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Genetic advances in the study of speech and language disorders.
Newbury DF, Monaco AP. Newbury DF, et al. Neuron. 2010 Oct 21;68(2):309-20. doi: 10.1016/j.neuron.2010.10.001. Neuron. 2010. PMID: 20955937 Free PMC article. Review.
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; International Molecular Genetic Study of Autism Consortium. Newbury DF, et al. Am J Hum Genet. 2002 May;70(5):1318-27. doi: 10.1086/339931. Epub 2002 Mar 13. Am J Hum Genet. 2002. PMID: 11894222 Free PMC article.
Molecular genetics of speech and language disorders.
Newbury DF, Monaco AP. Newbury DF, et al. Curr Opin Pediatr. 2002 Dec;14(6):696-701. doi: 10.1097/00008480-200212000-00009. Curr Opin Pediatr. 2002. PMID: 12436038 Review.
Talking genes - the molecular basis of language impairment.
Newbury DF, Monaco AP. Newbury DF, et al. Biologist (London). 2002 Dec;49(6):255-60. Biologist (London). 2002. PMID: 12486301 Review.
Genetic influences on language impairment and phonological short-term memory.
Newbury DF, Bishop DV, Monaco AP. Newbury DF, et al. Trends Cogn Sci. 2005 Nov;9(11):528-34. doi: 10.1016/j.tics.2005.09.002. Epub 2005 Sep 26. Trends Cogn Sci. 2005. PMID: 16188486 Review.
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
Falcaro M, Pickles A, Newbury DF, Addis L, Banfield E, Fisher SE, Monaco AP, Simkin Z, Conti-Ramsden G; SLI Consortium. Falcaro M, et al. Among authors: newbury df. Genes Brain Behav. 2008 Jun;7(4):393-402. doi: 10.1111/j.1601-183X.2007.00364.x. Epub 2007 Nov 12. Genes Brain Behav. 2008. PMID: 18005161
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. Among authors: newbury df. 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.
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
Newbury DF, Warburton PC, Wilson N, Bacchelli E, Carone S; International Molecular Genetic Study of Autism Consortium, Lamb JA, Maestrini E, Volpi EV, Mohammed S, Baird G, Monaco AP. Newbury DF, et al. Am J Med Genet A. 2009 Feb 15;149A(4):588-97. doi: 10.1002/ajmg.a.32704. Am J Med Genet A. 2009. PMID: 19267418 Free PMC article.
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
Winchester L, Newbury DF, Monaco AP, Ragoussis J. Winchester L, et al. Among authors: newbury df. Cytogenet Genome Res. 2008;123(1-4):322-32. doi: 10.1159/000184724. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287171
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, O'Hare A, Shaw D, Simkin Z, Simonoff E, Slonims V, Watson J, Ragoussis J, Fisher SE, Seckl JR, Helms PJ, Bolton PF, Pickles A, Conti-Ramsden G, Baird G, Bishop DV, Monaco AP. Newbury DF, et al. Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646677 Free PMC article.
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