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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)
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
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
Rohini, Murugeswari, Prajna, Lalitha, Muthukkaruppan
Matrix Metalloproteinases (MMP-8, MMP-9) and the Tissue Inhibitors of Metalloproteinases (Timp-1, Timp-2) in Keratitis Patients CORNEA 2007 Feb;26(2):207-11
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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