Myers J. J., Sperry R. W. Interhemispheric communication after section of the forebrain commissures // Cortex: A Journal Devoted to the Study of the Nervous System and Behavior. 1985. V. 21. № 2. P. 249–260.
Narberhaus A., Segarra D., Caldú X., Giménez M., Junqué C., Pueyo R., Botet F. Gestational age at preterm birth in relation to corpus callosum and general cognitive outcome in adolescents // Journal of Child Neurology. 2007. V. 22. № 6. P.761–765.
Narr K. L., Green M. F., Capetillo-Cunliffe L., Toga A. W., Zaidel E. Lateralized lexical decision in schizophrenia: Hemispheric specialization and interhemispheric lexicality priming // Journal of Abnormal Psychology. 2003. V. 112. № 4. P. 623–632.
Nosarti C., Rushe T. M., Woodruff P.W.R., Stewart A. L., Rifkin L., Murray R. M. Corpus callosum size and very preterm birth: relationship to neuropsychological outcome // Brain. 2004. V. 127. № 9. P. 2080–2089.
O'Brien G. The behavioral and developmental consequences of agenesis of the corpus callosum // Callosal Agenesis: A natural split brain? / M. Lassonde, M.A Jeeves (Eds.). – N.Y.: Plenum Press, 1994. P. 235–246.
O'Kusky J., Strauss E., Kosaka B., Wada J., Li D., Druhan M., Petrie J. The corpus callosum is larger with right-hemisphere cerebral speech dominance // Annals of Neurology. 1988. V. 24. № 3. P. 379–383.
Ottoson D. (Ed.). Duality and Unity of theBrain. – N.Y.: Macmillan. Publishing Co Inc; 1987. 436 p.
Pantev C, Oostenveld R., Engelien A., Ross B., Roberts L. E., Hoke M. Increased auditory cortical representation in musicians // Nature. 1998. V. 392. № 6678. P. 811–814.
Parker A., Dagnall N. Effects of handedness and saccadic bilateral eye movements on components of autobiographical recollection // Brain and Cognition. 2010. V. 73. № 2. P. 93–101.
Paul L. K., Brown W. S., Adolphs R., Tyszka J. M., Richards L. J., Mukherjee P., Sherr E. H. Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity // Nature Reviews Neuroscience. 2007. V. 8. № 4. P. 287–299.
Paul L. K., Schieffer B., Brown W. S. Social processing deficits in agenesis of the corpus callosum: Narratives from the Thematic Apperception Test // Archives of Clinical Neuropsychology. 2004. V. 19. № 2. P. 215–225.
Paul L. K., Van Lancker-Sidtis D., Schieffer B., Dietrich R., Brown W. S. Communicative deficits in agenesis of the corpus callosum: Nonliteral language and affective prosody // Brain and Language. 2003. V. 85. № 2. P. 313–324.
Pearson R. C., Esiri M. M., Hiorns R. W., Wilcock G. K., Powell T. P. Anatomical Correlates of the Distribution of the Pathological Changes in the Neocortex in Alzheimer Disease // Proceedings of National Academy of Sciences of the USA 1985. V. 82. № 13. P. 4531–4534.
Pennington B. F., Filipek PA., Ley D., Churchwell J., Kennedy D. N., Simon J. H., Filley C. M., Galaburda A., Alarcon M., DeFries J. C. Brain morphometry in reading-disabled twins // Neurology. 1999. V. 53. № 4. P. 723–729.
Phillips M. L., Woodruff P. W., David A. S. Stroop interference and facilitation in the cerebral hemispheres in schizophrenia // Schizophrenia Research. 1996. V. 20. № 1–2. P. 57–68.
Plessen K. J., Gruner R., Lundervold A., Hirsch L. G., Dongrong X. U., Bansal R., Peterson B. S., … et al. Reduced white matter connectivity in the corpus callosum of children with Tourette syndrome // Journal of Child Psychology Psychiatry. 2006. V. 47. №.12. P. 1013–1122.
Poirier P., Miljours S., Lassonde M., Lepore F. Sound localization in acallosal human listeners // Brain.1993. V. 116. Pt. 1. P. 53–69.
