-
1
-
-
0031455924
-
Prevalence of specific language impairment in kindergarten children
-
Tomblin JB, Records NL, Buckwalter P, Zhang X, Smith E, O'Brien M. Prevalence of specific language impairment in kindergarten children. J Speech Lang Hear Res 1997; 40: 1245-1260. (Pubitemid 28008821)
-
(1997)
Journal of Speech, Language, and Hearing Research
, vol.40
, Issue.6
, pp. 1245-1260
-
-
Tomblin, J.B.1
Records, N.L.2
Buckwalter, P.3
Zhang, X.4
Smith, E.5
O'Brien, M.6
-
3
-
-
0038571125
-
Deciphering the genetic basis of speech and language disorders
-
DOI 10.1146/annurev.neuro.26.041002.131144
-
Fisher SE, Lai CS, Monaco AP. Deciphering the genetic basis of speech and language disorders. Annu Rev Neurosci 2003; 26: 57-80. (Pubitemid 37064928)
-
(2003)
Annual Review of Neuroscience
, vol.26
, pp. 57-80
-
-
Fisher, S.E.1
Lai, C.S.L.2
Monaco, A.P.3
-
4
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
DOI 10.1038/35097076
-
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001; 413: 519-523. (Pubitemid 32938749)
-
(2001)
Nature
, vol.413
, Issue.6855
, pp. 519-523
-
-
Lai, C.S.L.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
5
-
-
33749867547
-
Functional genetic analysis of mutations implicated in a human speech and language disorder
-
DOI 10.1093/hmg/ddl392
-
Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM et al. Functional genetic analysis of mutations implicated in a human speech and language disorder. Hum Mol Genet 2006; 15: 3154-3167. (Pubitemid 44605496)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.21
, 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
Bird, L.E.7
Davies, K.E.8
Fisher, S.E.9
-
6
-
-
0036190947
-
Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia
-
Watkins KE, Dronkers NF, Vargha-Khadem F. Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain 2002; 125(Pt 3): 452-464. (Pubitemid 34194402)
-
(2002)
Brain
, vol.125
, Issue.3
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
7
-
-
13244292715
-
FOXP2 and the neuroanatomy of speech and language
-
DOI 10.1038/nrn1605
-
Vargha-Khadem F, Gadian DG, Copp A, Mishkin M. FOXP2 and the neuroanatomy of speech and language. Nat Rev Neurosci 2005; 6: 131-138. (Pubitemid 40188947)
-
(2005)
Nature Reviews Neuroscience
, vol.6
, Issue.2
, pp. 131-138
-
-
Vargha-Khadem, F.1
Gadian, D.G.2
Copp, A.3
Mishkin, M.4
-
8
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
DOI 10.1086/430841
-
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC et al. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet 2005; 76: 1074-1080. (Pubitemid 40705441)
-
(2005)
American Journal of Human Genetics
, vol.76
, Issue.6
, pp. 1074-1080
-
-
MacDermot, K.D.1
Bonora, E.2
Sykes, N.3
Coupe, A.-M.4
Lai, C.S.L.5
Vernes, S.C.6
Vargha-Khadem, F.7
McKenzie, F.8
Smith, R.L.9
Monaco, A.P.10
Fisher, S.E.11
-
9
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
DOI 10.1093/brain/awg247
-
Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 2003; 126(Pt 11): 2455-2462. (Pubitemid 37314435)
-
(2003)
Brain
, vol.126
, Issue.11
, pp. 2455-2462
-
-
Lai, C.S.L.1
Gerrelli, D.2
Monaco, A.P.3
Fisher, S.E.4
Copp, A.J.5
-
10
-
-
0036188886
-
MRI analysis of an inherited speech and language disorder: Structural brain abnormalities
-
Watkins KE, Vargha-Khadem F, Ashburner J, Passingham RE, Connelly A, Friston KJ et al. MRI analysis of an inherited speech and language disorder: structural brain abnormalities. Brain 2002; 125(Pt 3): 465-478. (Pubitemid 34194403)
-
(2002)
Brain
, vol.125
, Issue.3
, 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
Frackowiak, R.S.J.7
Mishkin, M.8
Gadian, D.G.9
-
11
-
-
13144255748
-
Neural basis of an inherited speech and language disorder
-
DOI 10.1073/pnas.95.21.12695
-
