메뉴 건너뛰기




Volumn 8, Issue JULY, 2014, Pages

Assessing the effects of common variation in the FOXP2 gene on human brain structure

Author keywords

Brain anatomy; FOXP2; Imaging genetics; Language; MRI; Transcription factor; VBM

Indexed keywords

DNA; TRANSCRIPTION FACTOR FOXP2;

EID: 84903695301     PISSN: None     EISSN: 16625161     Source Type: Journal    
DOI: 10.3389/fnhum.2014.00473     Document Type: Article
Times cited : (36)

References (51)
  • 1
    • 34548832230 scopus 로고    scopus 로고
    • A fast diffeomorphic image registration algorithm
    • doi: 10.1016/j.neuroimage.2007.07.007
    • Ashburner, J. (2007). A fast diffeomorphic image registration algorithm. Neuroimage 38, 95-113. doi: 10.1016/j.neuroimage.2007.07.007
    • (2007) Neuroimage , vol.38 , pp. 95-113
    • Ashburner, J.1
  • 2
    • 0037341876 scopus 로고    scopus 로고
    • Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia
    • doi: 10.1002/hbm.10093
    • Belton, E., Salmond, C. H., Watkins, K. E., Vargha-Khadem, F., and Gadian, D. G. (2003). Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia. Hum. Brain Mapp. 18, 194-200. doi: 10.1002/hbm.10093
    • (2003) Hum. Brain Mapp. , vol.18 , pp. 194-200
    • Belton, E.1    Salmond, C.H.2    Watkins, K.E.3    Vargha-Khadem, F.4    Gadian, D.G.5
  • 3
    • 80054815994 scopus 로고    scopus 로고
    • Association of the Alzheimer's Gene SORL1 with hippocampal volume in young, healthy adults
    • doi: 10.1176/appi.ajp.2011.10101509
    • Bralten, J., Arias-Vásquez, A., Makkinje, R., Veltman, J. A., Brunner, H. G., Fernández, G., et al. (2011). Association of the Alzheimer's Gene SORL1 with hippocampal volume in young, healthy adults. Am. J. Psychiatry 168, 1083-1089. doi: 10.1176/appi.ajp.2011.10101509
    • (2011) Am. J. Psychiatry , vol.168 , pp. 1083-1089
    • Bralten, J.1    Arias-Vásquez, A.2    Makkinje, R.3    Veltman, J.A.4    Brunner, H.G.5    Fernández, G.6
  • 4
    • 84876665206 scopus 로고    scopus 로고
    • Power failure: Why small sample size undermines the reliability of neuroscience
    • doi: 10.1038/nrn3475
    • Button, K. S., Ioannidis, J. P., Mokrysz, C., Nosek, B. A., Flint, J., Robinson, E. S., et al. (2013). Power failure: why small sample size undermines the reliability of neuroscience. Nat. Rev. Neurosci. 14, 365-376. doi: 10.1038/nrn3475
    • (2013) Nat. Rev. Neurosci. , vol.14 , pp. 365-376
    • Button, K.S.1    Ioannidis, J.P.2    Mokrysz, C.3    Nosek, B.A.4    Flint, J.5    Robinson, E.S.6
  • 5
    • 84870059030 scopus 로고    scopus 로고
    • Schizophrenia risk gene ZNF804A does not influence macroscopic brain structure: An MRI study in 892 volunteers
    • doi: 10.1038/mp.2011.181
    • Cousijn, H., Rijpkema, M., Harteveld, A., Harrison, P. J., Fernández, G., Franke, B., et al. (2012). Schizophrenia risk gene ZNF804A does not influence macroscopic brain structure: an MRI study in 892 volunteers. Mol. Psychiatry 17, 1155-1157. doi: 10.1038/mp.2011.181
    • (2012) Mol. Psychiatry , vol.17 , pp. 1155-1157
    • Cousijn, H.1    Rijpkema, M.2    Harteveld, A.3    Harrison, P.J.4    Fernández, G.5    Franke, B.6
  • 6
    • 84928589716 scopus 로고    scopus 로고
    • Neurogenomics of speech and language disorders: The road ahead
    • doi: 10.1186/gb-2013-14-4-204
    • Deriziotis, P., and Fisher, S. E. (2013). Neurogenomics of speech and language disorders: the road ahead. Genome Biol. 14:204. doi: 10.1186/gb-2013-14-4-204
    • (2013) Genome Biol. , vol.14 , pp. 204
