Ramesh A - Search Results

1

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.

Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ. Chen A, et al. Among authors: ramesh a. Am J Med Genet. 1997 Sep 5;71(4):467-71. Am J Med Genet. 1997. PMID: 9286457

2

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Chen A, O'Neill M, Van Camp G, Coucke P, Smith SD, Kenyon JB, et al. Fukushima K, et al. Among authors: ramesh a. Hum Mol Genet. 1995 Sep;4(9):1643-8. doi: 10.1093/hmg/4.9.1643. Hum Mol Genet. 1995. PMID: 8541854

3

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. Among authors: ramesh a. Genome Res. 1995 Oct;5(3):305-8. doi: 10.1101/gr.5.3.305. Genome Res. 1995. PMID: 8593615 Free article.

4

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

Greinwald JH Jr, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Skvorak AB, Van Camp G, Srisailapathy CR, Lovett M, Morton CC, Sheffield VC, Smith RJ. Greinwald JH Jr, et al. Among authors: ramesh a. Genome Res. 1997 Sep;7(9):879-86. doi: 10.1101/gr.7.9.879. Genome Res. 1997. PMID: 9314493 Free article.

5

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: ramesh a. Hum Mol Genet. 1998 Feb;7(2):285-90. doi: 10.1093/hmg/7.2.285. Hum Mol Genet. 1998. PMID: 9425236

6

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: ramesh a. 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

7

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss.

Scott DA, Kraft ML, Carmi R, Ramesh A, Elbedour K, Yairi Y, Srisailapathy CR, Rosengren SS, Markham AF, Mueller RF, Lench NJ, Van Camp G, Smith RJ, Sheffield VC. Scott DA, et al. Among authors: ramesh a. Hum Mutat. 1998;11(5):387-94. doi: 10.1002/(SICI)1098-1004(1998)11:5<387::AID-HUMU6>3.0.CO;2-8. Hum Mutat. 1998. PMID: 9600457

8

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

Greinwald JH Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ. Greinwald JH Jr, et al. Among authors: ramesh a. Am J Med Genet. 1998 Jun 30;78(2):107-13. Am J Med Genet. 1998. PMID: 9674898

9

Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.

Scott DA, Greinwald JH Jr, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, Van Gamp G, Lovett M, Deininger PL, Batzer MA, Morton CC, Keats BJ, Smith RJ, Sheffield VC. Scott DA, et al. Among authors: ramesh a. Gene. 1998 Jul 30;215(2):461-9. doi: 10.1016/s0378-1119(98)00316-3. Gene. 1998. PMID: 9758550

10

Refining the DFNB17 interval in consanguineous Indian families.

Guo Y, Pilipenko V, Lim LH, Dou H, Johnson L, Srisailapathy CR, Ramesh A, Choo DI, Smith RJ, Greinwald JH. Guo Y, et al. Among authors: ramesh a. Mol Biol Rep. 2004 Jun;31(2):97-105. doi: 10.1023/b:mole.0000031385.64105.61. Mol Biol Rep. 2004. PMID: 15293785

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