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Sankara Nethralaya
Sankara Nethralaya
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Department of Genetics and Molecular Biology
Research
List Of Publications
Tomas Aleman , Nagasamy Soumittra, Artur V. Cideciyan, Alexander Sumaroka, Vedam Ramprasad, Waldo Herrera, Elizabeth A.M. Windsor, Sharon B Schwartz, Robert C Russell, Alejandro J. Roman, Chris F. Inglehearn, Govindasamy Kumaramanickavel, Edwin M. Stone, Gerald A. Fishman, and Samuel G. Jacobson. CERKL Mutations Cause an Autosomal Recessive Cone-Rod Dystrophy With Inner Retinopathy. IOVS [in press]
Madhavan J,Mitra M, Mallikarjuna K,Pranav O, Srinivasan R, Nagpal A, Venkatesan P, Kumaramanickavel G. KIF14 and E2F3 mRNA expression in human retinoblastoma and its phenotype association. Molecular Vision 2009; 15:235-240.
Eranga N. Vithana, Patricio E. Morgan, Vedam Ramprasad, Donald T.H. Tan, Victor H.K Yong, Divya Venkataraman, Anandalakshmi Venkatraman, Gary H.F. Yam, Soumittra Nagasamy, Ricky W.K. Law, Rama Rajagopal, Chi P. Pang, Govindsamy Kumaramanickevel, Joseph R. Casey and Tin Aung. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum. Mol. Genet; 17: 656-66.
Ali M, Ramprasad VL, Soumittra N, Mohamed MD, Jafri H, Rashid Y, Danciger M, McKibbin M, Kumaramanickavel G, Inglehearn CF. A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. Mol Vis. 2008;14:1960-4. Epub 2008 Oct 30. PMID: 18978954 [PubMed - in process]
Raman R, Rani PK, Reddi Rachepalle S, Gnanamoorthy P, Uthra S, Kumaramanickavel G, Sharma T. Prevalence of Diabetic Retinopathy in India Sankara Nethralaya Diabetic Retinopathy Epidemiology and Molecular Genetics Study Report 2. Ophthalmology. 2008 Dec 11. [Epub ahead of print] PMID: 19084275 [PubMed - as supplied by publisher]
Sen P, Bhargava A, George R, Ve Ramesh S, Hemamalini A, Prema R, Kumaramanickavel G, Vijaya L. Prevalence of retinitis pigmentosa in South Indian population aged above 40 years. Ophthalmic Epidemiol. 2008 Jul-Aug;15(4):279-81. PMID: 18780262 [PubMed - indexed for MEDLINE]
Rani PK, Raman R, Subramani S, Perumal G, Kumaramanickavel G, Sharma T. Knowledge of diabetes and diabetic retinopathy among rural populations in India, and the influence of knowledge of diabetic retinopathy on attitude and practice. Rural Remote Health. 2008 Jul-Sep;8(3):838. Epub 2008 Jul 24.PMID: 18656993 [PubMed - indexed for MEDLINE]
Mamatha G, Srilekha S, Meenakshi S, Kumaramanickavel Govindasamy. Screening of the RPE65 gene in the Asian Indian patients with leber congenital amaurosis. Ophthalmic Genet. 2008 Jun;29(2):73-8. PMID: 18484312 [PubMed - indexed for MEDLINE]
Gandra M, Anandula V, Authiappan V, Sundaramurthy S, Raman R, Bhattacharya S, Kumaramanickavel G. Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from India. Mol Vis. 2008 Jun 14;14:1105-13. PMID: 18552984 [PubMed - indexed for MEDLINE]
Madhavan J, Ganesh A, Kumaramanickavel G. Retinoblastoma: from disease to discovery. Ophthalmic Res. 2008;40(5):221-6. Epub 2008 Apr 29. Review. PMID: 18446017 [PubMed - indexed for MEDLINE]
Uthra S, Raman R, Mukesh BN, Rajkumar SA, Padmaja KR, Paul PG, Lakshmipathy P, Gnanamoorthy P, Sharma T, McCarty CA, Kumaramanickavel G. Association of VEGF gene polymorphisms with diabetic retinopathy in a south Indian cohort. Ophthalmic Genet. 2008 Mar;29(1):11-5. PMID: 18363167 [PubMed - indexed for MEDLINE]
Ramprasad VL, Soumittra N, Nancarrow D, Sen P, McKibbin M, Williams GA, Arokiasamy T, Lakshmipathy P, Inglehearn CF, Kumaramanickavel G. Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis. Mol Vis. 2008 Mar 10;14:481-6. PMID: 18334959 [PubMed - indexed for MEDLINE]
