(Q34558530)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

KCNQ4: a gene for age-related hearing impairment? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

10

1 reference

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29 December 2019

Guy Van Camp

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

E Van Eyken

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

L Van Laer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

E Fransen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

V Topsakal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

N Lemkens

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

W Laureys

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

N Nelissen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

A Vandevelde

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

T Wienker

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

1 October 2006

1 reference

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29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

1007-1016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

Genomewide linkage analysis to presbycusis in the Framingham Heart Study.

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

The relation of hearing in the elderly to the presence of cardiovascular disease and cardiovascular risk factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

Genetic associations in age-related hearing thresholds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

GOLD--graphical overview of linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Focus on primary care. Thyroid function and dysfunction in women

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Glutathione S-transferase gene polymorphisms in presbycusis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

A nonsense mutation in the fibrillin-1 gene of a Marfan syndrome patient induces NMD and disrupts an exonic splicing enhancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Supporting cells contribute to control of hearing sensitivity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

A novel Z-score-based method to analyze candidate genes for age-related hearing impairment

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Prospective evaluation of associations between hearing sensitivity and selected cardiovascular risk factors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Estrogen and hearing: a summary of recent investigations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

A major gene affecting age-related hearing loss in C57BL/6J mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Ahl2, a second locus affecting age-related hearing loss in mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Description and primary results from an audiometric study of male twins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Efficient selective screening of haplotype tag SNPs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

The impact of SNP density on fine-scale patterns of linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Hearing threshold in patients with diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Tobacco smoking, ageing and health among the elderly: a longitudinal population study of 70-year-old men and an age cohort comparison

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Noise-induced transient microlesions in the cell membranes of auditory hair cells.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

The future of association studies: gene-based analysis and replication

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Ahl3, a third locus on mouse chromosome 17 affecting age-related hearing loss.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Perspectives on the past decade of asthma genetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Excitotoxicity, synaptic repair, and functional recovery in the mammalian cochlea: a review of recent findings

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Hearing: the effects of chemicals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Cochlear pathology in presbycusis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Haplotype association analysis of discrete and continuous traits using mixture of regression models.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Mechanisms of salicylate ototoxicity.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Candidate-gene approaches for studying complex genetic traits: practical considerations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

N-acetyltransferase 2 gene polymorphism and presbycusis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Is DFNA5 a susceptibility gene for age-related hearing impairment?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Role of glutathione in protection against noise-induced hearing loss

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20375

7 January 2021

Identifiers

DOI

10.1002/HUMU.20375

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16917933%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference