PubMed for id: 1812636094

Year	Number of Results
1993	1
1997	2
1998	2
1999	1
2017	1
2019	1
2020	1
2021	1
2022	1
2023	1
2024	0

1

Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.

Chen R, Diaz-Miranda MA, Aref-Eshghi E, Hartman TR, Griffith C, Morrison JL, Wheeler PG, Torti E, Richard G, Kenna M, Dechene ET, Spinner NB, Bai R, Conlin LK, Krantz ID, Amr SS, Luo M. Chen R, et al. Hum Mutat. 2022 Dec;43(12):1837-1843. doi: 10.1002/humu.24443. Epub 2022 Aug 2. Hum Mutat. 2022. PMID: 35870179

2

Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.

Mei X, Zhou Y, Amjad M, Yang W, Zhu R, Asif M, Hussain HMJ, Yang T, Iqbal F, Hu H. Mei X, et al. Neural Plast. 2021 Apr 22;2021:5528434. doi: 10.1155/2021/5528434. eCollection 2021. Neural Plast. 2021. PMID: 33976695 Free PMC article.

3

A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.

Walls WD, Moteki H, Thomas TR, Nishio SY, Yoshimura H, Iwasa Y, Frees KL, Nishimura CJ, Azaiez H, Booth KT, Marini RJ, Kolbe DL, Weaver AM, Schaefer AM, Wang K, Braun TA, Usami SI, Barr-Gillespie PG, Richardson GP, Smith RJ, Casavant TL. Walls WD, et al. Hum Genet. 2020 Oct;139(10):1315-1323. doi: 10.1007/s00439-020-02174-y. Epub 2020 May 7. Hum Genet. 2020. PMID: 32382995 Free PMC article.

4

[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene].

Zhou C, Li S, Song Q, Liu X, Miao Z. Zhou C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10;36(2):147-150. doi: 10.3760/cma.j.issn.1003-9406.2019.02.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30703234 Chinese.

5

Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.

Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, Ogawa K, Matsunaga T. Yamamoto N, et al. Orphanet J Rare Dis. 2017 Sep 25;12(1):157. doi: 10.1186/s13023-017-0708-z. Orphanet J Rare Dis. 2017. PMID: 28946916 Free PMC article.

6

Genetic Hearing Loss Overview.

Shearer AE, Hildebrand MS, Schaefer AM, Smith RJH. Shearer AE, et al. 1999 Feb 14 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1999 Feb 14 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301607 Free Books & Documents. Review.

7

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G. Verhoeven K, et al. Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60. Nat Genet. 1998. PMID: 9590290

8

Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.

Hughes DC, Legan PK, Steel KP, Richardson GP. Hughes DC, et al. Genomics. 1998 Feb 15;48(1):46-51. doi: 10.1006/geno.1997.5159. Genomics. 1998. PMID: 9503015

9

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ. Verhoeven K, et al. Am J Hum Genet. 1997 May;60(5):1168-73. Am J Hum Genet. 1997. PMID: 9150164 Free PMC article.

10

Nonsyndromic hearing impairment: unparalleled heterogeneity.

Van Camp G, Willems PJ, Smith RJ. Van Camp G, et al. Am J Hum Genet. 1997 Apr;60(4):758-64. Am J Hum Genet. 1997. PMID: 9106521 Free PMC article. Review. No abstract available.

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