    • Deriziotis, P.1    Fisher, S.E.2
  • 7
    • 34547145165 scopus 로고    scopus 로고
    • G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences
    • doi: 10.3758/BF03193146
    • Faul, F., Erdfelder, E., Lang, A. G., and Buchner, A. (2007). G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav. Res. Methods 39, 175-191. doi: 10.3758/BF03193146
    • (2007) Behav. Res. Methods , vol.39 , pp. 175-191
    • Faul, F.1    Erdfelder, E.2    Lang, A.G.3    Buchner, A.4
  • 8
    • 33747190655 scopus 로고    scopus 로고
    • Tangled webs: Tracing the connections between genes and cognition
    • doi: 10.1016/j.cognition.2006.04.004
    • Fisher, S. E. (2006). Tangled webs: tracing the connections between genes and cognition. Cognition 101, 270-297. doi: 10.1016/j.cognition.2006.04.004
    • (2006) Cognition , vol.101 , pp. 270-297
    • Fisher, S.E.1
  • 9
    • 63449102727 scopus 로고    scopus 로고
    • FOXP2 as a molecular window into speech and language
    • doi: 10.1016/j.tig.2009.03.002
    • Fisher, S. E., and Scharff, C. (2009). FOXP2 as a molecular window into speech and language. Trends Genet. 25, 166-177. doi: 10.1016/j.tig.2009.03.002
    • (2009) Trends Genet. , vol.25 , pp. 166-177
    • Fisher, S.E.1    Scharff, C.2
  • 10
    • 0031940694 scopus 로고    scopus 로고
    • Localisation of a gene implicated in a severe speech and language disorder
    • doi: 10.1038/ng0298-168
    • Fisher, S. E., Vargha-Khadem, F., Watkins, K. E., Monaco, A. P., and Pembrey, M. E. (1998). Localisation of a gene implicated in a severe speech and language disorder. Nat. Genet. 18, 168-170. doi: 10.1038/ng0298-168
    • (1998) Nat. Genet. , vol.18 , pp. 168-170
    • Fisher, S.E.1    Vargha-Khadem, F.2    Watkins, K.E.3    Monaco, A.P.4    Pembrey, M.E.5
  • 11
    • 77956174929 scopus 로고    scopus 로고
    • Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individuals
    • doi: 10.1016/j.biopsych.2010.05.037
    • Franke, B., Vasquez, A. A., Veltman, J. A., Brunner, H. G., Rijpkema, M., and Fernández, G. (2010). Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individuals. Biol. Psychiatry 68, 586-588. doi: 10.1016/j.biopsych.2010.05.037
    • (2010) Biol. Psychiatry , vol.68 , pp. 586-588
    • Franke, B.1    Vasquez, A.A.2    Veltman, J.A.3    Brunner, H.G.4    Rijpkema, M.5    Fernández, G.6
  • 12
    • 84867896115 scopus 로고    scopus 로고
    • An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
    • doi: 10.1038/mp.2011.105
    • French, C. A., Jin, X., Campbell, T. G., Gerfen, E., Groszer, M., Fisher, S. E., et al. (2012). An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. Mol. psychiatry 17, 1077-1085. doi: 10.1038/mp.2011.105
    • (2012) Mol. psychiatry , vol.17 , pp. 1077-1085
    • French, C.A.1    Jin, X.2    Campbell, T.G.3    Gerfen, E.4    Groszer, M.5    Fisher, S.E.6
  • 13
    • 84872857437 scopus 로고    scopus 로고
    • Decoding the genetics of speech and language
    • doi: 10.1016/j.conb.2012.11.006
    • Graham, S. A., and Fisher, S. E. (2013). Decoding the genetics of speech and language. Curr. Opin. Neurobiol. 23, 43-51. doi: 10.1016/j.conb.2012.11.006
    • (2013) Curr. Opin. Neurobiol. , vol.23 , pp. 43-51
    • Graham, S.A.1    Fisher, S.E.2
  • 14
    • 40149112272 scopus 로고    scopus 로고
    • Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
    • doi: 10.1016/j.cub.2008.01.060
    • Groszer, M., Keays, D. A., Deacon, R. M., De Bono, J. P., Prasad-Mulcare, S., Gaub, S., et al. (2008). Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr. Biol. 18, 354-362. doi: 10.1016/j.cub.2008.01.060
