Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 4
2001 1
2002 2
2003 1
2004 1
2005 2
2007 4
2008 4
2009 9
2010 11
2011 7
2012 5
2013 2
2014 2
2015 12
2016 8
2017 5
2018 10
2019 5
2020 7
2021 9
2022 8
2023 5
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

113 results

Results by year

Filters applied: . Clear all
Page 1
The natural history and genotype-phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis.
Colbert BM, Lanting C, Smeal M, Blanton S, Dykxhoorn DM, Tang PC, Getchell RL, Velde H, Fehrmann M, Thorpe R, Chapagain P, Elkhaligy H, Kremer H, Yntema H, Haer-Wigman L, Redfield S, Sun T, Bruijn S, Plomp A, Goderie T, van de Kamp J, Free RH, Wassink-Ruiter JK, Widdershoven J, Vanhoutte E, Rotteveel L, Kriek M, van Dooren M, Hoefsloot L, de Gier HHW; DOOFNL Consortium; Schaefer A, Kolbe D, Azaiez H, Rabie G, Aburayyan A, Kawas M, Kanaan M, Holder J, Usami SI, Chen Z, Dai P, Holt J, Nelson R, Choi BY, Shearer E, Smith RJH, Pennings R, Liu XZ. Colbert BM, et al. Hum Genet. 2024 Apr 30. doi: 10.1007/s00439-024-02648-3. Online ahead of print. Hum Genet. 2024. PMID: 38691166
Advances in cochlear gene therapies.
Klimara MJ, Smith RJH. Klimara MJ, et al. Curr Opin Pediatr. 2023 Dec 1;35(6):631-640. doi: 10.1097/MOP.0000000000001273. Epub 2023 Jul 6. Curr Opin Pediatr. 2023. PMID: 37417821 Review.
De novo variants are a common cause of genetic hearing loss.
Klimara MJ, Nishimura C, Wang D, Kolbe DL, Schaefer AM, Walls WD, Frees KL, Smith RJH, Azaiez H. Klimara MJ, et al. Genet Med. 2022 Dec;24(12):2555-2567. doi: 10.1016/j.gim.2022.08.028. Epub 2022 Oct 4. Genet Med. 2022. PMID: 36194208 Free PMC article.
The hearing-impaired patient: what the future holds.
Smith RJH. Smith RJH. Hum Genet. 2022 Apr;141(3-4):307-310. doi: 10.1007/s00439-022-02447-8. Epub 2022 Mar 15. Hum Genet. 2022. PMID: 35290517 Free PMC article. No abstract available.
113 results