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

2

FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India.

Nagarathinam I, Chong SS, B K T, Justin Margret J, Venkataraman V, Natarajan Padmavathy K, Srisailapathy CRS. Nagarathinam I, et al. Among authors: srisailapathy crs. Adv Genet (Hoboken). 2021 May 28;2(2):e10048. doi: 10.1002/ggn2.10048. eCollection 2021 Jun. Adv Genet (Hoboken). 2021. PMID: 36618123 Free PMC article.

3

Evaluation of recurrent GNPTAB, GNPTG, and NAGPA variants associated with stuttering.

Gunasekaran ND, Jayasankaran C, Justin Margret J, Krishnamoorthy M, Srisailapathy CRS. Gunasekaran ND, et al. Among authors: srisailapathy crs. Adv Genet (Hoboken). 2021 May 20;2(2):e10043. doi: 10.1002/ggn2.10043. eCollection 2021 Jun. Adv Genet (Hoboken). 2021. PMID: 36618124 Free PMC article.

4

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

5

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

6

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: srisailapathy cr. Genome Res. 1995 Oct;5(3):305-8. doi: 10.1101/gr.5.3.305. Genome Res. 1995. PMID: 8593615 Free article.

7

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

8

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: srisailapathy cr. Genome Res. 1997 Sep;7(9):879-86. doi: 10.1101/gr.7.9.879. Genome Res. 1997. PMID: 9314493 Free article.

9

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

10

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

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