Vargha-Khadem F - Search Results

1

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. MacDermot KD, et al. Am J Hum Genet. 2005 Jun;76(6):1074-80. doi: 10.1086/430841. Epub 2005 Apr 22. Am J Hum Genet. 2005. PMID: 15877281 Free PMC article.

2

Localisation of a gene implicated in a severe speech and language disorder.

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. Fisher SE, et al. Nat Genet. 1998 Feb;18(2):168-70. doi: 10.1038/ng0298-168. Nat Genet. 1998. PMID: 9462748

3

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. Lai CS, et al. Am J Hum Genet. 2000 Aug;67(2):357-68. doi: 10.1086/303011. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10880297 Free PMC article.

4

A forkhead-domain gene is mutated in a severe speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. Lai CS, et al. Nature. 2001 Oct 4;413(6855):519-23. doi: 10.1038/35097076. Nature. 2001. PMID: 11586359

5

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. Vargha-Khadem F, et al. Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):930-3. doi: 10.1073/pnas.92.3.930. Proc Natl Acad Sci U S A. 1995. PMID: 7846081 Free PMC article.

6

Neocerebellar Crus I Abnormalities Associated with a Speech and Language Disorder Due to a Mutation in FOXP2.

Argyropoulos GPD, Watkins KE, Belton-Pagnamenta E, Liégeois F, Saleem KS, Mishkin M, Vargha-Khadem F. Argyropoulos GPD, et al. Cerebellum. 2019 Jun;18(3):309-319. doi: 10.1007/s12311-018-0989-3. Cerebellum. 2019. PMID: 30460543 Free PMC article.

7

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia.

Belton E, Salmond CH, Watkins KE, Vargha-Khadem F, Gadian DG. Belton E, et al. Hum Brain Mapp. 2003 Mar;18(3):194-200. doi: 10.1002/hbm.10093. Hum Brain Mapp. 2003. PMID: 12599277 Free PMC article.

8

The speech gene FOXP2 is not imprinted.

Thomas AC, Frost JM, Ishida M, Vargha-Khadem F, Moore GE, Stanier P. Thomas AC, et al. J Med Genet. 2012 Nov;49(11):669-70. doi: 10.1136/jmedgenet-2012-101242. Epub 2012 Oct 2. J Med Genet. 2012. PMID: 23033221 No abstract available.

9

Neural basis of an inherited speech and language disorder.

Vargha-Khadem F, Watkins KE, Price CJ, Ashburner J, Alcock KJ, Connelly A, Frackowiak RS, Friston KJ, Pembrey ME, Mishkin M, Gadian DG, Passingham RE. Vargha-Khadem F, et al. Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12695-700. doi: 10.1073/pnas.95.21.12695. Proc Natl Acad Sci U S A. 1998. PMID: 9770548 Free PMC article.

10

FOXP2 and the neuroanatomy of speech and language.

Vargha-Khadem F, Gadian DG, Copp A, Mishkin M. Vargha-Khadem F, et al. Nat Rev Neurosci. 2005 Feb;6(2):131-8. doi: 10.1038/nrn1605. Nat Rev Neurosci. 2005. PMID: 15685218 Review.

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