Periasamy  Sundaresan
Periasamy Sundaresan
Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
Verified email at - Homepage
Cited by
Cited by
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
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), 755-757, 2006
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
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
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
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
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
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, 2010
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
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
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), 556-562, 2016
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), 1751-1758, 1999
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), 564-572, 1999
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
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
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
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
Mutational analysis of MIR184 in sporadic keratoconus and myopia
J Lechner, HA Bae, J Guduric-Fuchs, A Rice, G Govindarajan, S Siddiqui, ...
Investigative ophthalmology & visual science 54 (8), 5266-5272, 2013
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), 387-392, 2015
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
The system can't perform the operation now. Try again later.
Articles 1–20