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Publications

  1. Chandru Jayasankaran, Nandhini Devi G, Paridhy Vanniya S, Selvakumari M, Jeffrey J M, Sharanya N, Srikumari Srisailapathy CR. Absence of an Asian founder mutation c.100C > T (p.R34X) in TMC1 among a large cohort of prelingual non syndromic hearing loss from South India. Global Journal for Research Analysis. 2019; 8(8).

  2. Paridhy Vanniya. S, KunkaMohanramRamkumar, C. R. Srikumari Srisailapathy. Immune-mediated Sensorineural Hearing Loss: Patho-Mechanisms and Therapeutic Strategies. Turkish Journal of Immunology 2019; 7(1):S92−S98.

  3. G. Nandhini Devi, AnbupalamThalamuthu, S. Valarmathi, N. P. Karthikeyen and C. R. Srikumari Srisailapathy. Genetic epidemiology of stuttering among school children in the state of Tamil Nadu, India. Journal of fluency disorders. 2018;58:11-21.

  4. Pavithra Amritkumar, Justin Margret Jeffrey, Jayasankaran Chandru, Paridhy Vanniya.S,
    M. Kalaimathi, Rajagopalan Ramakrishnan; N.P. Karthikeyen; C.R.Srikumari Srisailapathy. Role of DFNB1 mutations in Hereditary Hearing Loss among Assortative Mating Hearing Impaired families from South India. BMC Medical Genetics. 2018;19(1):105

  5. Jeffrey J M , Chandru J , Pavithra A, Kalaimathi M, Indhumathi N, Ashraf P and C.R.Srikumari Srisailapathy. Exclusion of putative CATSPER2 & STRC gene deletion and FOXI1 gene mutations in a unique cohort with sensorineural deafness and male infertility from south India. Current Science. 2018; 114(12): 2538-42.

  6. Vanniya S, Srisailapathy CS,Mohanram RK. The tip link protein Cadherin-23: from hearing loss to cancer. Pharmacological Research. 2018 Feb 5. https://doi.org/10.1016/j.phrs.2018.01.026.

  7. Kalaimathi M, G. Nandhini Devi and C.R.Srikumari Srisailapathy. Study of DRD2 TaqA1 Polymorphism in Developmental Stuttering. Proceedings National Symposium on Genetics in Clinical Medicine, 2017, pp 89 – 92. ISBN: 978-93-5288-254-0.

  8. Nandhini Devi G and C R Srikumari Srisailapathy. Contribution of GNPTAB and GNPTG mutations to persistent stuttering. Proceedings National Symposium on Genetics in Clinical Medicine, 2017, pp 79 – 83. ISBN: 978-93-5288-254-0

  9. Jeffrey J M, Amrutha K, Charles S, Chandra R Samuel and C R Srikumari Srisailapathy. Screening for contiguous gene deletion in chromosome 15q15.3 among infertile males from Chennai - a pilot study. Proceedings National Symposium on Genetics in Clinical Medicine, 2017, pp 31-34. ISBN: 978-93-5288-254-0

  10. Paridhy Vanniya S, Selvakumari M, Sharanya N and C. R. Srikumari Srisailapathy. Prevalence of the CDH23 mutation p.D990N among South Indian Hearing Impaired Individuals. Int.J.Curr.Res.Aca.Rev.2017; Special Issue-4: 219-223. ISSN: 2347-3215.

  11. Vanniya S, Chandru J, Pavithra A, Jeffrey JM, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, CR Srikumari S. Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families–an evaluation. Annals of human genetics. 2017 Nov 17.

  12. Pavithra A, Chandru J, Jeffrey JM, Karthikeyen NP, Srisailapathy CS. Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family. European Archives of Oto-Rhino-Laryngology. 2017 Jan 1;274(1):119-25.

