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The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate.
Eur J Hum Genet. 2020 Jul;28(7):925-937. doi: 10.1038/s41431-020-0581-4. Epub 2020 May 28.
Eur J Hum Genet. 2020.
PMID: 32467599
Free PMC article.
A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect.
Abdelfatah N, Merner N, Houston J, Benteau T, Griffin A, Doucette L, Stockley T, Lauzon JL, Young TL.
Abdelfatah N, et al. Among authors: benteau t.
Hum Mutat. 2013 Jan;34(1):66-9. doi: 10.1002/humu.22205. Epub 2012 Oct 11.
Hum Mutat. 2013.
PMID: 22911656
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X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.
Stanton SG, Griffin A, Stockley TL, Brown C, Young TL, Benteau T, Abdelfatah N.
Stanton SG, et al. Among authors: benteau t.
Am J Audiol. 2014 Jun;23(2):190-200. doi: 10.1044/2014_AJA-13-0040.
Am J Audiol. 2014.
PMID: 24687041
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A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.
Pater JA, Benteau T, Griffin A, Penney C, Stanton SG, Predham S, Kielley B, Squires J, Zhou J, Li Q, Abdelfatah N, O'Rielly DD, Young TL.
Pater JA, et al. Among authors: benteau t.
Hum Genet. 2017 Jan;136(1):107-118. doi: 10.1007/s00439-016-1746-7. Epub 2016 Nov 12.
Hum Genet. 2017.
PMID: 27838790
Free PMC article.
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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.
Abdelfatah N, Mostafa AA, French CR, Doucette LP, Penney C, Lucas MB, Griffin A, Booth V, Rowley C, Besaw JE, Tranebjærg L, Rendtorff ND, Hodgkinson KA, Little LA, Agrawal S, Parnes L, Batten T, Moore S, Hu P, Pater JA, Houston J, Galutira D, Benteau T, MacDonald C, French D, O'Rielly DD, Stanton SG, Young TL.
Abdelfatah N, et al. Among authors: benteau t.
Hum Genet. 2022 Apr;141(3-4):965-979. doi: 10.1007/s00439-021-02381-1. Epub 2021 Oct 11.
Hum Genet. 2022.
PMID: 34633540
Free PMC article.
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Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.
Singh S, Penney C, Griffin A, Woodland G, Werdyani S, Benteau TA, Abdelfatah N, Squires J, King B, Houston J, Dyer MJ, Roslin NM, Vincent D, Marquis P, O'Rielly DD, Hodgkinson K, Burt T, Baker A, Stanton SG, Young TL.
Singh S, et al. Among authors: benteau ta.
Eur J Hum Genet. 2023 Jul;31(7):815-823. doi: 10.1038/s41431-023-01358-0. Epub 2023 Apr 19.
Eur J Hum Genet. 2023.
PMID: 37072551
Free PMC article.
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Impact of a mobile decision support tool on antimicrobial stewardship indicators in St. John's, Canada.
Doyle D, McDonald G, Pratt C, Rehan Z, Benteau T, Phillips J, Daley P.
Doyle D, et al. Among authors: benteau t.
PLoS One. 2021 Jun 16;16(6):e0252407. doi: 10.1371/journal.pone.0252407. eCollection 2021.
PLoS One. 2021.
PMID: 34133424
Free PMC article.
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