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

Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China.

JAMA network open - 1 Sept 2021

Zhu Qing-Wen, Li Mu-Ting, Zhuang Xun, Chen Kai, Xu Wan-Qing, Jiang Yin-Hua, Qin Gang

Abstract excerpt

Importance: Early identification and intervention for newborns with hearing loss (HL) may lead to improved physiological and social-emotional outcomes. The current newborn hearing screening is generally beneficial but improvements can be made. Objective: To assess feasibility and evaluate utility of a modified genetic and hearing screening program for newborn infants. Design, Setting, and Participants: This...

Read the complete abstract on PubMed

Topics

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

Share to Early Diagnosis
Share to Feasibility Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Hearing Loss

Share to Hearing Tests

Share to Infant, Newborn

Share to Neonatal Screening

Share to Pilot Projects

Source

Open in PubMed Open full text

Identifiers

PMID: 34533568
DOI: 10.1001/jamanetworkopen.2021.25544
PMCID: PMC8449278

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China.PMID 34533568Read ↗

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

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

Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow-up.Semantic proximity Read ↗

Characteristics of hearing loss-associated gene mutations: A multi-center study of 119,606 neonates in Gannan.Semantic proximity Read ↗

Genetic screening for hearing impairment and the genotype-phenotype correlation of GJB2 c.109G>A variants in 47,729 neonates: a population-based study in southern China.Semantic proximity Read ↗

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

Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program.Semantic proximity Read ↗

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

Disparities in deafness gene mutations between Han and Li ethnic newborns in Hainan, China: insights from a combined screening program.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 ↗

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

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

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