Ramprasad VL, George R, Soumittra N, Sharmila F, Vijaya L, Kumaramanickavel G. Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India. Mol Vis. 2008 Feb 9;14:318-22. PMID: 18334947 [PubMed - indexed for MEDLINE]
Prema R, George R, Sathyamangalam Ve R, Hemamalini A, Baskaran M, Kumaramanickavel G, Catherine M, Vijaya L. Comparison of refractive errors and factors associated with spectacle use in a rural and urban South Indian population. Indian J Ophthalmol. 2008 Mar-Apr;56(2):139-44. PMID: 18292625 [PubMed - in process]
Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum Mol Genet. 2008 Mar 1;17(5):656-66. Epub 2007 Nov 16. PMID: 18024964 [PubMed - indexed for MEDLINE]
Madhavan J, Ganesh A, Roy J, Biswas J, Kumaramanickavel G. The relationship between tumor cell differentiation and age at diagnosis in retinoblastoma. J Pediatr Ophthalmol Strabismus. 2008 Jan-Feb;45(1):22-5. PMID: 18286958 [PubMed - indexed for MEDLINE]
Uthra S, Raman R, Mukesh BN, Kumari RP, Sharma T, McCarty CA, Kumaramanickavel G. Genetics of diabetic retinopathy. Int J Hum Genet 2008 8(1-2):155-9.
Madhavan J, Coral K, Mallikarjuna K, Corson TW, Amit N, Khetan V, George R, Biswas J, Gallie BL, Kumaramanickavel G. High expression of KIF14 in retinoblastoma: association with older age at diagnosis. Invest Ophthalmol Vis Sci. 2007 Nov;48(11):4901-6. PMID: 17962437 [PubMed - indexed for MEDLINE]
Rani PK, Raman R, Sharma V, Mahuli SV, Tarigopala A, Sudhir RR, Kumaramanickavel G, Sharma T. Analysis of a comprehensive diabetic retinopathy screening model for rural and urban diabetics in developing countries. Br J Ophthalmol. 2007 Nov;91(11):1425-9. PMID: 17947265 [PubMed - indexed for MEDLINE]
Vijaya L, George R, Arvind H, Baskaran M, Ve Ramesh S, Raju P, Kumaramanickavel G, McCarty C. Prevalence of primary angle-closure disease in an urban south Indian population and comparison with a rural population. The Chennai Glaucoma Study. Ophthalmology. 2008 Apr;115(4):655-660.e1. Epub 2007 Sep 17. PMID: 17869343 [PubMed - indexed for MEDLINE]
Uthra S, Raman R, Mukesh BN, Rajkumar SA, Kumari R P, Agarwal S, Paul PG, Lakshmipathy P, Gnanamoorthy P, Sharma T, McCarty CA, Kumaramanickavel G. Diabetic retinopathy and IGF-1 gene polymorphic cytosine-adenine repeats in a Southern Indian cohort. Ophthalmic Res. 2007;39(5):294-9. Epub 2007 Sep 12. PMID: 17851271 [PubMed - indexed for MEDLINE]
Vijaya L, George R, Baskaran M, Arvind H, Raju P, Ramesh SV, Kumaramanickavel G, McCarty C. Prevalence of primary open-angle glaucoma in an urban south Indian population and comparison with a rural population. The Chennai Glaucoma Study. Ophthalmology. 2008 Apr;115(4):648-654.e1. Epub 2007 Jul 30. PMID: 17664010 [PubMed - indexed for MEDLINE]
Sripriya S, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Karthiyayini T, Vijaya L, Kumaramanickavel G. Transforming growth factor beta-1 -509C>T polymorphism in Indian patients with primary open angle glaucoma. Mol Diagn Ther. 2007;11(3):151-4. PMID: 17570736 [PubMed - indexed for MEDLINE]
Uthra S, Raman R, Mukesh BN, Padmaja Kumari R, Paul PG, Lakshmipathy P, Gnanamoorthy P, Sharma T, McCarty CA, Kumaramanickavel G. Intron 4 VNTR of endothelial nitric oxide synthase (eNOS) gene and diabetic retinopathy in type 2 patients in southern India. Ophthalmic Genet. 2007 Jun;28(2):77-81. PMID: 17558849 [PubMed - indexed for MEDLINE]
Ramprasad VL, George RJ, Sripriya S, Nirmaladevi J, Vijaya L, Kumaramanickavel G. Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling. Ophthalmic Genet. 2007 Mar;28(1):17-24. PMID: 17454743 [PubMed - indexed for MEDLINE]
Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online. Hum Mutat. 2007 May;28(5):522-3. PMID: 17397048 [PubMed - indexed for MEDLINE]
Joseph B, Kumaramanickavel G. ‘Insight’ into molecular genetic testing in retinoblastoma. Int J Hum Genet. 2007 Mar;7(1):23-8.
