Srisailapathy CR - Search Results

1

High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications.

Pavithra A, Jeffrey JM, Chandru J, Ramesh A, Srisailapathy CR. Pavithra A, et al. Among authors: srisailapathy cr. J Genet. 2014 Apr;93(1):207-13. doi: 10.1007/s12041-014-0338-3. J Genet. 2014. PMID: 24840842 Free article. No abstract available.

2

Association of ABO and Rh(D) blood groups with filariasis.

Srisailapathy CR, Ramesh A, Ganesan J. Srisailapathy CR, et al. Hum Hered. 1990;40(6):381-5. doi: 10.1159/000153962. Hum Hered. 1990. PMID: 2128074

3

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: srisailapathy cr. Hum Mol Genet. 1995 Sep;4(9):1643-8. doi: 10.1093/hmg/4.9.1643. Hum Mol Genet. 1995. PMID: 8541854

4

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.

Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR, et al. Jain PK, et al. Among authors: srisailapathy cr. Hum Mol Genet. 1995 Dec;4(12):2391-4. doi: 10.1093/hmg/4.12.2391. Hum Mol Genet. 1995. PMID: 8634715

5

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: srisailapathy cr. Am J Med Genet. 1997 Sep 5;71(4):467-71. Am J Med Genet. 1997. PMID: 9286457

6

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

7

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: srisailapathy cr. 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

8

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: srisailapathy cr. 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

9

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: srisailapathy cr. Am J Med Genet. 1998 Jun 30;78(2):107-13. Am J Med Genet. 1998. PMID: 9674898

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: srisailapathy cr. 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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