  13. Paridhy Vanniya S., SireeshDornadula, DhamodharanUmapathy, PonjayanthiBalashanmugam, Srikumari Srisailapathy C.R .and RamkumarKunkaMohanram. KEAP1. Book Chapter in Encyclopedia of Signaling Molecule Springer Science+Business Media LLC 2016 S. Choi (ed.), Encyclopedia of Signaling Molecules, DOI 10.1007/978-1- 4614-6438-9_101855- 1

  14. Subathra M, Ramesh A, Selvakumari M, Karthikeyen NP, Srisailapathy CR. Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired.. Annals of Human Genetics, 2016: 80;257-273.

  15. Pavithra A, Selvakumari M, Nityaa V, Sharanya N, Ramakrishnan R, Narasimhan M, Srisailapathy CR. Autosomal dominant hearing loss resulting from p. R75Q mutation in the GJB2 gene: nonsyndromic presentation in a South Indian family. Annals of human genetics. 2015 Jan 1;79(1):76-82.

  16. Sharanya Narasimhan, Chandru Jayasankaran, Ramakrishnan Rajagopalan, C.R.Srikumari Srisailapathy. The Public Health Significance and Issues Related to Noise-Induced Hearing Loss: The Indian Scenario. Public health research series, 2014, 264-277.

  17. Subathra M, Selvakumari M, Ramesh A, Ramakrishnan R, Karan KR, Kaur M, Manikandan M, Srikumari Srisailapathy CR. Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five Generational Indian Family with Mitochondrial 1555A> G Mutation and Postlingual Hearing Loss. Annals of human genetics. 2014 May 1;78(3):217-34.

  18. Pavithra A, Harini PT, Chandru J, Sarvani C, Rastogi A, Selvakumari M, Subathra M, Ramesh A, Srisailapathy CS. Is screening for mitochondrial A1555G mutation among assortative mating hearing impaired families important?: A prefatory quest. Research in Otolaryngology. 2014;3(1):1-7.

  19. Pavithra A, Jeffrey JM, Chandru J, Ramesh A, Srisailapathy CS. High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications. Journal of genetics. 2014 Apr 1;93(1):207-13.

  20. Ganapathy A, Pandey N, Srisailapathy CS, Jalvi R, Malhotra V, Venkatappa M, Chatterjee A, Sharma M, Santhanam R, Chadha S, Ramesh A. Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE. PLoS One. 2014 Jan 8;9(1):e84773.

  21. Paramasivam A, Raghunandhakumar S, Sambantham S, Safa B, Vijayashree-Priyadharsini J, Anandan B, Rajiv R, Srikumari-Srisailapathy CR. Induction of apoptosis in mouse neuroblastoma (Neuro-2a) cells by thymoquinone. Biomed. Prev. Nutr. 2 (2012): 223-227.

  22. Padmaja MV, Jayaraman M, Srinivasan AV, Srisailapathy CS, Ramesh A. PARK2 gene mutations in early onset Parkinson's disease patients of South India. Neuroscience letters. 2012 Aug 15;523(2):145-7

  23. Padmaja MV, Jayaraman M, Srinivasan AV, Srisailapathy CS, Ramesh A. The SNCA (A53T, A30P, E46K) and LRRK2 (G2019S) mutations are rare cause of Parkinson's disease in South Indian patients. Parkinsonism & related disorders. 2012 Jul 1;18(6):801-2

  24. Selvakumari M, Subathra M, Pavithra A and C.R. Srikumari Srisailapathy. Screening for deafness causing GJB2, GJB6 genes (Connexins) and mitochondrial DNA mutations among the prelingual childhood hearing impaired. Journal of Advanced Biotechnology, 2011. suppl.Vol 10 (10); 70-72.

  25. Suhasini G, Sonaa E, Shila S, Srikumari CR, Jayaraman G, Ramesh A. Genetic admixture studies on four in situ evolved, two migrant and twenty-one ethnic populations of Tamil Nadu, south India. Journal of Genetics. 2011 Aug 1;90(2):191-202.

  26. Charizopoulou N, Lelli A, Schraders M, Ray K, Hildebrand MS, Ramesh A, Srisailapathy CS, Oostrik J, Admiraal RJ, Neely HR, Latoche JR. Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. Nature communications. 2011 Feb 15;2:201.

