-
1
-
-
84872857437
-
Decoding the genetics of speech and language
-
Graham S.A., Fisher S.E. Decoding the genetics of speech and language. Curr Opin Neurobiol 2013, 23:43-51.
-
(2013)
Curr Opin Neurobiol
, vol.23
, pp. 43-51
-
-
Graham, S.A.1
Fisher, S.E.2
-
2
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai C.S., Fisher S.E., Hurst J.A., Vargha-Khadem F., Monaco A.P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001, 413:519-523.
-
(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
-
3
-
-
84881666129
-
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria
-
Turner S.J., Hildebrand M.S., Block S., Damiano J., Fahey M., Reilly S., Bahlo M., Scheffer I.E., Morgan A.T. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. Am J Med Genet A 2013, 161:2321-2326.
-
(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
Bahlo, M.7
Scheffer, I.E.8
Morgan, A.T.9
-
4
-
-
0036190947
-
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia
-
Watkins K.E., Dronkers N.F., Vargha-Khadem F. Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain 2002, 125:452-464.
-
(2002)
Brain
, vol.125
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
5
-
-
29244467422
-
The eloquent ape: genes, brains and the evolution of language
-
Fisher S.E., Marcus G.F. The eloquent ape: genes, brains and the evolution of language. Nat Rev Genet 2006, 7:9-20.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 9-20
-
-
Fisher, S.E.1
Marcus, G.F.2
-
6
-
-
13444311847
-
The faculty of language: what's special about it?
-
Pinker S., Jackendoff R. The faculty of language: what's special about it?. Cognition 2005, 95:201-236.
-
(2005)
Cognition
, vol.95
, pp. 201-236
-
-
Pinker, S.1
Jackendoff, R.2
-
7
-
-
84869219473
-
Birds, primates, and spoken language origins: behavioral phenotypes and neurobiological substrates
-
Petkov C.I., Jarvis E.D. Birds, primates, and spoken language origins: behavioral phenotypes and neurobiological substrates. Front Evol Neurosci 2012, 4:12.
-
(2012)
Front Evol Neurosci
, vol.4
, pp. 12
-
-
Petkov, C.I.1
Jarvis, E.D.2
-
8
-
-
13244292715
-
FOXP2 and the neuroanatomy of speech and language
-
Vargha-Khadem F., Gadian D.G., Copp A., Mishkin M. FOXP2 and the neuroanatomy of speech and language. Nat Rev Neurosci 2005, 6:131-138.
-
(2005)
Nat Rev Neurosci
, vol.6
, pp. 131-138
-
-
Vargha-Khadem, F.1
Gadian, D.G.2
Copp, A.3
Mishkin, M.4
-
9
-
-
33749867547
-
Functional genetic analysis of mutations implicated in a human speech and language disorder
-
Vernes S.C., Nicod J., Elahi F.M., Coventry J.A., Kenny N., Coupe A.M., Bird L.E., Davies K.E., Fisher S.E. Functional genetic analysis of mutations implicated in a human speech and language disorder. Hum Mol Genet 2006, 15:3154-3167.
-
(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
Bird, L.E.7
Davies, K.E.8
Fisher, S.E.9
-
10
-
-
84867581362
-
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
-
Bacon C., Rappold G.A. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders. Hum Genet 2012, 131:1687-1698.
-
(2012)
Hum Genet
, vol.131
, pp. 1687-1698
-
-
Bacon, C.1
Rappold, G.A.2
-
11
-
-
84355162792
-
Phenotype of FOXP2 haploinsufficiency in a mother and son
-
Rice G.M., Raca G., Jakielski K.J., Laffin J.J., Iyama-Kurtycz C.M., Hartley S.L., Sprague R.E., Heintzelman A.T., Shriberg L.D. Phenotype of FOXP2 haploinsufficiency in a mother and son. Am J Med Genet A 2012, 158A:174-181.
