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Publications 2008-09
Thanapal Amala Rajasundari, Periasamy Sundaresan, Perumalsamy Vijayalakshmi, David
WG Brown and Li Jin. Laboratory confirmation of congenital rubella syndrome in infants - an
Eye hospital based investigation J Med Virol, 2008: 80: 536-546
Moumné L, Batista F, Benayoun BA, Nallathambi J, Fellous M, Sundaresan P, Veitia RA.The
mutations and potential targets of the forkhead transcription factor FOXL2. Mol Cell
Endocrinol. 2008; 30:282(1-2):2-11
Sivagnanam Ananthi , Thangavel Chitra , Ramachandran Bini , Namperumalsamy
Prajna, Prajna Lalitha, Kuppamauthu Dharmaligam .Comparative Analysis of the
Tear Protein Profile in Mycotic keratitis patients. Molecular vision.2008; 14:500-507
Parthasarathy Arpitha, Namperumalsamy V Prajna, Muthiah Srinivasan, and Veerappan
Muthukkaruppan. A Method to Isolate Human Limbal Basal Cells Enriched for a Subset of
Epithelial Cells with a Large Nucleus/Cytoplasm Ratio Expressing High Levels of p63. Microscopy Research and Technique 2008; 71(6):469-76.
P. Murugeswari, Dhananjay Shukla, Anand Rajendran, R. Kim, P. Namperumalsamy, VR.
Muthukkaruppan, Pro-inflammatory cytokines, angiogenic and anti-angiogenic factors in
vitreous of patients with Proliferative Diabetic Retinopathy and Eales’ Disease – RETINA,
2008;28(6):817-824
Boomiraj Hemadevi, Reiner A Veitia, Muthiah Srinivasan, Jambulingam Arunkumar,
Namperumalsamy Venkatesh Prajna, Corinne Lesaffre and Periasamy Sundaresan.
Identification of mutations in SLC4A11gene in patients withRecessive Congenital Hereditary
Endothelial Dystrophy. Arch Ophthalmol. 2008 May; 126(5):700-8.
Jeyabalan Nallathambi, Paul Laissue, Frank Batista, Bérénice A. Benayoun
Corinne Lesaffre, Lara Moumné, PJ Eswari Pandaranayaka, Kim Usha, Sankaran
Krishnaswamy, Periasamy Sundaresan, Reiner A. Veitia. Differential functional
effects of novel mutations of the transcription factor FOXL2 in BPES patients.
Hum Mutat. 2008 May 16. [Epub ahead of print]
Parthasarathy Arpitha,Namperumalsamy V Prajna,Muthiah Srinivasan, and Veerappan
Muthukkaruppan A subset of Human Limbal Epithelial Cells with Greater Nucleus/Cytoplasm
Ratio Expressing High Levels of p63 Possesses Slow-Cycling Property CORNEA
2008;27(10):1164-70
Ashutosh Verma, S. R. Rathinam, C. Gowri Priya, V. R. Muthukkaruppan, Brian Stevenson,
and John F. Timoney LruA and LruB antibodies in sera of human cases of leptospiral uveitis Clinical and Vaccine Immunology 2008; 15; 1019–1023
P. J. Eswari Pandaranayaka P J. Kanagavalli J, S. R., Krishnadas P. Sundaresan, S.
Krishnaswamy Over expression and purification of recombinant human myocilin World J
Microbiol Biotechnol 2008; 24:903–907.
Ramachandran Ramya Devi,Wenliang Yao, Perumalsamy Vijayalakshmi, Yuri V. Sergeev,
Periasamy Sundaresan, J. Fielding Hejtmancik Crystallin Gene mutations in Indian
families with inherited pediatric cataract Molecular Vision 2008; 14:1157-1170
CG Priya, Rathinam SR, Muthukkaruppan VR Leptospiral Endotoxin as a Causative
Factor for Human Ocular Inflammation Invest Ophthalmol Vis Sci 2008;49(12):5419-24
Mika Asai-Coakwell, Curtis R. French, Ming Ye1, Kamal Garcha , Karin Bigot,Anoja G.
Perera, Karen Staehling-Hampton, Silvina C. Mema, Bhaskar Chanda,Arcady Mushegian,
Steven Bamforth, Michael R. Doschak, Guang Li, Matthew B. Dobbs,Philip F. Giampietro,
Brian P. Brooks, Perumalsamy Vijayalakshmi, Yves Sauve ,Marc Abitbo, Periasamy
Sundaresan, Veronica van Heyningen, Olivier Pourquie,T. Michael Underhill, Andrew J.
Waskiewicz and Ordan J. Lehmann Incomplete penetrance and phenotypic variability
characterize Gdf6-attributable oculo-skeletal phenotypes Human Molecular
Genetics 2009; 18:1110-1121
Guruswamy Neethirajan, Abraham Solomon, Krishnadas SR, Vijayalakshmi P and
Periasamy Sundaresan Genotype/ Phenotype Association in Indian congenital
Aniridia Indian Journal of Pediatrics 2009; 76(5):513-517
Publications 2007
Nallathambi J, Moumne L, De Baere E, Beysen D, Usha K, Sundaresan P, Veitia RA.
A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. Hum Genet. 2007 Mar;121(1):107-12.
Suganthalakshmi B, Shukla D, Rajendran A, Kim R, Nallathambi J, Sundaresan P.
Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis. Mol Vis. 2007 Apr 19;13:611-7.
Ramachandran RD, Perumalsamy V, Hejtmancik JF.
Autosomal recessive juvenile onset cataract associated with mutation in BFSP1. Hum Genet. 2007 May;121 (3-4):475-82.
Rohini G, Murugeswari P, Prajna NV, Lalitha P, Muthukkaruppan V.
Matrix metalloproteinases (MMP-8, MMP-9) and the tissue inhibitors of metalloproteinases (TIMP-1, TIMP-2) in patients with fungal keratitis. Cornea. 2007 Feb; 26(2):207-11.
Prajna VN, Nirmalan PK, Saravanan S, Srinivasan M.
Economic analysis of corneal ulcers in South India. Cornea. 2007 Feb;26(2):119-22.
Janakaraj Kanagavalli, P.J. Eswari Pandaranayaka, Subbaiah Ramasamy Krishnadas, Sankaran Krishnaswamy, Periasamy Sundaresan.
"In vitro and in vivo study on the secretion of the Gly367Arg mutant myocilin protein" Molecular Vision 2007; 13:1161-8
Jeyabalan Nallathambi Guruswamy Neethirajan, Kim Usha, Jethani Jitendra, Elfride De Baere, and Periasamy Sundaresan.
FOXL2 mutations in Indian families with Blepharophimosis-Ptosis- Epicanthus Inversus Syndrome. Journal of Genetics 2007Aug ; 80 (2)
Vasanthi, Namperumalsamy, Prajna, Lalitha, Kannan Mahadevan,Muthukkaruppan
A Pilot study on the infiltrating cells and cytokine levels in the tear of fungal Keratitis patients. Indian J Ophthalmol 2007;55:27-31
Publications 2006
Suganthalakshmi, Rajendran, Kim, Namperumalsamy, Sundaresan
Emerging Patterns of Possible Potential Candidate Gene Polymorphisms Associated with Diabetic Retinopathy – a review Asian J.Exp.Sci. 2006:20:15-28
Eranga Vithana, Morgan, Sundaresan, Ebenezer, Tan, Anand, Khine, Dhivya, Yong, salto Tellez, Anandalakshmi, Ke Guo, Hemadevi, Moin D. Mohamed, Srinivasan M, Prajna, Khine M, Casey J, Chris F. Inglehearn and Tin Aung .
Mutations in Na+-borate co-transporter SLC4A11 cause recessive Congenital Hereditary Endothelial Dystrophy CHED2. Nature Genetics 2006 Jul; 38 (7):755-7,
Neethirajan G, Nallathambi J, Krishnadas, Vijayalakshmi,Shashikanth, Jon Martin
Collinson and Sundaresan Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia. 2006. BMC J Ophthalmol 6:28
Suganthalakshmi B, Anand R, Kim R, Mahalakshmi R, Karthikprakash S, Namperumalsamy P, Sundareasan P.
Association of VEGF and eNOS gene polymorphisms in type 2 diabetic retinopathy. Mol Vision.2006; 12:336-41
Nallathambi J,Shukla,Rajendran,Namperumalsamy,Muthulakshmi,Sundaresan.
Identification of Novel FZD4 mutations in Indian Patients with Familial Exudative Vitreoretinopathy (FEVR) Mol Vision. 2006 12: 1086 - 1092.
Nallathambi J, Neethirajan G, Shashikant S, Vijayalakshmi P, Sundaresan P
PAX6 Missense Mutations Associated in patients with Optic Nerve Malformation Mol Vision. 2006:12:236-42
DeviRR, Vijayalakshmi P.
Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea Mol Vision. 2006;12:190-5
Amala, Keerthy, Vijayalakshmi, Muthukkaruppan
Immune Status of Health Care Personnel and Post vaccination analysis of immunity against Rubella in an Eye Hospital" 2006 Indian J Med Res, 2006 Nov;124(5):553-8.
P.Vijayalakshmi, VR.Muthukkaruppan, A.Rajasundari, G.Korukluoglu, W.Nigatu, L.A.Warrener,D.Samuel, D.W.G.Brown
Evaluation of a commercial rubella IgM assay for use on oral fluid samples for diagnosis and surveillance of congenital rubella syndrome and postnatal rubella 2006 J Clin Virol, 2006;37:265-8
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