Lin YH - Search Results

1

Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment.

Wu CC, Lin YH, Lu YC, Chen PJ, Yang WS, Hsu CJ, Chen PL. Wu CC, et al. Among authors: lin yh. PLoS One. 2013;8(2):e57369. doi: 10.1371/journal.pone.0057369. Epub 2013 Feb 22. PLoS One. 2013. PMID: 23451214 Free PMC article.

2

Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome.

Wang SH, Wu CC, Lu YC, Lin YH, Su YN, Hwu WL, Yu IS, Hsu CJ. Wang SH, et al. Among authors: lin yh. Laryngoscope. 2012 May;122(5):1130-6. doi: 10.1002/lary.23217. Epub 2012 Mar 23. Laryngoscope. 2012. PMID: 22447252

3

Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice.

Lu YC, Wu CC, Yang TH, Lin YH, Yu IS, Lin SW, Chang Q, Lin X, Wong JM, Hsu CJ. Lu YC, et al. Among authors: lin sw, lin x, lin yh. PLoS One. 2013 Jun 3;8(6):e64906. doi: 10.1371/journal.pone.0064906. Print 2014. PLoS One. 2013. PMID: 23755160 Free PMC article.

4

Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing.

Lin YH, Wu CC, Hsu TY, Chiu WY, Hsu CJ, Chen PL. Lin YH, et al. Mutat Res. 2015 Jan;771:1-5. doi: 10.1016/j.mrfmmm.2014.11.001. Epub 2014 Nov 13. Mutat Res. 2015. PMID: 25771973

5

Contribution of adiponectin and its type 1 receptor to age-related hearing impairment.

Wu CC, Tsai CH, Lu YC, Lin HC, Hwang JH, Lin YH, Yang WS, Chen PJ, Liao WC, Lee YL, Liu TC, Hsu CJ. Wu CC, et al. Among authors: lin yh, lin hc. Neurobiol Aging. 2015 Jun;36(6):2085-93. doi: 10.1016/j.neurobiolaging.2015.02.030. Epub 2015 Mar 5. Neurobiol Aging. 2015. PMID: 25911279

6

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing.

Wu CC, Lin YH, Liu TC, Lin KN, Yang WS, Hsu CJ, Chen PL, Wu CM. Wu CC, et al. Among authors: lin kn, lin yh. Medicine (Baltimore). 2015 Jul;94(27):e1073. doi: 10.1097/MD.0000000000001073. Medicine (Baltimore). 2015. PMID: 26166082 Free PMC article.

7

Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations.

Wu CM, Ko HC, Tsou YT, Lin YH, Lin JL, Chen CK, Chen PL, Wu CC. Wu CM, et al. Among authors: lin jl, lin yh. PLoS One. 2015 Sep 23;10(9):e0138575. doi: 10.1371/journal.pone.0138575. eCollection 2015. PLoS One. 2015. PMID: 26397989 Free PMC article.

8

Newborn genetic screening for hearing impairment: a population-based longitudinal study.

Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH, Huang FL, Tsao PN, Su YN, Lee YL, Hsieh WS, Hsu CJ. Wu CC, et al. Among authors: lin yh. Genet Med. 2017 Jan;19(1):6-12. doi: 10.1038/gim.2016.66. Epub 2016 Jun 16. Genet Med. 2017. PMID: 27308839 Free article.

9

Clinical heterogeneity of LRRK2 p.I2012T mutation.

Fan TS, Wu RM, Chen PL, Chen TF, Li HY, Lin YH, Chen CY, Chen ML, Tai CH, Lin HI, Lin CH. Fan TS, et al. Among authors: lin ch, lin hi, lin yh. Parkinsonism Relat Disord. 2016 Dec;33:36-43. doi: 10.1016/j.parkreldis.2016.09.008. Epub 2016 Sep 7. Parkinsonism Relat Disord. 2016. PMID: 27628070

10

Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss.

Lin PH, Hsu CJ, Lin YH, Lin YH, Lee HY, Wu CC, Liu TC. Lin PH, et al. Among authors: lin yh. JAMA Otolaryngol Head Neck Surg. 2017 Sep 1;143(9):912-919. doi: 10.1001/jamaoto.2017.0945. JAMA Otolaryngol Head Neck Surg. 2017. PMID: 28687817 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,858 results

Search Page

Filters