Oghalai JS - Search Results

1

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.

Haraksingh RR, Jahanbani F, Rodriguez-Paris J, Gelernter J, Nadeau KC, Oghalai JS, Schrijver I, Snyder MP. Haraksingh RR, et al. Among authors: oghalai js. BMC Genomics. 2014 Dec 20;15(1):1155. doi: 10.1186/1471-2164-15-1155. BMC Genomics. 2014. PMID: 25528277 Free PMC article.

2

DNA sequence analysis and genotype-phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy.

Tang HY, Fang P, Lin JW, Darilek S, Osborne BT, Haymond JA, Manolidis S, Roa BB, Oghalai JS, Alford RL. Tang HY, et al. Among authors: oghalai js. BMJ Open. 2015 May 19;5(5):e007506. doi: 10.1136/bmjopen-2014-007506. BMJ Open. 2015. PMID: 25991456 Free PMC article.

3

Otalgia, Facial Nerve Paralysis, and Hearing Loss.

Alyono JC, Corrales CE, Oghalai JS. Alyono JC, et al. Among authors: oghalai js. JAMA Otolaryngol Head Neck Surg. 2014 Jun;140(6):575-6. doi: 10.1001/jamaoto.2014.621. JAMA Otolaryngol Head Neck Surg. 2014. PMID: 24810396 No abstract available.

4

Mechanisms of hearing loss after blast injury to the ear.

Cho SI, Gao SS, Xia A, Wang R, Salles FT, Raphael PD, Abaya H, Wachtel J, Baek J, Jacobs D, Rasband MN, Oghalai JS. Cho SI, et al. Among authors: oghalai js. PLoS One. 2013 Jul 1;8(7):e67618. doi: 10.1371/journal.pone.0067618. Print 2013. PLoS One. 2013. PMID: 23840874 Free PMC article.

5

A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus).

Probst FJ, Corrigan RR, Del Gaudio D, Salinger AP, Lorenzo I, Gao SS, Chiu I, Xia A, Oghalai JS, Justice MJ. Probst FJ, et al. Among authors: oghalai js. PLoS One. 2013 Nov 26;8(11):e80408. doi: 10.1371/journal.pone.0080408. eCollection 2013. PLoS One. 2013. PMID: 24303013 Free PMC article.

6

New Web-Based Tool for Generating Scattergrams to Report Hearing Results.

Oghalai JS, Jackler RK. Oghalai JS, et al. Otolaryngol Head Neck Surg. 2016 Jun;154(6):981. doi: 10.1177/0194599816638314. Otolaryngol Head Neck Surg. 2016. PMID: 27251009 Review. No abstract available.

7

High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.

Tang HY, Xia A, Oghalai JS, Pereira FA, Alford RL. Tang HY, et al. Among authors: oghalai js. BMC Med Genet. 2005 Aug 8;6:30. doi: 10.1186/1471-2350-6-30. BMC Med Genet. 2005. PMID: 16086836 Free PMC article.

8

Chronic pachymeningitis presenting as asymmetric sensorineural hearing loss.

Oghalai JS, Ramirez AL, Hegarty JL, Jackler RK. Oghalai JS, et al. Otol Neurotol. 2004 Jul;25(4):616-21. doi: 10.1097/00129492-200407000-00033. Otol Neurotol. 2004. PMID: 15241244

9

Cognition in children with sensorineural hearing loss: etiologic considerations.

Pierson SK, Caudle SE, Krull KR, Haymond J, Tonini R, Oghalai JS. Pierson SK, et al. Among authors: oghalai js. Laryngoscope. 2007 Sep;117(9):1661-5. doi: 10.1097/MLG.0b013e3180ca7834. Laryngoscope. 2007. PMID: 17690618 Free PMC article.

10

Comprehensive diagnostic battery for evaluating sensorineural hearing loss in children.

Lin JW, Chowdhury N, Mody A, Tonini R, Emery C, Haymond J, Oghalai JS. Lin JW, et al. Among authors: oghalai js. Otol Neurotol. 2011 Feb;32(2):259-64. doi: 10.1097/MAO.0b013e31820160fa. Otol Neurotol. 2011. PMID: 21131880 Free PMC article.

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