  27. Indhumathi N, Deepika S, Chong SS, Thelma BK, Ramesh AR and Srikumari Srisailapathy CR. Fragile X repeat variation in Tamil Nadu, South India: A comparison of radioactive and methylation-specific polymerase chain reaction in CGG repeat sizing. Genetic Testing and Molecular Biomarkers, 2011 DOI: 10.1089/gtmb.2011.0102.

  28. Suhasini G, Sonaa E, Shila S, Srikumari CR, Jayaraman G, Ramesh A. Genetic admixture studies on four in situ evolved, two migrant and twenty-one ethnic populations of Tamil Nadu, south India. Journal of genetics. 2011 Aug 1;90(2):191-202.

  29. Mani RS, Ganapathy A, Jalvi R, Srisailapathy CS, Malhotra V, Chadha S, Agarwal A, Ramesh A, Rangasayee RR, Anand A. Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss. European Journal of Human Genetics. 2009 Apr;17(4):502.

  30. Vijaya M, Kanthimathi S, Srikumari CR, Reddy PG, Majumder PP, Ramesh A. A Study on Telugu–Speaking Immigrants of Tamil Nadu, South India. International Journal of Human Genetics. 2007 Dec 1;7(4):303-6.

  31. Kanthimathi S, Vijaya M, Srikumari CR, Reddy PG, Majumder PP, Ramesh A. A genetic structure of the early immigrants (Mukkalathor) of Tamil Nadu as inferred from autosomal loci. International Journal of Human Genetics. 2007 Jun 1;7(2):167-73.

  32. Khan SY, Ahmed ZM, Shabbir MI, Kitajiri SI, Kalsoom S, Tasneem S, Shayiq S, Ramesh A, Srisailapathy S, Khan SN, Smith RJ. Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus. Human Mutation. 2007 May 1;28(5):417-23.

  33. Guo Y, Pilipenko V, Lim LH, Dou H, Johnson L, Srisailapathy CS, Ramesh A, Choo DI, Smith RJ, Greinwald JH. Refining the DFNB17 interval in consanguineous Indian families. Molecular biology reports. 2004 Jun 1;31(2):97-105.

  34. Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailapathy S, Deshmukh D, Riazuddin S, Griffith AJ. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus. The American Journal of Human Genetics. 2002 Sep 1;71(3):632-6.

  35. Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, Polomeno R, Ramesh A, Schloss M, Srisailapathy CS, Wayne S. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. The American Journal of Human Genetics. 2001 Jan 31;68(1):26-37.

  36. Daryl A. Scott, S.Drury, R. A. Sundstrom, J. Bishop, R.E.Swiderski, R.Carmi, Arabandi Ramesh, C.R. Srikumari Srisailapathy, Khalil Elbedour, B.J.Keats, Val C.Sheffield, Richard J.H Smith, Refining the DFNB11 deafness locus using intra-genic polymorphism in a novel gene, TMEM2, Gene. 2000;246:265-274.

  37. Gu SM, Kumaramanickavel G, Srikumari CR, Denton MJ, Gal A. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family. Journal of Medical Genetics. 1999 Sep 1;36(9):705-7.

  38. Valenzuela CY, Srikumari CR, Csoknyay J, Pineda N. Annual menarche and scholar rhythms. REVISTA MEDICA DE CHILE. 1999 Feb 1;127(2):143-50

  39. Smith RJ, Ramesh A, Srikumari Srisailapathy CR, Fukushima K, Wayne S, Chen A, Van Laer L, Ashley J, Zbar RI, Lovett M, Van Camp G. Homozygosity mapping applied to hereditary hearing impairment-localizing recessive deafness genes. In Developments in genetic hearing impairment 1998 (pp. 77-89). Whurr Publishers.

  40. Scott DA, Greinwald JH, Marietta JR, Drury S, Swiderski RE, Vinas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K,  Srisailapathy CR. 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. Gene. 1998 Jul 30;215(2):461-9.

