Evidence map›Paper›PMID 23873582›Full record

ArticleAmerican journal of medical genetics. Part A2013

Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: further confirmation of pathogenicity and haplotype analysis in Asian populations.

Emily Gallant, Lauren Francey, Ellen A Tsai, Micah Berman, Yaru Zhao, Heather Fetting, Maninder Kaur, Matthew A Deardorff, Alisha Wilkens, Dinah Clark and 3 more

Abstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  4. TheGenes · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Emily GallantDivision of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Lauren Francey
Ellen A Tsai
Micah Berman
Yaru Zhao
Heather Fetting
Maninder Kaur
Matthew A Deardorff
Alisha Wilkens
Dinah Clark
Hakon Hakonarson
Heidi L Rehm
Ian D Krantz
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USChina Medical University · CNMass General Brigham · US

Funding

Audiological and Genetic Resource for Pediatric Hearing ResearchR24DC012207 · NIDCD · CHILDREN'S HOSP OF PHILADELPHIA · PI CRENSHAW, E BRYAN · 2012 to 2016
$3.9M
Audiological and Genetic Resource for Pediatric Hearing ResearchR33DC008630 · NIDCD · CHILDREN'S HOSP OF PHILADELPHIA · PI CRENSHAW, E BRYAN · 2009 to 2011
$2.1M
NIDCD NIH HHS R24 DC012207NIDCD NIH HHS R33 DC008630NIDCD NIH HHS R33DC008630
6 · The paper itself

Abstract

Hearing impairment affects 1 in 650 newborns, making it the most common congenital sensory impairment. Autosomal recessive nonsyndromic sensorineural hearing impairment (ARNSHI) comprises 80% of familial hearing impairment cases. Mutations in GJB2 account for a significant number of ARNSHI (and up to 50% of documented recessive (e.g., more than 1 affected sibling) hearing impairment in some populations). Mutations in the GJB2 gene are amongst the most common causes of hearing impairment in populations of various ethnic backgrounds. Two mutations of this gene, 35delG and 167delT, account for the majority of reported mutations in Caucasian populations, especially those of Mediterranean and Ashkenazi Jewish background. The 235delC mutation is most prevalent in East Asian populations. Some mutations are of less well-characterized significance. The V37I missense mutation, common in Asian populations, was initially described as a polymorphism and later as a potentially pathogenic mutation. We report here on 15 unrelated individuals with ARNSHI and homozygosity for the V37I GJB2 missense mutation. Nine individuals are of Chinese ancestry, two are of unspecified Asian descent, one is of Japanese descent, one individual is of Vietnamese ancestry, one of Philippine background and one of Italian and Cuban/Caucasian background. Homozygosity for the V37I GJB2 mutation may be a more common pathogenic missense mutation in Asian populations, resulting in mild to moderate sensorineural hearing impairment. We report a presumed haplotype block specific to East Asian individuals with the V37I mutation encompassing the GJB2 gene that may account for the high prevalence in East Asian populations.

Indexed as

HomozygoteMutationAdolescentAsian PeopleChildChild, PreschoolChromosome MappingCodonConnexin 26ConnexinsDNA Mutational AnalysisFemaleHaplotypesHearing Loss, SensorineuralHumansInfantCodonConnexin 26ConnexinsGJB2 protein, humanChinaGJB2haplotypehearing impairmentV37I

Identifiers

PMID23873582
PMCPMC3745519
OpenAlexW2144704308

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.