Vernes SC - Search Results

1

A functional genetic link between distinct developmental language disorders.

Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. Vernes SC, et al. N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5. N Engl J Med. 2008. PMID: 18987363 Free PMC article.

2

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. Among authors: vernes sc. 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.

3

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. Vernes SC, et al. Hum Mol Genet. 2006 Nov 1;15(21):3154-67. doi: 10.1093/hmg/ddl392. Epub 2006 Sep 19. Hum Mol Genet. 2006. PMID: 16984964

4

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 SC, Fisher SE, Ren B, Geschwind DH. Spiteri E, et al. Among authors: vernes sc. Am J Hum Genet. 2007 Dec;81(6):1144-57. doi: 10.1086/522237. Epub 2007 Oct 31. Am J Hum Genet. 2007. PMID: 17999357 Free PMC article.

5

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE. Vernes SC, et al. Am J Hum Genet. 2007 Dec;81(6):1232-50. doi: 10.1086/522238. Epub 2007 Oct 31. Am J Hum Genet. 2007. PMID: 17999362 Free PMC article.

6

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.

Vernes SC, MacDermot KD, Monaco AP, Fisher SE. Vernes SC, et al. Eur J Hum Genet. 2009 Oct;17(10):1354-8. doi: 10.1038/ejhg.2009.43. Epub 2009 Apr 8. Eur J Hum Genet. 2009. PMID: 19352412 Free PMC article.

7

Unravelling neurogenetic networks implicated in developmental language disorders.

Vernes SC, Fisher SE. Vernes SC, et al. Biochem Soc Trans. 2009 Dec;37(Pt 6):1263-9. doi: 10.1042/BST0371263. Biochem Soc Trans. 2009. PMID: 19909259

8

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, Massacrier A, Rudolf G, Khalife M, Hirsch E, Fisher SE, Szepetowski P. Roll P, et al. Among authors: vernes sc. Hum Mol Genet. 2010 Dec 15;19(24):4848-60. doi: 10.1093/hmg/ddq415. Epub 2010 Sep 21. Hum Mol Genet. 2010. PMID: 20858596 Free PMC article.

9

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.

Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, Ragoussis J, Davies KE, Geschwind DH, Fisher SE. Vernes SC, et al. PLoS Genet. 2011 Jul;7(7):e1002145. doi: 10.1371/journal.pgen.1002145. Epub 2011 Jul 7. PLoS Genet. 2011. PMID: 21765815 Free PMC article.

10

The DISC1 promoter: characterization and regulation by FOXP2.

Walker RM, Hill AE, Newman AC, Hamilton G, Torrance HS, Anderson SM, Ogawa F, Derizioti P, Nicod J, Vernes SC, Fisher SE, Thomson PA, Porteous DJ, Evans KL. Walker RM, et al. Among authors: vernes sc. Hum Mol Genet. 2012 Jul 1;21(13):2862-72. doi: 10.1093/hmg/dds111. Epub 2012 Mar 20. Hum Mol Genet. 2012. PMID: 22434823

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