Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Concurrent Hearing and Genetic Screening among Newborns in Ningbo, China.

Computational and mathematical methods in medicine - 1 Jan 2022

Guomei Cao, Luyan Zhang, Lingling Dai, Chunhong Huang, Shan Chen

Abstract excerpt

OBJECTIVE: To detect the carrier rates of deafness gene variants in populations in Ningbo and analyze the risk of hereditary hearing loss through concurrent hearing and genetic screening tests. METHODS: Two thousand one hundred and seventy-four newborns were enrolled from November 2018 to August 2019. All subjects underwent hearing screening and newborn deafness genetic screening with 15 variants in 4 genes, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Computational Biology
Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to DNA, Mitochondrial

Share to Hearing Tests

Share to Neonatal Screening

Share to Sulfate Transporters

Source

Open in PubMed Open full text

Identifiers

PMID: 35047053
DOI: 10.1155/2022/1713337
PMCID: PMC8763501

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Concurrent Hearing and Genetic Screening among Newborns in Ningbo, China.PMID 35047053Read ↗

Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns.Semantic proximity Read ↗

The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide.Semantic proximity Read ↗

Auditory screening concurrent deafness predisposing genes screening in 10,043 neonates in Gansu province, China.Semantic proximity Read ↗

Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns.Semantic proximity Read ↗

Combined hearing screening and genetic screening of deafness among Hakka newborns in China.Semantic proximity Read ↗

[Analysis of results of concurrent hearing and deafness genetic screening and follow up of 33 911 newborns].Semantic proximity Read ↗

Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.Semantic proximity Read ↗

Concurrent Hearing and Genetic Screening of 18 001 Neonates with Hearing Diagnose in Nantong, ChinaSemantic proximity Read ↗

[Results of combined newborn hearing and deafness gene screening in Yuncheng area of Shanxi Province].Semantic proximity Read ↗

Analysis of combined screening results of the hearing and deafness genes in 10754 newbornsSemantic proximity Read ↗

Optimized concurrent hearing and genetic screening in Beijing, China: A cross-sectional study.Semantic proximity Read ↗

[Current status of newborn deafness gene screeningin parts of China].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.