-
(2012)
Am J Med Genet A
, vol.158 A
, pp. 174-181
-
-
Rice, G.M.1
Raca, G.2
Jakielski, K.J.3
Laffin, J.J.4
Iyama-Kurtycz, C.M.5
Hartley, S.L.6
Sprague, R.E.7
Heintzelman, A.T.8
Shriberg, L.D.9
-
12
-
-
33749869970
-
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
-
Shriberg L.D., Ballard K.J., Tomblin J.B., Duffy J.R., Odell K.H., Williams C.A. Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. J Speech Lang Hear Res 2006, 49:500-525.
-
(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
-
13
-
-
70349459760
-
Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2
-
Tomblin J.B., O'Brien M., Shriberg L.D., Williams C., Murray J., Patil S., Bjork J., Anderson S., Ballard K. Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2. J Speech Lang Hear Res 2009, 52:1157-1174.
-
(2009)
J Speech Lang Hear Res
, vol.52
, pp. 1157-1174
-
-
Tomblin, J.B.1
O'Brien, M.2
Shriberg, L.D.3
Williams, C.4
Murray, J.5
Patil, S.6
Bjork, J.7
Anderson, S.8
Ballard, K.9
-
14
-
-
0037341876
-
Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia
-
Belton E., Salmond C.H., Watkins K.E., Vargha-Khadem F., Gadian D.G. Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia. Hum Brain Mapp 2003, 18:194-200.
-
(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
-
15
-
-
0036188886
-
MRI analysis of an inherited speech and language disorder: structural brain abnormalities
-
Watkins K.E., Vargha-Khadem F., Ashburner J., Passingham R.E., Connelly A., Friston K.J., Frackowiak R.S., Mishkin M., Gadian D.G. MRI analysis of an inherited speech and language disorder: structural brain abnormalities. Brain 2002, 125:465-478.
-
(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
Frackowiak, R.S.7
Mishkin, M.8
Gadian, D.G.9
-
16
-
-
0242290123
-
Language fMRI abnormalities associated with FOXP2 gene mutation
-
Liegeois F., Baldeweg T., Connelly A., Gadian D.G., Mishkin M., Vargha-Khadem F. Language fMRI abnormalities associated with FOXP2 gene mutation. Nat Neurosci 2003, 6:1230-1237.
-
(2003)
Nat Neurosci
, vol.6
, pp. 1230-1237
-
-
Liegeois, F.1
Baldeweg, T.2
Connelly, A.3
Gadian, D.G.4
Mishkin, M.5
Vargha-Khadem, F.6
-
17
-
-
79958801139
-
Endophenotypes of FOXP2: dysfunction within the human articulatory network
-
Liegeois F., Morgan A.T., Connelly A., Vargha-Khadem F. Endophenotypes of FOXP2: dysfunction within the human articulatory network. Eur J Paediatr Neurol 2011, 15:283-288.
-
(2011)
Eur J Paediatr Neurol
, vol.15
, pp. 283-288
-
-
Liegeois, F.1
Morgan, A.T.2
Connelly, A.3
Vargha-Khadem, F.4
-
18
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
Lai C.S., Gerrelli D., Monaco A.P., Fisher S.E., Copp A.J. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 2003, 126:2455-2462.
-
(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
-
19
-
-
58249090576
-
Conservation and diversity of Foxp2 expression in muroid rodents: functional implications
-
Campbell P., Reep R.L., Stoll M.L., Ophir A.G., Phelps S.M. Conservation and diversity of Foxp2 expression in muroid rodents: functional implications. J Comp Neurol 2009, 512:84-100.
-
(2009)
J Comp Neurol
, vol.512
, pp. 84-100
-
-
Campbell, P.1
Reep, R.L.2
Stoll, M.L.3
Ophir, A.G.4
Phelps, S.M.5
-
20
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
Ferland R.J., Cherry T.J., Preware P.O., Morrisey E.E., Walsh C.A. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J Comp Neurol 2003, 460:266-279.
