# Newborn hearing concurrent genetic screening for hearing impairment—A clinical practice in 58,397 neonates in Tianjin, China

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/newborn-hearing-concurrent-genetic-screening-for-hearing-impairment-a-clinical/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Junqing Zhang,Peng Wang,Bing Han,Yibing Ding,Lei Pan,Jing Zou,Haisheng Liu,Xinzhi Pang,Enqing Liu,Hongyue Wang,Hongyan Liu,Xudong Zhang,Cheng Xiu,Dafei Feng,Qian Li,Dayong Wang,Liang Zong,Yuting Yi,Ning Tian,Feng Mu,Tian Geng,Yaqiu Chen,Gongshu Liu,Fuxia Zhang,Xin Yi,Ling Yang,Qiuju Wang |
| Citations | 74 |
| DOI | 10.1016/j.ijporl.2013.08.038 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2088635199 |
| PMID | 24100002 |
| Type | article |
| Year | 2013 |

## Paper authors

- [Xin Yi](https://scholariq.org/researchers/xin-yi/)

## Paper journal

- [International Journal of Pediatric Otorhinolaryngology](https://scholariq.org/journals/international-journal-of-pediatric-otorhinolaryngology/)

## Paper primary topic

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)

## Paper topics

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.