MR/J003719/1/MRC_/Medical Research Council/United Kingdom[Grants and Funding] - Search Results

Year	Number of Results
2013	1
2014	5
2015	3
2016	4
2017	2
2018	2
2019	1
2020	1
2024	0

1

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

Devanna P, Chen XS, Ho J, Gajewski D, Smith SD, Gialluisi A, Francks C, Fisher SE, Newbury DF, Vernes SC. Devanna P, et al. Mol Psychiatry. 2018 May;23(5):1375-1384. doi: 10.1038/mp.2017.30. Epub 2017 Mar 14. Mol Psychiatry. 2018. PMID: 28289279 Free PMC article.

2

The Genetic Population Structure of Robinson Crusoe Island, Chile.

Mountford HS, Villanueva P, Fernández MA, Jara L, De Barbieri Z, Carvajal-Carmona LG, Cazier JB, Newbury DF. Mountford HS, et al. Front Genet. 2020 Jun 26;11:669. doi: 10.3389/fgene.2020.00669. eCollection 2020. Front Genet. 2020. PMID: 32676101 Free PMC article.

3

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

Pettigrew KA, Frinton E, Nudel R, Chan MTM, Thompson P, Hayiou-Thomas ME, Talcott JB, Stein J, Monaco AP, Hulme C, Snowling MJ, Newbury DF, Paracchini S. Pettigrew KA, et al. J Neurodev Disord. 2016 Jun 14;8:24. doi: 10.1186/s11689-016-9157-6. eCollection 2016. J Neurodev Disord. 2016. PMID: 27307794 Free PMC article.

4

Reading and language disorders: the importance of both quantity and quality.

Newbury DF, Monaco AP, Paracchini S. Newbury DF, et al. Genes (Basel). 2014 Apr 4;5(2):285-309. doi: 10.3390/genes5020285. Genes (Basel). 2014. PMID: 24705331 Free PMC article.

5

Candidate gene variant effects on language disorders in Robinson Crusoe Island.

Mountford HS, Villanueva P, Fernández MA, Barbieri Z, Cazier JB, Newbury DF. Mountford HS, et al. Ann Hum Biol. 2019 Mar;46(2):109-119. doi: 10.1080/03014460.2019.1622776. Epub 2019 Jun 19. Ann Hum Biol. 2019. PMID: 31132892

6

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.

7

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

Nudel R. Nudel R. J Neurodev Disord. 2016 Apr 5;8:13. doi: 10.1186/s11689-016-9146-9. eCollection 2016. J Neurodev Disord. 2016. PMID: 27053962 Free PMC article.

8

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation.

Prekovic S, Đurđević DF, Csifcsák G, Šveljo O, Stojković O, Janković M, Koprivšek K, Covill LE, Lučić M, Van den Broeck T, Helsen C, Ceroni F, Claessens F, Newbury DF. Prekovic S, et al. Sci Rep. 2016 Feb 3;6:20369. doi: 10.1038/srep20369. Sci Rep. 2016. PMID: 26838027 Free PMC article.

9

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Chen XS, Reader RH, Hoischen A, Veltman JA, Simpson NH, Francks C, Newbury DF, Fisher SE. Chen XS, et al. Sci Rep. 2017 Apr 25;7:46105. doi: 10.1038/srep46105. Sci Rep. 2017. PMID: 28440294 Free PMC article.

10

Family aggregation of language impairment in an isolated Chilean population from Robinson Crusoe Island.

De Barbieri Z, Fernández MA, Newbury DF, Villanueva P. De Barbieri Z, et al. Int J Lang Commun Disord. 2018 May;53(3):643-655. doi: 10.1111/1460-6984.12377. Epub 2018 Mar 25. Int J Lang Commun Disord. 2018. PMID: 29575355

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