-
(2003)
J Comp Neurol
, vol.460
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
Preware, P.O.3
Morrisey, E.E.4
Walsh, C.A.5
-
21
-
-
22144496080
-
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
-
Shu W., Cho J.Y., Jiang Y., Zhang M., Weisz D., Elder G.A., Schmeidler J., De Gasperi R., Sosa M.A., Rabidou D., et al. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proc Natl Acad Sci USA 2005, 102:9643-9648.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 9643-9648
-
-
Shu, W.1
Cho, J.Y.2
Jiang, Y.3
Zhang, M.4
Weisz, D.5
Elder, G.A.6
Schmeidler, J.7
De Gasperi, R.8
Sosa, M.A.9
Rabidou, D.10
-
22
-
-
40149112272
-
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
-
Groszer M., Keays D.A., Deacon R.M., de Bono J.P., Prasad-Mulcare S., Gaub S., Baum M.G., French C.A., Nicod J., Coventry J.A., 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
Baum, M.G.7
French, C.A.8
Nicod, J.9
Coventry, J.A.10
-
23
-
-
42949179575
-
Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
-
Fujita E., Tanabe Y., Shiota A., Ueda M., Suwa K., Momoi M.Y., Momoi T. Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. Proc Natl Acad Sci USA 2008, 105:3117-3122.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 3117-3122
-
-
Fujita, E.1
Tanabe, Y.2
Shiota, A.3
Ueda, M.4
Suwa, K.5
Momoi, M.Y.6
Momoi, T.7
-
24
-
-
34547653713
-
Generation of mice with a conditional Foxp2 null allele
-
French C.A., Groszer M., Preece C., Coupe A.M., Rajewsky K., Fisher S.E. Generation of mice with a conditional Foxp2 null allele. Genesis 2007, 45:440-446.
-
(2007)
Genesis
, vol.45
, pp. 440-446
-
-
French, C.A.1
Groszer, M.2
Preece, C.3
Coupe, A.M.4
Rajewsky, K.5
Fisher, S.E.6
-
25
-
-
63449102727
-
FOXP2 as a molecular window into speech and language
-
Fisher S.E., 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
-
26
-
-
79960253200
-
FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution
-
Enard W. FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution. Curr Opin Neurobiol 2011, 21:415-424.
-
(2011)
Curr Opin Neurobiol
, vol.21
, pp. 415-424
-
-
Enard, W.1
-
27
-
-
65849256049
-
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
-
Enard W., Gehre S., Hammerschmidt K., Holter S.M., Blass T., Somel M., Bruckner M.K., Schreiweis C., Winter C., Sohr R., et al. A humanized version of Foxp2 affects cortico-basal 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
Bruckner, M.K.7
Schreiweis, C.8
Winter, C.9
Sohr, R.10
-
28
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes S.C., Oliver P.L., Spiteri E., Lockstone H.E., Puliyadi R., Taylor J.M., Ho J., Mombereau C., Brewer A., Lowy E., et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet 2011, 7:e1002145.
-
(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
Ho, J.7
Mombereau, C.8
Brewer, A.9
Lowy, E.10
-
29
-
-
70449653431
-
Human-specific transcriptional regulation of CNS development genes by FOXP2
-
Konopka G., Bomar J.M., Winden K., Coppola G., Jonsson Z.O., Gao F., Peng S., Preuss T.M., Wohlschlegel J.A., Geschwind D.H. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature 2009, 462:213-217.
-
(2009)
Nature
, vol.462
, pp. 213-217
-
-
Konopka, G.1
Bomar, J.M.2
Winden, K.3
Coppola, G.4
Jonsson, Z.O.5
Gao, F.6
Peng, S.7
Preuss, T.M.8
Wohlschlegel, J.A.9
Geschwind, D.H.10
-
30
-
-
36749050396
-
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
-
Spiteri E., Konopka G., Coppola G., Bomar J., Oldham M., Ou J., Vernes S.C., Fisher S.E., Ren B., Geschwind D.H. 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.
