Fukushima K - Search Results

1

Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis.

Chen W, Meyer NC, McKenna MJ, Pfister M, McBride DJ Jr, Fukushima K, Thys M, Camp GV, Smith RJ. Chen W, et al. Among authors: fukushima k. Clin Genet. 2007 May;71(5):406-14. doi: 10.1111/j.1399-0004.2007.00794.x. Clin Genet. 2007. PMID: 17489845

2

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ. Chen AH, et al. Among authors: fukushima k. Hum Mol Genet. 1995 Jun;4(6):1073-6. doi: 10.1093/hmg/4.6.1073. Hum Mol Genet. 1995. PMID: 7655461

3

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.

van Camp G, Coucke P, Balemans W, van Velzen D, van de Bilt C, van Laer L, Smith RJ, Fukushima K, Padberg GW, Frants RR, et al. van Camp G, et al. Among authors: fukushima k. Hum Mol Genet. 1995 Nov;4(11):2159-63. doi: 10.1093/hmg/4.11.2159. Hum Mol Genet. 1995. PMID: 8589696

4

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER, Smith SD, Kenyon JB, Zbar RI, Smith RJ. Fukushima K, et al. Genome Res. 1995 Oct;5(3):305-8. doi: 10.1101/gr.5.3.305. Genome Res. 1995. PMID: 8593615 Free article.

5

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3.

Lesperance MM, Hall JW 3rd, Bess FH, Fukushima K, Jain PK, Ploplis B, San Agustin TB, Skarka H, Smith RJ, Wills M, et al. Lesperance MM, et al. Among authors: fukushima k. Hum Mol Genet. 1995 Oct;4(10):1967-72. doi: 10.1093/hmg/4.10.1967. Hum Mol Genet. 1995. PMID: 8595423

6

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.

O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ. O'Neill ME, et al. Among authors: fukushima k. Hum Mol Genet. 1996 Jun;5(6):853-6. doi: 10.1093/hmg/5.6.853. Hum Mol Genet. 1996. PMID: 8776603

7

Usher's syndrome type IC: clinical studies and fine-mapping the disease locus.

Marietta J, Walters KS, Burgess R, Ni L, Fukushima K, Moore KC, Hejtmancik JF, Smith RJ. Marietta J, et al. Among authors: fukushima k. Ann Otol Rhinol Laryngol. 1997 Feb;106(2):123-8. doi: 10.1177/000348949710600206. Ann Otol Rhinol Laryngol. 1997. PMID: 9041816

8

Localization of a gene for otosclerosis to chromosome 15q25-q26.

Tomek MS, Brown MR, Mani SR, Ramesh A, Srisailapathy CR, Coucke P, Zbar RI, Bell AM, McGuirt WT, Fukushima K, Willems PJ, Van Camp G, Smith RJ. Tomek MS, et al. Among authors: fukushima k. Hum Mol Genet. 1998 Feb;7(2):285-90. doi: 10.1093/hmg/7.2.285. Hum Mol Genet. 1998. PMID: 9425236

9

Passage to India: the search for genes causing autosomal recessive nonsyndromic hearing loss.

Zbar RI, Ramesh A, Srisailapathy CR, Fukushima K, Wayne S, Smith RJ. Zbar RI, et al. Among authors: fukushima k. Otolaryngol Head Neck Surg. 1998 Mar;118(3 Pt 1):333-7. doi: 10.1016/S0194-59989870311-0. Otolaryngol Head Neck Surg. 1998. PMID: 9527113

10

A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Fukushima K, Kasai N, Ueki Y, Nishizaki K, Sugata K, Hirakawa S, Masuda A, Gunduz M, Ninomiya Y, Masuda Y, Sato M, McGuirt WT, Coucke P, Van Camp G, Smith RJ. Fukushima K, et al. Am J Hum Genet. 1999 Jul;65(1):141-50. doi: 10.1086/302461. Am J Hum Genet. 1999. PMID: 10364526 Free PMC article.

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