Periasamy  Sundaresan
Periasamy Sundaresan
Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
Verified email at aravind.org - Homepage
TitleCited byYear
Systemic antitumor immunity in experimental brain tumor therapy using a multimutated, replication-competent herpes simplex virus
T Todo, SD Rabkin, P Sundaresan, A Wu, KR Meehan, HB Herscowitz, ...
Human gene therapy 10 (17), 2741-2755, 1999
2101999
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
EN Vithana, P Morgan, P Sundaresan, ND Ebenezer, DTH Tan, ...
Nature genetics 38 (7), 755, 2006
1992006
Local and systemic therapy of human prostate adenocarcinoma with the conditionally replicating herpes simplex virus vector G207
JR Walker, KG Mcgeagh, P Sundaresan, TJ Jorgensen, SD Rabkin, ...
Human gene therapy 10 (13), 2237-2243, 1999
1761999
Association of VEGF and eNOS gene polymorphisms in type 2 diabetic retinopathy
B Suganthalakshmi, R Anand, R Kim, R Mahalakshmi, S Karthikprakash, ...
Mol Vis 12 (1), 336-341, 2006
1552006
Crystallin gene mutations in Indian families with inherited pediatric cataract
RR Devi, W Yao, P Vijayalakshmi, YV Sergeev, P Sundaresan, ...
Molecular vision 14, 1157, 2008
1462008
Attenuated, replication-competent herpes simplex virus type 1 mutant G207: safety evaluation in mice
P Sundaresan, WD Hunter, RL Martuza, SD Rabkin
Journal of virology 74 (8), 3832-3841, 2000
1392000
In vivo immune evasion mediated by the herpes simplex virus type 1 immunoglobulin G Fc receptor
T Nagashunmugam, J Lubinski, L Wang, LT Goldstein, BS Weeks, ...
Journal of Virology 72 (7), 5351-5359, 1998
1351998
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies
M Ye, KM Berry-Wynne, M Asai-Coakwell, P Sundaresan, T Footz, ...
Human molecular genetics 19 (2), 287-298, 2009
1162009
Effect of prior exposure to herpes simplex virus 1 on viral vector-mediated tumor therapy in immunocompetent mice
A Chahlavi, SD Rabkin, T Todo, P Sundaresan, RL Martuza
Gene therapy 6 (10), 1751, 1999
911999
Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy
S Balasubbu, P Sundaresan, A Rajendran, K Ramasamy, G Govindarajan, ...
BMC medical genetics 11 (1), 158, 2010
882010
Hepatoma-specific antitumor activity of an albumin enhancer/promoter regulated herpes simplex virus in vivo
SI Miyatake, S Tani, F Feigenbaum, P Sundaresan, H Toda, O Narumi, ...
Gene therapy 6 (4), 564, 1999
871999
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes
M Asai-Coakwell, CR French, M Ye, K Garcha, K Bigot, AG Perera, ...
Human molecular genetics 18 (6), 1110-1121, 2009
852009
The mutations and potential targets of the forkhead transcription factor FOXL2
L Moumne, F Batista, BA Benayoun, J Nallathambi, M Fellous, ...
Molecular and cellular endocrinology 282 (1-2), 2-11, 2008
772008
ABCB6 mutations cause ocular coloboma
L Wang, F He, J Bu, X Liu, W Du, J Dong, JD Cooney, SK Dubey, Y Shi, ...
The American Journal of Human Genetics 90 (1), 40-48, 2012
762012
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
CC Khor, T Do, H Jia, M Nakano, R George, K Abu-Amero, R Duvesh, ...
Nature genetics 48 (5), 556, 2016
722016
A common variant near TGFBR3 is associated with primary open angle glaucoma
Z Li, RR Allingham, M Nakano, L Jia, Y Chen, Y Ikeda, B Mani, LJ Chen, ...
Human molecular genetics 24 (13), 3880-3892, 2015
682015
A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction
J Nallathambi, L Moumné, E De Baere, D Beysen, K Usha, P Sundaresan, ...
Human genetics 121 (1), 107-112, 2007
672007
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy
B Hemadevi, RA Veitia, M Srinivasan, J Arunkumar, NV Prajna, C Lesaffre, ...
Archives of Ophthalmology 126 (5), 700-708, 2008
602008
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
T Aung, M Ozaki, T Mizoguchi, RR Allingham, Z Li, A Haripriya, S Nakano, ...
Nature genetics 47 (4), 387, 2015
592015
Evaluation and understanding of myocilin mutations in Indian primary open angle glaucoma patients
J Kanagavalli, SR Krishnadas, E Pandaranayaka, S Krishnaswamy, ...
Mol Vis 9, 606-14, 2003
582003
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Articles 1–20