메뉴 건너뛰기




Volumn 25, Issue 9, 2010, Pages 563-581

Neurobiology and neurogenetics of dyslexia;Neurobiología y neurogenética de la dislexia

Author keywords

Animal models; Comorbidity; Dyslexia; Neurobiology; Neurogenetics

Indexed keywords

ARTICLE; AUDITORY SYSTEM; BRAIN CORTEX; BRAIN MALFORMATION; DYSLEXIA; DYX1 GENE; DYX2 GENE; DYX3 GENE; DYX4 GENE; DYX5 GENE; DYX6 GENE; DYX7 GENE; DYX8 GENE; DYX9 GENE; GENE LOCUS; GENETICS; LEARNING DISORDER; NEUROBIOLOGY; NONHUMAN; PHONETICS; READING;

EID: 78649329370     PISSN: 02134853     EISSN: 15781968     Source Type: Journal    
DOI: 10.1016/j.nrl.2009.12.010     Document Type: Short Survey
Times cited : (14)

References (196)
  • 2
    • 0028889053 scopus 로고
    • Defining and classifying learning disabilities and attention-deficit/hyperactivity disorder
    • Shaywitz B.A., Fletcher J., Shaywitz S.E. Defining and classifying learning disabilities and attention-deficit/hyperactivity disorder. J Child Neurol. 1995, 10:S50-S57.
    • (1995) J Child Neurol. , vol.10
    • Shaywitz, B.A.1    Fletcher, J.2    Shaywitz, S.E.3
  • 3
    • 20444409668 scopus 로고    scopus 로고
    • Dyslexia, (Specific Reading Disability)
    • Shaywitz S.E., Shaywitz B.A. Dyslexia, (Specific Reading Disability). Biol Psychiatry. 2005, 57:1301-1309.
    • (2005) Biol Psychiatry. , vol.57 , pp. 1301-1309
    • Shaywitz, S.E.1    Shaywitz, B.A.2
  • 4
    • 41549165267 scopus 로고    scopus 로고
    • The Education of dyslexic children from childhood to young adulthood
    • Shaywitz S., Morris R., Shaywitz B. The Education of dyslexic children from childhood to young adulthood. Annu Rev Psychol. 2008, 59:451-475.
    • (2008) Annu Rev Psychol. , vol.59 , pp. 451-475
    • Shaywitz, S.1    Morris, R.2    Shaywitz, B.3
  • 7
    • 33645174874 scopus 로고
    • Evidence that dyslexia may represent the lower tail of a normal distribution of reading ability
    • Shaywitz S., Escobar M., Shaywitz B., Fletcher J., Makuch R. Evidence that dyslexia may represent the lower tail of a normal distribution of reading ability. N Engl J Med. 1992, 326:145-150.
    • (1992) N Engl J Med. , vol.326 , pp. 145-150
    • Shaywitz, S.1    Escobar, M.2    Shaywitz, B.3    Fletcher, J.4    Makuch, R.5
  • 9
    • 33747161925 scopus 로고    scopus 로고
    • Genes, brain, and cognition: a roadmap for the cognitive scientist
    • Ramus F. Genes, brain, and cognition: a roadmap for the cognitive scientist. Cognition. 2006, 101:247-269.
    • (2006) Cognition. , vol.101 , pp. 247-269
    • Ramus, F.1
  • 11
    • 0033634772 scopus 로고    scopus 로고
    • The neurological basis of developmental dyslexia: an overview and working hypothesis
    • Habib M. The neurological basis of developmental dyslexia: an overview and working hypothesis. Brain. 2000, 123:2373-2399.
    • (2000) Brain. , vol.123 , pp. 2373-2399
    • Habib, M.1
  • 12
    • 0037378781 scopus 로고    scopus 로고
    • Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults
    • Ramus F., Rosen S., Dakin S.C., Day B.L., Castellote J.M., White S., et al. Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults. Brain. 2003, 126:841-865.
    • (2003) Brain. , vol.126 , pp. 841-865
    • Ramus, F.1    Rosen, S.2    Dakin, S.C.3    Day, B.L.4    Castellote, J.M.5    White, S.6
  • 13
    • 0034610301 scopus 로고    scopus 로고
    • Disruption of the neural response to rapid acoustic stimuli in dyslexia: evidence from functional MRI
    • Temple E., Poldrack R.A., Protopapas A., Nagarajan S., Salz T., Tallal P., et al. Disruption of the neural response to rapid acoustic stimuli in dyslexia: evidence from functional MRI. Proc Nat Acad Sci U S A. 2000, 97:13907-13912.
    • (2000) Proc Nat Acad Sci U S A. , vol.97 , pp. 13907-13912
    • Temple, E.1    Poldrack, R.A.2    Protopapas, A.3    Nagarajan, S.4    Salz, T.5    Tallal, P.6
  • 14
    • 0019215685 scopus 로고
    • Specific reading disability: differences in contrast sensitivity as a function of spatial frequency
    • Lovegrove W.J., Bowling A., Badcock D., Blackwood M. Specific reading disability: differences in contrast sensitivity as a function of spatial frequency. Science. 1980, 210:439-440.
    • (1980) Science. , vol.210 , pp. 439-440
    • Lovegrove, W.J.1    Bowling, A.2    Badcock, D.3    Blackwood, M.4
  • 16
    • 0026554483 scopus 로고
    • Working memory
    • Baddeley A. Working memory. Science. 1992, 255:556-559.
    • (1992) Science. , vol.255 , pp. 556-559
    • Baddeley, A.1
  • 17
    • 0031468533 scopus 로고    scopus 로고
    • Lobular patterns of cerebellar activation in verbal working memory and finger tapping tasks as revealed by functional MRI
    • Desmond J.E., Gabrieli J.D., Wagner A.D., Ginier B.L., Glover G.H. Lobular patterns of cerebellar activation in verbal working memory and finger tapping tasks as revealed by functional MRI. J Neurosci. 1997, 17:9675-9685.
    • (1997) J Neurosci. , vol.17 , pp. 9675-9685
    • Desmond, J.E.1    Gabrieli, J.D.2    Wagner, A.D.3    Ginier, B.L.4    Glover, G.H.5
  • 18
    • 0025874742 scopus 로고
    • Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia
    • Livingstone M.S., Rosen G.D., Drislane F.W., Galaburda A.M. Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia. Proc Natl Acad Sci U S A. 1991, 88:7943-7947.
    • (1991) Proc Natl Acad Sci U S A. , vol.88 , pp. 7943-7947
    • Livingstone, M.S.1    Rosen, G.D.2    Drislane, F.W.3    Galaburda, A.M.4
  • 19
    • 0031048442 scopus 로고    scopus 로고
    • To see but not to read: the magnocellular theory of dyslexia
    • Stein J., Walsh V. To see but not to read: the magnocellular theory of dyslexia. Trends Neurosci. 1997, 20:147-152.
    • (1997) Trends Neurosci. , vol.20 , pp. 147-152
    • Stein, J.1    Walsh, V.2
  • 22
    • 0032555155 scopus 로고    scopus 로고
    • Functional connectivity of the angular gyrus in normal reading and dyslexia
    • Horwitz B., Rumsey J.M., Donohue B.C. Functional connectivity of the angular gyrus in normal reading and dyslexia. Proc Natl Acad Sci U S A. 1998, 95:8939-8944.
    • (1998) Proc Natl Acad Sci U S A. , vol.95 , pp. 8939-8944
    • Horwitz, B.1    Rumsey, J.M.2    Donohue, B.C.3
  • 24
    • 0036237545 scopus 로고    scopus 로고
    • Language-specific tuning of visual cortex? Functional properties of the visual word form area
    • Cohen L., Lehericy S., Chochon F., Lemer C., Rivaud S., Dehaene S. Language-specific tuning of visual cortex? Functional properties of the visual word form area. Brain. 2002, 125:1054-1069.
    • (2002) Brain. , vol.125 , pp. 1054-1069
    • Cohen, L.1    Lehericy, S.2    Chochon, F.3    Lemer, C.4    Rivaud, S.5    Dehaene, S.6
  • 25
    • 0037675712 scopus 로고    scopus 로고
    • The visual word form area: expertise for reading in the fusiform gyrus
    • McCandliss B.D., Cohen L., Dehaene S. The visual word form area: expertise for reading in the fusiform gyrus. Trends Cogn Sci. 2003, 7:293-299.
    • (2003) Trends Cogn Sci. , vol.7 , pp. 293-299
    • McCandliss, B.D.1    Cohen, L.2    Dehaene, S.3
  • 26
  • 28
    • 0002573396 scopus 로고    scopus 로고
    • Phonological aspects of aphasia
    • Academic Press, San Diego, M.T. Sarno (Ed.)
