Ravindran RD, Sundaresan P, Tiruvengada Krishnan, Praveen Vashist, Maraini G, Saravanan V, Usha Chakravarthy, Liam Smeeth, Dorothea Nitsch, Ian S Young, Astrid E Fletcher “Genetic variants in a sodium-dependent vitamin C transporter gene and age-related cataract” Br J Ophthalmol 2019;103:1223–1227.
Manojkumar Kumaran, Umadevi Subramanian, Bharanidharan Devarajan “Performance Assessment of Variant Calling Pipelines using Human Whole Exome Sequencing and Simulated data” BMC Bioinformatics 2019 Jun 17;20(1):342.
Mohammed Razeeth Shait Mohammed, Muthukumar Balamurugan, Rabbind Singh Amrathlal, Priyadharshini Kannan, Jeya Maheshwari Jayapal, Venkatesh Prajna Namperumalsamy, Lalitha Prajna, Dharmalingam Kuppamuthu “Identification of the proteoforms of surface localized Rod A of Aspergillus flavus and determination of the mechanism of proteoform generation” Journal of Proteomics 193 (2019) 62–70
Mohammed Razeeth Shait Mohammed, Muthu Kumar, Rabbind Singh Amrathlal, Priya Kannan, Jeya Maheshwari Jayapal, Venkatesh Prajna Namperumalsamy, Lalitha Prajna, Dharmalingam Kuppamuthu “Data set for the spore surface proteome and Hydrophobin A/RodA proteoforms of A.flavus” Data in Brief 2019
Dharmalingam K. “Immunology of the eye”. In: Prajna NV, editor. Peyman’s principles & practice of ophthalmology. 2nd ed. 2 Vols. New Delhi: Jaypee Brothers Medical Publishers; 2019. p. 163-174.
Kim R, Krishnadas R, Dharmalingam K, Jeya Maheshwari J. “Proteomics of Neurodegenerative Disorders of the Eye”. In: Prakash G and Iwata T editor. Advances in Vision Research: genetic eye research in Asia and the Pacific Vol II. Singapore: Springer Nature . 2019 p. 393-402
Dharmaraj S, Anshuman Verma, Sundaresan P, Chitra Kannabiran “Leber Congenital Amaurosis in Asia”. In: Prakash G and Iwata T editor. Advances in Vision Research: genetic eye research in Asia and the Pacific Vol II. Singapore: Springer Nature 2019 p.191- 232
Usha Kim, Thirumalairaj K, Aloysius Abraham, Shanthi R, Bharanidharan D, Muthukkaruppan VR, Vanniarajan A. Genetics of Retinoblastoma: Basic Research and Clinical Applications. In: Prakash G and Iwata T editor. Advances in Vision Research: genetic eye research in Asia and the Pacific Vol II. Singapore: Springer Nature 2019 p.313-322
Prakadeeswari G, Haripriya A, Banushree R, Sundaresan P. Genetics of Exfoliation Syndrome in Asians. In: Prakash G and Iwata T editor. Advances in Vision Research: genetic eye research in Asia and the Pacific Vol II. Singapore: Springer Nature 2019 p.381-392
Bharanidharan D, Vanniarajan A, Sundaresan P. Genomic Approaches to Eye Diseases: An Asian Perspective. In: Prakash G and Iwata T editor. Advances in Vision Research: genetic eye research in Asia and the Pacific Vol II. Singapore: Springer Nature 2019 p.403-416
Amit Khedekar, Bharanidharan Devarajan, Kim Ramasamy, Veerappan Muthukkaruppan “Smartphone-based application improves the detection of Retinoblastoma” Eye (Lond). 2019 Jun;33(6):896-901
Velusamy Nithya, Sivakumar Rathinam, Rajapandian Siva Ganesa Karthikeyan, Prajna Lalitha. “A ten year study of prevalence, antimicrobial susceptibility pattern, and genotypic characterization of Methicillin resistant Staphylococcus aureus causing ocular infections in a tertiary eye care hospital in South India” Infection. Genetics and Evolution, 2019. 69, 203-210.
