Dawson S - Search Results

1

Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

Vuckovic D, Dawson S, Scheffer DI, Rantanen T, Morgan A, Di Stazio M, Vozzi D, Nutile T, Concas MP, Biino G, Nolan L, Bahl A, Loukola A, Viljanen A, Davis A, Ciullo M, Corey DP, Pirastu M, Gasparini P, Girotto G. Vuckovic D, et al. Among authors: dawson s. Hum Mol Genet. 2015 Oct 1;24(19):5655-64. doi: 10.1093/hmg/ddv279. Epub 2015 Jul 17. Hum Mol Genet. 2015. PMID: 26188009 Free PMC article.

2

Identification and functional analysis of common sequence variants in the DFNA15 gene, Brn-3c.

Nolan LS, Jagutpal SS, Cadge BA, Woo P, Dawson SJ. Nolan LS, et al. Among authors: dawson sj. Gene. 2007 Oct 1;400(1-2):89-97. doi: 10.1016/j.gene.2007.05.023. Epub 2007 Jun 12. Gene. 2007. PMID: 17611044

3

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss.

Linden Phillips L, Bitner-Glindzicz M, Lench N, Steel KP, Langford C, Dawson SJ, Davis A, Simpson S, Packer C. Linden Phillips L, et al. Among authors: dawson sj. Int J Audiol. 2013 Feb;52(2):124-33. doi: 10.3109/14992027.2012.733424. Epub 2012 Nov 7. Int J Audiol. 2013. PMID: 23131088 Free PMC article. Review.

4

A functional and genetic analysis of SOD2 promoter variants and their contribution to age-related hearing loss.

Nolan LS, Cadge BA, Gomez-Dorado M, Dawson SJ. Nolan LS, et al. Among authors: dawson sj. Mech Ageing Dev. 2013 Jul-Aug;134(7-8):298-306. doi: 10.1016/j.mad.2013.02.009. Epub 2013 Mar 13. Mech Ageing Dev. 2013. PMID: 23500038 Clinical Trial.

5

Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice.

Nolan LS, Maier H, Hermans-Borgmeyer I, Girotto G, Ecob R, Pirastu N, Cadge BA, Hübner C, Gasparini P, Strachan DP, Davis A, Dawson SJ. Nolan LS, et al. Among authors: dawson sj. Neurobiol Aging. 2013 Aug;34(8):2077.e1-9. doi: 10.1016/j.neurobiolaging.2013.02.009. Epub 2013 Mar 26. Neurobiol Aging. 2013. PMID: 23540940 Free PMC article.

6

Mutations and altered expression of SERPINF1 in patients with familial otosclerosis.

Ziff JL, Crompton M, Powell HR, Lavy JA, Aldren CP, Steel KP, Saeed SR, Dawson SJ. Ziff JL, et al. Hum Mol Genet. 2016 Jun 15;25(12):2393-2403. doi: 10.1093/hmg/ddw106. Epub 2016 Apr 7. Hum Mol Genet. 2016. PMID: 27056980 Free PMC article.

7

Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population.

Mowat AJ, Crompton M, Ziff JL, Aldren CP, Lavy JA, Saeed SR, Dawson SJ. Mowat AJ, et al. Hum Genet. 2018 May;137(5):357-363. doi: 10.1007/s00439-018-1889-9. Epub 2018 May 4. Hum Genet. 2018. PMID: 29728750 Free PMC article.

8

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes.

Lewis MA, Nolan LS, Cadge BA, Matthews LJ, Schulte BA, Dubno JR, Steel KP, Dawson SJ. Lewis MA, et al. Among authors: dawson sj. BMC Med Genomics. 2018 Sep 4;11(1):77. doi: 10.1186/s12920-018-0395-1. BMC Med Genomics. 2018. PMID: 30180840 Free PMC article.

9

GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.

Wells HRR, Freidin MB, Zainul Abidin FN, Payton A, Dawes P, Munro KJ, Morton CC, Moore DR, Dawson SJ, Williams FMK. Wells HRR, et al. Am J Hum Genet. 2019 Oct 3;105(4):788-802. doi: 10.1016/j.ajhg.2019.09.008. Epub 2019 Sep 26. Am J Hum Genet. 2019. PMID: 31564434 Free PMC article.

10

Targeted deletion of the RNA-binding protein Caprin1 leads to progressive hearing loss and impairs recovery from noise exposure in mice.

Nolan LS, Chen J, Gonçalves AC, Bullen A, Towers ER, Steel KP, Dawson SJ, Gale JE. Nolan LS, et al. Among authors: dawson sj. Sci Rep. 2022 Feb 14;12(1):2444. doi: 10.1038/s41598-022-05657-2. Sci Rep. 2022. PMID: 35165318 Free PMC article.

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