Kimberling WJ - Search Results

1

Is hearing loss due to mutations in the Connexin 26 gene progressive?

Gopalarao D, Kimberling WJ, Jesteadt W, Kelley PM, Beauchaine KL, Cohn ES. Gopalarao D, et al. Among authors: kimberling wj. Int J Audiol. 2008 Jan;47(1):11-20. doi: 10.1080/14992020701602087. Int J Audiol. 2008. PMID: 18196482

2

Expressivity of hearing loss in cases with Usher syndrome type IIA.

Sadeghi AM, Cohn ES, Kimberling WJ, Halvarsson G, Möller C. Sadeghi AM, et al. Among authors: kimberling wj. Int J Audiol. 2013 Dec;52(12):832-7. doi: 10.3109/14992027.2013.839885. Epub 2013 Oct 28. Int J Audiol. 2013. PMID: 24160897

3

Audiological findings in Usher syndrome types IIa and II (non-IIa).

Sadeghi M, Cohn ES, Kelly WJ, Kimberling WJ, Tranebjoerg L, Möller C. Sadeghi M, et al. Among authors: kimberling wj. Int J Audiol. 2004 Mar;43(3):136-43. doi: 10.1080/14992020400050019. Int J Audiol. 2004. PMID: 15198377

4

Audiological and vestibular features in affected subjects with USH3: a genotype/phenotype correlation.

Sadeghi M, Cohn ES, Kimberling WJ, Tranebjaerg L, Möller C. Sadeghi M, et al. Among authors: kimberling wj. Int J Audiol. 2005 May;44(5):307-16. doi: 10.1080/14992020500060610. Int J Audiol. 2005. PMID: 16028794

5

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Am J Hum Genet. 1998 Apr;62(4):792-9. doi: 10.1086/301807. Am J Hum Genet. 1998. PMID: 9529365 Free PMC article.

6

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).

Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, Schaefer GB, Gobar LS, Hahn FJ, Harris DJ, Kimberling WJ. Cohn ES, et al. Among authors: kimberling wj. Pediatrics. 1999 Mar;103(3):546-50. doi: 10.1542/peds.103.3.546. Pediatrics. 1999. PMID: 10049954

7

Prevalent connexin 26 gene (GJB2) mutations in Japanese.

Abe S, Usami S, Shinkawa H, Kelley PM, Kimberling WJ. Abe S, et al. Among authors: kimberling wj. J Med Genet. 2000 Jan;37(1):41-3. doi: 10.1136/jmg.37.1.41. J Med Genet. 2000. PMID: 10633133 Free PMC article.

8

Connexin 26: required for normal auditory function.

Kelley PM, Cohn E, Kimberling WJ. Kelley PM, et al. Among authors: kimberling wj. Brain Res Brain Res Rev. 2000 Apr;32(1):184-8. doi: 10.1016/s0165-0173(99)00080-6. Brain Res Brain Res Rev. 2000. PMID: 10751669 Review.

9

Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.

Abe S, Kelley PM, Kimberling WJ, Usami SI. Abe S, et al. Among authors: kimberling wj. Am J Med Genet. 2001 Nov 1;103(4):334-8. Am J Med Genet. 2001. PMID: 11746015

10

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.

Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ. Varga R, et al. Among authors: kimberling wj. J Med Genet. 2006 Jul;43(7):576-81. doi: 10.1136/jmg.2005.038612. Epub 2005 Dec 21. J Med Genet. 2006. PMID: 16371502 Free PMC article.

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