-
1
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
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;413:519-23.
-
(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
-
2
-
-
33751113031
-
Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia
-
Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K. Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia. Am J Hum Gen 2006;79:965-72.
-
(2006)
Am J Hum Gen
, vol.79
, pp. 965-972
-
-
Feuk, L.1
Kalervo, A.2
Lipsanen-Nyman, M.3
Skaug, J.4
Nakabayashi, K.5
Finucane, B.6
Hartung, D.7
Innes, M.8
Kerem, B.9
Nowaczyk, M.J.10
Rivlin, J.11
Roberts, W.12
Senman, L.13
Summers, A.14
Szatmari, P.15
Wong, V.16
Vincent, J.B.17
Zeesman, S.18
Osborne, L.R.19
Cardy, J.O.20
Kere, J.21
Scherer, S.W.22
Hannula-Jouppi, K.23
more..
-
3
-
-
79959984619
-
The parental antagonism theory of language evolution: preliminary evidence for the proposal
-
Brown WM. The parental antagonism theory of language evolution: preliminary evidence for the proposal. Human Biol 2011;83:213-45.
-
(2011)
Human Biol
, vol.83
, pp. 213-245
-
-
Brown, W.M.1
-
4
-
-
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;25:166-77.
-
(2009)
Trends Genet
, vol.25
, pp. 166-177
-
-
Fisher, S.E.1
Scharff, C.2
-
5
-
-
0037158715
-
Molecular evolution of FOXP2, a gene involved in speech and language
-
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 2002;418:869-72.
-
(2002)
Nature
, vol.418
, pp. 869-872
-
-
Enard, W.1
Przeworski, M.2
Fisher, S.E.3
Lai, C.S.4
Wiebe, V.5
Kitano, T.6
Monaco, A.P.7
Pääbo, S.8
-
6
-
-
22144496080
-
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
-
Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, Schmeidler J, De Gasperi R, Sosa MA, Rabidou D, Santucci AC, Perl D, Morrisey E, Buxbaum JD. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proc Natl Acad Sci USA 2005;102:9643-8.
-
(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
Santucci, A.C.11
Perl, D.12
Morrisey, E.13
Buxbaum, J.D.14
-
7
-
-
34547653713
-
Generation of mice with a conditional Foxp2 null allele
-
French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. Generation of mice with a conditional Foxp2 null allele. Genesis 2007;45:440-6.
-
(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
-
8
-
-
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, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol 2008;18:354-62.
-
(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
Enard, W.11
Fray, M.12
Brown, S.D.13
Nolan, P.M.14
Pääbo, S.15
Channon, K.M.16
Costa, R.M.17
Eilers, J.18
Ehret, G.19
Rawlins, J.N.20
Fisher, S.E.21
more..
-
9
-
-
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
-
10
-
-
78149339689
-
Epigenotype-phenotype correlations in Silver-Russell syndrome
-
Wakeling EL, Amero SA, Alders M, Bliek J, Forsythe E, Kumar S, Lim DH, MacDonald F, Mackay DJ, Maher ER, Moore GE, Poole RL, Price SM, Tangeraas T, Turner CL, Van Haelst MM, Willoughby C, Temple IK, Cobben JM. Epigenotype-phenotype correlations in Silver-Russell syndrome. J Med Genet 2010;47:760-8.
-
(2010)
J Med Genet
, vol.47
, pp. 760-768
-
-
Wakeling, E.L.1
Amero, S.A.2
Alders, M.3
Bliek, J.4
Forsythe, E.5
Kumar, S.6
Lim, D.H.7
MacDonald, F.8
Mackay, D.J.9
Maher, E.R.10
Moore, G.E.11
Poole, R.L.12
Price, S.M.13
Tangeraas, T.14
Turner, C.L.15
Van Haelst, M.M.16
Willoughby, C.17
Temple, I.K.18
Cobben, J.M.19
-
11
-
-
84355166477
-
Maternally and paternally inherited deletion of 7q31 involving the FOXP2 Gene in two families
-
Zilina O, Reimand T, Zjablovskaja Männik K, Männamaa M, Traat A, Puusepp-Benazzouz H, Kurg A, Ounap K. Maternally and paternally inherited deletion of 7q31 involving the FOXP2 Gene in two families. Am J Med Genetics 2011;158A:254-6.
-
(2011)
Am J Med Genetics
, vol.158 A
, pp. 254-256
-
-
Zilina, O.1
Reimand, T.2
Zjablovskaja Männik, K.3
Männamaa, M.4
Traat, A.5
Puusepp-Benazzouz, H.6
Kurg, A.7
Ounap, K.8
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