area: Maturation During Adolescence and Effects of ADHD

Tomasi, D. G., & Volkow, N. D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs382 · Cited by 144 · see citing works

In the Blink of an Eye: Relating Positive-Feedback Sensitivity to Striatal Dopamine D2-Like Receptors through Blink Rate

Groman, S. M., James, A. S., Seu, E., Tran, S., Clark, T. A., Harpster, S. N., Crawford, M. A., Burtner, J., Feiler, K., Roth, R. H., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3037-14.2014 · Cited by 143 · see citing works

Development of social functioning in preschizophrenia children and adolescents: A systematic review.

Tarbox, S. I., & Pogue‐Geile, M. F. (2008) · Psychological Bulletin · doi:10.1037/0033-2909.34.4.561 · Cited by 143 · see citing works

Experience during adolescence shapes brain development: From synapses and networks to normal and pathological behavior

Dow-Edwards, D. L., MacMaster, F. P., Peterson, B. S., Niesink, R. J. M., Andersen, S. L., & Braams, B. R. (2019) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2019.106834 · Cited by 146 · see citing works

Mesocorticolimbic Dopamine Pathways Across Adolescence: Diversity in Development

Reynolds, L. M., & Flores, C. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.735625 · Cited by 137 · see citing works

Developmental pathology, dopamine, and stress: a model for the age of onset of schizophrenia symptoms.

Thompson, J. L., Pogue-Geile, M., & Grace, A. (2004) · Schizophrenia bulletin · doi:10.1093/oxfordjournals.schbul.a007139 · Cited by 148 · see citing works

A study on neuroinflammation and NMDA receptor function in STZ (ICV) induced memory impaired rats

Rai, S., Kamat, P. K., Nath, C., & Shukla, R. (2012) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2012.08.008 · Cited by 129 · see citing works

Pubertal changes in emotional information processing: Pupillary, behavioral, and subjective evidence during emotional word identification

Silk, J. S., Siegle, G. J., Whalen, D. J., Ostapenko, L. J., Ladouceur, C. D., & Dahl, R. E. (2009) · Development and Psychopathology · doi:10.1017/s0954579409000029 · Cited by 127 · see citing works

Research on alcohol and adolescent brain development: opportunities and future directions

Witt, E. D. (2010) · Alcohol · doi:10.1016/j.alcohol.2009.08.011 · Cited by 125 · see citing works

Adolescence as a period of vulnerability and intervention in schizophrenia: Insights from the MAM model

Gomes, F. V., Rincón‐Cortés, M., & Grace, A. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.030 · Cited by 128 · see citing works

Intrinsic excitatory connections in the prefrontal cortex and the pathophysiology of schizophrenia

Lewis, D. A., & González‐Burgos, G. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00243-9 · Cited by 126 · see citing works

Cannabis use at a young age is associated with psychotic experiences

Schubart, C. D., van Gastel, W. A., Breetvelt, E., Beetz, S. L., Ophoff, R. A., Sommer, I. E., Kahn, R. S., & Boks, M. P. (2010) · Psychological Medicine · doi:10.1017/s003329171000187x · Cited by 123 · see citing works

Postnatal Development of Prefrontal Inhibitory Circuits and the Pathophysiology of Cognitive Dysfunction in Schizophrenia

Lewis, D. A., Cruz, D. A., Eggan, S. M., & Erickson, S. L. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1308.008 · Cited by 121 · see citing works

Studies of Brain and Cognitive Maturation Through Childhood and Adolescence: A Strategy for Testing Neurodevelopmental Hypotheses

Luna, B., & Sweeney, J. A. (2001) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a006886 · Cited by 122 · see citing works

Developmental Theory for a Cognitive Enhancement Therapy of Schizophrenia

Hogarty, G. E., & Flesher, S. (1999) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a033410 · Cited by 121 · see citing works

Cocaine and morphine-induced place conditioning in adolescent and adult rats

CAMPBELL, J., WOOD, R., & SPEAR, L. P. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00225-5 · Cited by 114 · 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

The development of antisocial behavior: What can we learn from functional neuroimaging studies?

Crowe, S. L., & Blair, J. (2008) · Development and Psychopathology · doi:10.1017/s0954579408000540 · Cited by 109 · see citing works

Gene expression in the prefrontal cortex during adolescence: implications for the onset of schizophrenia

Harris, L. W., Lockstone, H. E., Khaitovich, P., Weickert, C. S., Webster, M. J., & Bahn, S. (2009) · BMC Medical Genomics · doi:10.1186/1755-8794-2-28 · Cited by 112 · see citing works

Layer 3 Excitatory and Inhibitory Circuitry in the Prefrontal Cortex: Developmental Trajectories and Alterations in Schizophrenia

Hoftman, G. D., Datta, D., & Lewis, D. A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.022 · Cited by 109 · see citing works

Developmental regulation of the NMDA receptor subunits, NR3A and NR1, in human prefrontal cortex

Henson, M. A., Roberts, A. C., Salimi, K., Vadlamudi, S., Hamer, R. M., Gilmore, J. H., Jarskog, L. F., & Philpot, B. D. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn017 · Cited by 110 · see citing works

Abnormal Cortical Growth in Schizophrenia Targets Normative Modules of Synchronized Development

