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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.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, Baird G, Paracchini S, Fisher SE, Newbury DF; SLI Consortium. Simpson NH, et al. Dev Med Child Neurol. 2014 Apr;56(4):346-53. doi: 10.1111/dmcn.12294. Epub 2013 Oct 9. Dev Med Child Neurol. 2014. PMID: 24117048 Free PMC article.
Associations of HLA alleles with specific language impairment.
Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium; Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF. Nudel R, et al. J Neurodev Disord. 2014 Jan 17;6(1):1. doi: 10.1186/1866-1955-6-1. J Neurodev Disord. 2014. PMID: 24433325 Free PMC article.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Echeverry MM, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER; SLI Consortium; Palomino H, Carvajal-Carmona L, Veltman JA, Cazier JB, De Barbieri Z, Fisher SE, Newbury DF. Villanueva P, et al. PLoS Genet. 2015 Mar 17;11(3):e1004925. doi: 10.1371/journal.pgen.1004925. eCollection 2015 Mar. PLoS Genet. 2015. PMID: 25781923 Free PMC article.
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.
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.
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.
Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Magdalena Echeverry M, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER; SLI Consortium; Palomino H, Carvajal-Carmona L, Veltman JA, Cazier JB, De Barbieri Z, Fisher SE, Newbury DF. Villanueva P, et al. PLoS Genet. 2015 Jun 26;11(6):e1005336. doi: 10.1371/journal.pgen.1005336. eCollection 2015 Jun. PLoS Genet. 2015. PMID: 26114769 Free PMC article. No abstract available.
465 results