-
(2007)
Am J Hum Genet
, vol.81
, 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
-
31
-
-
36749013035
-
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
-
Vernes S.C., Spiteri E., Nicod J., Groszer M., Taylor J.M., Davies K.E., Geschwind D.H., Fisher S.E. 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.
-
(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
Geschwind, D.H.7
Fisher, S.E.8
-
32
-
-
78951481923
-
Humanized Foxp2 specifically affects cortico-basal ganglia circuits
-
Reimers-Kipping S., Hevers W., Paabo S., Enard W. Humanized Foxp2 specifically affects cortico-basal ganglia circuits. Neuroscience 2010, 175:75-84.
-
(2010)
Neuroscience
, vol.175
, pp. 75-84
-
-
Reimers-Kipping, S.1
Hevers, W.2
Paabo, S.3
Enard, W.4
-
33
-
-
84865230062
-
Convergent repression of Foxp2 3'UTR by miR-9 and miR-132 in embryonic mouse neocortex: implications for radial migration of neurons
-
Clovis Y.M., Enard W., Marinaro F., Huttner W.B., De Pietri Tonelli D. Convergent repression of Foxp2 3'UTR by miR-9 and miR-132 in embryonic mouse neocortex: implications for radial migration of neurons. Development 2012, 139:3332-3342.
-
(2012)
Development
, vol.139
, pp. 3332-3342
-
-
Clovis, Y.M.1
Enard, W.2
Marinaro, F.3
Huttner, W.B.4
De Pietri Tonelli, D.5
-
34
-
-
57149090343
-
A functional genetic link between distinct developmental language disorders
-
Vernes S.C., Newbury D.F., Abrahams B.S., Winchester L., Nicod J., Groszer M., Alarcon M., Oliver P.L., Davies K.E., Geschwind D.H., et al. A functional genetic link between distinct developmental language disorders. N Engl J Med 2008, 359:2337-2345.
-
(2008)
N 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
Alarcon, M.7
Oliver, P.L.8
Davies, K.E.9
Geschwind, D.H.10
-
35
-
-
79958067224
-
CNTNAP2 variants affect early language development in the general population
-
Whitehouse A.J., Bishop D.V., Ang Q.W., Pennell C.E., Fisher S.E. CNTNAP2 variants affect early language development in the general population. Genes Brain Behav 2011, 10:451-456.
-
(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
-
36
-
-
80051569371
-
Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk
-
Mukamel Z., Konopka G., Wexler E., Osborn G.E., Dong H., Bergman M.Y., Levitt P., Geschwind D.H. Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk. J Neurosci 2011, 31:11437-11442.
-
(2011)
J Neurosci
, vol.31
, pp. 11437-11442
-
-
Mukamel, Z.1
Konopka, G.2
Wexler, E.3
Osborn, G.E.4
Dong, H.5
Bergman, M.Y.6
Levitt, P.7
Geschwind, D.H.8
-
37
-
-
84863507705
-
The DISC1 promoter: characterization and regulation by FOXP2
-
Walker R.M., Hill A.E., Newman A.C., Hamilton G., Torrance H.S., Anderson S.M., Ogawa F., Derizioti P., Nicod J., Vernes S.C., et al. The DISC1 promoter: characterization and regulation by FOXP2. Hum Mol Genet 2012, 21:2862-2872.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 2862-2872
-
-
Walker, R.M.1
Hill, A.E.2
Newman, A.C.3
Hamilton, G.4
Torrance, H.S.5
Anderson, S.M.6
Ogawa, F.7
Derizioti, P.8
Nicod, J.9
Vernes, S.C.10
-
38
-
-
78649477258
-
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
-
Roll P., Vernes S.C., Bruneau N., Cillario J., Ponsole-Lenfant M., Massacrier A., Rudolf G., Khalife M., Hirsch E., Fisher S.E., et al. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Hum Mol Genet 2010, 19:4848-4860.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4848-4860
-
-
Roll, P.1
Vernes, S.C.2
Bruneau, N.3
Cillario, J.4
Ponsole-Lenfant, M.5
Massacrier, A.6
Rudolf, G.7
Khalife, M.8
Hirsch, E.9
Fisher, S.E.10
-
39
-
-
84888068454
-
The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice
-
Sia G.M., Clem R.L., Huganir R.L. The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice. Science 2013, 342:987-991.
