(Q26774741)

1

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Jun Yao

2

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Qin-Jun Wei

3

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Guang-Qian Xing

4

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Xin Cao

Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

5

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language of work or name

English

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publication date

December 2015

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1 December 2015

9 references

25 April 2019

20 June 2019

30 June 2019

14 September 2019

11 October 2019

28 November 2019

15 December 2019

6 November 2020

1 June 2022

9 references

25 April 2019

20 June 2019

30 June 2019

14 September 2019

11 October 2019

28 November 2019

15 December 2019

6 November 2020

1 June 2022

94

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page(s)

e2248

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issue

50

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copyright license

9 references

25 April 2019

20 June 2019

30 June 2019

14 September 2019

11 October 2019

28 November 2019

15 December 2019

6 November 2020

on focus list of Wikimedia project

1 June 2022

ScienceSource

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cites work

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7 April 2017

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Operating characteristics of a rank correlation test for publication bias

7 April 2017

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The SLC26 gene family of multifunctional anion exchangers

7 April 2017

1 reference

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Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

7 April 2017

1 reference

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Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China

7 April 2017

1 reference

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Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations

7 April 2017

1 reference

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Value of quantitative and qualitative analyses of circulating cell-free DNA as diagnostic tools for hepatocellular carcinoma: a meta-analysis

28 September 2017

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Variations in the cochlear implant experience in children with enlarged vestibular aqueduct

28 September 2017

1 reference

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KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects

28 September 2017

1 reference

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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study.

28 September 2017

1 reference

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Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China

28 September 2017

1 reference

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Genetic diagnosis and cochlear implantation for patients with nonsyndromic hearing loss and enlarged vestibular aqueduct

28 September 2017

1 reference

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Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

28 September 2017

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Identification of high-quality cancer prognostic markers and metastasis network modules

28 September 2017

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Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct

28 September 2017

1 reference

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Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

28 September 2017

1 reference

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Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

28 September 2017

1 reference

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Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

28 September 2017

1 reference

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Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Genotype-phenotype correlations for SLC26A4-related deafness.

28 September 2017

1 reference

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The diagnostic odds ratio: a single indicator of test performance

28 September 2017

1 reference

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Genetic screening for hearing loss.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Audiologic presentation of enlargement of the vestibular aqueduct according to the SLC26A4 genotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Vestibular Dysfunction in Patients with Enlarged Vestibular Aqueduct.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Spectrum and frequency of SLC26A4 mutations among Czech patients with early hearing loss with and without Enlarged Vestibular Aqueduct (EVA).

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Pendred syndrome and DFNB4-mutation screening ofSLC26A4by denaturing high-performance liquid chromatography and the identification of eleven novel mutations

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5058913

Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26683941

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26683941