Kannan Thirumalmuthu, Bharanidharan Devarajan, Lalitha Prajna and Vidyarani Mohankumar “Mechanisms of Fluoroquinolone and Aminoglycoside Resistance in Keratitis Associated Pseudomonas aeruginosa” Microbial Drug Resistance 2019 Jul/Aug; 25(6):813-823
Sara SH, Prajna NV, Senthil kumari S. “Human amniotic membrane as a drug carrier – An in‑vitro study using fortified cefazolin ophthalmic solution”. Indian J Ophthalmol 2019 Apr;67(4):472-475.
Aloysius Abraham, Kannan Thirumalai Raj, Namrata Gaikwad, Veerappan Muthukkaruppan, Alia G. Reddy, Kumarasamy Thangaraj, Usha Kim, Ayyasamy Vanniarajan “Retinoblastoma discordance in families with twins” Indian Journal of Ophthalmology 2019;67(3); p436-439
Bo Gong et al., “Mutant RAMP2 causes Primary Open Angle Glaucoma via the CRLR – cAMP axis” Genet Med 2019 Oct;21(10):2345-2354
Premanand Chandran, Prakash Chermakani, Prasanna Venkataraman, Siva rasanna Thilagar, Ganesh V Raman & Periasamy Sundaresan “A novel 5 bp homozygous deletion mutation in ASPH gene associates with Traboulsi syndrome” Ophthalmic Genetics 2019 Apr;40(2):185-187
T Daniel Berner et al., “The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling 1 pathway in pseudoexfoliation syndrome” Human Molecular Genetics 2019
Niranjana Parthiban, Nithya Lakshmi Sampath, Jayapal Jeya Maheshwari, Namperumalsamy Venkatesh Prajna, Prajna Lalitha, Kuppamuthu Dharmalingam “Quantitative Profiling of tear proteome reveals down regulation of Zinc alpha -2 glycoprotein inAspergillus flavus keratitis patients” Exp Eye Res. 2019 (Jun 21) E pub
Yogapriya Sundaresan , Ganesh Govardhan Gaikwad, Kishan Anilkumar Prajapati, N Venkatesh Prajna, Gowri Priya Chidambaranathan “Comparison of structural integrity and functional status of corneal endothelium stored in Cornisol and Optisol‑GS” Indian Journal of Ophthalmology 2019 Oct;67(10):1579-1584.
Yogapriya Sundaresan, Muthukkaruppan Veerappan, Krishnadas Subbiah Ramasamy, Gowri Priya Chidambaranathan “Identification, quantification and age related changes of human trabecular meshwork stem cells” Eye and Vision (2019) 6:31
Sivakumar Rathinam, Irene Daniel, Dharmalingam Kuppamuthu & Jeya Maheshwari Jayapal “Molecular Mimicry between Betaine Aldehyde Dehydrogenase of Leptospira and Retinal Dehydrogenase 1 of Human Lens: A Potential Trigger for Cataract Formation in Leptospiral Uveitis Patients” Ocular Immunology and Inflammation 2019 e pub
Yelchuri, Madhavi Latha; Madhavi, Bhagyashree; Gohil, Nilam ; Sajeev, Hitha Sara Venkatesh Prajna, N, Senthilkumari S “In Vitro Evaluation of the Drug Reservoir Function of Human Amniotic Membrane Using Moxifloxacin as a Model Drug” journal of Cornea 2017;0:1-6
Prakadeeswari G, Haripriya A, Sundaresan P. “MTHFR and MTHFD1 gene polymorphisms are not associated with pseudoexfoliation syndrome in South Indian population” Int Ophthalmol. 2017 Mar 15. [Epub ahead of print]
Durga M, Prajna NV, Lumbini Devi, Sundaresan P “Genetic Analysis of CHST6 Gene in Indian Families with Macular Corneal Dystrophy” Int J Gen Sci 4(1): 1-10.