Vargha-Khadem F, Watkins KE, Price CJ, Ashburner J, Alcock KJ, Connelly A et al. Neural basis of an inherited speech and language disorder. Proc Natl Acad Sci USA 1998; 95: 12695-12700. (Pubitemid 28483827)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.21
, pp. 12695-12700
-
-
Vargha-Khadem, F.1
Watkins, K.E.2
Price, C.J.3
Ashburner, J.4
Alcock, K.J.5
Connelly, A.6
Frackowiak, R.S.J.7
Friston, K.J.8
Pembrey, M.E.9
Mishkin, M.10
Gadian, D.G.11
Passingham, R.E.12
-
12
-
-
0242290123
-
Language fMRI abnormalities associated with FOXP2 gene mutation
-
DOI 10.1038/nn1138
-
Liegeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F. Language fMRI abnormalities associated with FOXP2 gene mutation. Nat Neurosci 2003; 6: 1230-1237. (Pubitemid 37346045)
-
(2003)
Nature Neuroscience
, vol.6
, Issue.11
, pp. 1230-1237
-
-
Liegeois, F.1
Baldeweg, T.2
Connelly, A.3
Gadian, D.G.4
Mishkin, M.5
Vargha-Khadem, F.6
-
13
-
-
3242716663
-
Learned birdsong and the neurobiology of human language
-
DOI 10.1196/annals.1298.038
-
Jarvis ED. Learned birdsong and the neurobiology of human language. Ann NY Acad Sci 2004; 1016: 749-777. (Pubitemid 38951495)
-
(2004)
Annals of the New York Academy of Sciences
, vol.1016
, pp. 749-777
-
-
Jarvis, E.D.1
-
14
-
-
0039482686
-
On the nature and evolution of the neural bases of human language
-
Lieberman P. On the nature and evolution of the neural bases of human language. Am J Phys Anthropol 2002; 35(Suppl): 36-62. (Pubitemid 36109382)
-
(2002)
American Journal of Physical Anthropology
, Issue.SUPPL. 35
, pp. 36-62
-
-
Lieberman, P.1
-
15
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
DOI 10.1002/cne.10654
-
Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J Comp Neurol 2003; 460: 266-279. (Pubitemid 36512935)
-
(2003)
Journal of Comparative Neurology
, vol.460
, Issue.2
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
Preware, P.O.3
Morrisey, E.E.4
Walsh, C.A.5
-
16
-
-
0038054082
-
Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum
-
DOI 10.1002/jnr.10638
-
Takahashi K, Liu FC, Hirokawa K, Takahashi H. Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum. J Neurosci Res 2003; 73: 61-72. (Pubitemid 36791370)
-
(2003)
Journal of Neuroscience Research
, vol.73
, Issue.1
, pp. 61-72
-
-
Takahashi, K.1
Liu, F.-C.2
Hirokawa, K.3
Takahashi, H.4
-
17
-
-
1842610982
-
Parallel FoxP1 and FoxP2 Expression in Songbird and Human Brain Predicts Functional Interaction
-
DOI 10.1523/JNEUROSCI.5589-03.2004
-
Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA. Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. J Neurosci 2004; 24: 3152-3163. (Pubitemid 38451882)
-
(2004)
Journal of Neuroscience
, vol.24
, Issue.13
, pp. 3152-3163
-
-
Teramitsu, I.1
Kudo, L.C.2
London, S.E.3
Geschwind, D.H.4
White, S.A.5
-
18
-
-
1842454166
-
FoxP2 Expression in Avian Vocal Learners and Non-Learners
-
DOI 10.1523/JNEUROSCI.4369-03.2004
-
Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED et al. FoxP2 expression in avian vocal learners and non-learners. J Neurosci 2004; 24: 3164-3175. (Pubitemid 38451883)
-
(2004)
Journal of Neuroscience
, vol.24
, Issue.13
, pp. 3164-3175
-
-
Haesler, S.1
Wada, K.2
Nshdejan, A.3
Morrisey, E.E.4
Lints, T.5
Jarvis, E.D.6
Scharff, C.7
-
19
-
-
0342614209
-
Unified nomenclature for the winged helix/forkhead transcription factors
-
Kaestner KH, Knochel W, Martinez DE. Unified nomenclature for the winged helix/forkhead transcription factors. Genes Dev 2000; 14: 142-146. (Pubitemid 30070978)
-
(2000)
Genes and Development
, vol.14
, Issue.2
, pp. 142-146
-
-
Kaestner, K.H.1
Knochel, W.2
Martinez, D.E.3
-
20
-
-
40149112272
-
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
-
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol 2008; 18: 354-362.