    • Blumstein S.E. Phonological aspects of aphasia. Acquired aphasia 1998, 157-185. Academic Press, San Diego. M.T. Sarno (Ed.).
    • (1998) Acquired aphasia , pp. 157-185
    • Blumstein, S.E.1
  • 29
    • 0032759487 scopus 로고    scopus 로고
    • The relation of phoneme discrimination, lexical access, and short-term memory: a case study and interactive activation account
    • Martin R.C., Breedin S.D., Damian M.F. The relation of phoneme discrimination, lexical access, and short-term memory: a case study and interactive activation account. Brain Lang. 1999, 70:437-482.
    • (1999) Brain Lang. , vol.70 , pp. 437-482
    • Martin, R.C.1    Breedin, S.D.2    Damian, M.F.3
  • 30
    • 0031877801 scopus 로고    scopus 로고
    • Neuroimaging studies of the cerebellum: language, learning and memory
    • Desmond J.E., Fiez J.A. Neuroimaging studies of the cerebellum: language, learning and memory. Trends Cogn Sci. 1998, 2:355-362.
    • (1998) Trends Cogn Sci. , vol.2 , pp. 355-362
    • Desmond, J.E.1    Fiez, J.A.2
  • 31
    • 0003340105 scopus 로고    scopus 로고
    • Broca's language area from a neuroanatomical and developmental perspective
    • Oxford University Press, Oxford, P. Hagoort, C. Brown (Eds.)
    • Uylings H.B.M., Malofeeva L.I., Bogolepova I.N., Amunts K., Zilles K. Broca's language area from a neuroanatomical and developmental perspective. Neurocognition of language processing 1999, 319-336. Oxford University Press, Oxford. P. Hagoort, C. Brown (Eds.).
    • (1999) Neurocognition of language processing , pp. 319-336
    • Uylings, H.B.M.1    Malofeeva, L.I.2    Bogolepova, I.N.3    Amunts, K.4    Zilles, K.5
  • 32
    • 0009769564 scopus 로고    scopus 로고
    • Storage and computation in the brain: a neuroimaging perspective
    • Kluwer, Dordrecht, S. Nooteboom, F. Weerman, F. Wijnen (Eds.)
    • Kaan E., Stowe L.A. Storage and computation in the brain: a neuroimaging perspective. Storage and computation in the language faculty 2002, 257-298. Kluwer, Dordrecht. S. Nooteboom, F. Weerman, F. Wijnen (Eds.).
    • (2002) Storage and computation in the language faculty , pp. 257-298
    • Kaan, E.1    Stowe, L.A.2
  • 33
    • 0034113215 scopus 로고    scopus 로고
    • The neurology of syntax: Language use without Broca's area
    • Grodzinsky Y. The neurology of syntax: Language use without Broca's area. Behav Brain Sci. 2000, 23:1-71.
    • (2000) Behav Brain Sci. , vol.23 , pp. 1-71
    • Grodzinsky, Y.1
  • 35
    • 0025648329 scopus 로고
    • Developmental dyslexia in women: neuropathological findings in three patients
    • Humphreys P., Kaufmann W.E., Galaburda A.M. Developmental dyslexia in women: neuropathological findings in three patients. Ann Neurol. 1990, 2:727-738.
    • (1990) Ann Neurol. , vol.2 , pp. 727-738
    • Humphreys, P.1    Kaufmann, W.E.2    Galaburda, A.M.3
  • 36
    • 0018356659 scopus 로고
    • Cytoarchitectonic abnormalities in developmental dyslexia: a case study
    • Galaburda A.M., Kemper T.L. Cytoarchitectonic abnormalities in developmental dyslexia: a case study. Ann Neurol. 1979, 6:94-100.
    • (1979) Ann Neurol. , vol.6 , pp. 94-100
    • Galaburda, A.M.1    Kemper, T.L.2
  • 37
    • 33644893384 scopus 로고    scopus 로고
    • Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia
    • Sokol D.K., Golomb M.R., Carvalho K.S., Edwards-Brown M. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology. 2006, 66:294.
    • (2006) Neurology. , vol.66 , pp. 294
    • Sokol, D.K.1    Golomb, M.R.2    Carvalho, K.S.3    Edwards-Brown, M.4
  • 38
    • 0033758190 scopus 로고    scopus 로고
    • Microstructure of temporo-parietal white matter as a basis for reading ability: evidence from diffusion tensor magnetic resonance imaging
    • Klingberg T., Hedehus M., Temple E., Salz T., Gabrieli J.D., Moseley M.E., et al. Microstructure of temporo-parietal white matter as a basis for reading ability: evidence from diffusion tensor magnetic resonance imaging. Neuron. 2000, 25:493-500.
    • (2000) Neuron. , vol.25 , pp. 493-500
    • Klingberg, T.1    Hedehus, M.2    Temple, E.3    Salz, T.4    Gabrieli, J.D.5    Moseley, M.E.6
  • 39
    • 17644382644 scopus 로고    scopus 로고
    • Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging
    • Deutsch G.K., Dougherty R.F., Bammer R., Siok W.T., Gabrieli J.D., Wandell B. Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging. Cortex. 2005, 41:354-363.
    • (2005) Cortex. , vol.41 , pp. 354-363
    • Deutsch, G.K.1    Dougherty, R.F.2    Bammer, R.3    Siok, W.T.4    Gabrieli, J.D.5    Wandell, B.6
  • 40
    • 67649644759 scopus 로고    scopus 로고
    • When all hypotheses are right: A multifocal account of dyslexia
    • Pernet C., Andersson J., Paulesu E., Demonet J.F. When all hypotheses are right: A multifocal account of dyslexia. Hum Brain Mapp. 2009, 30:2278-2292.
    • (2009) Hum Brain Mapp. , vol.30 , pp. 2278-2292
    • Pernet, C.1    Andersson, J.2    Paulesu, E.3    Demonet, J.F.4
  • 42
    • 3242749669 scopus 로고    scopus 로고
    • Neuroanatomical markers for dyslexia: a review of dyslexia structural imaging studies
    • Eckert M. Neuroanatomical markers for dyslexia: a review of dyslexia structural imaging studies. Neuroscientist. 2004, 10:362-371.
    • (2004) Neuroscientist. , vol.10 , pp. 362-371
    • Eckert, M.1
  • 45
    • 53449089443 scopus 로고    scopus 로고
    • Effective brain connectivity in children with reading difficulties during phonological processing
    • Cao F., Bitan T., Booth J.R. Effective brain connectivity in children with reading difficulties during phonological processing. Brain Lang. 2008, 107:91-101.
    • (2008) Brain Lang. , vol.107 , pp. 91-101
    • Cao, F.1    Bitan, T.2    Booth, J.R.3
  • 47
    • 20444419815 scopus 로고    scopus 로고
    • Subliminal convergence of kanji and kana words: further evidence for functional parcellation of the posterior temporal cortex in visual word perception
    • Nakamura K., Dehaene S., Jobert A., Le Bihan D., Kouider S. Subliminal convergence of kanji and kana words: further evidence for functional parcellation of the posterior temporal cortex in visual word perception. J Cogn Neurosci. 2005, 17:954-968.
    • (2005) J Cogn Neurosci. , vol.17 , pp. 954-968
    • Nakamura, K.1    Dehaene, S.2    Jobert, A.3    Le Bihan, D.4    Kouider, S.5
  • 48
    • 44449161302 scopus 로고    scopus 로고
    • A structural-functional basis for dyslexia in the cortex of Chinese readers
    • Siok W.T., Niu Z., Jin Z., Perfetti C.A., Tan L.H. A structural-functional basis for dyslexia in the cortex of Chinese readers. Proc Natl Acad Sci U S A. 2008, 105:5561-5566.
    • (2008) Proc Natl Acad Sci U S A. , vol.105 , pp. 5561-5566
    • Siok, W.T.1    Niu, Z.2    Jin, Z.3    Perfetti, C.A.4    Tan, L.H.5
  • 50
    • 0037418288 scopus 로고    scopus 로고
    • Neural deficits in children with dyslexia ameliorated by behavioral remediation: evidence from functional MRI
    • Temple E., Deutsch G.K., Poldrack R.A., Miller S.L., Tallal P., Merzenich M.M., et al. Neural deficits in children with dyslexia ameliorated by behavioral remediation: evidence from functional MRI. Proc Nat Acad Sci U S A. 2003, 100:2860-2865.