S Sripriya, R George, L Vijaya, G Kumaramanickavel (2007). Understanding the biology of glaucoma : The current scenario. Journal of Current Glaucoma Practice. 1: 7-16
Joseph B, Raman R, Uthra S, Jagadeesan M, Ganesh A, Paul PG, Sharma T, Kumaramanickavel G. Genotype-phenotype correlation analysis in retinoblastoma patients from India. Asian Pac J Cancer Prev. 2006 Oct-Dec;7(4):619-22. PMID: 17250439 [PubMed - indexed for MEDLINE]
Balasubramanian D, Kaufman PL, Wiggs JL, Kumaramanickavel G, Mandal A, Maumenee I, Nirmalan PK, Friedman D, Biswas J. Rao GN, Zack D. Research Opportunities in Vision: A Report of the US-Indo Workshops on Collaborative Research. Investigative ophthalmology and Visual Science 2006; 47:1717-1735.
Joseph B, Madhavan J, Mamatha G, Ramprasad VL, Gopal L, Kumaramanickavel G. Retinoblastoma: a diagnostic model for India. Asian Pac J Cancer Prev. 2006 Jul-Sep;7(3):485-8. PMID: 17059352 [PubMed - indexed for MEDLINE]
Agarwal S, Raman R, Kumari RP, Deshmukh H, Paul PG, Gnanamoorthy P, Kumaramanickavel G, Sharma T. Diabetic retinopathy in type II diabetics detected by targeted screening versus newly diagnosed in general practice. Ann Acad Med Singapore. 2006 Aug;35(8):531-5. PMID: 17006579 [PubMed - indexed for MEDLINE]
Sripriya S, Nirmaladevi J, George R, Hemamalini A, Baskaran M, Prema R, Ve Ramesh S, Karthiyayini T, Amali J, Job S, Vijaya L, Kumaramanickavel G. OPTN gene: profile of patients with glaucoma from India. Mol Vis. 2006 Jul 24;12:816-20. PMID: 16885925 [PubMed - indexed for MEDLINE]
Vijaya L, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Paul PG, Kumaramanickavel G, McCarty C. Prevalence and causes of blindness in the rural population of the Chennai Glaucoma Study. Br J Ophthalmol. 2006 Apr;90(4):407-10. PMID: 16547314 [PubMed - indexed for MEDLINE]
Vijaya L, George R, Arvind H, Baskaran M, Paul PG, Ramesh SV, Raju P, Kumaramanickavel G, McCarty C. Prevalence of angle-closure disease in a rural southern Indian population. Arch Ophthalmol. 2006 Mar;124(3):403-9. PMID: 16534061 [PubMed - indexed for MEDLINE]
Joseph B, Paul PG, Elamparithi A, Roy J, Vidhya A, Shanmugam MP, Kumaramanickavel G. Karyotyping in retinoblastoma--a statistical approach. Asian Pac J Cancer Prev. 2005 Oct-Dec;6(4):468-71. PMID: 16435993 [PubMed - indexed for MEDLINE]
Vijaya L, George R, Paul PG, Baskaran M, Arvind H, Raju P, Ramesh SV, Kumaramanickavel G, McCarty C. Prevalence of open-angle glaucoma in a rural south Indian population. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4461-7. PMID: 16303934 [PubMed - indexed for MEDLINE]
Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. Mol Vis. 2005 Nov 3;11:934-40. PMID: 16288197 [PubMed - indexed for MEDLINE]
Agarwal S, Mahajan S, Rani PK, Raman R, Paul PG, Kumaramanickavel G, Sharma T. How high is the non-response rate of patients referred for eye examination from diabetic screening camps? Ophthalmic Epidemiol. 2005 Dec;12(6):393-4. PMID: 16283991 [PubMed - indexed for MEDLINE]
