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Year Number of Results
2010 4
2011 1
2014 2
2015 2
2021 0
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8 results
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Page 1
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.
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.
Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE; SLI Consortium, Whitehouse AJ, Snowling MJ, Newbury DF, Paracchini S. Pettigrew KA, et al. Genes Brain Behav. 2015 Apr;14(4):369-76. doi: 10.1111/gbb.12213. Epub 2015 Apr 1. Genes Brain Behav. 2015. PMID: 25778778 Free PMC article.
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC; SLI Consortium, Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF. Simpson NH, et al. Eur J Hum Genet. 2015 Oct;23(10):1370-7. doi: 10.1038/ejhg.2014.296. Epub 2015 Jan 14. Eur J Hum Genet. 2015. PMID: 25585696 Free PMC article.
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H; IMGSAC; SLI Consortium; WGS500 Consortium, Parr J, Pagnamenta AT, Maestrini E, Bacchelli E, Fisher SE, Newbury DF. Ceroni F, et al. Eur J Hum Genet. 2014 Oct;22(10):1165-71. doi: 10.1038/ejhg.2014.4. Epub 2014 Feb 12. Eur J Hum Genet. 2014. PMID: 24518835 Free PMC article.
Identification of candidate genes for dyslexia susceptibility on chromosome 18.
Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ. Scerri TS, et al. PLoS One. 2010 Oct 28;5(10):e13712. doi: 10.1371/journal.pone.0013712. PLoS One. 2010. PMID: 21060895 Free PMC article.
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Nudel R, et al. Genes Brain Behav. 2014 Apr;13(4):418-29. doi: 10.1111/gbb.12127. Epub 2014 Mar 24. Genes Brain Behav. 2014. PMID: 24571439 Free PMC article.
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP. Newbury DF, et al. Behav Genet. 2011 Jan;41(1):90-104. doi: 10.1007/s10519-010-9424-3. Epub 2010 Dec 17. Behav Genet. 2011. PMID: 21165691 Free PMC article.
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Horn D, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco AP, Bonin M, Riess O, Wohlleber E, Illig T, Bezzina CR, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold GA, Strom TM. Horn D, et al. Hum Mutat. 2010 Nov;31(11):E1851-60. doi: 10.1002/humu.21362. Hum Mutat. 2010. PMID: 20848658 Free PMC article.
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