Анализ связи латеральных предпочтений и функциональной асимметрии с языковыми проблемами в детстве

Обзор литературных источников


  • Елена Ивановна Николаева Российский государственный педагогический университет им. А. И. Герцена https://orcid.org/0000-0001-8363-8496



Библиографические ссылки

Abou-Khalil, B. (2007) Methods for determination of language dominance: The Wada test and proposed noninvasive alternatives. Current Neurology and Neuroscience Reports, vol. 7, pp. 483–490. PMID: 17999894. DOI: 10.1007/s11910-007-0075-6 (In English)

Alarcón, M., Abrahams, B. S., Stone, J. L. et al. (2008) Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics, vol. 82, no. 1, pp. 150–159. PMID: 18179893. DOI: 10.1016/j.ajhg.2007.09.005 (In English)

Annett, M. (1985) Left, right, hand and brain: The Right shift theory. London; Hillsdale, N. J.: Lawrence Erlbaum Associates, 474 p. (In English)

Anney, R., Klei, L., Pinto, D. et al. (2012) Individual common variants exert weak effects on the risk for autism spectrum disorders. Human Molecular Genetics, vol. 21, no. 21, pp. 4781–4792. PMID: 22843504. DOI: 10.1093/hmg/dds301 (In English)

Arking, D. E., Cutler, D. J., Brune, C. W. et al. (2008) A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, vol. 82, no. 1, pp. 160–164. PMID: 18179894. DOI: 10.1016/j.ajhg.2007.09.015 (In English)

Badcock, N., Bishop, D., Hardiman, M. et al. (2011) Co-localisation of abnormal brain structure and function in specific language impairment. Brain and Language, vol. 120, no. 3, pp. 310–320. PMID: 22137677. DOI: 10.1016/j.bandl.2011.10.006 (In English)

Badzakova-Trajkov, G., Häberling, I. S., Corballis, M. C. (2010) Cerebral asymmetries in monozygotic twins: An fMRI study. Neuropsychologia, vol. 48, no. 10, pp. 3086–3093. PMID: 20600189. DOI: 10.1016/j.neuropsychologia.2010.06.020 (In English)

Bishop, D. V. M. (2009) Genes, cognition and communication: Insights from neurodevelopmental disorders. Annals of the New York Academy of Sciences, vol. 1156, no. 1, pp. 1–18. PMID: 19338500. DOI: 10.1111/j.1749-6632.2009.04419.x (In English)

Bishop, D. V. M. (2013) Cerebral asymmetry and language development: Cause, correlate or consequence? Science, vol. 340, no. 6138, article 1230531. PMID: 23766329. DOI: 10.1126/science.1230531 (In English)Комплексные исследования детства, 2020, т. 2, № 1 63

Bishop, D. V. M., Snowling, M. J. (2004) Developmental dyslexia and specific language impairment: Same or different? Psychological Bulletin, vol. 130, no. 6, pp. 858–886. PMID: 15535741. DOI: 10.1037/0033-2909.130.6.858 (In English)

Bishop, D. V. M. (2006) What causes specific language impairment in children? Current Directions in Psychological Science, vol. 15, no. 5, pp. 217–221. PMID: 19009045. DOI: 10.1111/j.1467-8721.2006.00439.x (In English)

Brown, T. T., Lugar, H. M., Coalson, R. S. et al. (2005) Developmental changes in human cerebral functional organization for word generation. Cerebral Cortex, vol. 15, no. 3, pp. 275–290. PMID: 15297366. DOI: 10.1093/cercor/bhh129 (In English)

Catani, M. (2007) Symmetries in human brain language pathways correlate with verbal recall. Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 43, pp. 17163–17168. PMID: 17939998. DOI: 10.1073/pnas.0702116104 (In English)

Darki, F., Peyrard-Janvid, M., Matsson, H. et al. (2012) Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure. Biological Psychiatry, vol. 72, no. 8, pp. 671–676. PMID: 22683091. DOI: 10.1016/j.biopsych.2012.05.008 (In English)

de Guibert, C., Maumet, C., Jannin, P. et al. (2011) Abnormal functional lateralization and activity of language brain areas in typical specific language impairment (developmental dysphasia). Brain, vol. 134, no. 10, pp. 3044–3058. PMID: 21719430. DOI: 10.1093/brain/awr141 (In English)