Rani PK, Raman R, Agarwal S, Paul PG, Uthra S, Margabandhu G, Senthilkumar D, Kumaramanickavel G, Sharma T. Diabetic retinopathy screening model for rural population: awareness and screening methodology. Rural Remote Health. 2005 Oct-Dec;5(4):350. Epub 2005 Oct 10. PMID: 16212469 [PubMed - indexed for MEDLINE]
Paul PP, George RJ, Arvind H, Raj M, Augustian, Ramesh SV, Sriram P, Kumaramanickavel G, McCarthy C, Vijaya L. A comparison of participants and non-participants in the Chennai Glaucoma Study-rural population. Ophthalmic Epidemiol. 2005 Apr;12(2):125-35. PMID: 16028345 [PubMed - indexed for MEDLINE]
Agarwal S, Raman R, Paul PG, Rani PK, Uthra S, Gayathree R, McCarty C, Kumaramanickavel G, Sharma T. Sankara Nethralaya-Diabetic Retinopathy Epidemiology and Molecular Genetic Study (SN-DREAMS 1): study design and research methodology. Ophthalmic Epidemiol. 2005 Apr;12(2):143-53. PMID: 16019696 [PubMed - indexed for MEDLINE]
Joseph B, Shanmugam MP, Srinivasan MK, Kumaramanickavel G. Retinoblastoma: genetic testing versus conventional clinical screening in India. Mol Diagn. 2004;8(4):237-43. PMID: 15887979 [PubMed - indexed for MEDLINE]
Madhavan C, Bhende P, Gopal L, Vasanthi SB, Kumaramanickavel G. Retinitis pigmentosa patients with sickle cell disease and dextrocardia and situs inversus syndrome. Indian J Ophthalmol. 2001 Sep;49(3):193-5. PMID: 15887731 [PubMed - indexed for MEDLINE]
Harini R, Ata-ur-Rasheed M, Shanmugam MP, Amali J, Das D, Kumaramanickavel G. Genetic profile of 81 retinoblastoma patients from a referral hospital in southern India. Indian J Ophthalmol. 2001 Mar;49(1):37-42. PMID: 15887714 [PubMed - indexed for MEDLINE]
Ramprasad VL, Thool A, Murugan S, Nancarrow D, Vyas P, Rao SK, Vidhya A, Ravishankar K, Kumaramanickavel G. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):17-23. PMID: 15623749 [PubMed - indexed for MEDLINE]
Joseph B, Narayana KS, Mamatha G et al. Mutational Screening of RB1 gene by multiplex PCR. Ind J Biotech. 2005 Apr;4(2):194-200.
Raju P, Ramesh SV, Arvind H, George R, Baskaran M, Paul PG, Kumaramanickavel G, McCarty C, Vijaya L. Prevalence of refractive errors in a rural South Indian population. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4268-72. PMID: 15557431 [PubMed - indexed for MEDLINE]
Sripriya S, Uthra S, Sangeetha R, George RJ, Hemamalini A, Paul PG, Amali J, Vijaya L, Kumaramanickavel G. Low frequency of myocilin mutations in Indian primary open-angle glaucoma patients. Clin Genet. 2004 Apr;65(4):333-7. PMID: 15025728 [PubMed - indexed for MEDLINE]
Kumaramanickavel G (2004). Genetic Diseases of the Eye in India. Genetic Disorders of the Indian Subcontinent. (Ed Dhavendra Kumar) pp 369-398, Springer, 2004. ISBN 1402012152, 9781402012150.