  41. Van Hauwe P, Everett LA, Coucke P, Scott DA, Kraft ML, Ris-Stalpers C, Bolder C, Otten B, de Vijlder JJ, Dietrich NL, Ramesh A, Srisailapathy CR. Two frequent missense mutations in Pendred syndrome. Human Molecular Genetics. 1998 Jul 1;7(7):1099-104.

  42. Greinwald JH, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. American Journal of Medical Genetics Part A. 1998 Jun 30;78(2):107-13.

  43. Zbar RI, Ramesh A, Srisailapathy CS, Fukushima K, Wayne S, Smith RJ. Passage to India: the search for genes causing autosomal recessive nonsyndromic hearing loss. Otolaryngology—Head and Neck Surgery. 1998 Mar;118(3):333-7.

  44. Tomek MS, Brown MR, Mani SR, Ramesh A, Srikumari Srisailapathy CR, Coucke P, Zbar RI, Bell AM, McGuirt WT, Fukushima K, Willems PJ. Localization of a gene for otosclerosis to chromosome 15q25–q26. Human molecular genetics. 1998 Feb 1;7(2):285-90.

  45. Daryl Scott DA, Kraft ML, Carmi R, Ramesh A, Elbedour K, Yairi Y, Srisailapathy CS,Rosengren SS, Markham AF, Mueller RF, Lench NJ. Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. Human mutation. 1998 Jan 1;11(5):387

  46. Gu SM, Thompson DA, Srikumari CS, Lorenz B, Finckh U, Nicoletti A, Murthy KR, Rathmann M, Kumaramanickavel G, Denton MJ, Gal A. Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy. Nature genetics. 1997 Oct 1;17(2):194-7.

  47. Greinwald JH, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Srisailapathy CS,. Construction of P1-Derived Artificial Chromosome and Yeast Artificial Chromosome Contigs Encompassing the DFNB7 andDFNB11 Region of Chromosome 9q13–21. Genome research. 1997 Sep 1;7(9):879-86.

  48. Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Hauwe PV, Zbar RI, Ashley J, Lovett M. New gene for autosomal recessive non‐syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics Part A. 1997 Sep 5;71(4):467-71.

  49. CY Valenzuela CY, Srikumari CR, Gopinath PM, Ghose N, Gajalakshmi P, Csoknyay J. New evidence of non seasonal factors in the menarche rhythm. Biological research. 1996;29:245-52.

  50. Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Ploplis B, Skarka H, Srisailapathy CS, Wayne S. A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus. Human Molecular Genetics. 1995 Dec 1;4(12):2391-4.

  51. Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER. An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6. Genome research. 1995 Oct 1;5(3):305-8.

  52. Fukushima K, Ramesh A, Srisailapathy CS, Ni L, Chen A, O'Neill M, Camp GV, Coucke P, D. Smith S, B. Kenyon J, Jain P. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Human molecular genetics. 1995 Sep 1;4(9):1643-8.

  53. Kumaramanickavel G, Maw M, Denton MJ, John S, Srikumari CS, Orth U, Oehlmann R, Gal A. Missense rhodopsin mutation in a family with recessive RP. Nature genetics. 1994 Sep;8(1):10.

  54. Thangaraj K, Srikumari CR, Ramesh A. The genetic composition of an endogamous Adi-Dravidar population of Tamil Nadu. Gene geography: a computerized bulletin on human gene frequencies. 1992;6(1-2):27-30.

  55. Kumari JR, Srikumari CR, Valenzuela CY. ABO segregation distortion in Visakhapatnam, India. AnthropologischerAnzeiger. 1992 Dec 1:307-14.

  56. Rao TV, Srikumari CR and JS Murthy. Inbreeding and Genetic load among Brahmins of coastal Andhra Pradesh . Genetic studies in India- Impact of Haldane. 1991;113-120.