-
(2013)
Science
, vol.342
, pp. 987-991
-
-
Sia, G.M.1
Clem, R.L.2
Huganir, R.L.3
-
40
-
-
70350532596
-
Differential gene expression in the developing lateral geniculate nucleus and medial geniculate nucleus reveals novel roles for Zic4 and Foxp2 in visual and auditory pathway development
-
Horng S., Kreiman G., Ellsworth C., Page D., Blank M., Millen K., Sur M. Differential gene expression in the developing lateral geniculate nucleus and medial geniculate nucleus reveals novel roles for Zic4 and Foxp2 in visual and auditory pathway development. J Neurosci 2009, 29:13672-13683.
-
(2009)
J Neurosci
, vol.29
, pp. 13672-13683
-
-
Horng, S.1
Kreiman, G.2
Ellsworth, C.3
Page, D.4
Blank, M.5
Millen, K.6
Sur, M.7
-
41
-
-
68649090782
-
Modified sound-evoked brainstem potentials in Foxp2 mutant mice
-
Kurt S., Groszer M., Fisher S.E., Ehret G. Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain Res 2009, 1289:30-36.
-
(2009)
Brain Res
, vol.1289
, pp. 30-36
-
-
Kurt, S.1
Groszer, M.2
Fisher, S.E.3
Ehret, G.4
-
42
-
-
84857853508
-
Foxp2 mutations impair auditory-motor association learning
-
Kurt S., Fisher S.E., Ehret G. Foxp2 mutations impair auditory-motor association learning. PLOS ONE 2012, 7:e33130.
-
(2012)
PLOS ONE
, vol.7
-
-
Kurt, S.1
Fisher, S.E.2
Ehret, G.3
-
43
-
-
83455212153
-
FoxP2 expression in the cerebellum and inferior olive: development of the transverse stripe-shaped expression pattern in the mouse cerebellar cortex
-
Fujita H., Sugihara I. FoxP2 expression in the cerebellum and inferior olive: development of the transverse stripe-shaped expression pattern in the mouse cerebellar cortex. J Comp Neurol 2012, 520:656-677.
-
(2012)
J Comp Neurol
, vol.520
, pp. 656-677
-
-
Fujita, H.1
Sugihara, I.2
-
44
-
-
0038054082
-
Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum
-
Takahashi K., Liu F.C., 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.
-
(2003)
J Neurosci Res
, vol.73
, pp. 61-72
-
-
Takahashi, K.1
Liu, F.C.2
Hirokawa, K.3
Takahashi, H.4
-
45
-
-
55449107738
-
A translational profiling approach for the molecular characterization of CNS cell types
-
Heiman M., Schaefer A., Gong S., Peterson J.D., Day M., Ramsey K.E., Suarez-Farinas M., Schwarz C., Stephan D.A., Surmeier D.J., et al. A translational profiling approach for the molecular characterization of CNS cell types. Cell 2008, 135:738-748.
-
(2008)
Cell
, vol.135
, pp. 738-748
-
-
Heiman, M.1
Schaefer, A.2
Gong, S.3
Peterson, J.D.4
Day, M.5
Ramsey, K.E.6
Suarez-Farinas, M.7
Schwarz, C.8
Stephan, D.A.9
Surmeier, D.J.10
-
46
-
-
0034667966
-
Pitch and timing abilities in inherited speech and language impairment
-
Alcock K.J., Passingham R.E., Watkins K., Vargha-Khadem F. Pitch and timing abilities in inherited speech and language impairment. Brain Lang 2000, 75:34-46.
