Evidence map›Paper›PMID 33745059›Full record

ArticleHuman genetics2021

Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.

Shadi Ahmadmehrabi, Binglan Li, Joseph Park, Batsal Devkota, Marijana Vujkovic, Yi-An Ko, David Van Wagoner, W H Wilson Tang, Ian Krantz, Marylyn Ritchie and 5 more

Abstract read
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In one paragraph

Article in Human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Rare and low-frequency variants in families with otitis media.Journal of molecular medicine (Berlin, Germany) · 2025
    Article
  2. Deep metabolic phenotyping of humans with protein-altering variants inJHEP reports : innovation in hepatology · 2025
    Article
  3. Article
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  6. Review
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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

15 authors at 6 institutions in 1 country.

Shadi AhmadmehrabiCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Binglan LiDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Joseph ParkDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Batsal DevkotaDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Marijana VujkovicDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Yi-An KoDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
David Van WagonerDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, Cleveland, OH, USA.
W H Wilson TangCleveland Clinic, Heart and Vascular Institute, Cleveland, OH, USA.
Ian KrantzDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Marylyn RitchieDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Regeneron Genetics Center
Jason BrantCorporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Michael J RuckensteinDepartment of Otorhinolaryngology Head and Neck Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Douglas J EpsteinDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Daniel J RaderDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. rader@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-9245-9876
University of Pennsylvania · USChildren's Hospital of Philadelphia · USCleveland Clinic · USPhiladelphia VA Medical Center · USCleveland Clinic Lerner College of Medicine · USTranslational Therapeutics (United States) · US

Funding

Sensory cell fate specification in the inner earR01DC006254 · NIDCD · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, DOUGLAS J · 2003 to 2023
$7.6M
NIDCD NIH HHS R01 DC006254
6 · The paper itself

Abstract

While newborns and children with hearing loss are routinely offered genetic testing, adults are rarely clinically tested for a genetic etiology. One clinically actionable result from genetic testing in children is the discovery of variants in syndromic hearing loss genes. EYA4 is a known hearing loss gene which is also involved in important pathways in cardiac tissue. The pleiotropic effects of rare EYA4 variants are poorly understood and their prevalence in a large cohort has not been previously reported. We investigated cardio-auditory phenotypes in 11,451 individuals in a large biobank using a rare variant, genome-first approach to EYA4. We filtered 256 EYA4 variants carried by 6737 participants to 26 rare and predicted deleterious variants carried by 42 heterozygotes. We aggregated predicted deleterious EYA4 gene variants into a combined variable (i.e. "gene burden") and performed association studies across phenotypes compared to wildtype controls. We validated findings with replication in three independent cohorts and human tissue expression data. EYA4 gene burden was significantly associated with audiometric-proven HL (p = [Formula: see text], Mobitz Type II AV block (p = [Formula: see text]) and the syndromic presentation of HL and primary cardiomyopathy (p = 0.0194). Analyses on audiogram, echocardiogram, and electrocardiogram data validated these associations. Prior reports have focused on identifying variants in families with severe or syndromic phenotypes. In contrast, we found, using a genotype-first approach, that gene burden in EYA4 is associated with more subtle cardio-auditory phenotypes in an adult medical biobank population, including cardiac conduction disorders which have not been previously reported. We show the value of using a focused approach to uncover human disease related to pleiotropic gene variants and suggest a role for genetic testing in adults presenting with hearing loss.

Indexed as

Genome, HumanMutationAudiometryBiological Specimen BanksBlack or African AmericanBlack PeopleCardiomyopathiesEchocardiographyElectrocardiographyExome SequencingGene ExpressionHearing LossHumansMalePennsylvaniaPhenotypeEYA4 protein, humanTrans-Activators

Identifiers

PMID33745059
OpenAlexW3138594469

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.