    • (2008) Curr. Biol. , vol.18 , pp. 354-362
    • Groszer, M.1    Keays, D.A.2    Deacon, R.M.3    De Bono, J.P.4    Prasad-Mulcare, S.5    Gaub, S.6
  • 15
    • 84902205457 scopus 로고    scopus 로고
    • Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets
    • doi: 10.1002/hbm.22401
    • Guadalupe, T., Zwiers, M. P., Teumer, A., Wittfeld, K., Vasquez, A. A., Hoogman, M., et al. (2014). Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets. Hum. Brain Mapp. 35, 3277-3289. doi: 10.1002/hbm.22401
    • (2014) Hum. Brain Mapp. , vol.35 , pp. 3277-3289
    • Guadalupe, T.1    Zwiers, M.P.2    Teumer, A.3    Wittfeld, K.4    Vasquez, A.A.5    Hoogman, M.6
  • 16
    • 38549176222 scopus 로고    scopus 로고
    • Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X
    • doi: 10.1371/journal.pbio.0050321
    • Haesler, S., Rochefort, C., Georgi, B., Licznerski, P., Osten, P., and Scharff, C. (2007). Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS Biol. 5:e321. doi: 10.1371/journal.pbio.0050321
    • (2007) PLoS Biol. , vol.5
    • Haesler, S.1    Rochefort, C.2    Georgi, B.3    Licznerski, P.4    Osten, P.5    Scharff, C.6
  • 17
    • 2942595874 scopus 로고    scopus 로고
    • Nonstationary cluster-size inference with random field and permutation methods
    • doi: 10.1016/j.neuroimage.2004.01.041
    • Hayasaka, S., Phan, K. L., Liberzon, I., Worsley, K. J., and Nichols, T. E. (2004). Nonstationary cluster-size inference with random field and permutation methods. Neuroimage 22, 676-687. doi: 10.1016/j.neuroimage.2004.01.041
    • (2004) Neuroimage , vol.22 , pp. 676-687
    • Hayasaka, S.1    Phan, K.L.2    Liberzon, I.3    Worsley, K.J.4    Nichols, T.E.5
  • 18
    • 62749102750 scopus 로고    scopus 로고
    • MRI-derived measurements of human subcortical, ventricular and intracranial brain volumes: Reliability effects of scan sessions, acquisition sequences, data analyses, scanner upgrade, scanner vendors and field strengths
    • doi: 10.1016/j.neuroimage.2009.02.010
    • Jovicich, J., Czanner, S., Han, X., Salat, D., Van Der Kouwe, A., Quinn, B., et al. (2009). MRI-derived measurements of human subcortical, ventricular and intracranial brain volumes: reliability effects of scan sessions, acquisition sequences, data analyses, scanner upgrade, scanner vendors and field strengths. Neuroimage 46, 177-192. doi: 10.1016/j.neuroimage.2009.02.010
    • (2009) Neuroimage , vol.46 , pp. 177-192
    • Jovicich, J.1    Czanner, S.2    Han, X.3    Salat, D.4    Van Der Kouwe, A.5    Quinn, B.6
  • 19
    • 40349083853 scopus 로고    scopus 로고
    • De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment
    • doi: 10.1097/MCD.0b013e3282f17688
    • Kosho, T., Sakazume, S., Kawame, H., Wakui, K., Wada, T., Okoshi, Y., et al. (2008). De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment. Clin. Dysmorphol. 17, 31-34. doi: 10.1097/MCD.0b013e3282f17688
    • (2008) Clin. Dysmorphol. , vol.17 , pp. 31-34
    • Kosho, T.1    Sakazume, S.2    Kawame, H.3    Wakui, K.4    Wada, T.5    Okoshi, Y.6
  • 20
    • 84857853508 scopus 로고    scopus 로고
    • Foxp2 mutations impair auditory-motor association learning
    • doi: 10.1371/journal.pone.0033130
    • Kurt, S., Fisher, S. E., and Ehret, G. (2012). Foxp2 mutations impair auditory-motor association learning. PloS ONE 7:e33130. doi: 10.1371/journal.pone.0033130
    • (2012) PloS ONE , vol.7