    • (2003) Proc Nat Acad Sci U S A. , vol.100 , pp. 2860-2865
    • Temple, E.1    Deutsch, G.K.2    Poldrack, R.A.3    Miller, S.L.4    Tallal, P.5    Merzenich, M.M.6
  • 51
    • 0030022626 scopus 로고    scopus 로고
    • Temporal processing deficits of language -learning impaired children ameliorated by training
    • Merzenich M.M., Jenkins W.M., Johnston P., Schreiner C., Miller S.L., Tallal P. Temporal processing deficits of language -learning impaired children ameliorated by training. Science. 1996, 271:76-80.
    • (1996) Science. , vol.271 , pp. 76-80
    • Merzenich, M.M.1    Jenkins, W.M.2    Johnston, P.3    Schreiner, C.4    Miller, S.L.5    Tallal, P.6
  • 52
    • 0030023111 scopus 로고    scopus 로고
    • Language comprehension in language -learning impaired children improved with acoustically modified speech
    • Tallal P., Miller S.L., Bedi G., Byma G., Wang X., Nagarajan S.S., et al. Language comprehension in language -learning impaired children improved with acoustically modified speech. Science. 1996, 271:81-83.
    • (1996) Science. , vol.271 , pp. 81-83
    • Tallal, P.1    Miller, S.L.2    Bedi, G.3    Byma, G.4    Wang, X.5    Nagarajan, S.S.6
  • 53
    • 0002717148 scopus 로고    scopus 로고
    • A behavioral-genetic analysis of reading disabilities and component processes
    • MIT Press, Cambridge, R. Klein, P. McMullen (Eds.)
    • Olson R.K., Datta H., Gayan J., DeFries J.C. A behavioral-genetic analysis of reading disabilities and component processes. Converging methods for understanding reading and dyslexia 1999, 133-155. MIT Press, Cambridge. R. Klein, P. McMullen (Eds.).
    • (1999) Converging methods for understanding reading and dyslexia , pp. 133-155
    • Olson, R.K.1    Datta, H.2    Gayan, J.3    DeFries, J.C.4
  • 54
    • 33644753148 scopus 로고    scopus 로고
    • Psychiatric endophenotypes and the development of valid animal models
    • Gould T.D., Gottesman I.I. Psychiatric endophenotypes and the development of valid animal models. Genes Brain Behav. 2006, 5:113-119.
    • (2006) Genes Brain Behav. , vol.5 , pp. 113-119
    • Gould, T.D.1    Gottesman, I.I.2
  • 55
    • 0023179955 scopus 로고
    • Evidence for a genetic aetiology in reading disability of twins
    • DeFries J.C., Fulker D.W., Labuda M.C. Evidence for a genetic aetiology in reading disability of twins. Nature. 1987, 329:537-539.
    • (1987) Nature. , vol.329 , pp. 537-539
    • DeFries, J.C.1    Fulker, D.W.2    Labuda, M.C.3
  • 56
    • 0345865996 scopus 로고
    • Genetic influences of subtypes of dyslexia
    • Gayan J., Forsberg H., Olson R.K. Genetic influences of subtypes of dyslexia. Behav Genet. 1994, 24:513.
    • (1994) Behav Genet. , vol.24 , pp. 513
    • Gayan, J.1    Forsberg, H.2    Olson, R.K.3
  • 57
    • 0023299180 scopus 로고
    • A twin study of genetic influences on reading and spelling ability and disability
    • Stevenson J., Graham P., Fredman G., McLoughlin V. A twin study of genetic influences on reading and spelling ability and disability. J Child Psych Psychol. 1987, 28:229-247.
    • (1987) J Child Psych Psychol. , vol.28 , pp. 229-247
    • Stevenson, J.1    Graham, P.2    Fredman, G.3    McLoughlin, V.4
  • 58
    • 0030992259 scopus 로고    scopus 로고
    • Phonological and orthographic components of word recognition: a PET-rCBF study
    • Rumsey J.M., Horwitz B., Donohue B.C., Nace K., Maisog J.M., Andreason P. Phonological and orthographic components of word recognition: a PET-rCBF study. Brain. 1997, 120:739-759.
    • (1997) Brain. , vol.120 , pp. 739-759
    • Rumsey, J.M.1    Horwitz, B.2    Donohue, B.C.3    Nace, K.4    Maisog, J.M.5    Andreason, P.6
  • 59
    • 0033087303 scopus 로고    scopus 로고
    • The structure of genetic influences on general cognitive, language, phonological and reading abilities
    • Hohnen B., Stevenson J. The structure of genetic influences on general cognitive, language, phonological and reading abilities. Dev Psychol. 1999, 35:590-603.
    • (1999) Dev Psychol. , vol.35 , pp. 590-603
    • Hohnen, B.1    Stevenson, J.2
  • 61
    • 57349157021 scopus 로고    scopus 로고
    • Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
    • Paracchini S., Steer C.D., Buckingham L.L., Morris A.P., Ring S., Scerri T., et al. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry. 2008, 165:1576-1584.
    • (2008) Am J Psychiatry. , vol.165 , pp. 1576-1584
    • Paracchini, S.1    Steer, C.D.2    Buckingham, L.L.3    Morris, A.P.4    Ring, S.5    Scerri, T.6
  • 64
    • 0001815958 scopus 로고    scopus 로고
    • Genetic aetiologies of reading and spelling deficits: developmental differences
    • Whurr, Londres, C. Hulme, M. Snowling (Eds.)
    • DeFries J.C., Alarcon M., Olson R.C. Genetic aetiologies of reading and spelling deficits: developmental differences. Dyslexia: biology, cognition and intervention 1997, 20-37. Whurr, Londres. C. Hulme, M. Snowling (Eds.).
    • (1997) Dyslexia: biology, cognition and intervention , pp. 20-37
    • DeFries, J.C.1    Alarcon, M.2    Olson, R.C.3
  • 65
    • 0035257236 scopus 로고    scopus 로고
    • Association study designs for complex diseases
    • Cardon L.R., Bell J.L. Association study designs for complex diseases. Nat Rev Genet. 2001, 2:91-99.
    • (2001) Nat Rev Genet. , vol.2 , pp. 91-99
    • Cardon, L.R.1    Bell, J.L.2
  • 66
    • 45549105578 scopus 로고    scopus 로고
    • The human lexinome: genes of language and reading
    • Gibson C.J., Gruen J.R. The human lexinome: genes of language and reading. J Commun Disord. 2008, 41:409-420.
    • (2008) J Commun Disord. , vol.41 , pp. 409-420
    • Gibson, C.J.1    Gruen, J.R.2
  • 67
    • 78649320940 scopus 로고    scopus 로고
    • Benítez-Burraco A. ¿Hasta qué punto son específicos los trastornos específicos del lenguaje? Implicaciones para una caracterización biológica de la facultad lingüística humana. Ludus Vitalis.
    • Benítez-Burraco A. ¿Hasta qué punto son específicos los trastornos específicos del lenguaje? Implicaciones para una caracterización biológica de la facultad lingüística humana. Ludus Vitalis. 2009;XVI:101-34.
    • (2009) , vol.16 , pp. 101-134
  • 68
    • 0028340175 scopus 로고
    • The genetic basis of complex human behaviors
    • Plomin R., Owen M.J., McGuffin P. The genetic basis of complex human behaviors. Science. 1994, 264:1733-1739.
    • (1994) Science. , vol.264 , pp. 1733-1739
    • Plomin, R.1    Owen, M.J.2    McGuffin, P.3
  • 69
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
    • Lander E., Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995, 11:241-247.
    • (1995) Nat Genet. , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 70
    • 0037220422 scopus 로고    scopus 로고
    • Functional genomics of neural and behavioral plasticity
    • Hofmann H.A. Functional genomics of neural and behavioral plasticity. J Neurobiol. 2003, 54:272-282.
    • (2003) J Neurobiol. , vol.54 , pp. 272-282
    • Hofmann, H.A.1
  • 71
    • 33747190655 scopus 로고    scopus 로고
    • Tangled webs: tracing the connections between genes and cognition
    • Fisher S.E. Tangled webs: tracing the connections between genes and cognition. Cognition. 2006, 101:270-297.
    • (2006) Cognition. , vol.101 , pp. 270-297
    • Fisher, S.E.1
  • 72
    • 33744455435 scopus 로고    scopus 로고
    • The genetics of developmental dyslexia
    • Williams J., O'Donovan M.C. The genetics of developmental dyslexia. Eur J Hum Genet. 2006, 4:681-689.