Kumaramanickavel G, Joseph B, Vidhya A, Arokiasamy T, Shridhara Shetty N. Consanguinity and ocular genetic diseases in South India: analysis of a five-year study. Community Genet. 2002;5(3):182-5.PMID: 14960889 [PubMed]
Joseph B, Mamatha G, Raman G, Shanmugam MP, Kumaramanickavel G. Methylation status of RB1 promoter in Indian retinoblastoma patients. Cancer Biol Ther. 2004 Feb;3(2):184-7. Epub 2004 Feb 1. PMID: 14726655 [PubMed - indexed for MEDLINE]
Kumaramanickavel G, Joseph B, Narayana K, Natesh S, Mamatha G, Shanmugam MP, Elamparathi A, Biswas J. Molecular-genetic analysis of two cases with retinoblastoma: benefits for disease management. J Genet. 2003 Apr-Aug;82(1-2):39-44. PMID: 14631101 [PubMed - indexed for MEDLINE]
Arvind H, Paul PG, Raju P, Baskaran M, George R, Balu S, Sripriya S, Ramesh SV, Mukesh BN, Vijaya L, Kumaramanickavel G, McCarty C. Methods and design of the Chennai Glaucoma Study. Ophthalmic Epidemiol. 2003 Dec;10(5):337-48. PMID: 14566635 [PubMed - indexed for MEDLINE]
Kumaramanickavel G, Sripriya S, Ramprasad VL, Upadyay NK, Paul PG, Sharma T. Z-2 aldose reductase allele and diabetic retinopathy in India. Ophthalmic Genet. 2003 Mar;24(1):41-8. PMID: 12660865 [PubMed - indexed for MEDLINE]
Ramprasad VL, Rao SK, Ravishankar K, Kumaramanickavel G. Genetic studies in age related cataract: Problems encountered. Invest Ophthalmol Vis Sci. (9 Oct 2003) E letters to the editor.
Kumaramanickavel G, Ramprasad VL, Sripriya S, Upadyay NK, Paul PG, Sharma T. Association of Gly82Ser polymorphism in the RAGE gene with diabetic retinopathy in type II diabetic Asian Indian patients. J Diabetes Complications. 2002 Nov-Dec;16(6):391-4. PMID: 12477623 [PubMed - indexed for MEDLINE]
Joseph B, Srinivasan A, Soumittra N, Vidhya A, Shetty NS, Uthra S, Kumaramanickavel G. RPE65 gene: multiplex PCR and mutation screening in patients from India with retinal degenerative diseases. J Genet. 2002 Apr;81(1):19-23. PMID: 12357075 [PubMed - indexed for MEDLINE]
Kumaramanickavel G, Sripriya S, Vellanki RN, Upadyay NK, Badrinath SS, Rajendran V, Sukumar B, Ramprasad VL, Sharma T. Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients. Clin Genet. 2002 May;61(5):344-8. PMID: 12081717 [PubMed - indexed for MEDLINE]
Dollfus H, Biswas P, Kumaramanickavel G, Stoetzel C, Quillet R, Biswas J, Lajeunie E, Renier D, Perrin-Schmitt F. Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation. Am J Med Genet. 2002 May 1;109(3):218-25. PMID: 11977182 [PubMed - indexed for MEDLINE]
Joseph B, Shrinivasan A, Kumaramanickavel G. Microarray ‘Chipping’ in genomics. Ind J Biotech. 2002 Jul;1(3):245-54.
