Karthikeyen NP - Search Results

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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: karthikeyen np. 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

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: karthikeyen np. 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.

Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.

Subathra M, Ramesh A, Selvakumari M, Karthikeyen NP, Srisailapathy CR. Subathra M, et al. Among authors: karthikeyen np. Ann Hum Genet. 2016 Sep;80(5):257-73. doi: 10.1111/ahg.12161. Ann Hum Genet. 2016. PMID: 27530448

Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India.

Chandru J, Jeffrey JM, Pavithra A, Vanniya SP, Devi GN, Mahalingam S, Karthikeyen NP, Srisailapathy CRS. Chandru J, et al. Among authors: karthikeyen np. Eur Arch Otorhinolaryngol. 2020 Nov;277(11):3021-3035. doi: 10.1007/s00405-020-06026-3. Epub 2020 May 16. Eur Arch Otorhinolaryngol. 2020. PMID: 32417962

Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family.

Pavithra A, Chandru J, Jeffrey JM, Karthikeyen NP, Srisailapathy CRS. Pavithra A, et al. Among authors: karthikeyen np. Eur Arch Otorhinolaryngol. 2017 Jan;274(1):119-125. doi: 10.1007/s00405-016-4229-5. Epub 2016 Aug 1. Eur Arch Otorhinolaryngol. 2017. PMID: 27481527

Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families - an evaluation.

Vanniya S P, Chandru J, Pavithra A, Jeffrey JM, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, C R Srikumari S. Vanniya S P, et al. Among authors: karthikeyen np. Ann Hum Genet. 2018 Mar;82(2):119-126. doi: 10.1111/ahg.12228. Epub 2017 Nov 17. Ann Hum Genet. 2018. PMID: 29148562

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