-
(2000)
Brain Lang
, vol.75
, pp. 34-46
-
-
Alcock, K.J.1
Passingham, R.E.2
Watkins, K.3
Vargha-Khadem, F.4
-
47
-
-
84867896115
-
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
-
French C.A., Jin X., Campbell T.G., Gerfen E., Groszer M., Fisher S.E., Costa R.M. An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. Mol Psychiatry 2011, 17:1077-1085.
-
(2011)
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
Costa, R.M.7
-
48
-
-
84902103855
-
Foxp2 regulates neuronal differentiation and neuronal subtype specification
-
Chiu Y.C., Li M.Y., Liu Y.H., Ding J.Y., Yu J.Y., Wang T.W. Foxp2 regulates neuronal differentiation and neuronal subtype specification. Dev Neurobiol 2014, 74:723-738.
-
(2014)
Dev Neurobiol
, vol.74
, pp. 723-738
-
-
Chiu, Y.C.1
Li, M.Y.2
Liu, Y.H.3
Ding, J.Y.4
Yu, J.Y.5
Wang, T.W.6
-
49
-
-
84871770267
-
FoxP2 regulates neurogenesis during embryonic cortical development
-
Tsui D., Vessey J.P., Tomita H., Kaplan D.R., Miller F.D. FoxP2 regulates neurogenesis during embryonic cortical development. J Neurosci 2013, 33:244-258.
-
(2013)
J Neurosci
, vol.33
, pp. 244-258
-
-
Tsui, D.1
Vessey, J.P.2
Tomita, H.3
Kaplan, D.R.4
Miller, F.D.5
-
50
-
-
84860310017
-
Foxp-mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS
-
Rousso D.L., Pearson C.A., Gaber Z.B., Miquelajauregui A., Li S., Portera-Cailliau C., Morrisey E.E., Novitch B.G. Foxp-mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS. Neuron 2012, 74:314-330.
-
(2012)
Neuron
, vol.74
, pp. 314-330
-
-
Rousso, D.L.1
Pearson, C.A.2
Gaber, Z.B.3
Miquelajauregui, A.4
Li, S.5
Portera-Cailliau, C.6
Morrisey, E.E.7
Novitch, B.G.8
-
51
-
-
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
-
52
-
-
84890493080
-
Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability
-
Murugan M., Harward S., Scharff C., Mooney R. Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability. Neuron 2013, 80:1464-1476.
-
(2013)
Neuron
, vol.80
, pp. 1464-1476
-
-
Murugan, M.1
Harward, S.2
Scharff, C.3
Mooney, R.4
-
53
-
-
13644263307
-
Infant rodent ultrasounds-a gate to the understanding of sound communication
-
Ehret G. Infant rodent ultrasounds-a gate to the understanding of sound communication. Behav Genet 2005, 35:19-29.
-
(2005)
Behav Genet
, vol.35
, pp. 19-29
-
-
Ehret, G.1
-
54
-
-
77952992862
-
The structure of innate vocalizations in Foxp2-deficient mouse pups
-
Gaub S., Groszer M., Fisher S.E., Ehret G. The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes Brain Behav 2010, 9:390-401.
-
(2010)
Genes Brain Behav
, vol.9
, pp. 390-401
-
-
Gaub, S.1
Groszer, M.2
Fisher, S.E.3
Ehret, G.4
-
55
-
-
84874199672
-
Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval
-
Bowers J.M., Perez-Pouchoulen M., Edwards N.S., McCarthy M.M. Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval. J Neurosci 2013, 33:3276-3283.
-
(2013)
J Neurosci
, vol.33
, pp. 3276-3283
-
-
Bowers, J.M.1
Perez-Pouchoulen, M.2
Edwards, N.S.3
McCarthy, M.M.4
-
56
-
-
67049165175
-
Analysis of Foxp2 expression in the cerebellum reveals a possible sex difference
-
Hamson D.K., Csupity A.S., Gaspar J.M., Watson N.V. Analysis of Foxp2 expression in the cerebellum reveals a possible sex difference. Neuroreport 2009, 20:611-616.
