-
1
-
-
0001328240
-
Six cases of congenital word-blindness affecting three generations of one family
-
Stephenson S: Six cases of congenital word-blindness affecting three generations of one family. Ophthalmoscope 1907;5:482-484.
-
(1907)
Ophthalmoscope
, vol.5
, pp. 482-484
-
-
Stephenson, S.1
-
2
-
-
0001667268
-
Congenital 'word-blindness' and its treatment
-
Thomas CJ: Congenital 'word-blindness' and its treatment. Ophthalmoscope 1905;3:380-385.
-
(1905)
Ophthalmoscope
, vol.3
, pp. 380-385
-
-
Thomas, C.J.1
-
3
-
-
20444409668
-
Dyslexia (specific reading disability)
-
Shaywitz SE, Shaywitz BA: Dyslexia (specific reading disability). Biol Psychiatry 2005;57:1301-1309.
-
(2005)
Biol Psychiatry
, vol.57
, pp. 1301-1309
-
-
Shaywitz, S.E.1
Shaywitz, B.A.2
-
4
-
-
0022790723
-
Family history of children with developmental language disorders
-
Neils J, Aram DM: Family history of children with developmental language disorders. Percept Mot Skills 1986;63:655-658.
-
(1986)
Percept Mot Skills
, vol.63
, pp. 655-658
-
-
Neils, J.1
Aram, D.M.2
-
6
-
-
0024510587
-
Familial aggregation in specific language impairment
-
Tallal P, Ross R, Curtiss S: Familial aggregation in specific language impairment. J Speech Hear Disord 1989;54:167-173.
-
(1989)
J Speech Hear Disord
, vol.54
, pp. 167-173
-
-
Tallal, P.1
Ross, R.2
Curtiss, S.3
-
7
-
-
0024507073
-
Familial concentration of developmental language impairment
-
Tomblin JB: Familial concentration of developmental language impairment. J Speech Hear Disord 1989;54:287-295.
-
(1989)
J Speech Hear Disord
, vol.54
, pp. 287-295
-
-
Tomblin, J.B.1
-
8
-
-
0029005821
-
Specific language impairment: Preliminary investigation of factors associated with family history and with patterns of language performance
-
Lahey M, Edwards J: Specific language impairment: preliminary investigation of factors associated with family history and with patterns of language performance. J Speech Hear Res 1995;38:643-657.
-
(1995)
J Speech Hear Res
, vol.38
, pp. 643-657
-
-
Lahey, M.1
Edwards, J.2
-
9
-
-
0026499677
-
A study of developmental speech and language disorders in twins
-
Lewis BA, Thompson LA: A study of developmental speech and language disorders in twins. J Speech Hear Res 1992;35:1086-1094.
-
(1992)
J Speech Hear Res
, vol.35
, pp. 1086-1094
-
-
Lewis, B.A.1
Thompson, L.A.2
-
10
-
-
0028872434
-
Genetic basis of specific language impairment: Evidence from a twin study
-
Bishop DV, North T, Donlan C: Genetic basis of specific language impairment: evidence from a twin study. Dev Med Child Neurol 1995;37:56-71.
-
(1995)
Dev Med Child Neurol
, vol.37
, pp. 56-71
-
-
Bishop, D.V.1
North, T.2
Donlan, C.3
-
11
-
-
0031890655
-
Heritability of poor language achievement among twins
-
Tomblin JB, Buckwalter PR: Heritability of poor language achievement among twins. J Speech Lang Hear Res 1998;41:188-199.
-
(1998)
J Speech Lang Hear Res
, vol.41
, pp. 188-199
-
-
Tomblin, J.B.1
Buckwalter, P.R.2
-
12
-
-
33644666549
-
Genetic influence on language delay in two-year-old children
-
Dale PS, Simonoff E, Bishop DV, Eley TC, Oliver B, Price TS, Purcell S, Stevenson J, Plomin R: Genetic influence on language delay in two-year-old children. Nat Neurosci 1998;1:324-328.
