Srikumari Srisailapathy CR - Search Results

1

Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.

Amritkumar P, Jeffrey JM, Chandru J, Vanniya S P, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, Srikumari Srisailapathy CR. Amritkumar P, et al. Among authors: srikumari srisailapathy cr. BMC Med Genet. 2018 Jun 19;19(1):105. doi: 10.1186/s12881-018-0609-6. BMC Med Genet. 2018. PMID: 29921236 Free PMC article.

2

Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.

Subathra M, Selvakumari M, Ramesh A, Ramakrishnan R, Karan KR, Kaur M, Manikandan M, Srikumari Srisailapathy CR. Subathra M, et al. Among authors: srikumari srisailapathy cr. Ann Hum Genet. 2014 May;78(3):217-34. doi: 10.1111/ahg.12061. Epub 2014 Mar 24. Ann Hum Genet. 2014. PMID: 24660976

3

Genetic epidemiology of stuttering among school children in the state of Tamil Nadu, India.

Nandhini Devi G, Thalamuthu A, Valarmathi S, Karthikeyen NP, Srikumari Srisailapathy CR. Nandhini Devi G, et al. Among authors: srikumari srisailapathy cr. J Fluency Disord. 2018 Dec;58:11-21. doi: 10.1016/j.jfludis.2018.10.001. Epub 2018 Oct 11. J Fluency Disord. 2018. PMID: 30343931

4

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss.

Mani RS, Ganapathy A, Jalvi R, Srikumari Srisailapathy CR, Malhotra V, Chadha S, Agarwal A, Ramesh A, Rangasayee RR, Anand A. Mani RS, et al. Among authors: srikumari srisailapathy cr. Eur J Hum Genet. 2009 Apr;17(4):502-9. doi: 10.1038/ejhg.2008.179. Epub 2008 Oct 22. Eur J Hum Genet. 2009. PMID: 18941476 Free PMC article.

5

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2.

Scott DA, Drury S, Sundstrom RA, Bishop J, Swiderski RE, Carmi R, Ramesh A, Elbedour K, Srikumari Srisailapathy CR, Keats BJ, Sheffield VC, Smith RJ. Scott DA, et al. Among authors: srikumari srisailapathy cr. Gene. 2000 Apr 4;246(1-2):265-74. doi: 10.1016/s0378-1119(00)00090-1. Gene. 2000. PMID: 10767548

6

The SNCA (A53T, A30P, E46K) and LRRK2 (G2019S) mutations are rare cause of Parkinson's disease in South Indian patients.

Vishwanathan Padmaja M, Jayaraman M, Srinivasan AV, Srikumari Srisailapathy CR, Ramesh A. Vishwanathan Padmaja M, et al. Among authors: srikumari srisailapathy cr. Parkinsonism Relat Disord. 2012 Jul;18(6):801-2. doi: 10.1016/j.parkreldis.2012.02.012. Epub 2012 Mar 20. Parkinsonism Relat Disord. 2012. PMID: 22436655 No abstract available.

7

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: srikumari srisailapathy cr. Gene. 1998 Jul 30;215(2):461-9. doi: 10.1016/s0378-1119(98)00316-3. Gene. 1998. PMID: 9758550

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

7 results

Search Page