    • (2006) Eur J Hum Genet. , vol.4 , pp. 681-689
    • Williams, J.1    O'Donovan, M.C.2
  • 73
    • 0031027824 scopus 로고    scopus 로고
    • Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
    • Grigorenko E.L., Wood F.B., Meyer M.S., Hart L.A., Speed W.C., Shuster A., et al. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet. 1997, 60:27-39.
    • (1997) Am J Hum Genet. , vol.60 , pp. 27-39
    • Grigorenko, E.L.1    Wood, F.B.2    Meyer, M.S.3    Hart, L.A.4    Speed, W.C.5    Shuster, A.6
  • 75
    • 0034701254 scopus 로고    scopus 로고
    • Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
    • Morris D.W., Robinson L., Turic D., Duke M., Webb V., Milham C., et al. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Hum Molec Genet. 2000, 9:843-848.
    • (2000) Hum Molec Genet. , vol.9 , pp. 843-848
    • Morris, D.W.1    Robinson, L.2    Turic, D.3    Duke, M.4    Webb, V.5    Milham, C.6
  • 76
    • 0141482054 scopus 로고    scopus 로고
    • A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
    • Taipale M., Kaminen N., Nopola-Hemmi J., Haltia T., Myllyluoma B., Lyytinen H., et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci U S A. 2003, 100:11553-11558.
    • (2003) Proc Natl Acad Sci U S A. , vol.100 , pp. 11553-11558
    • Taipale, M.1    Kaminen, N.2    Nopola-Hemmi, J.3    Haltia, T.4    Myllyluoma, B.5    Lyytinen, H.6
  • 77
    • 0344496513 scopus 로고    scopus 로고
    • The tetratricopeptide repeat: a structural motif mediating protein-protein interactions
    • Blatch G.L., Lässle M. The tetratricopeptide repeat: a structural motif mediating protein-protein interactions. BioEssays. 1999, 21:932-939.
    • (1999) BioEssays. , vol.21 , pp. 932-939
    • Blatch, G.L.1    Lässle, M.2
  • 78
    • 48749084615 scopus 로고    scopus 로고
    • The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
    • Tapia-Páez I., Tammimies K., Massinen S., Roy A.L., Kere J. The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. FASEB J. 2008, 22:3001-3009.
    • (2008) FASEB J. , vol.22 , pp. 3001-3009
    • Tapia-Páez, I.1    Tammimies, K.2    Massinen, S.3    Roy, A.L.4    Kere, J.5
  • 79
    • 35148851563 scopus 로고    scopus 로고
    • Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations
    • Rosen G.D., Bai J., Wang Y., Fiondella C.G., Threlkeld S.W., LoTurco J.J., et al. Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cereb Cortex. 2007, 17:2562-2572.
    • (2007) Cereb Cortex. , vol.17 , pp. 2562-2572
    • Rosen, G.D.1    Bai, J.2    Wang, Y.3    Fiondella, C.G.4    Threlkeld, S.W.5    LoTurco, J.J.6
  • 81
    • 33846440958 scopus 로고    scopus 로고
    • Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1
    • Threlkeld S.W., McClure M.M., Bai J., Wang Y., LoTurco J.J., Rosen G.D., et al. Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. Brain Res Bull. 2007, 71:508-514.
    • (2007) Brain Res Bull. , vol.71 , pp. 508-514
    • Threlkeld, S.W.1    McClure, M.M.2    Bai, J.3    Wang, Y.4    LoTurco, J.J.5    Rosen, G.D.6
  • 82
    • 0034629007 scopus 로고    scopus 로고
    • Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: abolition by NMDA receptor blockade
    • Cammarota M., Bevilaqua L.R.M., Ardenghi P., Paratcha G., Levi de Stein M., Izquierdo I., et al. Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: abolition by NMDA receptor blockade. Mol Brain Res. 2000, 76:36-46.
    • (2000) Mol Brain Res. , vol.76 , pp. 36-46
    • Cammarota, M.1    Bevilaqua, L.R.M.2    Ardenghi, P.3    Paratcha, G.4    Levi de Stein, M.5    Izquierdo, I.6
  • 83
    • 0037229762 scopus 로고    scopus 로고
    • Modulation of taste-induced Elk-1 activation by identified neurotransmitter systems in the insular cortex of the behaving rat
    • Berman D.E. Modulation of taste-induced Elk-1 activation by identified neurotransmitter systems in the insular cortex of the behaving rat. Neurobiol Learn Mem. 2003, 79:122-126.
    • (2003) Neurobiol Learn Mem. , vol.79 , pp. 122-126
    • Berman, D.E.1
  • 84
    • 34748875368 scopus 로고    scopus 로고
    • Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
    • Marino C., Citterio A., Giorda R., Facoetti A., Menozzi G., Vanzin L., et al. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav. 2007, 6:640-646.
    • (2007) Genes Brain Behav. , vol.6 , pp. 640-646
    • Marino, C.1    Citterio, A.2    Giorda, R.3    Facoetti, A.4    Menozzi, G.5    Vanzin, L.6
  • 86
    • 0141594625 scopus 로고    scopus 로고
    • The first candidate gene for dyslexia: Turning the page of a new chapter of research
    • Grigorenko E.L. The first candidate gene for dyslexia: Turning the page of a new chapter of research. Proc Natl Acad Sci U S A. 2003, 100:11190-11192.
    • (2003) Proc Natl Acad Sci U S A. , vol.100 , pp. 11190-11192
    • Grigorenko, E.L.1
  • 87
    • 0033366739 scopus 로고    scopus 로고
    • A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
    • Fisher S.E., Marlow A.J., Lamb J., Maestrini E., Williams D.F., Richardson A.J., et al. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet. 1999, 64:146-156.
    • (1999) Am J Hum Genet. , vol.64 , pp. 146-156
    • Fisher, S.E.1    Marlow, A.J.2    Lamb, J.3    Maestrini, E.4    Williams, D.F.5    Richardson, A.J.6
  • 88
    • 0033364213 scopus 로고    scopus 로고
    • Quantitative-trait locus for specific language and reading deficits on chromosome 6p
    • Gayan J., Smith S.D., Cherny S.S., Cardon L.R., Fulker D.W., Brower A.M., et al. Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet. 1999, 64:157-164.
    • (1999) Am J Hum Genet. , vol.64 , pp. 157-164
    • Gayan, J.1    Smith, S.D.2    Cherny, S.S.3    Cardon, L.R.4    Fulker, D.W.5    Brower, A.M.6
  • 90
    • 3543029197 scopus 로고    scopus 로고
    • Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses
    • Deffenbacher K.E., Kenyon J.B., Hoover D.M., Olson R.K., Pennington B.F., DeFries J.C., et al. Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet. 2004, 115:128-138.
    • (2004) Hum Genet. , vol.115 , pp. 128-138
    • Deffenbacher, K.E.1    Kenyon, J.B.2    Hoover, D.M.3    Olson, R.K.4    Pennington, B.F.5    DeFries, J.C.6
  • 91
    • 28044465597 scopus 로고    scopus 로고
    • DCDC2 is associated with reading disability and modulates neuronal development in the brain
    • Meng H., Smith S.D., Hager K., Held M., Liu J., Olson R.K., et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Nat Acad Sci U S A. 2005, 102:17053-17058.
    • (2005) Proc Nat Acad Sci U S A. , vol.102 , pp. 17053-17058
    • Meng, H.1    Smith, S.D.2    Hager, K.3    Held, M.4    Liu, J.5    Olson, R.K.6
  • 92
    • 0034462394 scopus 로고    scopus 로고
    • Male sexual dysfunction in mice bearing targeted mutant alleles of the PEA3 ets gene
    • Laing M.A., Coonrod S., Hinton B.T., Downie J.W., Tozer R., Rudnicki M.A., et al. Male sexual dysfunction in mice bearing targeted mutant alleles of the PEA3 ets gene. Mol Cell Biol. 2000, 20:9337-9345.
    • (2000) Mol Cell Biol. , vol.20 , pp. 9337-9345
    • Laing, M.A.1    Coonrod, S.2    Hinton, B.T.3    Downie, J.W.4    Tozer, R.5    Rudnicki, M.A.6
  • 93
    • 0037806030 scopus 로고    scopus 로고
    • Neurotrophins and netrins require calcineurin/NFAT signaling to stimulate outgrowth of embryonic axons
    • Graef I.A., Wang F., Charron F., Chen L., Neilson J., Tessier-Lavigne M., et al. Neurotrophins and netrins require calcineurin/NFAT signaling to stimulate outgrowth of embryonic axons. Cell. 2003, 113:657-670.