-
(1998)
Nat Neurosci
, vol.1
, pp. 324-328
-
-
Dale, P.S.1
Simonoff, E.2
Bishop, D.V.3
Eley, T.C.4
Oliver, B.5
Price, T.S.6
Purcell, S.7
Stevenson, J.8
Plomin, R.9
-
13
-
-
0032930791
-
Different origin of auditory and phonological processing problems in children with language impairment: Evidence from a twin study
-
Bishop DV, Bishop SJ, Bright P, James C, Delaney T, Tallal P: Different origin of auditory and phonological processing problems in children with language impairment: evidence from a twin study. J Speech Lang Hear Res 1999;42:155-168.
-
(1999)
J Speech Lang Hear Res
, vol.42
, pp. 155-168
-
-
Bishop, D.V.1
Bishop, S.J.2
Bright, P.3
James, C.4
Delaney, T.5
Tallal, P.6
-
14
-
-
1242321354
-
Genetic and environmental influence on language impairment in 4-year-old same-sex and opposite-sex twins
-
Viding E, Spinath FM, Price TS, Bishop DV, Dale PS, Plomin R: Genetic and environmental influence on language impairment in 4-year-old same-sex and opposite-sex twins. J Child Psychol Psychiatry 2004;45:315-325.
-
(2004)
J Child Psychol Psychiatry
, vol.45
, pp. 315-325
-
-
Viding, E.1
Spinath, F.M.2
Price, T.S.3
Bishop, D.V.4
Dale, P.S.5
Plomin, R.6
-
15
-
-
33747190655
-
Tangled webs: Tracing the connections between genes and cognition
-
Fisher SE: Tangled webs: tracing the connections between genes and cognition. Cognition 2006;101:270-297.
-
(2006)
Cognition
, vol.101
, pp. 270-297
-
-
Fisher, S.E.1
-
16
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Botstein D, Risch N: Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 2003;33(suppl):228-237.
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
17
-
-
85015078040
-
The double helix in clinical practice
-
Bell JI: The double helix in clinical practice. Nature 2003;421:414-416.
-
(2003)
Nature
, vol.421
, pp. 414-416
-
-
Bell, J.I.1
-
18
-
-
22844440427
-
Identification of hundreds of conserved and nonconserved human microRNAs
-
Bentwich I, Avniel A, Karov Y, Aharonov R, Gilad S, Barad O, Barzilai A, Einat P, Einav U, Meiri E, Sharon E, Spector Y, Bentwich Z: Identification of hundreds of conserved and nonconserved human microRNAs. Nat Genet 2005;37:766-770.
-
(2005)
Nat Genet
, vol.37
, pp. 766-770
-
-
Bentwich, I.1
Avniel, A.2
Karov, Y.3
Aharonov, R.4
Gilad, S.5
Barad, O.6
Barzilai, A.7
Einat, P.8
Einav, U.9
Meiri, E.10
Sharon, E.11
Spector, Y.12
Bentwich, Z.13
-
19
-
-
33751548288
-
Diversity of microRNAs in human and chimpanzee brain
-
Berezikov E, Thuemmler F, van Laake LW, Kondova I, Bontrop R, Cuppen E, Plasterk RH: Diversity of microRNAs in human and chimpanzee brain. Nat Genet 2006;38:1375-1377.
-
(2006)
Nat Genet
, vol.38
, pp. 1375-1377
-
-
Berezikov, E.1
Thuemmler, F.2
van Laake, L.W.3
Kondova, I.4
Bontrop, R.5
Cuppen, E.6
Plasterk, R.H.7
-
20
-
-
33745286231
-
TUF love for 'junk' DNA
-
Willingham AT, Gingeras TR: TUF love for 'junk' DNA. Cell 2006;125:1215-1220.
-
(2006)
Cell
, vol.125
, pp. 1215-1220
-
-
Willingham, A.T.1
Gingeras, T.R.2
-
22
-
-
79959524146
-
A haplotype map of the human genome
-
International Hapmap Consortium
-
International Hapmap Consortium: A haplotype map of the human genome. Nature 2005;437:1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
23
-
-
33751329250
-
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME: Global variation in copy number in the human genome. Nature 2006;444:444-454.
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME: Global variation in copy number in the human genome. Nature 2006;444:444-454.
-
-
-
-
24
-
-
0035451780
-
On the allelic spectrum of human disease
-
Reich DE, Lander ES: On the allelic spectrum of human disease. Trends Genet 2001;17:502-510.
