# Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/genome-sequencing-identifies-coding-and-non-coding-variants-for-non-syndromic/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Memoona Ramzan,Duygu Duman,LeShon Chere Peart Hendricks,Shengru Guo,Ahmet Mutlu,M. Tayyar Kalcıoğlu,Serhat Seyhan,Claudia Carranza,Murtaza Bonyadi,Nejat Mahdieh,Muzeyyen Yildirim‐Baylan,Erick Figueroa-Ildefonso,Özgül M. Alper,Tahir Atık,Abdurrahman Ayral,Nazım Bozan,Burhan Balta,Christian Rivas,Gabrielle Novais Manzoli,Fabiola Huesca-Hernández,Raja A. H. Kuchay,Merve Durgut,Güney Bademci,Mustafa Tekin |
| Citations | 12 |
| DOI | 10.1038/s10038-023-01159-9 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W4377226496 |
| PMID | 37217689 |
| Type | article |
| Year | 2023 |

## Paper authors

- [Ahmet Mutlu](https://scholariq.org/researchers/ahmet-mutlu/)

## 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/)
- [Ear Surgery and Otitis Media](https://scholariq.org/topics/ear-surgery-and-otitis-media/)
- [Connexins and lens biology](https://scholariq.org/topics/connexins-and-lens-biology/)

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