    • Kurt, S.1    Fisher, S.E.2    Ehret, G.3
  • 21
    • 84869074313 scopus 로고    scopus 로고
    • Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization
    • doi: 10.1038/gim.2012.72
    • Laffin, J. J., Raca, G., Jackson, C. A., Strand, E. A., Jakielski, K. J., and Shriberg, L. D. (2012). Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization. Genet. Med. 14, 928-936. doi: 10.1038/gim.2012.72
    • (2012) Genet. Med. , vol.14 , pp. 928-936
    • Laffin, J.J.1    Raca, G.2    Jackson, C.A.3    Strand, E.A.4    Jakielski, K.J.5    Shriberg, L.D.6
  • 22
    • 0035807360 scopus 로고    scopus 로고
    • A forkhead-domain gene is mutated in a severe speech and language disorder
    • doi: 10.1038/35097076
    • Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F., and Monaco, A. P. (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413, 519-523. doi: 10.1038/35097076
    • (2001) Nature , vol.413 , pp. 519-523
    • Lai, C.S.1    Fisher, S.E.2    Hurst, J.A.3    Vargha-Khadem, F.4    Monaco, A.P.5
  • 23
    • 0142153166 scopus 로고    scopus 로고
    • FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
    • doi: 10.1093/brain/awg247
    • Lai, C. S., Gerrelli, D., Monaco, A. P., Fisher, S. E., and Copp, A. J. (2003). FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 126, 2455-2462. doi: 10.1093/brain/awg247
    • (2003) Brain , vol.126 , pp. 2455-2462
    • Lai, C.S.1    Gerrelli, D.2    Monaco, A.P.3    Fisher, S.E.4    Copp, A.J.5
  • 25
    • 21044445447 scopus 로고    scopus 로고
    • Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
    • doi: 10.1086/430841
    • MacDermot, K. D., Bonora, E., Sykes, N., Coupe, A. M., Lai, C. S., Vernes, S. C., et al. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am. J. Hum. Genet. 76, 1074-1080. doi: 10.1086/430841
    • (2005) Am. J. Hum. Genet. , vol.76 , pp. 1074-1080
    • McDermot, K.D.1    Bonora, E.2    Sykes, N.3    Coupe, A.M.4    Lai, C.S.5    Vernes, S.C.6
  • 26
    • 84890493080 scopus 로고    scopus 로고
    • Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability
    • doi: 10.1016/j.neuron.2013.09.021
    • Murugan, M., Harward, S., Scharff, C., and Mooney, R. (2013). Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability. Neuron 80, 1464-1476. doi: 10.1016/j.neuron.2013.09.021
    • (2013) Neuron , vol.80 , pp. 1464-1476
    • Murugan, M.1    Harward, S.2    Scharff, C.3    Mooney, R.4
  • 27
    • 84880889694 scopus 로고    scopus 로고
    • FOXP2 variation modulates functional hemispheric asymmetries for speech perception
    • doi: 10.1016/j.bandl.2013.07.001
    • Ocklenburg, S., Arning, L., Gerding, W. M., Epplen, J. T., Gunturkun, O., and Beste, C. (2013). FOXP2 variation modulates functional hemispheric asymmetries for speech perception. Brain Lang. 126, 279-284. doi: 10.1016/j.bandl.2013.07.001
    • (2013) Brain Lang. , vol.126 , pp. 279-284
    • Ocklenburg, S.1    Arning, L.2    Gerding, W.M.3    Epplen, J.T.4    Gunturkun, O.5    Beste, C.6
  • 28
    • 78650659382 scopus 로고    scopus 로고
    • The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration
    • doi: 10.3233/JAD-2010-101206
    • Padovani, A., Cosseddu, M., Premi, E., Archetti, S., Papetti, A., Agosti, C., et al. (2010). The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration. J. Alzheimers Dis. 22, 923-931. doi: 10.3233/JAD-2010-101206
    • (2010) J. Alzheimers Dis. , vol.22 , pp. 923-931
    • Padovani, A.1    Cosseddu, M.2    Premi, E.3    Archetti, S.4    Papetti, A.5    Agosti, C.6