-
(2001)
Trends Genet
, vol.17
, pp. 502-510
-
-
Reich, D.E.1
Lander, E.S.2
-
25
-
-
33645130154
-
Mendelian disorders deserve more attention
-
Antonarakis SE, Beckmann JS: Mendelian disorders deserve more attention. Nat Rev Genet 2006;7:277-282.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 277-282
-
-
Antonarakis, S.E.1
Beckmann, J.S.2
-
26
-
-
0038571125
-
Deciphering the genetic basis of speech and language disorders
-
Fisher SE, Lai CS, Monaco AP: Deciphering the genetic basis of speech and language disorders. Annu Rev Neurosci 2003;26:57-80.
-
(2003)
Annu Rev Neurosci
, vol.26
, pp. 57-80
-
-
Fisher, S.E.1
Lai, C.S.2
Monaco, A.P.3
-
27
-
-
0036302206
-
A major susceptibility locus for specific language impairment is located on 13q21
-
Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM: A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet 2002;71:45-55.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 45-55
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Vieland, V.J.4
Bassett, A.S.5
Tallal, P.6
Brzustowicz, L.M.7
-
28
-
-
2342592462
-
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment
-
Bartlett CW, Flax JF, Logue MW, Smith BJ, Vieland VJ, Tallal P, Brzustowicz LM: Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment. Hum Hered 2004;57:10-20.
-
(2004)
Hum Hered
, vol.57
, pp. 10-20
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Smith, B.J.4
Vieland, V.J.5
Tallal, P.6
Brzustowicz, L.M.7
-
29
-
-
18244408330
-
A genomewide scan identifies two novel loci involved in specific language impairment
-
The SLI Consortium
-
The SLI Consortium: A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet 2002;70:384-398.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 384-398
-
-
-
30
-
-
2442657674
-
Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment
-
The SLI Consortium
-
The SLI Consortium: Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. Am J Hum Genet 2004;74:1225-1238.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1225-1238
-
-
-
31
-
-
27544444173
-
Genetic influences on language impairment and phonological short-term memory
-
Newbury DF, Bishop DV, Monaco AP: Genetic influences on language impairment and phonological short-term memory. Trends Cogn Sci 2005;9:528-534.
-
(2005)
Trends Cogn Sci
, vol.9
, pp. 528-534
-
-
Newbury, D.F.1
Bishop, D.V.2
Monaco, A.P.3
-
32
-
-
0029865799
-
Nonword repetition as a behavioural marker for inherited language impairment: Evidence from a twin study
-
Bishop DV, North T, Donlan C: Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study. J Child Psychol Psychiatry 1996;37:391-403.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 391-403
-
-
Bishop, D.V.1
North, T.2
Donlan, C.3
-
33
-
-
0028458282
-
The Children's Test of Nonword Repetition: A test of phonological working memory
-
Gathercole SE, Willis CS, Baddeley AD, Emslie H: The Children's Test of Nonword Repetition: a test of phonological working memory. Memory 1994;2: 103-127.
-
(1994)
Memory
, vol.2
, pp. 103-127
-
-
Gathercole, S.E.1
Willis, C.S.2
Baddeley, A.D.3
Emslie, H.4
-
34
-
-
0004899128
-
Phonological memory deficits in language disordered children - is there a causal connection?
-
Gathercole SE, Baddeley AD: Phonological memory deficits in language disordered children - is there a causal connection? J Memory Lang 1990;29:336-360.
-
(1990)
J Memory Lang
, vol.29
, pp. 336-360
-
-
Gathercole, S.E.1
Baddeley, A.D.2
-
35
-
-
0035080409
-
Genetic influences on language impairment and literacy problems in children: Same or different?
-
Bishop DV: Genetic influences on language impairment and literacy problems in children: same or different? J Child Psychol Psychiatry 2001;42:189-198.
-
(2001)
J Child Psychol Psychiatry
, vol.42
, pp. 189-198
-
-
Bishop, D.V.1
-
36
-
-
33847757519
-
The genetic bases of speech sound disorders: Evidence from spoken and written language
-
Lewis BA, Shriberg LD, Freebairn LA, Hansen AJ, Stein CM, Taylor HG, Iyengar SK: The genetic bases of speech sound disorders: evidence from spoken and written language. J Speech Lang Hear Res 2006;49:1294-1312.