Alexander‐Bloch, A. F., Reiss, P. T., Rapoport, J. L., Mcadams, H., Giedd, J. N., Bullmore, E. T., & Gogtay, N. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.02.010 · Cited by 108 · see citing works

Development of calcium‐permeable AMPA receptors and their correlation with NMDA receptors in fast‐spiking interneurons of rat prefrontal cortex

Wang, H. X., & Gao, W. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.187591 · Cited by 109 · see citing works

Non-Human Primates: Model Animals for Developmental Psychopathology

Nelson, E. E., & Winslow, J. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.150 · Cited by 110 · see citing works

Adolescent Maturation of Cortical Dopamine

O’Donnell, P. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9157-3 · Cited by 107 · see citing works

The relationship between dorsolateral prefrontal N-acetylaspartate measures and striatal dopamine activity in schizophrenia.

Bertolino, A., Knable, M., Saunders, R., Callicott, J., Kolachana, B., Mattay, V., Bachevalier, J., Frank, J., Egan, M., & Weinberger, D. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00380-1 · Cited by 110 · see citing works

Chronic Cold Stress Alters Prefrontal Cortical Modulation of Amygdala Neuronal Activity in Rats

Correll, C. M., Rosenkranz, J. A., & Grace, A. A. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.04.009 · Cited by 106 · see citing works

Utilization of Animal Studies to Determine the Effects and Human Risks of Environmental Toxicants (Drugs, Chemicals, and Physical Agents)

Brent, R. L. (2004) · PEDIATRICS · doi:10.1542/peds.113.s3.984 · Cited by 106 · see citing works

Adolescent Initiation of Cannabis use and Early-Onset Psychosis

Bagot, K. S., Milin, R., & Kaminer, Y. (2015) · Substance Abuse · doi:10.1080/08897077.2014.995332 · Cited by 105 · see citing works

Perinatal risks and childhood premorbid indicators of later psychosis: Next steps for early psychosocial interventions

Liu, C. H., Keshavan, M. S., Tronick, E., & Seidman, L. J. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv047 · Cited by 104 · see citing works

Neural systems supporting cognitive-affective interactions in adolescence: the role of puberty and implications for affective disorders

Ladouceur, C. D. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00065 · Cited by 104 · see citing works

Significance of Adolescent Neurodevelopment for the Neural Circuitry of Bipolar Disorder

Blumberg, H. P., Kaufman, J., Martin, A., Charney, D. S., Krystal, J. H., & Peterson, B. S. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1308.048 · Cited by 103 · see citing works

Nicotinic actions on neuronal networks for cognition: General principles and long-term consequences

Poorthuis, R. B., Goriounova, N. A., Couey, J. J., & Mansvelder, H. D. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.04.031 · Cited by 102 · see citing works

The impact of junk foods on the adolescent brain

Reichelt, A. C., & Rank, M. M. (2017) · Birth Defects Research · doi:10.1002/bdr2.1173 · Cited by 102 · see citing works

Early exposure to cannabis and risk for psychosis in young adolescents in Trinidad

Konings, M., Henquet, C., Maharajh, H. D., Hutchinson, G. A., & van Os, J. (2008) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2008.01202.x · Cited by 101 · see citing works

The role of prefrontal catecholamines in attention and working memory

Clark, K., & Noudoost, B. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00033 · Cited by 101 · see citing works

Arg Kinase Regulates Prefrontal Dendritic Spine Refinement and Cocaine-Induced Plasticity

Gourley, S. L., Olevska, A., Warren, M. S., Taylor, J. R., & Koleske, A. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2730-11.2012 · Cited by 98 · see citing works

Blockade of Phencyclidine-Induced Cortical Apoptosis and Deficits in Prepulse Inhibition by M40403, a Superoxide Dismutase Mimetic

Wang, C., McInnis, J., West, J. B., Bao, J., Anastasio, N. C., Guidry, J. A., Ye, Y., Salvemini, D., & Johnson, K. M. (2003) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.041798 · Cited by 98 · see citing works

Unmasking Schizophrenia: Synaptic Pruning in Adolescence Reveals a Latent Physiological Vulnerability in Prefrontal Recurrent Networks

Chafee, M. V., & Averbeck, B. B. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.06.023 · Cited by 26 · see citing works

Is schizophrenia due to excessive synaptic pruning in the prefrontal cortex? The Feinberg hypothesis revisited

Keshavan, M. S., Anderson, S., & Pettergrew, J. W. (1994) · Journal of Psychiatric Research · doi:10.1016/0022-3956(94)90009-4 · Cited by 525 · see citing works

Schizophrenia and the normal functional development of the prefrontal cortex

Breslin, N. A., & Weinberger, D. R. (1990) · Development and Psychopathology · doi:10.1017/s0954579400005800 · Cited by 15 · see citing works

Cognitive functions associated with developing prefrontal cortex during adolescence and developmental neuropsychiatric disorders

Sakurai, T., & Gamo, N. J. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.11.007 · Cited by 49 · see citing works

Schizophrenia: a tale of two critical periods for prefrontal cortical development

Selemon, L. D., & Zecevic, N. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.115 · Cited by 336 · see citing works