These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
219 related articles for article (PubMed ID: 29293505)
1. Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss. Likar T; Hasanhodžić M; Teran N; Maver A; Peterlin B; Writzl K PLoS One; 2018; 13(1):e0188578. PubMed ID: 29293505 [TBL] [Abstract][Full Text] [Related]
2. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Sansović I; Meašić AM; Bobinec A; Morožin Pohovski L; Odak L; Vulin K; Lozić B; Kero M; Huljev Frković S; Pušeljić S Croat Med J; 2024 Jun; 65(3):198-208. PubMed ID: 38868966 [TBL] [Abstract][Full Text] [Related]
3. Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients. Cabanillas R; Diñeiro M; Cifuentes GA; Castillo D; Pruneda PC; Álvarez R; Sánchez-Durán N; Capín R; Plasencia A; Viejo-Díaz M; García-González N; Hernando I; Llorente JL; Repáraz-Andrade A; Torreira-Banzas C; Rosell J; Govea N; Gómez-Martínez JR; Núñez-Batalla F; Garrote JA; Mazón-Gutiérrez Á; Costales M; Isidoro-García M; García-Berrocal B; Ordóñez GR; Cadiñanos J BMC Med Genomics; 2018 Jul; 11(1):58. PubMed ID: 29986705 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing. Safka Brozkova D; Poisson Marková S; Mészárosová AU; Jenčík J; Čejnová V; Čada Z; Laštůvková J; Rašková D; Seeman P Clin Genet; 2020 Dec; 98(6):548-554. PubMed ID: 32860223 [TBL] [Abstract][Full Text] [Related]
6. Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria. Frohne A; Vrabel S; Laccone F; Neesen J; Roesch S; Dossena S; Schoefer C; Frei K; Parzefall T Eur Arch Otorhinolaryngol; 2024 Jul; 281(7):3577-3586. PubMed ID: 38400873 [TBL] [Abstract][Full Text] [Related]
7. Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations. Gu X; Guo L; Ji H; Sun S; Chai R; Wang L; Li H Clin Genet; 2015 Jun; 87(6):588-93. PubMed ID: 24853665 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families. Doll J; Vona B; Schnapp L; Rüschendorf F; Khan I; Khan S; Muhammad N; Alam Khan S; Nawaz H; Khan A; Ahmad N; Kolb SM; Kühlewein L; Labonne JDJ; Layman LC; Hofrichter MAH; Röder T; Dittrich M; Müller T; Graves TD; Kong IK; Nanda I; Kim HG; Haaf T Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33187236 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Sadeghian L; Tabatabaiefar MA; Fattahi N; Pourreza MR; Tahmasebi P; Alavi Z; Hashemzadeh Chaleshtori M Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():99-105. PubMed ID: 31176026 [TBL] [Abstract][Full Text] [Related]
12. Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss. Hofrichter MAH; Doll J; Habibi H; Enayati S; Vahidi Mehrjardi MY; Müller T; Dittrich M; Haaf T; Vona B Eur J Med Genet; 2019 Oct; 62(10):103724. PubMed ID: 31315069 [TBL] [Abstract][Full Text] [Related]
13. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss. Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population. Feng H; Huang S; Ma Y; Yang J; Chen Y; Wang G; Han M; Kang D; Zhang X; Dai P; Yuan Y Orphanet J Rare Dis; 2024 Sep; 19(1):342. PubMed ID: 39272213 [TBL] [Abstract][Full Text] [Related]
16. Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center: An Eight-year Study. Tropitzsch A; Schade-Mann T; Gamerdinger P; Dofek S; Schulte B; Schulze M; Battke F; Fehr S; Biskup S; Heyd A; Müller M; Löwenheim H; Vona B; Holderried M Ear Hear; 2022; 43(3):1049-1066. PubMed ID: 34753855 [TBL] [Abstract][Full Text] [Related]
17. Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing. Liu Y; Tan M; Cai L; Lv L; Chen Q; Chen W; Yang H; Xu Y Gene; 2022 Apr; 819():146258. PubMed ID: 35114279 [TBL] [Abstract][Full Text] [Related]
18. Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis. Alerasool M; Eslahi A; Vona B; Kahaei MS; Mojaver NK; Rajati M; Pasdar A; Ghasemi MM; Saburi E; Ardehaie RM; Aval MH; Tale MR; Nourizadeh N; Afzalzadeh MR; Niknezhad HT; Mojarrad M Clin Genet; 2024 Dec; 106(6):693-701. PubMed ID: 39107234 [TBL] [Abstract][Full Text] [Related]
19. Systematic Review of Hearing Loss Genes in the African American Population. Worden CP; Jeyakumar A Otol Neurotol; 2019 Jun; 40(5):e488-e496. PubMed ID: 31083078 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]