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PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.
Ann Hum Genet. 2022 Jan;86(1):1-13. doi: 10.1111/ahg.12442. Epub 2021 Aug 9.
Ann Hum Genet. 2022.
PMID: 34374074
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.
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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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: vanniya s p.
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.
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The tip link protein Cadherin-23: From Hearing Loss to Cancer.
Vanniya S P, Srisailapathy CRS, Kunka Mohanram R.
Vanniya S P, et al.
Pharmacol Res. 2018 Apr;130:25-35. doi: 10.1016/j.phrs.2018.01.026. Epub 2018 Feb 5.
Pharmacol Res. 2018.
PMID: 29421162
Review.
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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.
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
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