  • 29
    • 84855256715 scopus 로고    scopus 로고
    • Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment
    • doi: 10.1542/peds.2010-2094
    • Palka, C., Alfonsi, M., Mohn, A., Cerbo, R., Guanciali Franchi, P., Fantasia, D., et al. (2012). Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. Pediatrics 129, e183-e188. doi: 10.1542/peds.2010-2094
    • (2012) Pediatrics , vol.129
    • Palka, C.1    Alfonsi, M.2    Mohn, A.3    Cerbo, R.4    Guanciali Franchi, P.5    Fantasia, D.6
  • 30
    • 79952706051 scopus 로고    scopus 로고
    • Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
    • doi: 10.1007/s11689-010-9065-0
    • Peter, B., Raskind, W. H., Matsushita, M., Lisowski, M., Vu, T., Berninger, V. W., et al. (2011). Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. J. Neurodev. Disord. 3, 39-49. doi: 10.1007/s11689-010-9065-0
    • (2011) J. Neurodev. Disord. , vol.3 , pp. 39-49
    • Peter, B.1    Raskind, W.H.2    Matsushita, M.3    Lisowski, M.4    Vu, T.5    Berninger, V.W.6
  • 31
    • 84856002114 scopus 로고    scopus 로고
    • Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions
    • doi: 10.1523/JNEUROSCI.5996-10.2012
    • Pinel, P., Fauchereau, F., Moreno, A., Barbot, A., Lathrop, M., Zelenika, D., et al. (2012). Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. J. Neurosci. 32, 817-825. doi: 10.1523/JNEUROSCI.5996-10.2012
    • (2012) J. Neurosci. , vol.32 , pp. 817-825
    • Pinel, P.1    Fauchereau, F.2    Moreno, A.3    Barbot, A.4    Lathrop, M.5    Zelenika, D.6
  • 32
    • 84858023007 scopus 로고    scopus 로고
    • FOXP2, APOE, and PRNP: New modulators in primary progressive aphasia
    • doi: 10.3233/JAD-2011-111541
    • Premi, E., Pilotto, A., Alberici, A., Papetti, A., Archetti, S., Seripa, D., et al. (2012). FOXP2, APOE, and PRNP: new modulators in primary progressive aphasia. J. Alzheimers Dis. 28, 941-950. doi: 10.3233/JAD-2011-111541
    • (2012) J. Alzheimers Dis. , vol.28 , pp. 941-950
    • Premi, E.1    Pilotto, A.2    Alberici, A.3    Papetti, A.4    Archetti, S.5    Seripa, D.6
  • 33
    • 34548292504 scopus 로고    scopus 로고
    • PLINK: A tool set for whole-genome association and population-based linkage analyses
    • doi: 10.1086/519795
    • Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A., Bender, D., et al. (2007). PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559-575. doi: 10.1086/519795
    • (2007) Am. J. Hum. Genet. , vol.81 , pp. 559-575
    • Purcell, S.1    Neale, B.2    Todd-Brown, K.3    Thomas, L.4    Ferreira, M.A.5    Bender, D.6
  • 35
    • 33749253516 scopus 로고    scopus 로고
    • Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations
    • doi: 10.1097/01.ypg.0000185029.35558.bb
    • Sanjuán, J., Tolosa, A., González, J. C., Aguilar, E. J., Pérez-Tur, J., Nájera, C., et al. (2006). Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. Psychiatr. Genet. 16, 67-72. doi: 10.1097/01.ypg.0000185029.35558.bb
    • (2006) Psychiatr. Genet. , vol.16 , pp. 67-72
    • Sanjuán, J.1    Tolosa, A.2    González, J.C.3    Aguilar, E.J.4    Pérez-Tur, J.5    Nájera, C.6
  • 36
    • 77958498211 scopus 로고    scopus 로고
    • Knockdown of FoxP2 alters spine density in Area X of the zebra finch
    • doi: 10.1111/j.1601-183X.2010.00607.x
    • Schulz, S. B., Haesler, S., Scharff, C., and Rochefort, C. (2010). Knockdown of FoxP2 alters spine density in Area X of the zebra finch. Genes Brain Behav. 9, 732-740. doi: 10.1111/j.1601-183X.2010.00607.x