-
(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
-
21
-
-
65849256049
-
A humanized version of Foxp2 affects corticobasal ganglia circuits in mice
-
Enard W, Gehre S, Hammerschmidt K, Holter SM, Blass T, Somel M et al. A humanized version of Foxp2 affects corticobasal ganglia circuits in mice. Cell 2009; 137: 961-971.
-
(2009)
Cell
, vol.137
, pp. 961-971
-
-
Enard, W.1
Gehre, S.2
Hammerschmidt, K.3
Holter, S.M.4
Blass, T.5
Somel, M.6
-
22
-
-
38549176222
-
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X
-
Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS Biol 2007; 5: e321.
-
(2007)
PLoS Biol
, vol.5
-
-
Haesler, S.1
Rochefort, C.2
Georgi, B.3
Licznerski, P.4
Osten, P.5
Scharff, C.6
-
23
-
-
3142570811
-
Differential corticostriatal plasticity during fast and slow motor skill learning in mice
-
DOI 10.1016/j.cub.2004.06.053, PII S0960982204004658
-
Costa RM, Cohen D, Nicolelis MA. Differential corticostriatal plasticity during fast and slow motor skill learning in mice. Curr Biol 2004; 14: 1124-1134. (Pubitemid 38893975)
-
(2004)
Current Biology
, vol.14
, Issue.13
, pp. 1124-1134
-
-
Costa, R.M.1
Cohen, D.2
Nicolelis, M.A.L.3
-
24
-
-
33947235559
-
Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: Revisited
-
DOI 10.1007/s00335-006-0065-z
-
Keays DA, Clark TG, Campbell TG, Broxholme J, Valdar W. Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited. Mamm Genome 2007; 18: 123-124. (Pubitemid 46425381)
-
(2007)
Mammalian Genome
, vol.18
, Issue.2
, pp. 123-124
-
-
Keays, D.A.1
Clark, T.G.2
Campbell, T.G.3
Broxholme, J.4
Valdar, W.5
-
25
-
-
0036509698
-
A gene-driven approach to the identification of ENU mutants in the mouse
-
Coghill EL, Hugill A, Parkinson N, Davison C, Glenister P, Clements S et al. A gene-driven approach to the identification of ENU mutants in the mouse. Nat Genet 2002; 30: 255-256.
-
(2002)
Nat Genet
, vol.30
, pp. 255-256
-
-
Coghill, E.L.1
Hugill, A.2
Parkinson, N.3
Davison, C.4
Glenister, P.5
Clements, S.6
-
26
-
-
60749136245
-
Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill
-
Yin HH, Mulcare SP, Hilario MR, Clouse E, Holloway T, Davis MI et al. Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill. Nat Neurosci 2009; 12: 333-341.
-
(2009)
Nat Neurosci
, vol.12
, pp. 333-341
-
-
Yin, H.H.1
Mulcare, S.P.2
Hilario, M.R.3
Clouse, E.4
Holloway, T.5
Davis, M.I.6
-
27
-
-
33745760564
-
The role of the basal ganglia in habit formation
-
DOI 10.1038/nrn1919, PII NRN1919
-
Yin HH, Knowlton BJ. The role of the basal ganglia in habit formation. Nat Rev Neurosci 2006; 7: 464-476. (Pubitemid 44012286)
-
(2006)
Nature Reviews Neuroscience
, vol.7
, Issue.6
, pp. 464-476
-
-
Yin, H.H.1
Knowlton, B.J.2
-
28
-
-
56349143278
-
Striatal plasticity and basal ganglia circuit function
-
Kreitzer AC, Malenka RC. Striatal plasticity and basal ganglia circuit function. Neuron 2008; 60: 543-554.