-
(2006)
J Speech Lang Hear Res
, vol.49
, pp. 1294-1312
-
-
Lewis, B.A.1
Shriberg, L.D.2
Freebairn, L.A.3
Hansen, A.J.4
Stein, C.M.5
Taylor, H.G.6
Iyengar, S.K.7
-
38
-
-
10744233099
-
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading
-
Stein CM, Schick JH, Gerry Taylor H, Shriberg LD, Millard C, Kundtz-Kluge A, Russo K, Minich N, Hansen A, Freebairn LA, Elston RC, Lewis BA, Iyengar SK: Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am J Hum Genet 2004;74:283-297.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 283-297
-
-
Stein, C.M.1
Schick, J.H.2
Gerry Taylor, H.3
Shriberg, L.D.4
Millard, C.5
Kundtz-Kluge, A.6
Russo, K.7
Minich, N.8
Hansen, A.9
Freebairn, L.A.10
Elston, R.C.11
Lewis, B.A.12
Iyengar, S.K.13
-
39
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher SE, DeFries JC: Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci 2002;3:767-780.
-
(2002)
Nat Rev Neurosci
, vol.3
, pp. 767-780
-
-
Fisher, S.E.1
DeFries, J.C.2
-
40
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC: Quantitative trait locus for reading disability on chromosome 6. Science 1994;266:276-279.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
41
-
-
0020622130
-
Specific reading disability: Identification of an inherited form through linkage analysis
-
Smith SD, Kimberling WJ, Pennington BF, Lubs HA: Specific reading disability: identification of an inherited form through linkage analysis. Science 1983;219:1345-1347.
-
(1983)
Science
, vol.219
, pp. 1345-1347
-
-
Smith, S.D.1
Kimberling, W.J.2
Pennington, B.F.3
Lubs, H.A.4
-
42
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J: Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 2005;76:581-591.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 581-591
-
-
Cope, N.1
Harold, D.2
Hill, G.3
Moskvina, V.4
Stevenson, J.5
Holmans, P.6
Owen, M.J.7
O'Donovan, M.C.8
Williams, J.9
-
43
-
-
8844258018
-
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
-
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP: A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 2004;75:1046-1058.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1046-1058
-
-
Francks, C.1
Paracchini, S.2
Smith, S.D.3
Richardson, A.J.4
Scerri, T.S.5
Cardon, L.R.6
Marlow, A.J.7
MacPhie, I.L.8
Walter, J.9
Pennington, B.F.10
Fisher, S.E.11
Olson, R.K.12
DeFries, J.C.13
Stein, J.F.14
Monaco, A.P.15
-
44
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR: DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 2005;102:17053-17058.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
Held, M.4
Liu, J.5
Olson, R.K.6
Pennington, B.F.7
DeFries, J.C.8
Gelernter, J.9
O'Reilly-Pol, T.10
Somlo, S.11
Skudlarski, P.12
Shaywitz, S.E.13
Shaywitz, B.A.14
Marchione, K.15
Wang, Y.16
Paramasivam, M.17
LoTurco, J.J.18
Page, G.P.19
Gruen, J.R.20
more..
-
45
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hulsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Korne G, Nothen MM, Kere J: Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 2006;78:52-62.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
Hulsmann, J.11
Cichon, S.12
Lindgren, C.M.13
Propping, P.14
Zucchelli, M.15
Ziegler, A.16
Peyrard-Janvid, M.17
Schulte-Korne, G.18
Nothen, M.M.19
Kere, J.20
more..
-
46
-
-
33744920683
-
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
-
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, LoTurco JJ, Monaco AP: The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 2006;15:1659-1666.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
Lai, C.4
Paramasivam, M.5
Wang, Y.6
Keating, B.J.7
Taylor, J.M.8
Hacking, D.F.9
Scerri, T.10
Francks, C.11
Richardson, A.J.12
Wade-Martins, R.13
Stein, J.F.14
Knight, J.C.15
Copp, A.J.16
LoTurco, J.J.17
Monaco, A.P.18
-
47
-
-
33744925717
-
Genes, cognition and dyslexia: Learning to read the genome
-
Fisher SE, Francks C: Genes, cognition and dyslexia: learning to read the genome. Trends Cogn Sci 2006;10:250-257.