Dorsaint-Pierre, R., Penhune, V. B., Watkins, K. E. et al. (2006) Asymmetries of the planum temporale and Heschl’s gyrus: Relationship to language lateralization. Brain, vol. 129, no. 5, pp. 1164–1174. PMID: 16537567. DOI: 10.1093/brain/awl055 (In English)

Eckert, M. (2004) Neuroanatomical markers for dyslexia: A review of dyslexia structural imaging studies. The Neuroscientist, vol. 10, no. 4, pp. 362–371. PMID: 15271263. DOI: 10.1177/1073858404263596 (In English)

Eckert, M. A., Leonard, C. M. (2000) Structural imaging in dyslexia: The planum temporale. Mental Retardation and Developmental Disabilities Research Reviews, vol. 6, no. 3, pp. 198–206. PMID: 10982497. DOI: 10.1002/1098-2779(2000)6:3<198::AID-MRDD7>3.0.CO;2-1 (In English)

Geschwind, D. H., Miller, B. L., DeCarli, Ch., Carmelli, D. (2002) Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness. Proceedings of the National Academy of Sciences, vol. 99, no. 5, pp. 3176–3181. PMID: 11867730. DOI: 10.1073/pnas.052494999 (In English)

Green, A. E., Munafò, M., DeYoung, C. (2008) Using genetic data in cognitive neuroscience: From growing pains to genuine insights. Nature Reviews Neuroscience, vol. 9, no. 9, pp. 710–720. DOI: 10.1038/nrn2461 (In English)

Groen, M. A., Whitehouse, A. J. O., Badcock, N. A., Bishop, D. V. M. (2012) Does cerebral lateralisation develop? A study using functional transcranial Doppler ultrasound assessing lateralisation for language production and visuospatial memory. Brain and Behavior, vol. 2, no. 3, pp. 256–269. PMID: 22741100. DOI: 10.1002/brb3.56 (In English)

Häberling, I. S., Badzakova-Trajkov, G., Corballis, M. C. (2013) Asymmetries of the arcuate fasciculus in monozygotic twins: Genetic and nongenetic influences. PLOS ONE, vol. 8, no. 1, article e52315. PMID: 23300971. DOI: 10.1371/journal.pone.0052315 (In English)

Keller, S. S., Roberts, N., García-Fiñana, M. et al. (2011) Can the language-dominant hemisphere be predicted by brain anatomy? Journal of Cognitive Neuroscience, vol. 23, no. 8, pp. 2013–2029. PMID: 20807056. DOI: 10.1162/jocn.2010.21563 (In English)

Knecht, S., Deppe, M., Ringelstein, E.-B. et al. (1998) Reproducibility of functional transcranial Doppler sonography in determining hemispheric language lateralization. Stroke, vol. 29, no. 6, pp. 1155–1159. PMID: 9626288. DOI: 10.1161/01.STR.29.6.1155 (In English)

Knecht, S., Dräger, B., Flöel, A. et al. (2001) Behavioural relevance of atypical language lateralization in healthy subjects. Brain, vol. 124, no. 8, pp. 1657–1665. PMID: 11459756. DOI: 10.1093/brain/124.8.1657 (In English)

Lebel, C., Beaulieu C. (2009) Lateralization of the arcuate fasciculus from childhood to adulthood and its relation to cognitive abilities in children. Human Brain Mapping, vol. 30, no. 11, pp. 3563–3573. PMID: 19365801. DOI: 10.1002/hbm.20779 (In English)

Leonard, C. M., Lombardino, L. J., Walsh, K. et al. (2002) Anatomical risk factors that distinguish dyslexia from SLI predict reading skill in normal children. Journal of Communication Disorders, vol. 35, no. 6, pp. 501–531. PMID: 12443050. DOI: 10.1016/s0021-9924(02)00120-x (In English)

Levina, R. E. (ed.). (1968) Osnovy teorii i praktiki logopedii [The basis of the theory and practice of the speech therapy]. Moscow: Prosveshchenie Publ., 367 р. (In Russian)

Ligthart, L., Boomsma, D. I. (2012) Causes of comorbidity: Pleiotropy or causality? Shared genetic and environmental influences on migraine and neuroticism. Twin Research and Human Genetics, vol. 15, no. 2, pp. 158–165. PMID: 22856357. DOI: 10.1375/twin.15.2.158 (In English)

Medland, S. E., Duffy, D. L., Wright, M. J. et al. (2009) Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, vol. 47, no. 2, pp. 330–337. PMID: 18824185. DOI: 10.1016/j. neuropsychologia.2008.09.005 (In English)