-
(2008)
Neuron
, vol.60
, pp. 543-554
-
-
Kreitzer, A.C.1
Malenka, R.C.2
-
29
-
-
33749591279
-
Rapid Alterations in Corticostriatal Ensemble Coordination during Acute Dopamine-Dependent Motor Dysfunction
-
DOI 10.1016/j.neuron.2006.07.030, PII S0896627306006295
-
Costa RM, Lin SC, Sotnikova TD, Cyr M, Gainetdinov RR, Caron MG et al. Rapid alterations in corticostriatal ensemble coordination during acute dopamine-dependent motor dysfunction. Neuron 2006; 52: 359-369. (Pubitemid 44548339)
-
(2006)
Neuron
, vol.52
, Issue.2
, pp. 359-369
-
-
Costa, R.M.1
Lin, S.-C.2
Sotnikova, TatyanaD.3
Cyr, M.4
Gainetdinov, RaulR.5
Caron, MarcG.6
Nicolelis, MiguelA.L.7
-
30
-
-
77954444666
-
Dissociable effects of dopamine on neuronal firing rate and synchrony in the dorsal striatum
-
Burkhardt JM, Jin X, Costa RM. Dissociable effects of dopamine on neuronal firing rate and synchrony in the dorsal striatum. Front Integr Neurosci 2009; 3: 28.
-
(2009)
Front Integr Neurosci
, vol.3
, pp. 28
-
-
Burkhardt, J.M.1
Jin, X.2
Costa, R.M.3
-
31
-
-
34547653713
-
Generation of mice with a conditional Foxp2 null allele
-
DOI 10.1002/dvg.20305
-
French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. Generation of mice with a conditional Foxp2 null allele. Genesis 2007; 45: 440-446. (Pubitemid 47221804)
-
(2007)
Genesis
, vol.45
, Issue.7
, pp. 440-446
-
-
French, C.A.1
Groszer, M.2
Preece, C.3
Coupe, A.-M.4
Rajewsky, K.5
Fisher, S.E.6
-
32
-
-
0347986673
-
Transcriptional and DNA Binding Activity of the Foxp1/2/4 Family Is Modulated by Heterotypic and Homotypic Protein Interactions
-
DOI 10.1128/MCB.24.2.809-822.2004
-
Li S, Weidenfeld J, Morrisey EE. Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions. Mol Cell Biol 2004; 24: 809-822. (Pubitemid 38057931)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.2
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
33
-
-
36749050396
-
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
-
DOI 10.1086/522237
-
Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J et al. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. Am J Hum Genet 2007; 81: 1144-1157. (Pubitemid 350211446)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1144-1157
-
-
Spiteri, E.1
Konopka, G.2
Coppola, G.3
Bomar, J.4
Oldham, M.5
Ou, J.6
Vernes, S.C.7
Fisher, S.E.8
Ren, B.9
Geschwind, D.H.10
-
34
-
-
36749013035
-
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 SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE et al. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Am J Hum Genet 2007; 81: 1232-1250. (Pubitemid 350211452)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1232-1250
-
-
Vernes, S.C.1
Spiteri, E.2
Nicod, J.3
Groszer, M.4
Taylor, J.M.5
Davies, K.E.6
Geschwind, D.H.7
Fisher, S.E.8
-
35
-
-
63449102727
-
FOXP2 as a molecular window into speech and language
-
Fisher SE, Scharff C. FOXP2 as a molecular window into speech and language. Trends Genet 2009; 25: 166-177.
-
(2009)
Trends Genet
, vol.25
, pp. 166-177
-
-
Fisher, S.E.1
Scharff, C.2
|