Similar articles for PMID: 15638823

Year	Number of Results
1993	1
1997	1
1998	2
1999	3
2000	6
2001	6
2002	9
2003	9
2004	23
2005	20
2006	13
2007	17
2008	13
2009	20
2010	19
2011	22
2012	23
2013	19
2014	16
2015	18
2016	18
2017	12
2018	7
2019	15
2020	10
2021	13
2022	7
2023	1
2024	0

1

Double heterozygosity with mutations involving both the GJB2 and GJB6 genes is a possible, but very rare, cause of congenital deafness in the Czech population.

Seeman P, Bendová O, Rasková D, Malíková M, Groh D, Kabelka Z. Seeman P, et al. Ann Hum Genet. 2005 Jan;69(Pt 1):9-14. doi: 10.1046/j.1529-8817.2003.00120.x. Ann Hum Genet. 2005. PMID: 15638823

2

Mosaic GJB2 mutation A88V leading to diffuse neonatal hyperkeratosis and porokeratotic hamartoma.

Letertre O, Jullie ML, Reboul MP, Leclerc-Mercier S, Charbit F, Boralevi F, Labrèze C, Hadj-Rabia S, Morice-Picard F. Letertre O, et al. J Eur Acad Dermatol Venereol. 2023 Jun;37(6):e801-e803. doi: 10.1111/jdv.18935. Epub 2023 Feb 17. J Eur Acad Dermatol Venereol. 2023. PMID: 36734293 No abstract available.

3

[Meta-analysis for the association of GJB2 gene p.V37I variant and its types with the risk of deafness].

Wang Z, Shao Y, Li J. Wang Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Dec 10;39(12):1313-1318. doi: 10.3760/cma.j.cn511374-20220321-00186. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36453950 Chinese.

4

GJB2 and GJB6 gene transcripts in the human cochlea: A study using RNAscope, confocal, and super-resolution structured illumination microscopy.

Liu W, Rask-Andersen H. Liu W, et al. Front Mol Neurosci. 2022 Sep 20;15:973646. doi: 10.3389/fnmol.2022.973646. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36204137 Free PMC article.

5

The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of GJB2 Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome.

Xu Y, Wang M, Huang L, Hu J. Xu Y, et al. Ann Dermatol. 2022 Oct;34(5):382-386. doi: 10.5021/ad.20.278. Ann Dermatol. 2022. PMID: 36198631 Free PMC article.

6

A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.

Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Khusnutdinova EK, Poliakov A, Metspalu M, Posukh OL, Barashkov NA, Fedorova SA. Solovyev AV, et al. Hum Genet. 2022 Apr;141(3-4):697-707. doi: 10.1007/s00439-021-02405-w. Epub 2021 Nov 27. Hum Genet. 2022. PMID: 34839402

7

Genetic etiology of non-syndromic hearing loss in Latin America.

Lezirovitz K, Mingroni-Netto RC. Lezirovitz K, et al. Hum Genet. 2022 Apr;141(3-4):539-581. doi: 10.1007/s00439-021-02354-4. Epub 2021 Oct 15. Hum Genet. 2022. PMID: 34652575 Review.

8

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.

Batissoco AC, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, da Silva de Oliveira Longati EU, Mariano D, Hoshino ACH, Tsuji RK, Jesus-Santos R, Abath-Neto O, Bento RF, Oiticica J, Lezirovitz K. Batissoco AC, et al. Hum Genet. 2022 Apr;141(3-4):519-538. doi: 10.1007/s00439-021-02372-2. Epub 2021 Oct 1. Hum Genet. 2022. PMID: 34599368

9

Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family.

Ortore RP, Leone MP, Palumbo O, Petracca A, Trecca EMC, D'Ecclesia A, Vigliaroli CL, Micale L, Longo F, Melchionda S, Castori M. Ortore RP, et al. Audiol Res. 2021 Sep 9;11(3):443-451. doi: 10.3390/audiolres11030041. Audiol Res. 2021. PMID: 34562879 Free PMC article.

10

Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?

Lin YH, Wu PC, Tsai CY, Lin YH, Lo MY, Hsu SJ, Lin PH, Erdenechuluun J, Wu HP, Hsu CJ, Wu CC, Chen PL. Lin YH, et al. J Mol Diagn. 2021 Oct;23(10):1279-1291. doi: 10.1016/j.jmoldx.2021.07.007. Epub 2021 Jul 27. J Mol Diagn. 2021. PMID: 34325055 Free article.

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