Browse by UCL people
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Number of items: 22.
Article
Abidin, FNZ;
Wells, HRR;
Altmann, A;
Dawson, SJ;
(2021)
Hearing difficulty is linked to Alzheimer’s disease by common genetic vulnerability, not shared genetic architecture.
npj Aging and Mechanisms of Disease
, 7
(1)
, Article 17. 10.1038/s41514-021-00069-4.
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Cherny, SS;
Livshits, G;
Wells, HRR;
Freidin, MB;
Malkin, I;
Dawson, SJ;
Williams, FMK;
(2020)
Self-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank.
European Journal of Human Genetics
10.1038/s41431-020-0603-2.
(In press).
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Cipriani, V;
Vestito, L;
Magavern, EF;
Jacobsen, JOB;
Arno, G;
Behr, ER;
Benson, KA;
... Smedley, D; + view all
(2025)
Rare disease gene association discovery in the 100,000 Genomes Project.
Nature
10.1038/s41586-025-08623-w.
(In press).
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Crompton, M;
Cadge, BA;
Ziff, JL;
Mowat, AJ;
Nash, R;
Lavy, JA;
Powell, HRF;
... Dawson, SJ; + view all
(2019)
The Epidemiology of Otosclerosis in a British Cohort.
Otology & Neurotology
, 40
(1)
pp. 22-30.
10.1097/MAO.0000000000002047.
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Dawson, SJ;
Bowl, MR;
(2019)
Age-Related Hearing Loss.
Cold Spring Harbor perspectives in medicine
, 9
, Article a033217. 10.1101/cshperspect.a033217.
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Dunbar, LA;
Patni, P;
Aguilar, C;
Mburu, P;
Corns, L;
Wells, HR;
Delmaghani, S;
... Bowl, MR; + view all
(2019)
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
EMBO Molecular Medicine
, Article e10288. 10.15252/emmm.201910288.
(In press).
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Forge, A;
Taylor, RR;
Dawson, SJ;
Lovett, M;
Jagger, DJ;
(2017)
Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear.
PLoS Genetics
, 13
(3)
, Article e1006692. 10.1371/journal.pgen.1006692.
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Gómez-Dorado, M;
Daudet, N;
Gale, JE;
Dawson, SJ;
(2021)
Differential regulation of mammalian and avian ATOH1 by E2F1 and its implication for hair cell regeneration in the inner ear.
Scientific Reports
, 11
(1)
, Article 19368. 10.1038/s41598-021-98816-w.
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Gonçalves, AC;
Towers, ER;
Haq, N;
Porco, JA;
Pelletier, J;
Dawson, SJ;
Gale, JE;
(2019)
Drug-induced Stress Granule Formation Protects Sensory Hair Cells in Mouse Cochlear Explants During Ototoxicity.
Scientific Reports
, 9
(1)
, Article 12501. 10.1038/s41598-019-48393-w.
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Ingham, NJ;
Carlisle, F;
Pearson, S;
Lewis, MA;
Buniello, A;
Chen, J;
Isaacson, RL;
... Steel, KP; + view all
(2016)
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.
Scientific Reports
, 6
, Article 28964. 10.1038/srep28964.
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Ingham, NJ;
Pearson, SA;
Vancollie, VE;
Rook, V;
Lewis, MA;
Chen, J;
Buniello, A;
... Steel, KP; + view all
(2019)
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
PLoS Biology
, 17
(4)
, Article e3000194. 10.1371/journal.pbio.3000194.
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Lewis, MA;
Nolan, LS;
Cadge, BA;
Matthews, LJ;
Schulte, BA;
Dubno, JR;
Steel, KP;
(2018)
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.
BMC Medical Genomics
, 11
(1)
, Article 77. 10.1186/s12920-018-0395-1.
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Martin, Jack L;
Terry, Stephen J;
Gale, Jonathan E;
Dawson, Sally J;
(2023)
The ototoxic drug cisplatin localises to stress granules altering their dynamics and composition.
Journal of Cell Science
, 136
(14)
, Article jcs.260590. 10.1242/jcs.260590.
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Mowat, AJ;
Crompton, M;
Ziff, JL;
Aldren, CP;
Lavy, JA;
Saeed, SR;
Dawson, SJ;
(2018)
Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population.
Human Genetics
, 137
(5)
pp. 357-363.
10.1007/s00439-018-1889-9.
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Nolan, LS;
Maier, H;
Hermans-Borgmeyer, I;
Girotto, G;
Ecob, R;
Pirastu, N;
Cadge, BA;
... Dawson, SJ; + view all
(2013)
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice.
Neurobiol Aging
, 34
(8)
2077.e1 - 2077.e9.
10.1016/j.neurobiolaging.2013.02.009.
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Tornari, C;
Towers, ER;
Gale, JE;
Dawson, SJ;
(2014)
Regulation of the Orphan Nuclear Receptor Nr2f2 by the DFNA15 Deafness Gene Pou4f3.
PLoS One
, 9
(11)
, Article e112247 . 10.1371/journal.pone.0112247.
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Towers, ER;
Kelly, JJ;
Sud, R;
Gale, JE;
Dawson, SJ;
(2011)
Caprin-1 is a target of the deafness gene Pou4f3 and is recruited to stress granules in cochlear hair cells in response to ototoxic damage.
Journal of Cell Science
, 124
(7)
1145 - 1155.
10.1242/jcs.076141.
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Vuckovic, D;
Dawson, S;
Scheffer, DI;
Rantanen, T;
Morgan, A;
Di Stazio, M;
Vozzi, D;
... Girotto, G; + view all
(2015)
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.
Human Molecular Genetics
, 24
(19)
pp. 5655-5664.
10.1093/hmg/ddv279.
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Wells, HRR;
Abidin, FNZ;
Freidin, MB;
Williams, FMK;
Dawson, SJ;
(2021)
Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank.
Scientific Reports
, 11
(1)
, Article 6470. 10.1038/s41598-021-85871-6.
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Wells, HRR;
Freidin, MB;
Abidin, FNZ;
Payton, A;
Dawes, P;
Munro, KJ;
Morton, CC;
... Williams, FMK; + view all
(2019)
GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
The American Journal of Human Genetics
, 105
(4)
pp. 788-802.
10.1016/j.ajhg.2019.09.008.
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Zainul Abidin, FN;
Scelsi, MA;
Dawson, S;
Altmann, A;
(2021)
Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort.
NeuroImage: Clinical
, 32
, Article 102823. 10.1016/j.nicl.2021.102823.
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Ziff, JL;
Crompton, M;
Powell, HR;
Lavy, JA;
Aldren, CP;
Steel, KP;
Saeed, SR;
(2016)
Mutations and altered expression of SERPINF1 in patients with familial otosclerosis.
Human Molecular Genetics
, 25
(12)
pp. 2393-2403.
10.1093/hmg/ddw106.
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