Price G., Bagary M. S., Cercignani M., Altmann D. R., Ron M. A. The Corpus Callosum in First-Episode Schizophrenia: A Diffusion Tensor Imaging Study // Journal of Neurology, Neurosurgery, and Psychiatry. 2005. V. 76. № 4. P. 585–587.
Price G., Cercignani M., Parker G. J., Altmann D. R., Barnes T. R., Barker G. J., Joyce E. M., Ron M. A. Abnormal brain connectivity in first-episode psychosis: A diffusion MRI tractography study of the corpus callosum // Neuroimage. 2007. V. 35. № 2. P. 458–466.
Pribram K. H., McGuiness D. Arousal, activation and effort in the control of attention // Psychological Review. 1975. V. 82. № 2. P. 116–149.
Prokop A., Dehmichen M., Zilles K. Geschlechtsdimorphismus des corpus callosum? // Beitrage zur Gerichtlichen Medizin. 1990. V. 48. P. 263–270.
Pujol J., Vendrell P., Junque C., Marti-Vilalta J. L., Capdevila A. When does human brain development end? Evidence of corpus callosum growth up to adulthood // Annals of Neurology. 1993. V. 34. № 1. P. 71–75.
Raine A., Lencz T., Taylor K., Hellige J. B., Bihrle S., Lacasse L., Lee M., Ishikawa S., Colletti P. Corpus callosum abnormalities in psychopathic antisocial individuals // Archives of General Psychiatry. 2003. V. 60. № 11. P. 1134–1142.
Rauch R. A., Jinkins J. R. Analysis of cross-sectional area measurements of the corpus callosum adjusted for brain size in male and female subjects from childhood to adulthood // Behavioral Brain Research. 1994. V. 64. № 1–2. P. 65–78.
Reynvoet B., Ratinckx E., Notebaert K. Intra– and interhemispheric number priming: evidence for rapid integration of magnitude information between hemispheres // Cortex. 2008. V. 44. № 6. P. 728–736.
Roessner V., Banaschewski T., Uebel H., Becker A., Rothenberger A. Neuronal network models of ADHD – lateralization with respect to interhemispheric connectivity reconsidered // European Child and Adolescent Psychiatry. 2004. V. 13. № 1. P. 171–179.
Rosenthal R., Bigelow L. B. Quantitative brain measurements in chronic schizophrenia // The British Journal of Psychiatry. 1972. V. 121. № 562. P. 259–264.
Rumsey J. M., Casanova M., Mannheim G. B., Patronas N., DeVaughn N., Hamburger S. D., Aquino T. Corpus callosum morphology, as measured with MRI, in dyslexic men // Biological Psychiatry. 1996. V. 39. № 9. P. 769–775.
Sanders R. D. Sentence comprehension following agenesis of the corpus callosum // Brain and Language. 1989. V. 37. № 1. P. 59–72.
Satoh M., Furukawa K., Takeda K., Kuzuhara S. Left hemianomia of musical symbols caused by callosal infarction // Journal of Neurology, Neurosurgery and Psychiatry. 2006. V. 77. № 5. P. 705–706.
Sauerwein H. C., Lassonde M. Cognitive and sensori-motor functionning in the absence of corpus callosum: Neuropsychological studies in callosal agenesis and callosotomised patients // Behavioral Brain Research. 1994. V. 64. № 1–2. P. 229–240.
Sauerwein H. C., Nolin P., Lassonde M. Cognitive functioning in callosal agenesis // Callosal Agenesis: A Natural Split Brain? / M. Lassonde, M. A. Jeeves (Eds.). – N.Y.: Plenum Press, 1994. P. 221–233.
Schaefer G. B., Bodensteiner J. B., Buehler B. A., Lin A., Cole T. R. The neuroimaging findings in Sotos syndrome // American Journal of Medical Genetics. 1997. V. 68. № 4. P. 462–465.
Schilmoeller G. L., Schilmoeller, K. J. Filling the void: Facilitating family support through networking for children with rare disorder // Family Science Review. 2000. V. 13. № 3–4. P. 224–233.
Schlaug G., Jancke L., Huang Y., Steinmetz H. In vivo evidence of structural brain asymmetry in musicians // Science. 1995. V. 267. № 5198. P. 699–701.