    • (2003) Cell. , vol.113 , pp. 657-670
    • Graef, I.A.1    Wang, F.2    Charron, F.3    Chen, L.4    Neilson, J.5    Tessier-Lavigne, M.6
  • 94
    • 0033153135 scopus 로고    scopus 로고
    • Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons
    • Francis F., Koulakoff A., Boucher D., Chafey P., Schaar B., Vinet M.C., et al. Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons. Neuron. 1999, 23:247-256.
    • (1999) Neuron. , vol.23 , pp. 247-256
    • Francis, F.1    Koulakoff, A.2    Boucher, D.3    Chafey, P.4    Schaar, B.5    Vinet, M.C.6
  • 95
    • 17444444915 scopus 로고    scopus 로고
    • A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
    • Des Portes V., Pinard J.M., Billuart P., Vinet M.C., Koulakoff A., Carrie A., et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell. 1998, 92:51-61.
    • (1998) Cell. , vol.92 , pp. 51-61
    • Des Portes, V.1    Pinard, J.M.2    Billuart, P.3    Vinet, M.C.4    Koulakoff, A.5    Carrie, A.6
  • 96
    • 40949114128 scopus 로고    scopus 로고
    • Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat
    • Burbridge T.J., Wang Y., Volz A.J., Peschansky V.J., Lisann L., Galaburda A.M., et al. Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. Neuroscience. 2008, 152:723-733.
    • (2008) Neuroscience. , vol.152 , pp. 723-733
    • Burbridge, T.J.1    Wang, Y.2    Volz, A.J.3    Peschansky, V.J.4    Lisann, L.5    Galaburda, A.M.6
  • 99
    • 8844258018 scopus 로고    scopus 로고
    • A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
    • Francks C., Paracchini S., Smith S.D., Richardson A.J., Scerri T.S., Cardon L.R., et al. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet. 2004, 75:1046-1058.
    • (2004) Am J Hum Genet. , vol.75 , pp. 1046-1058
    • Francks, C.1    Paracchini, S.2    Smith, S.D.3    Richardson, A.J.4    Scerri, T.S.5    Cardon, L.R.6
  • 100
    • 15944372645 scopus 로고    scopus 로고
    • Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
    • Cope N., Harold D., Hill G., Moskvina V., Stevenson J., Holmans P., et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet. 2005, 76:581-591.
    • (2005) Am J Hum Genet. , vol.76 , pp. 581-591
    • Cope, N.1    Harold, D.2    Hill, G.3    Moskvina, V.4    Stevenson, J.5    Holmans, P.6
  • 101
    • 9144269126 scopus 로고    scopus 로고
    • A transcription map of the 6p22.3 reading disability locus identifying candidate genes
    • Londin E.R., Meng H., Gruen J.R. A transcription map of the 6p22.3 reading disability locus identifying candidate genes. BMC Genomics. 2003, 4:25.
    • (2003) BMC Genomics. , vol.4 , pp. 25
    • Londin, E.R.1    Meng, H.2    Gruen, J.R.3
  • 102
    • 33744920683 scopus 로고    scopus 로고
    • The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
    • Paracchini S., Thomas A., Castro S., Lai C., Paramasivam M., Wang Y., et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet. 2006, 15:1659-1666.
    • (2006) Hum Mol Genet. , vol.15 , pp. 1659-1666
    • Paracchini, S.1    Thomas, A.2    Castro, S.3    Lai, C.4    Paramasivam, M.5    Wang, Y.6
  • 103
    • 40549144021 scopus 로고    scopus 로고
    • The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms
    • Velayos-Baeza A., Toma C., Paracchini S., Monaco A.P. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Hum Mol Genet. 2008, 17:859-871.
    • (2008) Hum Mol Genet. , vol.17 , pp. 859-871
    • Velayos-Baeza, A.1    Toma, C.2    Paracchini, S.3    Monaco, A.P.4
  • 105
    • 33845246158 scopus 로고    scopus 로고
    • Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
    • Harold D., Paracchini S., Scerri T., Dennis M., Cope N., Hill G., et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry. 2006, 11:1085-1091.
    • (2006) Mol Psychiatry. , vol.11 , pp. 1085-1091
    • Harold, D.1    Paracchini, S.2    Scerri, T.3    Dennis, M.4    Cope, N.5    Hill, G.6
  • 106
    • 34548473808 scopus 로고    scopus 로고
    • A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
    • Luciano M., Lind P.A., Duffy D.L., Castles A., Wright M.J., Montgomery G.W., et al. A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry. 2007, 62:811-817.
    • (2007) Biol Psychiatry. , vol.62 , pp. 811-817
    • Luciano, M.1    Lind, P.A.2    Duffy, D.L.3    Castles, A.4    Wright, M.J.5    Montgomery, G.W.6
  • 108
    • 33744925717 scopus 로고    scopus 로고
    • Genes, cognition and dyslexia: learning to read the genome
    • Fisher S.E., Francks C. Genes, cognition and dyslexia: learning to read the genome. Trends Cogn Sci. 2006, 10:250-257.
    • (2006) Trends Cogn Sci. , vol.10 , pp. 250-257
    • Fisher, S.E.1    Francks, C.2
  • 110
    • 0038577166 scopus 로고    scopus 로고
    • A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
    • Kaminen N., Hannula-Jouppi K., Kestila M., Lahermo P., Muller K., Kaaranen M., et al. A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J Med Genet. 2003, 40:340-345.
    • (2003) J Med Genet. , vol.40 , pp. 340-345
    • Kaminen, N.1    Hannula-Jouppi, K.2    Kestila, M.3    Lahermo, P.4    Muller, K.5    Kaaranen, M.6
  • 111
    • 21844460777 scopus 로고    scopus 로고
    • A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
    • Raskind W.H., Igo R.P., Chapman N.H., Berninger V.W., Thomson J.B., Matsushita M., et al. A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. Mol Psychiatry. 2005, 10:699-711.
    • (2005) Mol Psychiatry. , vol.10 , pp. 699-711
    • Raskind, W.H.1    Igo, R.P.2    Chapman, N.H.3    Berninger, V.W.4    Thomson, J.B.5    Matsushita, M.6
  • 112
    • 0036217207 scopus 로고    scopus 로고
    • Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1
    • Francks C., Fisher S.E., Olson R.K., Pennington B.F., Smith S.D., Defries J.C., et al. Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric Genet. 2002, 12:35-41.
    • (2002) Psychiatric Genet. , vol.12 , pp. 35-41
    • Francks, C.1    Fisher, S.E.2    Olson, R.K.3    Pennington, B.F.4    Smith, S.D.5    Defries, J.C.6
  • 113
    • 34247092473 scopus 로고    scopus 로고
    • A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
    • Anthoni H., Zucchelli M., Matsson H., et al. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet. 2007, 16:667-677.
    • (2007) Hum Mol Genet. , vol.16 , pp. 667-677
    • Anthoni, H.1    Zucchelli, M.2    Matsson, H.3
  • 114
    • 0035416644 scopus 로고    scopus 로고
    • The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders
    • Kenmochi N., Suzuki T., Uechi T., Magoori M., Kuniba M., Higa S., et al. The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders. Genomics. 2001, 77:65-70.
    • (2001) Genomics. , vol.77 , pp. 65-70
    • Kenmochi, N.1    Suzuki, T.2    Uechi, T.3    Magoori, M.4    Kuniba, M.5    Higa, S.6
  • 115
    • 0032853876 scopus 로고    scopus 로고
    • Molecular analysis of the GCF gene identifies revisions to the cDNA and amino acid sequences
    • Takimoto M., Mao P., Wei G., Yamazaki H., Miura T., Johnson A.C., et al. Molecular analysis of the GCF gene identifies revisions to the cDNA and amino acid sequences. Biochim Biophys Acta. 1999, 1447:125-131.
    • (1999) Biochim Biophys Acta. , vol.1447 , pp. 125-131
    • Takimoto, M.1    Mao, P.2    Wei, G.3    Yamazaki, H.4    Miura, T.5    Johnson, A.C.6
  • 118
    • 33746263663 scopus 로고    scopus 로고
    • Breakthroughs in the search for dyslexia candidate genes
    • McGrath L.M., Smith S.D., Pennington B.F. Breakthroughs in the search for dyslexia candidate genes. Trends Mol Med. 2006, 12:333-341.
    • (2006) Trends Mol Med. , vol.12 , pp. 333-341
    • McGrath, L.M.1    Smith, S.D.2    Pennington, B.F.3
  • 119
    • 0032559219 scopus 로고    scopus 로고
    • Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors
    • Kidd T., Brose K., Mitchell K.J., Fetter R.D., Tessier-Lavigne M., Goodman C.S., et al. Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors. Cell. 1998, 92:205-215.