Mohd Hussain Shah, Noemi Tabanera, Subbaiah Ramasamy Krishnadas, Manju R. Pillai, Paola Bovolenta, Periasamy Sundaresan “Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma” 2017 E Pub Molecular Genetics & Genomic Medicine
Roopam Duvesh, Venkatesh R, Kavitha S, Pradeep Y. Ramulu, Krishnadas, SR, and Sundaresan P “Genetic Complexity of Primary Angle-Closure Glaucoma in Asians”in Advances in Vision Research, Volume I Part of the series Essentials in Ophthalmology p 291-313. ( Book Chapter)
Renugadevi K, Asim Kumar Sil, Vijayalakshmi P, and Sundaresan P “Molecular Genetic Analysis and Diagnosis of Albinism Patients in India” JSM Genet Genomics 2017 4(1): 1024
Tin Aung1, Mineo Ozaki, Mei Chin Lee et al “Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci” Nature Genetics 2017
Boomiraj Hemadevi, Prajna NV, Srinivasan M, Sundaresan P “Genetic Perspective of Corneal Endothelial Dystrophies”journals of JSM Genet Genomics 2017
Bhagya S, Lalitha P, Lalan Kumar Arya, Rathinam S. “Polymerase Chain Reaction and its Correlation with Clinical Features and Treatment Response in Tubercular Uveitis” Journal of Ocul Immunol Inflamm. 2017 Jun 30:1-8.
Gowthaman G, Saumi Mathews, Karthik Srinivasan, Kim Ramasamy, Sundaresan P “Establishment of human retinal mitoscriptome gene expression signature for diabetic retinopathy using cadaver eyes” Journal of Mitochondrion E pub 2017 July
Lakshmi Priya Jeganathan, Lalitha Prajna, VidyaraniMohankumar. “Genotypic and “Phenotypic Characterization of Pseudomonas aeruginosa isolates from post-cataract endophthalmitis patients” Microbial Pathogenesis 2015; 78;67-73
SivaganesaKarthikeyan R, Vareechon C , Prajna NV , Dharmalingam, K Pearlman E, and Lalitha P“IL-17 expression in peripheral blood neutrophils from fungal keratitis patients and healthy cohorts in South India” Journal of Infect Dis. 2015 Jan 1;211(1):130–4.
Sundaresan P, Simpson DA, Sambare C, Duffy S, Lechner J, Dastane A, Dervan EW, Vallabh N, Chelerkar V, Deshpande M, O’Brien C, McKnight A J, Willoughby CE. “Whole-mitochondrial genome sequencing in primary open-angle glaucoma using massively parallel sequencing identifies novel and known pathogenic variants” Genet Med.2015 Apr;17(4):279–84.
Selvam RM, Nithya R, Devi PN, Shree RS, Nila MV, Demonte NL, ThangavelC,Maheshwari JJ, Lalitha P, Prajna NV, Dharmalingam K. “Exoproteome of Aspergillusflavus corneal isolates and saprophytes: Identification of proteoforms of an oversecreted alkaline protease” J Proteomics. 2015;115:23-35
Selvam RM, Nithya R, Devi PN, Shree RS, Nila MV, Demonte NL, ThangavelC,Maheshwari JJ, Lalitha P, Prajna NV, Dharmalingam K. “Data set for the mass spectrometry based exoproteome analysis of Aspergillusflavusisolates” Data in Brief. 2015; 2: 42-47
Sushil Kumar Dubey, Mahalakshmi, PerumalsamyVijayalakshmi, PeriasamySundaresan “Mutational analysis and genotype-phenotype correlations in sporadic and familial aniridia patients from southern India” Molecular Vision 2015;21:88-97
Saumi Mathews, Jaya Devi Chidambaram, ShrutiLanjewar, JeenaMascarenhas, Namperumalsamy Venkatesh Prajna, VeerappanMuthukkaruppan, Gowri Priya Chidambaranathan, “In vivo confocal microscopic analysis of normal human anterior limbalstroma” Cornea 2015;34:464–470
Tin Aung et al., “A common variant mapping to CACNA1A is associated with susceptibility to Exfoliation syndrome” NATURE GENETICS 2015 Apr;47(4):387–92.