Schlaug G., Norton A., Overy R., Winner E. Effects of Music Training on the Child's Brain and Cognitive Development // Annals of the New York Academy of Sciences. The Neurosciences and Music II: From Perception to Performance. 2005. V. 1060. P. 219–230.
Seidman L. J., Valera E. M., Makris N. Structural brain imaging of attention-deficit hyperactivity disorder // Biological Psychiatry. 2005. V. 57. № 11. P. 1263–1272.
Semrud-Clikeman M. S., Filipek P. A., Biederman J., Steingard R., Kennedy D., Renshaw P., Bekken K. Attention-deficit hyperactivity disorder: Magnetic resonance imaging morphometric analysis of the corpus callosum // Journal of the American Academy of Child Adolescent Psychiatry. 1994. V. 33. № 6. P. 875–881.
Sergent J. Furtive incursions into bicameral minds. Integrative and coordinating role of subcortical structures // Brain. 1990. V. 113. Pt. 3. P. 537–568.
Shammi P., Stuss D. T. Humour appreciation: a role of the right frontal lobe // Brain. 1999. V. 122. № 4. P. 657–666.
Shevell M. I. Clinical and Diagnostic Profile of Agenesis of the Corpus Callosum // Journal of Child Neurology. 2002. V. 17. № 12. P. 895–899.
Silver P. H. Motor coordination in callosal agenesis // Callosal Agenesis: A Natural Split Brain? / M. Lassonde, M. A. Jeeves (Eds.). – N.Y.: Plenium Press, 1994. P. 207–219.
Smith K. M., Ohkubo Y., Maragnoli M. E., Rasin M. R., Schwartz M. L., Sestan N., Vaccarino F. M. Midline radial glia translocation and corpus callosum formation require FGF signaling // Nature Neuroscience. 2006. V. 9. № 6. P. 787–797.
Sotozaki H., Parlow S. Interhemispheric communication involving multiple tasks: A study of children with dyslexia // Brain and Language. 2006. V. 98. № 1. P. 89–101.
Sowell E. R., Mattson S. N., Thompson P. M., Jernigan T. L., Riley E. P., Toga A. W. Mapping Corpus Callosum Morphology and its Neurocognitive Correlates: The Effects of Prenatal Alcohol Exposure // Neurology. 2001. V. 57. № 2. P. 235–244.
Sperry R. W. The great cerebral commissure // Scientific American. 1964. V. 210. № 1. P. 42–52.
Sperry R. W. Brain bisection and mechanisms of consciousness // Brain and Conscious Experience / J. C. Eccles (Ed.). – Heidelberg: Springer-Verlag, 1966. P. 298–313.
Stein B. E., Price D. D., Gazzaniga M. S. Pain perception in a man with total corpus callosum transaction // Pain. 1989. V. 38. № 1. P. 51–56.
Stickles J. L., Schilmoeller G. L., Schilmoeller, K.J. A 23-year review of communication development in an individual with agenesis of the corpus callosum // International Journal of Disability, Development, and Education. 2002. V. 49. № 4. P. 367–383.
Suls J. M. A two-stage model for the appreciation of jokes and cartoons: an information processing analysis // The Psychology of Humor: Theoretical Perspectives and Empirical Issues / J. H. Goldstein, P. E. McGhee (Eds.). – N. Y. Academic Press, 1972. P. 81– 100.
Tabibnia G., Zaidel E. Alexithymia, interhemispheric transfer, and right hemispheric specialization: a critical review // Psychotherapy and Psychosomatics. 2005. V. 74. № 2. P. 81–92.
Taylor M., David A. S. Agenesis of the corpus callosum: a United Kingdom series of 56 cases // Journal of Neurology, Neurosurgery, and Psychiatry. 1998. V. 64. № 1. P. 131–134.
Temple C. M., Jeeves M. A., Vilarroya O. Reading in callosal agenesis // Brain and Language. 1990. V. 39. № 2. P. 235–253.