    • (1998) Cell. , vol.92 , pp. 205-215
    • Kidd, T.1    Brose, K.2    Mitchell, K.J.3    Fetter, R.D.4    Tessier-Lavigne, M.5    Goodman, C.S.6
  • 120
    • 0037122889 scopus 로고    scopus 로고
    • Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain
    • Bagri A., Marin O., Plump A.S., Mak J., Pleasure S.J., Rubenstein J.L.R., et al. Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain. Neuron. 2002, 33:233-248.
    • (2002) Neuron. , vol.33 , pp. 233-248
    • Bagri, A.1    Marin, O.2    Plump, A.S.3    Mak, J.4    Pleasure, S.J.5    Rubenstein, J.L.R.6
  • 121
    • 0035831296 scopus 로고    scopus 로고
    • Hierarchical organization of guidance receptors: silencing of netrin attraction by Slit through a Robo/DCC receptor complex
    • Stein E., Tessier-Lavigne M. Hierarchical organization of guidance receptors: silencing of netrin attraction by Slit through a Robo/DCC receptor complex. Science. 2001, 291:1928-1938.
    • (2001) Science. , vol.291 , pp. 1928-1938
    • Stein, E.1    Tessier-Lavigne, M.2
  • 123
    • 0032761073 scopus 로고    scopus 로고
    • Prevalence of speech delay in 6-year-old children and comorbidity with language impairment
    • Shriberg L.D., Tomblin J.B., McSweeny J.L. Prevalence of speech delay in 6-year-old children and comorbidity with language impairment. J Speech Lang Hear Res. 1999, 42:1461-1481.
    • (1999) J Speech Lang Hear Res. , vol.42 , pp. 1461-1481
    • Shriberg, L.D.1    Tomblin, J.B.2    McSweeny, J.L.3
  • 125
    • 18544365699 scopus 로고    scopus 로고
    • Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
    • Fisher S.E., Francks C., Marlow A.J., MacPhie I.L., Newbury D.F., Cardon L.R., et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet. 2002, 30:86-91.
    • (2002) Nat Genet. , vol.30 , pp. 86-91
    • Fisher, S.E.1    Francks, C.2    Marlow, A.J.3    MacPhie, I.L.4    Newbury, D.F.5    Cardon, L.R.6
  • 126
    • 0036779497 scopus 로고    scopus 로고
    • Developmental dyslexia: genetic dissection of a complex cognitive trait
    • Fisher S.E., DeFries J.C. Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci. 2002, 3:767-780.
    • (2002) Nat Rev Neurosci. , vol.3 , pp. 767-780
    • Fisher, S.E.1    DeFries, J.C.2
  • 128
    • 0343729909 scopus 로고    scopus 로고
    • Secretin, glucagon, gastric inhibitory polypeptide, parathyroid hormone, and related peptides in the regulation of the hypothalamus-pituitary-adrenal axis
    • Nussdorfer G.G., Bahcelioglu M., Neri G., Malendowicz L.K. Secretin, glucagon, gastric inhibitory polypeptide, parathyroid hormone, and related peptides in the regulation of the hypothalamus-pituitary-adrenal axis. Peptides. 2000, 21:309-324.
    • (2000) Peptides. , vol.21 , pp. 309-324
    • Nussdorfer, G.G.1    Bahcelioglu, M.2    Neri, G.3    Malendowicz, L.K.4
  • 130
    • 0030588129 scopus 로고    scopus 로고
    • Molecular cloning of a novel human gene (D11S4896E) at chromosomal region 11p15.5
    • Parker N.J., Begley C.G., Smith P.J., Fox R.M. Molecular cloning of a novel human gene (D11S4896E) at chromosomal region 11p15.5. Genomics. 1996, 37:253-256.
    • (1996) Genomics. , vol.37 , pp. 253-256
    • Parker, N.J.1    Begley, C.G.2    Smith, P.J.3    Fox, R.M.4
  • 131
    • 0033958493 scopus 로고    scopus 로고
    • Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression
    • Prawitt D., Enklaar T., Klemm G., Gartner B., Spangenberg C., Winterpacht A., et al. Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression. Hum Mol Genet. 2000, 9:203-216.
    • (2000) Hum Mol Genet. , vol.9 , pp. 203-216
    • Prawitt, D.1    Enklaar, T.2    Klemm, G.3    Gartner, B.4    Spangenberg, C.5    Winterpacht, A.6
  • 132
    • 0037162696 scopus 로고    scopus 로고
    • Ras and Rap control AMPA receptor trafficking during synaptic plasticity
    • Zhu J.J., Qin Y., Zhao M., Van Aelst L., Malinow R. Ras and Rap control AMPA receptor trafficking during synaptic plasticity. Cell. 2002, 110:443-555.
    • (2002) Cell. , vol.110 , pp. 443-555
    • Zhu, J.J.1    Qin, Y.2    Zhao, M.3    Van Aelst, L.4    Malinow, R.5
  • 134
    • 0034640706 scopus 로고    scopus 로고
    • A haplotype relative risk study of the dopamine D4 receptor (DRD4) exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD)
    • Eisenberg J., Zohar A., Mei-Tal G., Steinberg A., Tartakovsky E., Gritsenko I., et al. A haplotype relative risk study of the dopamine D4 receptor (DRD4) exon III repeat polymorphism and attention deficit hyperactivity disorder (ADHD). Am J Med Genet. 2000, 96:258-261.
    • (2000) Am J Med Genet. , vol.96 , pp. 258-261
    • Eisenberg, J.1    Zohar, A.2    Mei-Tal, G.3    Steinberg, A.4    Tartakovsky, E.5    Gritsenko, I.6
  • 135
    • 0033804337 scopus 로고    scopus 로고
    • Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD)
    • McCracken J.T., Smalley S.L., McGough J.J., Crawford L., Del'Homme M., Cantor R.M., et al. Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD). Mol Psychiatry. 2000, 5:531-536.
    • (2000) Mol Psychiatry. , vol.5 , pp. 531-536
    • McCracken, J.T.1    Smalley, S.L.2    McGough, J.J.3    Crawford, L.4    Del'Homme, M.5    Cantor, R.M.6
  • 136
    • 0035827817 scopus 로고    scopus 로고
    • Attention-deficit hyperactivity disorder: A study of association with both the dopamine transporter gene and the dopamine D4 receptor gene
    • Roman T., Schmitz M., Polanczyk G., Eizirik M., Rohde L.A., Hutz M.H. Attention-deficit hyperactivity disorder: A study of association with both the dopamine transporter gene and the dopamine D4 receptor gene. Am J Med Genet. 2001, 105:471-478.
    • (2001) Am J Med Genet. , vol.105 , pp. 471-478
    • Roman, T.1    Schmitz, M.2    Polanczyk, G.3    Eizirik, M.4    Rohde, L.A.5    Hutz, M.H.6
  • 137
    • 0034991683 scopus 로고    scopus 로고
    • Association of DRD4 with attention problems in normal childhood development
    • Schmidt L.A., Fox N.A., Perez-Edgar K., Hu S., Hamer D.H. Association of DRD4 with attention problems in normal childhood development. Psychiatr Genet. 2001, 11:25-29.
    • (2001) Psychiatr Genet. , vol.11 , pp. 25-29
    • Schmidt, L.A.1    Fox, N.A.2    Perez-Edgar, K.3    Hu, S.4    Hamer, D.H.5
  • 138
    • 0030888131 scopus 로고    scopus 로고
    • Language abilities in children with attention deficit hyperactivity disorder, reading disabilities, and normal controls
    • Purvis K.L., Tannock R. Language abilities in children with attention deficit hyperactivity disorder, reading disabilities, and normal controls. J Abnorm Child Psychol. 1997, 25:133-144.
    • (1997) J Abnorm Child Psychol. , vol.25 , pp. 133-144
    • Purvis, K.L.1    Tannock, R.2
  • 140
    • 34548676377 scopus 로고    scopus 로고
    • Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder
    • Willcutt E.G., Pennington B.F., Olson R.K., DeFries J.C. Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2007, 144:709-714.
    • (2007) Am J Med Genet B Neuropsychiatr Genet. , vol.144 , pp. 709-714
    • Willcutt, E.G.1    Pennington, B.F.2    Olson, R.K.3    DeFries, J.C.4
  • 142
    • 0030754103 scopus 로고    scopus 로고
    • II. Localization and characterization of dopamine D4binding sites in rat and human brain by use of the novel D4receptor-selective ligand [3H]NGD 94-1
    • Primus R.J., Thurkauf A., Xu J., Yevich E., McInerney S., Shaw K., et al. II. Localization and characterization of dopamine D4binding sites in rat and human brain by use of the novel D4receptor-selective ligand [3H]NGD 94-1. J Pharmacol Exp Ther. 1997, 282:1020-1027.
