170 related articles for article (PubMed ID: 34519870)
1. Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation.
Rim JH; Noh B; Koh YI; Joo SY; Oh KS; Kim K; Kim JA; Kim DH; Kim HY; Yoo JE; Lee ST; Bok JW; Lee MG; Jung J; Choi JY; Gee HY
Hum Genet; 2022 Apr; 141(3-4):915-927. PubMed ID: 34519870
[TBL] [Abstract][Full Text] [Related]
2. Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.
Liu C; Huang Y; Zhang Y; Ding H; Yu L; Wang A; Wang Y; Zeng Y; Liu L; Liu Y; Qi Y; Li F; Wu J; Du L; Mai F; Zhang Q; Wang X; Yin A
Int J Pediatr Otorhinolaryngol; 2022 Oct; 161():111258. PubMed ID: 35939872
[TBL] [Abstract][Full Text] [Related]
3. Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss.
Perry J; Redfield S; Oza A; Rouse S; Stewart C; Khela H; Srinivasan T; Albano V; Shearer E; Kenna M
Laryngoscope; 2023 Sep; 133(9):2417-2424. PubMed ID: 36515421
[TBL] [Abstract][Full Text] [Related]
4. How Does the "Cookie-Bite" Audiogram Shape Perform in Discriminating Genetic Hearing Loss in Adults?
Ahmadmehrabi S; Li B; Epstein DJ; Ruckenstein MJ; Brant JA
Otolaryngol Head Neck Surg; 2022 Mar; 166(3):537-539. PubMed ID: 34058916
[TBL] [Abstract][Full Text] [Related]
5. Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.
Sheppard S; Biswas S; Li MH; Jayaraman V; Slack I; Romasko EJ; Sasson A; Brunton J; Rajagopalan R; Sarmady M; Abrudan JL; Jairam S; DeChene ET; Ying X; Choi J; Wilkens A; Raible SE; Scarano MI; Santani A; Pennington JW; Luo M; Conlin LK; Devkota B; Dulik MC; Spinner NB; Krantz ID
Genet Med; 2018 Dec; 20(12):1663-1676. PubMed ID: 29907799
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Mohseni M; Babanejad M; Booth KT; Jamali P; Jalalvand K; Davarnia B; Ardalani F; Khoshaeen A; Arzhangi S; Ghodratpour F; Beheshtian M; Jahanshad F; Otukesh H; Bahrami F; Seifati SM; Bazazzadegan N; Habibi F; Behravan H; Mirzaei S; Keshavarzi F; Nikzat N; Mehrjoo Z; Thiele H; Nothnagel M; Azaiez H; Smith RJ; Kahrizi K; Najmabadi H
Clin Genet; 2021 Jul; 100(1):59-78. PubMed ID: 33713422
[TBL] [Abstract][Full Text] [Related]
7. Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss.
Gan NS; Oziębło D; Skarżyński H; Ołdak M
Audiol Neurootol; 2023; 28(5):327-337. PubMed ID: 37121227
[TBL] [Abstract][Full Text] [Related]
8. Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss.
Pavlenkova Z; Varga L; Borecka S; Karhanek M; Huckova M; Skopkova M; Profant M; Gasperikova D
Sci Rep; 2021 Nov; 11(1):22488. PubMed ID: 34795337
[TBL] [Abstract][Full Text] [Related]
9. Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.
Guan J; Wang H; Lan L; Wu Y; Chen G; Zhao C; Wang D; Wang Q
Mol Genet Genomic Med; 2020 Aug; 8(8):e1367. PubMed ID: 32567228
[TBL] [Abstract][Full Text] [Related]
10. Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.
Kannan-Sundhari A; Yan D; Saeidi K; Sahebalzamani A; Blanton SH; Liu XZ
Genet Test Mol Biomarkers; 2020 Oct; 24(10):674-680. PubMed ID: 32991204
[No Abstract] [Full Text] [Related]
11. Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.
Noman M; Ishaq R; Bukhari SA; Ahmed ZM; Riazuddin S
Genes (Basel); 2019 Dec; 10(12):. PubMed ID: 31835641
[TBL] [Abstract][Full Text] [Related]
12. Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF.
Khalil A; Karroum SB; Barake R; Dunya G; Abou-Rizk S; Kamar A; Nemer G; Bassim M
BMC Med Genet; 2020 Jan; 21(1):1. PubMed ID: 31898538
[TBL] [Abstract][Full Text] [Related]
13. Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss.
Lewis MA; Schulte J; Matthews L; Vaden KI; Steves CJ; Williams FMK; Schulte BA; Dubno JR; Steel KP
PLoS Genet; 2023 Nov; 19(11):e1011058. PubMed ID: 38011198
[TBL] [Abstract][Full Text] [Related]
14. Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.
Ramzan M; Zafeer MF; Abad C; Guo S; Owrang D; Alper O; Mutlu A; Atik T; Duman D; Bademci G; Vona B; Kalcioglu MT; Walz K; Tekin M
Eur J Hum Genet; 2024 Jun; 32(6):639-646. PubMed ID: 38374469
[TBL] [Abstract][Full Text] [Related]
15. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.
Kitano T; Miyagawa M; Nishio SY; Moteki H; Oda K; Ohyama K; Miyazaki H; Hidaka H; Nakamura KI; Murata T; Matsuoka R; Ohta Y; Nishiyama N; Kumakawa K; Furutate S; Iwasaki S; Yamada T; Ohta Y; Uehara N; Noguchi Y; Usami SI
PLoS One; 2017; 12(5):e0177636. PubMed ID: 28545070
[TBL] [Abstract][Full Text] [Related]
16. Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield.
Yamamoto N; Balciuniene J; Hartman T; Diaz-Miranda MA; Bedoukian E; Devkota B; Lawrence A; Golenberg N; Patel M; Tare A; Chen R; Schindler E; Choi J; Kaur M; Charles S; Chen J; Fanning EA; Dechene E; Cao K; Jill MR; Rajagopalan R; Bayram Y; Dulik MC; Germiller J; Conlin LK; Krantz ID; Luo M
J Pediatr; 2023 Nov; 262():113620. PubMed ID: 37473993
[TBL] [Abstract][Full Text] [Related]
17. Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss.
D'Aguillo C; Bressler S; Yan D; Mittal R; Fifer R; Blanton SH; Liu X
Int J Audiol; 2019 Dec; 58(12):834-850. PubMed ID: 31264897
[No Abstract] [Full Text] [Related]
18. A novel MYH9 mutation related to non-syndromic delayed post-lingual sensorineural hearing loss.
Pan C; Zhang Y; Yang S; Chen C; Wang J; Shi C; Yu Y
Eur Arch Otorhinolaryngol; 2022 Jun; 279(6):2811-2817. PubMed ID: 34228168
[TBL] [Abstract][Full Text] [Related]
19. Identification of Hearing Loss-Associated Variants of
Mahmood U; Bukhari SA; Ali M; Ahmed ZM; Riazuddin S
Biomed Res Int; 2021; 2021():5584788. PubMed ID: 33997018
[TBL] [Abstract][Full Text] [Related]
20. Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Clabout T; Maes L; Acke F; Wuyts W; Van Schil K; Coucke P; Janssens S; De Leenheer E
Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672845
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