  57. Ramesh A, Srikumari CR, Ferrell RE. pDL32B (D12S7) detects a 2-allele PstI polymorphism. Nucleic acids research. 1991 Sep 11;19(17):4789.

  58. Rajanikumari J, Srisailapathy CR. Gene differentiation at the ABO locus among six castes of Shudras, Andhra Pradesh, India. Gene geography: a computerized bulletin on human gene frequencies. 1991;5(1-2):51-4.

  59. RajaniKumari J, Srikumari CR, and Rao TV. Inheritance of anti- A and anti B isoagglutinins – family and twin study. Bionature. 1991;11(1): 9-12.

  60. Ramesh A, Srikumari CR and Mythili Ezekiel. Genetic load due to over dominant Genes : An observation in some populations of Madras City . Genetics: Perspective in man and environment. ST Santhya, R Malathi and G Jayaraman (Eds) University of Madras. 1990; 97-99.

  61. Srisailapathy S,  Ramesh A, Ganesan J. Association of ABO and Rh (D) blood groups with filariasis. Human heredity. 1990;40(6):381-5.

  62. Ramesh A, Srikumari CR, Sukumar S. Parallel cousin marriages in Madras, Tamil Nadu: new trends in Dravidian kinship. Social biology. 1989 Sep 1;36(3-4):248-54.

  63. Rajanikumari J, Srikumari CR. Segregation distortion in Rh polymorphism. AnthropologischerAnzeiger. 1987 Dec 1:331-5

  64. Rajanikumari J, Srikumari CR. Gene differentiation at the ABO locus in twenty castes and twenty two tribes of Andhra Pradesh, India. American journal of physical anthropology. 1987 Jan 1;72(1):95-9.

  65. Srikumari CR,Rajanikumari J, Rao TV. Acuity of selective mechanisms operating on ABO, Rh, and MN blood groups. American journal of physical anthropology. 1987 Jan 1;72(1):117-21.

  66. Srikumari CR, Rajanikumari J, Rao TV. Gene differentiation in four subcastes of Brahmins from Visakhapatnam, Andhra Pradesh. Human heredity. 1986;36(6):373-8.

  67. Rajanikumari J, Rao TV, Srikumari CR. Proportion of low birth weight infants in Visakhapatnam (India) and its relationsship with maternal age, parity and infants survival. AnthropologischerAnzeiger. 1986 Mar 1:13-8.

  68. Srikumari CR,,Rajanikumari J, and Devi MR. Calcar patterns – A familial study in Andhra Pradesh, India.  Dermatoglyphics. 1985; 13(1 & 2):19 – 21.

  69. Rajanikumari J, Srikumari CR, Devi MR. Absence of d triradius on the palms normal people in Andhra Pradesh, India. Dermatoglyphics 1985;13(1 & 2):15-18.

  70. Rajanikumari J, Srikumari CR, Devi MR. Inheritance Study of Seam Figures in the Hallucal Area. Mankind quarterly. 1985 Apr 1;25(3):303.

  71. Srikumari CR,Rajanikumari J, Rao TV. Variability of genetic load with changing socio-cultural environment. Human heredity. 1985;35(6):388-93.

  72. Rajanikumari J, Srikumari CR, Rao V. Variability of selection opportunities with changing socio-cultural environments. Human heredity. 1985;35(4):218-22.

  73. Devi MR, Kumari JR, Srikumari CR. Fertility and mortality differences in relation to maternal body size. Annals of Human Biology. 1985 Jan 1;12(5):479-84.

  74. Srikumari CR,Rajanikumari J, Rao TV. Familial appraisal of colorblindness in school children of an Indian population. Journal of Heredity. 1985 Jan 1;76(1):69-70.

  75. VR Reddy, CR Srikumari and BKC Reddy (1981) Acuity of smell sensitivity to sodium cyanide, acetic acid and ammonia among the Muslims of Vayalpadu, Andhra Pradesh. South East Asian Anthropologist 2(1): 23-25.

© 2020 by Dr. Srikumari Srisailapathy. All rights reserved.

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