    • (1997) J Pharmacol Exp Ther. , vol.282 , pp. 1020-1027
    • Primus, R.J.1    Thurkauf, A.2    Xu, J.3    Yevich, E.4    McInerney, S.5    Shaw, K.6
  • 143
    • 0027256723 scopus 로고
    • Cosegregation of balanced translocation (1,2) with retarded speech development and dyslexia
    • Froster U., Schulte-Körne G., Hebebrand J., Remschmidt H. Cosegregation of balanced translocation (1,2) with retarded speech development and dyslexia. Lancet. 1993, 342:178-179.
    • (1993) Lancet. , vol.342 , pp. 178-179
    • Froster, U.1    Schulte-Körne, G.2    Hebebrand, J.3    Remschmidt, H.4
  • 144
    • 0027213075 scopus 로고
    • Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
    • Rabin M., Wen X.L., Hepburn M., Lubs H.A., Feldman E., Duara R. Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet. 1993, 342:178.
    • (1993) Lancet. , vol.342 , pp. 178
    • Rabin, M.1    Wen, X.L.2    Hepburn, M.3    Lubs, H.A.4    Feldman, E.5    Duara, R.6
  • 145
    • 57649136416 scopus 로고    scopus 로고
    • The KIAA0319-like (KIAA0319L) Gene on chromosome 1p34 as a candidate for reading disabilities
    • Couto J.M., Gomez L., Wigg K., Cate-Carter T., Archibald J., Anderson B., et al. The KIAA0319-like (KIAA0319L) Gene on chromosome 1p34 as a candidate for reading disabilities. J Neurogenet. 2008, 22:295-313.
    • (2008) J Neurogenet. , vol.22 , pp. 295-313
    • Couto, J.M.1    Gomez, L.2    Wigg, K.3    Cate-Carter, T.4    Archibald, J.5    Anderson, B.6
  • 146
    • 46349103630 scopus 로고    scopus 로고
    • Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings
    • Zhou K., Asherson P., Sham P., Franke B., Anney R.J., Buitelaar J., et al. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biol Psychiatry. 2008, 64:571-576.
    • (2008) Biol Psychiatry. , vol.64 , pp. 571-576
    • Zhou, K.1    Asherson, P.2    Sham, P.3    Franke, B.4    Anney, R.J.5    Buitelaar, J.6
  • 147
    • 4444356020 scopus 로고    scopus 로고
    • Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. J Med Genet.
    • De Kovel CGF, Hol FA, Heister JG AM, Willemen JJ HT, Sandkuijl LA, Franke B, et al. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. J Med Genet. 2004; 41:652-7.
    • (2004) , vol.41 , pp. 652-657
    • De Kovel, C.G.F.1    Hol, F.A.2    Heister, J.G.A.M.3    Willemen, J.J.H.T.4    Sandkuijl, L.A.5    Franke, B.6
  • 148
    • 2442721228 scopus 로고    scopus 로고
    • Common and specific gender influences on individual differences in reading performance: a twin study
    • Knopnik V.S., Alarcón M., DeFries J.C. Common and specific gender influences on individual differences in reading performance: a twin study. Pers Individ Dif. 1998, 25:269-277.
    • (1998) Pers Individ Dif. , vol.25 , pp. 269-277
    • Knopnik, V.S.1    Alarcón, M.2    DeFries, J.C.3
  • 150
  • 151
    • 0029123145 scopus 로고
    • Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome
    • Lugenbeel K.A., Peier A.M., Carson N.L., Chudley A.E., Nelson D.L. Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome. Nat Genet. 1995, 10:483-485.
    • (1995) Nat Genet. , vol.10 , pp. 483-485
    • Lugenbeel, K.A.1    Peier, A.M.2    Carson, N.L.3    Chudley, A.E.4    Nelson, D.L.5
  • 155
    • 0034639857 scopus 로고    scopus 로고
    • Understanding the molecular basis of fragile X syndrome
    • Jin P., Warren S.T. Understanding the molecular basis of fragile X syndrome. Hum Mol Genet. 2000, 9:901-908.
    • (2000) Hum Mol Genet. , vol.9 , pp. 901-908
    • Jin, P.1    Warren, S.T.2
  • 156
    • 0034690063 scopus 로고    scopus 로고
    • Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo
    • Lendvai B., Stern E.A., Chen B., Svoboda K. Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo. Nature. 2000, 404:876-881.
    • (2000) Nature. , vol.404 , pp. 876-881
    • Lendvai, B.1    Stern, E.A.2    Chen, B.3    Svoboda, K.4
  • 157
    • 0036301947 scopus 로고    scopus 로고
    • A decade of molecular studies of fragile X syndrome
    • O'Donnell W.T., Warren S.T. A decade of molecular studies of fragile X syndrome. Annu Rev Neurosci. 2002, 25:315-338.
    • (2002) Annu Rev Neurosci. , vol.25 , pp. 315-338
    • O'Donnell, W.T.1    Warren, S.T.2
  • 162
    • 33644860165 scopus 로고    scopus 로고
    • Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
    • Zeesman S., Nowaczyk M.J., Teshima I., Roberts W., Cardy J.O., Brian J., et al. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A. 2006, 140:509-514.
    • (2006) Am J Med Genet A. , vol.140 , pp. 509-514
    • Zeesman, S.1    Nowaczyk, M.J.2    Teshima, I.3    Roberts, W.4    Cardy, J.O.5    Brian, J.6
  • 163
    • 24944473188 scopus 로고    scopus 로고
    • Benítez-Burraco A. FOXP2: del trastorno específico a la biología molecular del lenguaje. I. Aspectos etiológicos, neuroanatómicos, neurofisiológicos y moleculares. Rev Neurol.a
    • Benítez-Burraco A. FOXP2: del trastorno específico a la biología molecular del lenguaje. I. Aspectos etiológicos, neuroanatómicos, neurofisiológicos y moleculares. Rev Neurol. 2005a;40:671-82.
    • (2005) , vol.40 , pp. 671-682
  • 164
    • 25144440534 scopus 로고    scopus 로고
    • Benítez-Burraco A. FOXP2: del trastorno específico a la biología molecular del lenguaje. II. Implicaciones para la ontogenia y la filogenia del lenguaje. Rev Neurol., b
    • Benítez-Burraco A. FOXP2: del trastorno específico a la biología molecular del lenguaje. II. Implicaciones para la ontogenia y la filogenia del lenguaje. Rev Neurol. 2005b;41:37-44.
    • (2005) , vol.41 , pp. 37-44
  • 165
    • 41849089694 scopus 로고    scopus 로고
    • Benítez-Burraco A. FOXP2 y la biología molecular del lenguaje: nuevas evidencias. I. Aspectos fenotípicos y modelos animales. Rev Neurol.a
    • Benítez-Burraco A. FOXP2 y la biología molecular del lenguaje: nuevas evidencias. I. Aspectos fenotípicos y modelos animales. Rev Neurol. 2008a;46:289-98.
    • (2008) , vol.46 , pp. 289-298
  • 166
    • 41849097045 scopus 로고    scopus 로고
    • Benítez-Burraco A. FOXP2 y la biología molecular del lenguaje: nuevas evidencias. II. Aspectos moleculares e implicaciones para la ontogenia y la filogenia del lenguaje. Rev Neurol.b
    • Benítez-Burraco A. FOXP2 y la biología molecular del lenguaje: nuevas evidencias. II. Aspectos moleculares e implicaciones para la ontogenia y la filogenia del lenguaje. Rev Neurol. 2008b;46:351-9.
    • (2008) , vol.46 , pp. 351-359
  • 167
    • 0038571125 scopus 로고    scopus 로고
    • Deciphering the genetic basis of speech and language disorders
    • Fisher S.E., Lai C.S.L., Monaco A.P. Deciphering the genetic basis of speech and language disorders. Annu Rev Neurosci. 2003, 26:57-80.
    • (2003) Annu Rev Neurosci. , vol.26 , pp. 57-80
    • Fisher, S.E.1    Lai, C.S.L.2    Monaco, A.P.3
  • 168
    • 27544444173 scopus 로고    scopus 로고
    • Genetic influences on language impairment and phonological short-term memory
    • Newbury D.F., Bishop D.V., Monaco A.P. Genetic influences on language impairment and phonological short-term memory. Trends Cogn Sci. 2005, 9:528-534.
