-
1
-
-
34548832230
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
24
-
-
0242290123
-
Language fMRI abnormalities associated with FOXP2 gene mutation
-
doi: 10.1038/nn1138
-
Liégeois, F., Baldeweg, T., Connelly, A., Gadian, D. G., Mishkin, M., and Vargha-Khadem, F. (2003). Language fMRI abnormalities associated with FOXP2 gene mutation. Nat. Neurosci. 6, 1230-1237. doi: 10.1038/nn1138
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 1230-1237
-
-
Liégeois, F.1
Baldeweg, T.2
Connelly, A.3
Gadian, D.G.4
Mishkin, M.5
Vargha-Khadem, F.6
-
25
-
-
21044445447
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
34
-
-
84355162792
-
Phenotype of FOXP2 haploinsufficiency in a mother and son
-
doi: 10.1002/ajmg.a.34354
-
Rice, G. M., Raca, G., Jakielski, K. J., Laffin, J. J., Iyama-Kurtycz, C. M., Hartley, S. L., et al. (2012). Phenotype of FOXP2 haploinsufficiency in a mother and son. Am. J. Med. Genet. A 158A, 174-181. doi: 10.1002/ajmg.a.34354
-
(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
-
35
-
-
33749253516
-
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
-
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
-
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
-
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
-
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
-
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
-
41
-
-
13144255748
-
Neural basis of an inherited speech and language disorder
-
doi: 10.1073/pnas.95.21.12695
-
Vargha-Khadem, F., Watkins, K. E., Price, C. J., Ashburner, J., Alcock, K. J., Connelly, A., et al. (1998). Neural basis of an inherited speech and language disorder. Proc. Natl. Acad. Sci. U.S.A. 95, 12695-12700. doi: 10.1073/pnas.95.21.12695
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, 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
-
42
-
-
57149090343
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
49
-
-
84855790585
-
Imaging genetics of FOXP2 in dyslexia
-
doi: 10.1038/ejhg.2011.160
-
Wilcke, A., Ligges, C., Burkhardt, J., Alexander, M., Wolf, C., Quente, E., et al. (2012). Imaging genetics of FOXP2 in dyslexia. Eur. J. Hum. Genet. 20, 224-229. doi: 10.1038/ejhg.2011.160
-
(2012)
Eur. J. Hum. Genet.
, vol.20
, pp. 224-229
-
-
Wilcke, A.1
Ligges, C.2
Burkhardt, J.3
Alexander, M.4
Wolf, C.5
Quente, E.6
-
50
-
-
33644860165
-
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
-
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
|