TenHouten W. D., Walter D. O., Hoppe K. D., Bogen J. E. Alexithymia and the split brain: V. EEG alpha-band interhemispheric coherence analysis // Psychotherapy and Psychosomatics. 1987. V. 47. № 1. P. 1–10.
Thatcher R. W., Walker R. A., Guidice S. Human cerebral hemispheres develop at different rates and ages // Science. 1987. V. 236. № 4805. P. 1110–1113.
Thompson P. M., Giedd J. N., Woods R. P., MacDonald D., Evans A. S., Toga A. W. Growth patterns in the developing brain detected by using continuum – mechanical tensor maps // Nature. 2000. V. 404. № 6774. P. 190–193.
Thut G., Halsband U., Regard M., Mayer E., Leenders K. L., Landis T. What is the role of the corpus callosum in intermanual transfer of motor skills? A study of three cases with callosal pathology // Experimental Brain Research. 1997.V. 113. № 2. P. 365–370.
Tibbo P., Nopoulos P., Arndt S., Andreasen N. Corpus callosum shape and size in male patients with schizophrenia // Biological Psychiatry. 1998. V. 44. №.6. P. 405–412.
Tovar-Moll F., Moll J., de Oliveira-Souza R, Bramati I. E., Andreiuolo P. A., Lent R. Neuroplasticity in human callosal dysgenesis: a diffusion tensor imaging study // Cerebral Cortex. 2007. V. 17. № 3. P. 531–541.
Trevarthen C. B. Two mechanisms of vision in primates // Psychologische Forschung. 1968. V. 31. № 2. P. 299–337.
Tulving E., Kapur S., Craik F.I.M., Moscovitch M., Houle S. Hemispheric encoding/retrieval asymmetry in episodic memory: Positron emission tomography findings // Proceedings of the National Academy of Sciences of the United States of America. 1994. V. 91. № 6. P. 2016–2020.
Velichkovsky B. M. Heterarchy of cognition: The depths and the highs of a framework for memory research // Memory. 2002. V. 10. № 5–6. P. 405–419.
Vergani P., Ghidini A., Strobelt N., Locatelli A., Mariani S., Bertalero C., Cavallone M. Prognostic indicators in the prenatal diagnosis of agenesis of the corpus callosum // American Journal of Obstetrics and Gynecology. 1994. V. 170. № 3. P. 753–758.
Vidal C. N., Nicolson R., DeVito T., Hayashi K. M., Drost D. J., Williamson P. C. et al. Mapping corpus callosum deficits in autism: an index of aberrant cortical connectivity // Biological Psychiatry. 2006. V. 60. № 3. P. 218–225.
Voneida T. J. Performance of a visual conditioned response in split-brain cats // Experimental Neurology. 1963. V. 8. № 6. P. 493–504.
Van Wagenen W. P., Herren R. Y. Surgical division of the commissural pathways in the corpus callosum. Relation to spread of an epileptic attack // Archives of Neurology and Psychiatry. 1940. V. 44. № 4. P. 740–759.
Walterfang M., Wood A. G., Reutens D. C., Wood S. J., Chen J., Velakoulis D., McGorry P. D., Pantelis C. Corpus callosum size and shape in first-episode affective and schizophrenia-spectrum psychosis // Psychiatry Research. 2009. V. 173. № 1. P. 77–82.
Wapner W., Hamby S., Gardner H. The role of the right hemisphere in the apprehension of complex linguistic materials // Brain and Language. 1981. Sep. 14(1). P. 15–33.
Watson R. T., Heilman K. M. Callosal apraxia // Brain. 1983 V. 106. № 2. P. 391–403.
Westerhausen R., Kreuder F., Dos Santos Sequeira S., Walter C., Woerner W., Wittling R. A., Schweiger E., Wittling W. Effects of handedness and gender on macro– and microstructure of the corpus callosum and its subregions: a combined high-resolution and diffusion-tensor MRI study // Brain Research Cognitive Brain Research. 2004. V. 21. № 3. P. 418–426.
Wilkemeyer M. F., Chen S., Menkari C. E., Brenneman D. E., Sulik K. K., Charness M. E. Differential effects of ethanol antagonism and neuroprotection in peptide fragment NAPVSIPQ prevention of ethanol-induced developmental toxicity // Proceedings of the National Academy of Sciences of the United States of America. 2003. V. 100. № 14. P. 8543–8548.