Sushil K. Dubey, James F. Hejtmancik, Subbaiah R. Krishnadas, Rajendrababu Sharmila, Aravind Haripriya,PeriasamySundaresan “Evaluation of Genetic Polymorphisms in Clusterin and Tumor Necrosis Factor-Alpha Genes in South Indian Individuals with Pseudoexfoliation Syndrome” Current Eye Research, Early Online, 1–7, 2015
Li Z, Allingham RR, Nakano M, Jia L, Chen Y, Ikeda Y, Mani B, Chen LJ, Kee C, Garway-Heath DF, Sripriya S, Fuse N, Abu-Amero KK, Huang C, Namburi P, Burdon K, Perera SA, Gharahkhani P, Lin Y, Ueno M, Ozaki M, Mizoguchi T, Krishnadas SR, Osman EA, Lee MC, Chan AS, Tajudin LS, Do T, Goncalves A, Reynier P, Zhang H, Bourne R, Goh D, Broadway D, Husain R, Negi AK, Su DH, Ho CL, Blanco AA, Leung CK, Wong TT, Yakub A, Liu Y, Nongpiur ME, Han JC, Hon DN, Shantha B, Zhao B, Sang J, Zhang N, Sato R, Yoshii K, Panda-Jonas S, Ashley Koch AE, Herndon LW, Moroi SE, Challa P, Foo JN, Bei JX, Zeng YX, Simmons CP, BichChau TN, Sharmila PF, Chew M, Lim B, Tam PO, Chua E, Ng XY, Yong VH, Chong YF, Meah WY, Vijayan S, Seongsoo S, Xu W, Teo YY, Cooke Bailey JN, Kang JH, Haines JL, Cheng CY, Saw SM, Tai ES; ICAARE-Glaucoma consortium; NEIGHBORHOOD consortium, Richards JE, Ritch R, Gaasterland DE, Pasquale LR, Liu J, Jonas JB, Milea D, George R, Al-Obeidan SA, Mori K, MacGregor S, Hewitt AW, Girkin CA, Zhang M, Sundaresan P,Vijaya L, Mackey DA, Wong TY, Craig JE, Sun X, Kinoshita S, Wiggs JL, Khor CC, Yang Z, Pang CP, Wang N, Hauser MA, Tashiro K, Aung T, Vithana EN. “A common variant near TGFBR3 is associated with primary open angle glaucoma” Hum Mol Genet. 2015 Jul 1;24(13):3880–92.
Bharanidharan Devarajan, Logambiga Prakash, Thirumalai Raj Kannan, Aloysius A Abraham, Usha Kim, VeerappanMuthukkaruppan and AyyasamyVanniarajan “Targeted next generation sequencing of RB1 gene for the molecular diagnosis of Retinoblastoma” BMC Cancer. 2015 Apr 28;15(1):320.