-
(2006)
Trends Cogn Sci
, vol.10
, pp. 250-257
-
-
Fisher, S.E.1
Francks, C.2
-
48
-
-
33746263663
-
Breakthroughs in the search for dyslexia candidate genes
-
McGrath LM, Smith SD, Pennington BF: Breakthroughs in the search for dyslexia candidate genes. Trends Mol Med 2006;12:333-341.
-
(2006)
Trends Mol Med
, vol.12
, pp. 333-341
-
-
McGrath, L.M.1
Smith, S.D.2
Pennington, B.F.3
-
49
-
-
0025335054
-
An extended family with a dominantly inherited speech disorder
-
Hurst JA, Baraitser M, Auger E, Graham F, Norell S: An extended family with a dominantly inherited speech disorder. Dev Med Child Neurol 1990;32:352-355.
-
(1990)
Dev Med Child Neurol
, vol.32
, pp. 352-355
-
-
Hurst, J.A.1
Baraitser, M.2
Auger, E.3
Graham, F.4
Norell, S.5
-
50
-
-
0025343411
-
Feature-blind grammar and dysphasia
-
Gopnik M: Feature-blind grammar and dysphasia. Nature 1990;344:715.
-
(1990)
Nature
, vol.344
, pp. 715
-
-
Gopnik, M.1
-
51
-
-
0026145984
-
Familial aggregation of a developmental language disorder
-
Gopnik M, Crago MB: Familial aggregation of a developmental language disorder. Cognition 1991;39:1-50.
-
(1991)
Cognition
, vol.39
, pp. 1-50
-
-
Gopnik, M.1
Crago, M.B.2
-
52
-
-
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;125:452-464.
-
(2002)
Brain
, vol.125
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
53
-
-
0028870054
-
Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
-
Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R: Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc Natl Acad Sci USA 1995;92:930-933.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 930-933
-
-
Vargha-Khadem, F.1
Watkins, K.2
Alcock, K.3
Fletcher, P.4
Passingham, R.5
-
55
-
-
0038202901
-
FOXP2 in focus: What can genes tell us about speech and language?
-
Marcus GF, Fisher SE: FOXP2 in focus: what can genes tell us about speech and language? Trends Cogn Sci 2003;7:257-262.
-
(2003)
Trends Cogn Sci
, vol.7
, pp. 257-262
-
-
Marcus, G.F.1
Fisher, S.E.2
-
56
-
-
0031940694
-
Localisation of a gene implicated in a severe speech and language disorder
-
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME: Localisation of a gene implicated in a severe speech and language disorder. Nat Genet 1998;18:168-170.
-
(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
-
57
-
-
0033865944
-
The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
-
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP: The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Am J Hum Genet 2000;67:357-368.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 357-368
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Levy, E.R.4
Hodgson, S.5
Fox, M.6
Jeremiah, S.7
Povey, S.8
Jamison, D.C.9
Green, E.D.10
Vargha-Khadem, F.11
Monaco, A.P.12
-
58
-
-
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;413:519-523.
-
(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
-
59
-
-
33749867547
-
Functional genetic analysis of mutations implicated in a human speech and language disorder
-
Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, Bird LE, Davies KE, Fisher SE: 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
-
60
-
-
12444297502
-
Dissection of molecular mechanisms underlying speech and language disorders
-
Fisher SE: Dissection of molecular mechanisms underlying speech and language disorders. Appl Psycholing 2005;26:111-128.
-
(2005)
Appl Psycholing
, vol.26
, pp. 111-128
-
-
Fisher, S.E.1
-
61
-
-
0037341876
-
Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia
-
Belton E, Salmond CH, Watkins KE, Vargha-Khadem F, Gadian DG: 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
-
62
-
-
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, Frackowiak RS, Mishkin M, Gadian DG: 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
-
63
-
-
0242290123
-
Language fMRI abnormalities associated with FOXP2 gene mutation
-
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.
-
(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
-
64
-
-
0036387193
-
Forkhead transcription factors: Key players in development and metabolism
-
Carlsson P, Mahlapuu M: Forkhead transcription factors: key players in development and metabolism. Dev Biol 2002;250:1-23.
-
(2002)
Dev Biol
, vol.250
, pp. 1-23
-
-
Carlsson, P.1
Mahlapuu, M.2
-
65
-
-
0037866671
-
Fox's in development and disease
-
Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS: Fox's in development and disease. Trends Genet 2003;19:339-344.