    • (2005) Trends Cogn Sci. , vol.9 , pp. 528-534
    • Newbury, D.F.1    Bishop, D.V.2    Monaco, A.P.3
  • 169
    • 0035080409 scopus 로고    scopus 로고
    • Genetic influences on language impairment and literacy problems in child
    • Bishop D.V.M. Genetic influences on language impairment and literacy problems in child. J Child Psychol Psychiatry. 2001, 42:189-198.
    • (2001) J Child Psychol Psychiatry. , vol.42 , pp. 189-198
    • Bishop, D.V.M.1
  • 170
  • 172
    • 0028829319 scopus 로고
    • The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in children
    • Swillen A., Glorieux N., Peeters M., Fryns J.-P. The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in children. Clin Genet. 1995, 48:177-182.
    • (1995) Clin Genet. , vol.48 , pp. 177-182
    • Swillen, A.1    Glorieux, N.2    Peeters, M.3    Fryns, J.-P.4
  • 174
    • 0037810302 scopus 로고    scopus 로고
    • Molecular genetic delineation of a deletion of chromosome 13q12-q13 in a patient with autism and auditory processing deficits
    • Smith M., Woodroffe A., Smith R., Holguin S., Martinez J., Filipek P.A., et al. Molecular genetic delineation of a deletion of chromosome 13q12-q13 in a patient with autism and auditory processing deficits. Cytogenet Genome Res. 2002, 98:233-239.
    • (2002) Cytogenet Genome Res. , vol.98 , pp. 233-239
    • Smith, M.1    Woodroffe, A.2    Smith, R.3    Holguin, S.4    Martinez, J.5    Filipek, P.A.6
  • 175
    • 38549106474 scopus 로고    scopus 로고
    • Autismo y lenguaje: aspectos moleculares
    • Benítez-Burraco A. Autismo y lenguaje: aspectos moleculares. Rev Neurol. 2008, 46:40-48.
    • (2008) Rev Neurol. , vol.46 , pp. 40-48
    • Benítez-Burraco, A.1
  • 176
    • 20144386602 scopus 로고    scopus 로고
    • A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
    • Bond J., Roberts E., Springell K., Lizarraga S., Scott S., Higgins J., et al. A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nat Genet. 2005, 37:353-355.
    • (2005) Nat Genet. , vol.37 , pp. 353-355
    • Bond, J.1    Roberts, E.2    Springell, K.3    Lizarraga, S.4    Scott, S.5    Higgins, J.6
  • 177
    • 0033800738 scopus 로고    scopus 로고
    • Protein 4.1 R-135 interacts with a novel centrosomal protein (CPAP) which is associated with the gamma-tubulin complex
    • Hung L.-Y., Tang C-JC, Tang T.K. Protein 4.1 R-135 interacts with a novel centrosomal protein (CPAP) which is associated with the gamma-tubulin complex. Molec Cell Biol. 2000, 20:7813-7825.
    • (2000) Molec Cell Biol. , vol.20 , pp. 7813-7825
    • Hung, L.-Y.1    Tang, C.-J.C.2    Tang, T.K.3
  • 178
    • 2542483497 scopus 로고    scopus 로고
    • Identification of a novel microtubule-destabilizing motif in CPAP that binds to tubulin heterodimers and inhibits microtubule assembly
    • Hung L.-Y., Chen H.-L., Chang C.-W., Li B.-R., Tang T.K. Identification of a novel microtubule-destabilizing motif in CPAP that binds to tubulin heterodimers and inhibits microtubule assembly. Molec Biol Cell. 2004, 15:2697-2706.
    • (2004) Molec Biol Cell. , vol.15 , pp. 2697-2706
    • Hung, L.-Y.1    Chen, H.-L.2    Chang, C.-W.3    Li, B.-R.4    Tang, T.K.5
  • 179
    • 0036837664 scopus 로고    scopus 로고
    • Primary microcephaly: new approaches for an old disorder
    • Dobyns W.B. Primary microcephaly: new approaches for an old disorder. Am J Hum Genet. 2002, 112:315-317.
    • (2002) Am J Hum Genet. , vol.112 , pp. 315-317
    • Dobyns, W.B.1
  • 181
    • 52549109216 scopus 로고    scopus 로고
    • Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci
    • Brkanac Z., Chapman N.H., Igo R.P., Matsushita M.M., Nielsen K., Berninger V.W., et al. Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci. Behav Genet. 2008, 38:462-475.
    • (2008) Behav Genet. , vol.38 , pp. 462-475
    • Brkanac, Z.1    Chapman, N.H.2    Igo, R.P.3    Matsushita, M.M.4    Nielsen, K.5    Berninger, V.W.6
  • 183
    • 0035944532 scopus 로고    scopus 로고
    • Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, coactivates transcription with DLX homeodomain proteins
    • Yu G., Zerucha T., Ekker M., Rubenstein J.L.R. Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, coactivates transcription with DLX homeodomain proteins. Brain Res Dev Brain Res. 2001, 130:217-230.
    • (2001) Brain Res Dev Brain Res. , vol.130 , pp. 217-230
    • Yu, G.1    Zerucha, T.2    Ekker, M.3    Rubenstein, J.L.R.4
  • 184
    • 0041660965 scopus 로고    scopus 로고
    • Functional roles of protein interactions with AMPA and kainate receptors
    • Collingridge G.L., Isaac J.T.R. Functional roles of protein interactions with AMPA and kainate receptors. Neurosci Res. 2003, 47:3-15.
    • (2003) Neurosci Res. , vol.47 , pp. 3-15
    • Collingridge, G.L.1    Isaac, J.T.R.2
  • 185
    • 33744527050 scopus 로고    scopus 로고
    • Do different components of working memory underlie different subgroups of reading disabilities?
    • Swanson H.L., Howard C.B., Saez L. Do different components of working memory underlie different subgroups of reading disabilities?. J Learn Disabil. 2006, 39:252-269.
    • (2006) J Learn Disabil. , vol.39 , pp. 252-269
    • Swanson, H.L.1    Howard, C.B.2    Saez, L.3
  • 186
    • 0037178271 scopus 로고    scopus 로고
    • Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog
    • Mukhopadhyay M., Pelka P., DeSousa D., Kablar B., Schindler A., Rudnicki M.A., et al. Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog. Gene. 2002, 293:59-65.
    • (2002) Gene. , vol.293 , pp. 59-65
    • Mukhopadhyay, M.1    Pelka, P.2    DeSousa, D.3    Kablar, B.4    Schindler, A.5    Rudnicki, M.A.6
  • 187
    • 0034705117 scopus 로고    scopus 로고
    • Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin
    • Flory M.R., Moser M.J., Monnat R.J., Davis T.N. Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin. Proc Nat Acad Sci U S A. 2000, 97:5919-5923.
    • (2000) Proc Nat Acad Sci U S A. , vol.97 , pp. 5919-5923
    • Flory, M.R.1    Moser, M.J.2    Monnat, R.J.3    Davis, T.N.4
  • 189
    • 31144442752 scopus 로고    scopus 로고
    • Dyslexia-a molecular disorder of neuronal migration: the 2004 Norman Geschwind Memorial Lecture
    • Galaburda A.M. Dyslexia-a molecular disorder of neuronal migration: the 2004 Norman Geschwind Memorial Lecture. Ann Dyslexia. 2005, 55:151-165.
    • (2005) Ann Dyslexia. , vol.55 , pp. 151-165
    • Galaburda, A.M.1
  • 191
    • 0032422555 scopus 로고    scopus 로고
    • Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
    • Fox J.W., Lamperti E.D., Eksioglu Y.Z., Hong S.E., Feng Y., Graham D.A., et al. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron. 1998, 21:1315-1325.
    • (1998) Neuron. , vol.21 , pp. 1315-1325
    • Fox, J.W.1    Lamperti, E.D.2    Eksioglu, Y.Z.3    Hong, S.E.4    Feng, Y.5    Graham, D.A.6
  • 192
    • 20044379739 scopus 로고    scopus 로고
    • Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia
    • Chang B.S., Ly J., Appignani B., Bodell A., Apse K.A., Ravenscroftet R.S., et al. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology. 2005, 64:799-803.
    • (2005) Neurology. , vol.64 , pp. 799-803
    • Chang, B.S.1    Ly, J.2    Appignani, B.3    Bodell, A.4    Apse, K.A.5    Ravenscroftet, R.S.6
  • 193
    • 0031557531 scopus 로고    scopus 로고
    • Genetic dysphasia and linguistic theory
    • Newmeyer F.J. Genetic dysphasia and linguistic theory. J Neurolinguistics. 1997, 10:47-73.
    • (1997) J Neurolinguistics. , vol.10 , pp. 47-73
    • Newmeyer, F.J.1
  • 194


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.