Kumaramanickavel G, Sripriya S, Vellanki RN, Upadyay NK, Badrinath SS, Arokiasamy T, Sukumar B, Vidhya A, Joseph B, Sharma T, Gopal L. Tumor necrosis factor allelic polymorphism with diabetic retinopathy in India. Diabetes Res Clin Pract. 2001 Nov;54(2):89-94. PMID: 11640992 [PubMed - indexed for MEDLINE]
Dollfus H, Kumaramanickavel G, Biswas P, Stoetzel C, Quillet R, Denton M, Maw M, Perrin-Schmitt F. Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22. J Med Genet. 2001 Jul;38(7):470-2. No abstract available. PMID: 11474656 [PubMed - indexed for MEDLINE]
Maw MA, Corbeil D, Koch J, Hellwig A, Wilson-Wheeler JC, Bridges RJ, Kumaramanickavel G, John S, Nancarrow D, Röper K, Weigmann A, Huttner WB, Denton MJ. A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. Hum Mol Genet. 2000 Jan 1;9(1):27-34. PMID: 10587575 [PubMed - indexed for MEDLINE]
Gu S, 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. J Med Genet. 1999 Sep;36(9):705-7. PMID: 10507729 [PubMed - indexed for MEDLINE]
Klintworth GK, Sommer JR, Obrian G, Han L, Ahmed MN, Qumsiyeh MB, Lin PY, Basti S, Reddy MK, Kanai A, Hotta Y, Sugar J, Kumaramanickavel G, Munier F, Schorderet DF, El Matri L, Iwata F, Kaiser-Kupfer M, Nagata M, Nakayasu K, Hejtmancik JF, Teng CT. Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene. Mol Vis. 1998 Dec 31;4:31. PMID: 9873069 [PubMed - indexed for MEDLINE]
Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3. Genomics. 1998 Mar 15;48(3):341-5. PMID: 9545639 [PubMed - indexed for MEDLINE]
Vijaya R, Gupta R, Panda G, Ravishankar K, Kumaramanickavel G. Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital. Clin Genet. 1997 Dec;52(6):427-31. PMID: 9520253 [PubMed - indexed for MEDLINE]
Maw M, Kumaramanickavel G, Kar B, John S, Bridges R, Denton M. Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination. Hum Mutat. 1998;Suppl 1:S317-9. No abstract available. PMID: 9452120 [PubMed - indexed for MEDLINE]
Gu SM, Thompson DA, Srikumari CR, 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. Nat Genet. 1997 Oct;17(2):194-7. PMID: 9326941 [PubMed - indexed for MEDLINE]
Maw M, Kar B, Biswas J, Biswas P, Nancarrow D, Bridges R, Kumaramanickavel G, Denton M, Badrinath SS. Linkage of blepharophimosis syndrome in a large Indian pedigree to chromosome 7p. Hum Mol Genet. 1996 Dec;5(12):2049-54. PMID: 8968762 [PubMed - indexed for MEDLINE]
Maw MA, John S, Jablonka S, Müller B, Kumaramanickavel G, Oehlmann R, Denton MJ, Gal A. Oguchi disease: suggestion of linkage to markers on chromosome 2q. J Med Genet. 1995 May;32(5):396-8. PMID: 7616550 [PubMed - indexed for MEDLINE]
Kar B, John S, Kumaramanickavel G. Retinitis pigmentosa in India: a genetic and segregation analysis. Clin Genet. 1995 Feb;47(2):75-9. PMID: 7606847 [PubMed - indexed for MEDLINE]
Kumaramanickavel G, Maw M, Denton MJ, John S, Srikumari CR, Orth U, Oehlmann R, Gal A. Missense rhodopsin mutation in a family with recessive RP. Nat Genet. 1994 Sep;8(1):10-1. No abstract available. PMID: 7987385 [PubMed - indexed for MEDLINE]
Crawford AM, Tate ML, McEwan JC, Kumaramanickavel G, McEwan KM, Dodds KG, Swarbrick PA, Thompson P (1993). How reliable are sheep pedigrees? Proc N Z Soc Anim Prod 53:363–366.
Chand A, Kumaramanickavel G, Abraham M, Gahlot DK, Apte BN, Denton MJ (1991). Indian recessive pedigrees with recessive retinitis pigmentosa: A potential for homozygosity mapping. in Degenerative Retinopathies: Advances in Clinical and Genetic Research (Eds Humphries P, Battacharya S and Bird A), CRC press, Florida, pp.35-40. ISBN 0849301874, 9780849301872.