-
(2003)
Trends Genet
, vol.19
, pp. 339-344
-
-
Lehmann, O.J.1
Sowden, J.C.2
Carlsson, P.3
Jordan, T.4
Bhattacharya, S.S.5
-
66
-
-
33644800026
-
Structure of the forkhead domain of FOXP2 bound to DNA
-
Stroud JC, Wu Y, Bates DL, Han A, Nowick K, Paabo S, Tong H, Chen L: Structure of the forkhead domain of FOXP2 bound to DNA. Structure 2006;14:159-166.
-
(2006)
Structure
, vol.14
, pp. 159-166
-
-
Stroud, J.C.1
Wu, Y.2
Bates, D.L.3
Han, A.4
Nowick, K.5
Paabo, S.6
Tong, H.7
Chen, L.8
-
67
-
-
0037487188
-
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder
-
Gauthier J, Joober R, Mottron L, Laurent S, Fuchs M, De Kimpe V, Rouleau GA: Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. Am J Med Genet A 2003;118:172-175.
-
(2003)
Am J Med Genet A
, vol.118
, pp. 172-175
-
-
Gauthier, J.1
Joober, R.2
Mottron, L.3
Laurent, S.4
Fuchs, M.5
De Kimpe, V.6
Rouleau, G.A.7
-
68
-
-
18344368187
-
FOXP2 is not a major susceptibility gene for autism or specific language impairment
-
Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP: FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet 2002;70:1318-1327.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1318-1327
-
-
Newbury, D.F.1
Bonora, E.2
Lamb, J.A.3
Fisher, S.E.4
Lai, C.S.5
Baird, G.6
Jannoun, L.7
Slonims, V.8
Stott, C.M.9
Merricks, M.J.10
Bolton, P.F.11
Bailey, A.J.12
Monaco, A.P.13
-
69
-
-
0037043075
-
Evaluation of FOXP2 as an autism susceptibility gene
-
Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, Sheffield VC: Evaluation of FOXP2 as an autism susceptibility gene. Am J Med Genet 2002;114:566-569.
-
(2002)
Am J Med Genet
, vol.114
, pp. 566-569
-
-
Wassink, T.H.1
Piven, J.2
Vieland, V.J.3
Pietila, J.4
Goedken, R.J.5
Folstein, S.E.6
Sheffield, V.C.7
-
70
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE: Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet 2005;76:1074-1080.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1074-1080
-
-
MacDermot, K.D.1
Bonora, E.2
Sykes, N.3
Coupe, A.M.4
Lai, C.S.5
Vernes, S.C.6
Vargha-Khadem, F.7
McKenzie, F.8
Smith, R.L.9
Monaco, A.P.10
Fisher, S.E.11
-
71
-
-
33749869970
-
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
-
Shriberg LD, Ballard KJ, Tomblin JB, Duffy JR, Odell KH, Williams CA: 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
-
72
-
-
33644860165
-
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
-
Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW: Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A 2006;140:509-514.
-
(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
Senman, L.7
Feuk, L.8
Osborne, L.R.9
Scherer, S.W.10
-
73
-
-
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 Genet 2006;79:965-972.
-
(2006)
Am J Hum Genet
, 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..
-
74
-
-
33646510364
-
Genome-wide analysis of protein-DNA interactions
-
Kim TH, Ren B: Genome-wide analysis of protein-DNA interactions. Annu Rev Genomics Hum Genet 2006;7:81-102.
-
(2006)
Annu Rev Genomics Hum Genet
, vol.7
, pp. 81-102
-
-
Kim, T.H.1
Ren, B.2
-
75
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
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;126:2455-2462.
-
(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
-
76
-
-
1842610982
-
Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction
-
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.
-
(2004)
J Neurosci
, vol.24
, pp. 3152-3163
-
-
Teramitsu, I.1
Kudo, L.C.2
London, S.E.3
Geschwind, D.H.4
White, S.A.5
-
77
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
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.
-
(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
-
78
-
-
1842454166
-
FoxP2 expression in avian vocal learners and nonlearners
-
Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED, Scharff C: FoxP2 expression in avian vocal learners and nonlearners. J Neurosci 2004;24:3164-3175.
