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A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions.
Nudel R, Zetterberg R, Hemager N, Christiani CAJ, Ohland J, Burton BK, Greve AN, Spang KS, Ellersgaard D, Gantriis DL, Bybjerg-Grauholm J, Plessen KJ, Jepsen JRM, Thorup AAE, Werge T, Mors O, Nordentoft M. Nudel R, et al. Behav Brain Funct. 2022 Dec 1;18(1):14. doi: 10.1186/s12993-022-00198-0. Behav Brain Funct. 2022. PMID: 36457050 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.
Genome-Wide Studies of Specific Language Impairment.
Reader RH, Covill LE, Nudel R, Newbury DF. Reader RH, et al. Among authors: nudel r. Curr Behav Neurosci Rep. 2014;1(4):242-250. doi: 10.1007/s40473-014-0024-z. Curr Behav Neurosci Rep. 2014. PMID: 25411653 Free PMC article. Review.
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. Among authors: nudel r. 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.
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.
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.
49 results