Marita S Bady-Khoo
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Explore the profile of Marita S Bady-Khoo including associated specialties, affiliations and a list of published articles.
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5
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39
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Recent Articles
1.
Danilchenko V, Zytsar M, Maslova E, Bady-Khoo M, Barashkov N, Morozov I, et al.
Diagnostics (Basel)
. 2021 Dec;
11(12).
PMID: 34943614
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the prevalence of different HL forms significantly varies among populations worldwide. Investigation of region-specific landscapes of hereditary HL...
2.
Zytsar M, Bady-Khoo M, Danilchenko V, Maslova E, Barashkov N, Morozov I, et al.
Genes (Basel)
. 2020 Jul;
11(7).
PMID: 32708339
The mutations in the gene (13q12.11, MIM 121011) encoding transmembrane protein connexin 26 (Cx26) account for a significant portion of hereditary hearing loss worldwide. Earlier we found a high prevalence...
3.
Posukh O, Zytsar M, Bady-Khoo M, Danilchenko V, Maslova E, Barashkov N, et al.
Genes (Basel)
. 2019 Jun;
10(6).
PMID: 31195736
Mutations in the gene are the main cause for nonsyndromic autosomal recessive deafness 1A (DFNB1A) in many populations. mutational spectrum and pathogenic contribution are widely varying in different populations. Significant...
4.
Zytsar M, Barashkov N, Bady-Khoo M, Shubina-Olejnik O, Danilenko N, Bondar A, et al.
BMC Med Genet
. 2018 Aug;
19(1):138.
PMID: 30086704
Background: Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations...
5.
Solovyev A, Dzhemileva L, Posukh O, Barashkov N, Bady-Khoo M, Lobov S, et al.
J Community Genet
. 2017 Mar;
8(3):167-171.
PMID: 28324246
Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test systems....