    • (2010) Genes Brain Behav. , vol.9 , pp. 732-740
    • Schulz, S.B.1    Haesler, S.2    Scharff, C.3    Rochefort, C.4
  • 37
    • 33749869970 scopus 로고    scopus 로고
    • Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
    • doi: 10.1044/1092-4388(2006/038)
    • Shriberg, L. D., Ballard, K. J., Tomblin, J. B., Duffy, J. R., Odell, K. H., and Williams, C. A. (2006). Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. J. Speech Lang. Hear. Res. 49, 500-525. doi: 10.1044/1092-4388(2006/038)
    • (2006) J. Speech Lang. Hear. Res. , vol.49 , pp. 500-525
    • Shriberg, L.D.1    Ballard, K.J.2    Tomblin, J.B.3    Duffy, J.R.4    Odell, K.H.5    Williams, C.A.6
  • 38
    • 79952899733 scopus 로고    scopus 로고
    • Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients
    • doi: 10.1016/j.neulet.2011.02.024
    • Španiel, F., Horáček, J., Tintěra, J., Ibrahim, I., Novák, T., Čermák, J., et al. (2011). Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients. Neurosci. Lett. 493, 131-135. doi: 10.1016/j.neulet.2011.02.024
    • (2011) Neurosci. Lett. , vol.493 , pp. 131-135
    • Španiel, F.1    Horáček, J.2    Tintěra, J.3    Ibrahim, I.4    Novák, T.5    Čermák, J.6
  • 39
    • 77954803062 scopus 로고    scopus 로고
    • FOXP2 gene and language impairment in schizophrenia: Association and epigenetic studies
    • doi: 10.1186/1471-2350-11-114
    • Tolosa, A., Sanjuán, J., Dagnall, A. M., Moltó, M. D., Herrero, N., and De Frutos, R. (2010). FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies. BMC Med. Genet. 11:114. doi: 10.1186/1471-2350-11-114
    • (2010) BMC Med. Genet. , vol.11 , pp. 114
    • Tolosa, A.1    Sanjuán, J.2    Dagnall, A.M.3    Moltó, M.D.4    Herrero, N.5    De Frutos, R.6
  • 40
    • 84881666129 scopus 로고    scopus 로고
    • Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria
    • doi: 10.1002/ajmg.a.36055
    • Turner, S. J., Hildebrand, M. S., Block, S., Damiano, J., Fahey, M., Reilly, S., et al. (2013). Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. Am. J. Med. Genet. A 161, 2321-2326. doi: 10.1002/ajmg.a.36055
    • (2013) Am. J. Med. Genet. A , vol.161 , pp. 2321-2326
    • Turner, S.J.1    Hildebrand, M.S.2    Block, S.3    Damiano, J.4    Fahey, M.5    Reilly, S.6
  • 42
    • 57149090343 scopus 로고    scopus 로고
    • A functional genetic link between distinct developmental language disorders
    • doi: 10.1056/NEJMoa0802828
    • Vernes, S. C., Newbury, D. F., Abrahams, B. S., Winchester, L., Nicod, J., Groszer, M., et al. (2008). A functional genetic link between distinct developmental language disorders. New Engl. J. Med. 359, 2337-2345. doi: 10.1056/NEJMoa0802828
    • (2008) New Engl. J. Med. , vol.359 , pp. 2337-2345
    • Vernes, S.C.1    Newbury, D.F.2    Abrahams, B.S.3    Winchester, L.4    Nicod, J.5    Groszer, M.6
  • 43
    • 33749867547 scopus 로고    scopus 로고
    • Functional genetic analysis of mutations implicated in a human speech and language disorder
    • doi: 10.1093/hmg/ddl392
    • Vernes, S. C., Nicod, J., Elahi, F. M., Coventry, J. A., Kenny, N., Coupe, A. M., et al. (2006). Functional genetic analysis of mutations implicated in a human speech and language disorder. Hum. Mol. Genet. 15, 3154-3167. doi: 10.1093/hmg/ddl392
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 3154-3167
    • Vernes, S.C.1    Nicod, J.2    Elahi, F.M.3    Coventry, J.A.4    Kenny, N.5    Coupe, A.M.6
  • 44
    • 79960955811 scopus 로고    scopus 로고
    • Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
    • doi: 10.1371/journal.pgen.1002145
    • Vernes, S. C., Oliver, P. L., Spiteri, E., Lockstone, H. E., Puliyadi, R., Taylor, J. M., et al. (2011). Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet. 7:e1002145. doi: 10.1371/journal.pgen.1002145
    • (2011) PLoS Genet. , vol.7
    • Vernes, S.C.1    Oliver, P.L.2    Spiteri, E.3    Lockstone, H.E.4    Puliyadi, R.5    Taylor, J.M.6
  • 45
    • 36749013035 scopus 로고    scopus 로고
    • High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
    • doi: 10.1086/522238
    • Vernes, S. C., Spiteri, E., Nicod, J., Groszer, M., Taylor, J. M., Davies, K. E., et al. (2007). High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Am. J. Hum. Genet. 81, 1232-1250. doi: 10.1086/522238
    • (2007) Am. J. Hum. Genet. , vol.81 , pp. 1232-1250
    • Vernes, S.C.1    Spiteri, E.2    Nicod, J.3    Groszer, M.4    Taylor, J.M.5    Davies, K.E.6
  • 46
    • 0036190947 scopus 로고    scopus 로고
    • Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia
    • doi: 10.1093/brain/awf058
    • Watkins, K. E., Dronkers, N. F., and Vargha-Khadem, F. (2002a). Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain 125, 452-464. doi: 10.1093/brain/awf058
    • (2002) Brain , vol.125 , pp. 452-464
    • Watkins, K.E.1    Dronkers, N.F.2    Vargha-Khadem, F.3
  • 47
    • 0036188886 scopus 로고    scopus 로고
    • MRI analysis of an inherited speech and language disorder: Structural brain abnormalities
    • doi: 10.1093/brain/awf057
    • Watkins, K. E., Vargha-Khadem, F., Ashburner, J., Passingham, R. E., Connelly, A., Friston, K. J., et al. (2002b). MRI analysis of an inherited speech and language disorder: structural brain abnormalities. Brain 125, 465-478. doi: 10.1093/brain/awf057
    • (2002) Brain , vol.125 , pp. 465-478
    • Watkins, K.E.1    Vargha-Khadem, F.2    Ashburner, J.3    Passingham, R.E.4    Connelly, A.5    Friston, K.J.6
  • 48
    • 79958067224 scopus 로고    scopus 로고
    • CNTNAP2 variants affect early language development in the general population
    • doi: 10.1111/j.1601-183X.2011.00684.x
    • Whitehouse, A. J., Bishop, D. V., Ang, Q. W., Pennell, C. E., and Fisher, S. E. (2011). CNTNAP2 variants affect early language development in the general population. Genes Brain Behav. 10, 451-456. doi: 10.1111/j.1601-183X.2011.00684.x
    • (2011) Genes Brain Behav. , vol.10 , pp. 451-456
    • Whitehouse, A.J.1    Bishop, D.V.2    Ang, Q.W.3    Pennell, C.E.4    Fisher, S.E.5
  • 50
    • 33644860165 scopus 로고    scopus 로고
    • Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
    • doi: 10.1002/ajmg.a.31110
    • Zeesman, S., Nowaczyk, M. J., Teshima, I., Roberts, W., Cardy, J. O., Brian, J., et al. (2006). Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am. J. Med. Genet. A 140, 509-514. doi: 10.1002/ajmg.a.31110
    • (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
  • 51
    • 84355166477 scopus 로고    scopus 로고
    • Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families
    • doi: 10.1002/ajmg.a.34378
    • Zilina, O., Reimand, T., Zjablovskaja, P., Mannik, K., Mannamaa, M., Traat, A., et al. (2012). Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families. Am. J. Med. Genet. A 158A, 254-256. doi: 10.1002/ajmg.a.34378
    • (2012) Am. J. Med. Genet. A , vol.158 A , pp. 254-256
    • Zilina, O.1    Reimand, T.2    Zjablovskaja, P.3    Mannik, K.4    Mannamaa, M.5    Traat, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.