KannanThirumalairaj, Aloysius Abraham, Bharanidharan Devarajan, NamrataGaikwad, Usha Kim,VeerappanMuthukkaruppanand AyyasamyVanniarajan “A stepwise strategy for rapid and cost-effective RB1 screening in Indian retinoblastoma patients”Journal of Human Genetics 2015; 1-6
Gowri Priya Chidambaranathan, Saumi Mathews, Arun Kumar Panigrahi, JeenaMascarenhas, Venkatesh Prajna Namperumalsamy, MuthukkaruppanVeerappan, “In vivo confocal microscopic analysis of limbalstroma in limbal stem cell deficient patients” CORNEA 2015; August 26 (E Pub ahead of print)
Kathryn P. Burdon, Rhys D. Fogarty, WeiyongShen, SotoodehAbhary, Georgia Kaidonis, BinoyAppukuttan, Alex W. Hewitt, Shiwani Sharma, Mark Daniell, RohanW. Essex, John H. Chang, Sonja Klebe, Stewart R. Lake, Bishwanath Pal, Alicia Jenkins, GowthamanGovindarjan, PeriasamySundaresan, Ecosse L. Lamoureux, Kim Ramasamy, Maria Pefkianaki, Philip G. Hykin, Nikolai Petrovsky, Matthew A. Brown, Mark C. Gillies, Jamie E. Craig “Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene” Diabetologia 2015; 19th July (E Pub ahead of print)
Yu Zhou, Bibhuti B Saikia, Zhilin Jiang, Xiong Zhu, Yuqing Liu, Lulin Huang, Ramasamy Kim, Yin Yang, Chao Qu, Fang Hao, Bo Gong,Zhengfu Tai, LihongNiu, Zhenglin Yang, PeriasamySundaresan and Xianjun Zhu “Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population”Journal of J Hum Genet. 2015 Aug 6. (Epub ahead of print)
Namrata G, Vanniarajan A ,Akram Husain, Jeyaram I, Thirumalairaj K Santhi,R, Muthukkaruppan V,Usha Kim “Knudson’s hypothesis revisited in Indian retinoblastoma patients” Asia-Pac J ClinOncol 2015(Epub ahead of print)
SrinivasanSenthilkumari, Mohan Neethu, RadhakrishnanSanthi, SubbiahRamaswami Krishnadas, VeerappanMuthukkaruppan.”Identification of glaucomatous optic nerve head changes in Indian donor eyes without clinical history” Indian J Ophthalmol 2015;63:600-5.
ShirishDongare, Sharmila Rajendran, S Senthilkumari, Suresh K Gupta, RajaniMathur, RohitSaxena, SushmaSrivastava. “Genistein Alleviates high glucose induced toxicity and angiogenesis in cultured human RPE cells” Int J Pharm PharmSci, Vol 7, Issue 8, 294-298
HemadeviBoomiraj, VidyaraniMohankumar, LalithaPrajna. Bharanidharan Devarajan “Human corneal microRNA expression profile in fungal keratitis” Invest Ophthalmol Vis Sci.2015;56:7939–7946.
Anand Rajendran; Pankaja Dhoble; Sundaresan P; Saravanan V; Praveen Vashist; Dorothea Nitsch; Liam Smeeth; Usha Chakravarthy; Ravilla D Ravindran; Astrid E Fletcher. “Genetic risk factors for late age-related macular degeneration in India” British Journal of ophthalmology 2018 Sep;102(9):1213-1217.
Kotnala A., Senthilkumari S., Halder N., Kumar A. Velpandian T. “Microwave assisted synthesis for A2E and development of LC-ESI–MS method for quantification of ocular bisretinoids in human retina” Journal of Chromatography B 1073 (2018) 10–18
Nongpiur ME, Cheng CY, Duvesh R, Vijayan S, Baskaran M, Khor CC, Allen J, Kavitha S, Venkatesh R, Goh D, Husain R, Boey PY, Quek D, Ho CL, Wong TT, Perera S, Wong TY, Krishnadas SR, Sundaresan P, Aung T, Vithana EN. “Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease” Ophthalmology. 2018 May;125(5):664-670
Prakadeeswari G, Haripriya A, Sundaresan P. “MTHFR and MTHFD1 gene polymorphisms are not associated with pseudoexfoliation syndrome in South Indian population” Int Ophthalmol. 2018 Apr;38(2):599-606
Li S, Yang M, Liu W, Liu Y, Zhang L, Yang Y, Sundaresan P, Yang Z, Zhu X. Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa. Genet Test Mol Biomarkers. 2018 Feb; 22(2):109-114.
Raj RK, Prakadeeswari G, Vijayalakshmi P, Sundaresan P. Decoding of Tyrosinase Leads to Albinism in a Nonidentical Twin. J Clin Neonatol 2018;7:59-62.