-
(2009)
Neuroreport
, vol.20
, pp. 611-616
-
-
Hamson, D.K.1
Csupity, A.S.2
Gaspar, J.M.3
Watson, N.V.4
-
57
-
-
59649125005
-
Putative sex differences in verbal abilities and language cortex: a critical review
-
Wallentin M. Putative sex differences in verbal abilities and language cortex: a critical review. Brain Lang 2009, 108:175-183.
-
(2009)
Brain Lang
, vol.108
, pp. 175-183
-
-
Wallentin, M.1
-
58
-
-
78751685886
-
Ultrasonic vocalizations in mouse models for speech and socio-cognitive disorders: insights into the evolution of vocal communication
-
Fischer J., Hammerschmidt K. Ultrasonic vocalizations in mouse models for speech and socio-cognitive disorders: insights into the evolution of vocal communication. Genes Brain Behav 2010, 10:17-27.
-
(2010)
Genes Brain Behav
, vol.10
, pp. 17-27
-
-
Fischer, J.1
Hammerschmidt, K.2
-
59
-
-
29144444606
-
Ultrasonic songs of male mice
-
Holy T.E., Guo Z. Ultrasonic songs of male mice. PLoS Biol 2005, 3:e386.
-
(2005)
PLoS Biol
, vol.3
-
-
Holy, T.E.1
Guo, Z.2
-
60
-
-
84871877593
-
Mouse vocal communication system: are ultrasounds learned or innate?
-
Arriaga G., Jarvis E.D. Mouse vocal communication system: are ultrasounds learned or innate?. Brain Lang 2013, 124:96-116.
-
(2013)
Brain Lang
, vol.124
, pp. 96-116
-
-
Arriaga, G.1
Jarvis, E.D.2
-
61
-
-
84891634357
-
Defining functional gene-circuit interfaces in the mouse nervous system
-
Soden M.E., Gore B.B., Zweifel L.S. Defining functional gene-circuit interfaces in the mouse nervous system. Genes Brain Behav 2014, 13:2-12.
-
(2014)
Genes Brain Behav
, vol.13
, pp. 2-12
-
-
Soden, M.E.1
Gore, B.B.2
Zweifel, L.S.3
-
62
-
-
84875659006
-
Nanotools for neuroscience and brain activity mapping
-
Alivisatos A.P., Andrews A.M., Boyden E.S., Chun M., Church G.M., Deisseroth K., Donoghue J.P., Fraser S.E., Lippincott-Schwartz J., Looger L.L., et al. Nanotools for neuroscience and brain activity mapping. ACS Nano 2013, 7:1850-1866.
-
(2013)
ACS Nano
, vol.7
, pp. 1850-1866
-
-
Alivisatos, A.P.1
Andrews, A.M.2
Boyden, E.S.3
Chun, M.4
Church, G.M.5
Deisseroth, K.6
Donoghue, J.P.7
Fraser, S.E.8
Lippincott-Schwartz, J.9
Looger, L.L.10
-
63
-
-
3943066275
-
A gene-driven ENU-based approach to generating an allelic series in any gene
-
Quwailid M.M., Hugill A., Dear N., Vizor L., Wells S., Horner E., Fuller S., Weedon J., McMath H., Woodman P., et al. A gene-driven ENU-based approach to generating an allelic series in any gene. Mamm Genome 2004, 15:585-591.
-
(2004)
Mamm Genome
, vol.15
, pp. 585-591
-
-
Quwailid, M.M.1
Hugill, A.2
Dear, N.3
Vizor, L.4
Wells, S.5
Horner, E.6
Fuller, S.7
Weedon, J.8
McMath, H.9
Woodman, P.10
|