Wisniewski A. B. Sexually-dimorphic patterns of cortical asymmetry, and the role for sex steroid hormones in determining cortical patterns of lateralization // Psychoneuroendocrinology. 1998. V. 23. № 5. P. 519–547.
Wisniewski K. E., Jeret J. S. Callosal agenesis: A review of the clinical, pathological and cytogenetic features // Callosal Agenesis: A natural split brain? / M. Lassonde, M. A. Jeeves (Eds.). – N.Y.: Plenum Press, 1994. P. 1–6.
Witelson S. F. The brain connection: the corpus callosum is larger in left-handers // Science. 1985. V. 229. № 4714. P. 665–668.
Witelson S. F. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study // Brain. 1989. V. 112. № 3. P. 799–835.
Witelson SF. Neural sexual mosaicism: sexual differentiation of the human temporo-parietal region for functional asymmetry // Psychoneuroendocrinology. 1991. V. 16. № 1–3. P. 131–153.
Witelson S. F., Goldsmith C. H. The relationship of hand preference to anatomy of the corpus callosum in men // Brain Research. 1991. V. 545. № 1–2. P. 175–182.
Woodruff P. W., McManus I.C., David A. S. Meta-analysis of corpuscallosum size in schizophrenia // Journal of Neurology, Neurosurgery and Psychiatry. 1995. V. 58. № 4. P. 457–461.
Woodruff P. W., Phillips M. L., Rushe T., Wright I. C., Murray R. M., David A. S. Corpus callosum size and inter-hemispheric function in schizophrenia // Schizophrenia Research. 1997. V. 23. № 3. P. 189–196.
Yakovlev P. I., Lecours A. R. The myelogenetic cycles of regional maturation of the brain // Regional Development of the brain in early life / Minkowski A. (Ed). – Boston (MA): Blackwell Scientific Publications, 1967. P. 3–70.
Yazgan Y., Kinsbourne M. Functional consequences of changes in callosal area in Tourette's syndrome and Attention Deficit/ Hyperactivity Disorder // The Parallel Brain: The Cognitive Neuroscience of the Corpus Callosum (Issues in Clinical and Cognitive Neuropsychology) / E. Zaidel, M. Iacoboni (Eds.). – Cambridge (MA): The MIT Press, 2003. P. 423–432.
Zaidel D. W. The case for a relationship between human memory, hippocampus, and corpus callosum // Biological Research. 1995. V. 28. P. 51–57.
Zaidel E., Aboitiz F., Clarke J. Sexual dimorphism in interhemispheric relations: anatomical-behavioral convergence // Biological Research. 1995. V. 28. № 1. P. 27–43.
Zaidel E., Iacoboni M. New insights in callosal anatomy and morphometry // The Parallel Brain: The Cognitive Neuroscience of the Corpus Callosum (Issues in Clinical and Cognitive Neuropsychology) / E. Zaidel, M. Iacoboni (Eds.). – Cambridge (MA): The MIT Press, 2003. P. 131–136.
Zaidel D. W., Sperry R. W. Memory impairment after commissurotomy in man // Brain. 1974. V. 97. № 1. P. 263–272.
Zweier C., Thiel C. T., Dufke A., Crow Y. J., Meinecke P., Suri M., Ala-Mello S., Beemer F., Bernasconi S., Bianchi P., Bier A., Devriendt K., Dimitrov B., Firth H., Gallagher R. C., Garavelli L., Gillessen-Kaesbach G., Hudgins L., Kaariainen H., Karstens S., Krantz I., Mannhardt A., Medne L., Mucke J., Kibaek M., Krogh L. N., Peippo M., Rittinger O., Schulz S., Schelley S. L., Temple I. K., Dennis N. R., Van der Knaap M. S., Wheeler P., Yerushalmi B., Zenker M., Seidel H., Lachmeijer A., Prescott T., Kraus C., Lowry R. B., Rauch A. Clinical and mutational spectrum of Mowat-Wilson syndrome // European Journal of Medical Genetics. 2005. V. 48. № 2. P. 97–111.