Evidence map›Paper›PMID 41181184›Full record

ArticleFrontiers in pediatrics2025

Analysis of deafness gene screening results in 15771 newborn cases in Anyang city of Henan.

Yanchao Mu, Meiqing Han, Yang Li, Hua Di, Zhengxin Li, Haiyan Li, Dawei Wang, Xue Li, Lei Zhang, Huiping An

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Yanchao Mu *Prenatal Diagnosis Center, Anyang Key Laboratory of Prenatal Diagnosis, Anyang Maternal and Child Health Hospital, Anyang, China.
Meiqing Han *Laboratory Medicine Department, Anyang Maternal and Child Health Hospital, Anyang, China.
Yang LiPrenatal Diagnosis Center, Anyang Key Laboratory of Prenatal Diagnosis, Anyang Maternal and Child Health Hospital, Anyang, China.
Hua DiPrenatal Diagnosis Center, Anyang Key Laboratory of Prenatal Diagnosis, Anyang Maternal and Child Health Hospital, Anyang, China.
Zhengxin LiPrenatal Diagnosis Center, Anyang Key Laboratory of Prenatal Diagnosis, Anyang Maternal and Child Health Hospital, Anyang, China.
Haiyan LiNeonatal ICU, Anyang Maternal and Child Health Hospital, Anyang, China.
Dawei WangLaboratory Medicine Department, Anyang Maternal and Child Health Hospital, Anyang, China.
Xue LiDepartment of Health, Anyang Maternal and Child Health Hospital, Anyang, China.
Lei ZhangDepartment of Otolaryngology, Anyang Maternal and Child Health Hospital, Anyang, China.
Huiping AnNeonatal ICU, Anyang Maternal and Child Health Hospital, Anyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To analyze the prevalence and mutation spectrum of deafness-associated genes among newborns in Anyang City. Methods: Heel blood samples were collected from 15,771 newborns. Thirteen mutation sites across four genes associated with hereditary deafness ( Results: A total of 605 newborns were identified as carriers of pathogenic variants, yielding an overall carrier rate of 3.836%. Specifically, 254 newborns carried Conclusion: Implementing newborn genetic screening for deafness in this region facilitates the early identification of individuals at risk for congenital, delayed-onset, and aminoglycoside-induced hearing loss, enabling timely intervention and follow-up.

Indexed as

deafness genegenetic screeninghereditary hearing lossnewbornvariant locus

Identifiers

PMID41181184
PMCPMC12571625

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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.