Orton, S. T. (1925) “Word blindness” in school children. Archives of Neurology and Psychiatry, vol. 14, no. 5, pp. 581–615. DOI: 10.1001/archneurpsyc.1925.02200170002001 (In English)64 DOI: 10.33910/2687-0223-2020-2-1-58-64

Pennington, B. F., Bishop, D. V. M. (2009) Relations among speech, language, and reading disorders. Annual Review of Psychology, vol. 60, pp. 283–306. PMID: 18652545. DOI: 10.1146/annurev.psych.60.110707.163548 (In English)

Pernet, C., Poline, J., Demonet, J., Rousselet, G. (2009) Brain classification reveals the right cerebellum as the best biomarker of dyslexia. BMC Neuroscience, vol. 10, article 67. PMID: 19555471. DOI: 10.1186/1471-2202-10-67 (In English)

Pinel, P., Fauchereau, F., Moreno, A. et al. (2012) Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. Journal of Neuroscience, vol. 32, no. 3, pp. 817–825. PMID: 22262880. DOI: 10.1523/JNEUROSCI.5996-10.2012 (In English)

Plante, E., Almryde, K., Patterson, D. K. et al. (2015) Language lateralization shifts with learning by adults. Laterality: Asymmetries of Body, Brain and Cognition, vol. 20, no. 3, pp. 306–325. PMID: 25285756. DOI: 10.1080/1357650X.2014.963597 (In English)

Previc, F. H. (1991) A general theory concerning the prenatal origins of cerebral lateralization in humans. Psychological Review, vol. 98, no. 3, pp. 299–334. PMID: 1891521. DOI: 10.1037/0033-295x.98.3.299 (In English)

Raj, A., van Oudenaarden, A. (2008) Nature, nurture, or chance: Stochastic gene expression and its consequences. Cell, vol. 135, no. 2, pp. 216–226. PMID: 18957198. DOI: 10.1016/j.cell.2008.09.050 (In English)

Rice, M. L., Smith, S. D., Gayán, J. (2009) Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment. Journal of Neurodevelopmental Disorders, vol. 1, no. 4, pp. 264–282. PMID: 19997522. DOI: 10.1007/s11689-009-9031-x (In English)

Scerri, T. S., Brandler, W. M., Paracchini, S. et al. (2011) PCSK6 is associated with handedness in individuals with dyslexia. Human Molecular Genetics, vol. 20, no. 3, pp. 608–614. PMID: 21051773. DOI: 10.1093/hmg/ddq475 (In English)

Scott-Van Zeeland, A. A., Abrahams, B. S., Alvarez-Retuerto, A. I. et al. (2010) Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Science Translational Medicine, vol. 2, no. 56, pp. 56ra80. PMID: 21048216. DOI: 10.1126/scitranslmed.3001344 (In English)

Steinmetz, H., Herzog, A., Schlaug, G. et al. (1995) Brain (a)symmetry in monozygotic twins. Cerebral Cortex, vol. 5, no. 4, pp. 296–300. PMID: 7580122. DOI: 10.1093/cercor/5.4.296 (In English)

Vernes, S. C., Newbury, D. F., Abrahams, B. S. et al. (2008) A functional genetic link between distinct developmental language disorders. New England Journal of Medicine, vol. 359, no. 22, pp. 2337–2345. PMID: 18987363. DOI: 10.1056/NEJMoa0802828 (In English)

Webster, R. I., Shevell, M. I. (2004) Neurobiology of specific language impairment. Journal of Child Neurology, vol. 19, no. 7, pp. 471–481. PMID: 15526950. DOI: 10.1177/08830738040190070101 (In English)

Whalley, H. C., O’Connell, G., Sussmann, J. E. et al. (2011) Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, vol. 156, no. 8, pp. 941–948. PMID: 21987501. DOI: 10.1002/ajmg.b.31241 (In English)

Whitehouse, A. J. O., Bishop, D. V. M. (2008) Cerebral dominance for language function in adults with specific language impairment or autism. Brain, vol. 131, no. 12, pp. 3193–3200. DOI: 10.1093/brain/awn266 (In English)

Whitehouse, A. J. O., Bishop, D. V. M., Ang, Q. W. et al. (2011) CNTNAP2 variants affect early language development in the general population. Genes, Brain and Behavior, vol. 10, no. 4, pp. 451–456. PMID: 21310003. DOI: 10.1111/j.1601-183X.2011.00684.x (In English)






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