-
(2004)
J Neurosci
, vol.24
, 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
-
79
-
-
27444435989
-
Molecular cloning and developmental expression of foxP2 in zebrafish
-
Bonkowsky JL, Chien CB: Molecular cloning and developmental expression of foxP2 in zebrafish. Dev Dyn 2005;234:740-746.
-
(2005)
Dev Dyn
, vol.234
, pp. 740-746
-
-
Bonkowsky, J.L.1
Chien, C.B.2
-
80
-
-
29244467422
-
The eloquent ape: Genes, brains and the evolution of language
-
Fisher SE, Marcus GF: 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
-
81
-
-
0035920153
-
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
-
Shu W, Yang H, Zhang L, Lu MM, Morrisey EE: Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors. J Biol Chem 2001;276:27488-27497.
-
(2001)
J Biol Chem
, vol.276
, pp. 27488-27497
-
-
Shu, W.1
Yang, H.2
Zhang, L.3
Lu, M.M.4
Morrisey, E.E.5
-
82
-
-
33749836933
-
Singing mice, songbirds, and more: Models for FOXP2 function and dysfunction in human speech and language
-
White SA, Fisher SE, Geschwind DH, Scharff C, Holy TE: Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language. J Neurosci 2006;26:10376-10379.
-
(2006)
J Neurosci
, vol.26
, pp. 10376-10379
-
-
White, S.A.1
Fisher, S.E.2
Geschwind, D.H.3
Scharff, C.4
Holy, T.E.5
-
83
-
-
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;102:9643-9648.
-
(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
Santucci, A.C.11
Perl, D.12
Morrisey, E.13
Buxbaum, J.D.14
-
84
-
-
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, Paabo S: Molecular evolution of FOXP2, a gene involved in speech and language. Nature 2002;418:869-872.
-
(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
Paabo, S.8
-
85
-
-
0036959262
-
Accelerated protein evolution and origins of human-specific features: Foxp2 as an example
-
Zhang J, Webb DM, Podlaha O: Accelerated protein evolution and origins of human-specific features: Foxp2 as an example. Genetics 2002;162:1825-1835.
-
(2002)
Genetics
, vol.162
, pp. 1825-1835
-
-
Zhang, J.1
Webb, D.M.2
Podlaha, O.3
-
86
-
-
26844496418
-
Severe expressive-language delay related to duplication of the Williams-Beuren locus
-
Somerville MJ, Mervis CB, Young EJ, Seo EJ, del Campo M, Bamforth S, Peregrine E, Loo W, Lilley M, Perez-Jurado LA, Morris CA, Scherer SW, Osborne LR: Severe expressive-language delay related to duplication of the Williams-Beuren locus. N Engl J Med 2005;353:1694-1701.
-
(2005)
N Engl J Med
, vol.353
, pp. 1694-1701
-
-
Somerville, M.J.1
Mervis, C.B.2
Young, E.J.3
Seo, E.J.4
del Campo, M.5
Bamforth, S.6
Peregrine, E.7
Loo, W.8
Lilley, M.9
Perez-Jurado, L.A.10
Morris, C.A.11
Scherer, S.W.12
Osborne, L.R.13
-
87
-
-
33845889998
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
-
Durand CM, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsater H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Roge B, Heron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T: Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet 2007;39:25-27.
-
(2007)
Nat Genet
, vol.39
, pp. 25-27
-
-
Durand, C.M.1
Betancur, C.2
Boeckers, T.M.3
Bockmann, J.4
Chaste, P.5
Fauchereau, F.6
Nygren, G.7
Rastam, M.8
Gillberg, I.C.9
Anckarsater, H.10
Sponheim, E.11
Goubran-Botros, H.12
Delorme, R.13
Chabane, N.14
Mouren-Simeoni, M.C.15
de Mas, P.16
Bieth, E.17
Roge, B.18
Heron, D.19
Burglen, L.20
Gillberg, C.21
Leboyer, M.22
Bourgeron, T.23
more..
-
88
-
-
26844582888
-
On genes, speech, and language
-
Fisher SE: On genes, speech, and language. N Engl J Med 2005;353:1655-1657.
-
(2005)
N Engl J Med
, vol.353
, pp. 1655-1657
-
-
Fisher, S.E.1
|