Zhou Y, Li S, Huang L, Yang Y, Zhang L, Yang M, Liu W, Kim R, Jiang Z Sundaresan P, Zhu X, Yang Z.” A splicing mutation in Aryl Hydrocarbon Receptor associated with retinitis pigmentosa:. Hum Mol Genet. 2018 May 2. [Epub]
Vidyarani M, Sangeetha R, Gowri Priya C, Lalitha Prajna. ”Autophagy induced by type III secretion system toxins enhances clearance of Pseudomonas aeruginosa from human corneal epithelial cells”. Biochem Biophys Res Commun. 2018:1-6. [Epub]
Soundararajan Ashwinbalaji, Srinivasan Senthilkumari, Chidambaranathan Gowripriya, Subbaiah Krishnadas, B’ Ann T. Gabelt, Paul L. Kaufman & Veerappan Muthukkaruppan “SB772077B, A New Rho Kinase Inhibitor Enhances Aqueous Humour Outflow Facility in Human Eyes” Scientific Reports | (2018) 8:15472
Lalan Kumar Arya, Sivakumar R. Rathinam, Prajna Lalitha, Usha R. Kim, SudeepGhatani, Veena Tandon “Trematode Fluke Procerovumvariumas Cause of Ocular Inflammation in Children, South India” Emerging Infectious Diseases Vol. 22, No. 2, February 2016; 192-199
Yanan Di, Lulin Huang, PeriasamySundaresan, Shujin Li, Ramasamy Kim, Bibhuti Ballav Saikia, Chao Qu, Xiong Zhu, Yu Zhou, Zhilin Jiang, Lin Zhang, Ying Lin, Dingding Zhang, Yuanfen Li, Houbin Zhang, Yibing Yin, Fang Lu, Xianjun Zhu &Zhenglin Yang “Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population”Scientific Reports | 6:19432 | DOI: 10.1038/srep19432
ChieaChuenKhor et al., “Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma” Nature Genetics (published online 4 April 2016)
KarthikeyanArcotSadagopan, Renukadevi Kathirvel, Rosanne B. Keep, P. Sundaresan, Hui Huang, Arndt Rolfs, KannanParthiban& P. Vijayalakshmi “Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism” Ophthalmic Genet. 2016 May 13:1-3.
Zhang L, Yang Y, Li S, Tai Z, Huang L, Liu Y, Zhu X, Di Y, Qu C, Jiang Z, Li Y, Zhang G, Kim R, Sundaresan P, Yang Z, Zhu X.“Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy”Genet Test Mol Biomarkers. 2016 May 26. [Epub ahead of print]
Mohideen Abdul Kader, PrasanthiNamburi, SarikaRamugade, R. Ramakrishnan, Subbiah R. Krishnadas, Ben R. Roos, SundaresanPeriasamy, Alan L. Robin&John H. Fingert “Clinical and genetic characterization of a large primary open angle glaucoma pedigree”Ophthalmic Genetics 2016
Yin Yang, Yeming Yang, Lulin Huang, YaruZhai, Jie Li, Zhilin Jiang, Bo Gong, Hao Fang, Ramasamy Kim , Zhenglin Yang, PeriasamySundaresan, Xianjun Zhu & Yu Zhou “Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa” Scientific Reports | 6:33681 | DOI: 10.1038/srep33681
JeyalakshmiKandhavelu, Naveen Luke Demonte, Venkatesh Prajna Namperumalsamy, Lalitha Prajna, Chitra Thangavel, Jeya Maheshwari Jayapal,Dharmalingam Kuppamuthu “Aspergillusflavusinduced alterations in tear protein profile reveal pathogen induced host response to fungal infection” Journal of Proteomics 2016 (accepted 19th Oct 2016)
Bibhuti BS, Sushil Kumar Dubey, Mahesh Kumar S, SundaresanP “Whole mitochondrial genome analysis in South Indian patients with Leber’s hereditary optic neuropathy” Journal of Mitochondrion 2016
Senthilkumari S, Sharmila R, GowripriyaC, Vanniarajan A. “Epalrestat, an Aldose Reductase Inhibitor Prevents Glucose-Induced Toxicity in Human Retinal Pigment Epithelial Cells”In Vitro’ J OculPharmacolTher. (2016 E pub Nov 11)