Traboulsi syndrome: A rare eye disease and its genetic association
Chermakani, Prakash, Sundaresan, Periasamy
Published in TNOA Journal of Ophthalmic Science and Research (01.01.2023)
Published in TNOA Journal of Ophthalmic Science and Research (01.01.2023)
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Journal Article
Mutational screening of LCA genes emphasizing RPE65 in South Indian cohort of patients
Verma, Anshuman, Perumalsamy, Vijayalakshmi, Shetty, Shashikant, Kulm, Maigi, Sundaresan, Periasamy
Published in PloS one (16.09.2013)
Published in PloS one (16.09.2013)
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Journal Article
Association of ABCA4 Gene Variants in Patients with Autosomal Recessive Cone-Rod Dystrophy and Retinitis Pigmentosa Cohorts from South India
Kadarkarai Raj Rajendran, Chermakani, Prakash, Anjanamurthy, Rupa, Rencilin, Clayton Fernando, Sundaresan, Periasamy
Published in Cytology and genetics (01.06.2023)
Published in Cytology and genetics (01.06.2023)
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Journal Article
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Gong, Bo, Zhang, Houbin, Huang, Lulin, Chen, Yuhong, Shi, Yi, Tam, Pancy Oi-Sin, Zhu, Xianjun, Huang, Yi, Lei, Bo, Sundaresan, Periasamy, Li, Xi, Jiang, Linxin, Yang, Jialiang, Lin, Ying, Lu, Fang, Chen, Lijia, Li, Yuanfeng, Leung, Christopher Kai-Shun, Guo, Xiaoxin, Zhang, Shanshan, Huang, Guo, Wu, Yaqi, Zhou, Tongdan, Shuai, Ping, Tham, Clement Chee-Yung, Weisschuh, Nicole, Krishnadas, Subbaiah Ramasamy, Mardin, Christian, Reis, André, Yang, Jiyun, Zhang, Lin, Zhou, Yu, Wang, Ziyan, Qu, Chao, Shaw, Peter X., Pang, Chi-Pui, Sun, Xinghuai, Zhu, Weiquan, Li, Dean Yaw, Pasutto, Francesca, Yang, Zhenglin
Published in Genetics in medicine (01.10.2019)
Published in Genetics in medicine (01.10.2019)
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Journal Article
Whole-mitochondrial genome sequencing in primary open-angle glaucoma using massively parallel sequencing identifies novel and known pathogenic variants
Sundaresan, Periasamy, Simpson, David A., Sambare, Chitra, Duffy, Seamus, Lechner, Judith, Dastane, Aditi, Dervan, Edward W., Vallabh, Neeru, Chelerkar, Vidya, Deshpande, Madan, O'Brien, Colm, McKnight, Amy Jayne, Willoughby, Colin E.
Published in Genetics in medicine (01.04.2015)
Published in Genetics in medicine (01.04.2015)
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Journal Article
Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy
Balasubbu, Suganthalakshmi, Sundaresan, Periasamy, Rajendran, Anand, Ramasamy, Kim, Govindarajan, Gowthaman, Perumalsamy, Namperumalsamy, Hejtmancik, J Fielding
Published in BMC genetics (10.11.2010)
Published in BMC genetics (10.11.2010)
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Journal Article
Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India
Viswarubhiny, Sriee, Anjanamurthy, Rupa, Vanniarajan, Ayyasamy, Bharanidharan, Devarajan, Perumalsamy, Vijayalakshmi, Sundaresan, Periasamy
Published in Eye and vision (Novato, Calif.) (06.05.2021)
Published in Eye and vision (Novato, Calif.) (06.05.2021)
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Journal Article
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies
Asai-Coakwell, Mika, March, Lindsey, Dai, Xiao Hua, Duval, Michele, Lopez, Irma, French, Curtis R, Famulski, Jakub, De Baere, Elfride, Francis, Peter J, Sundaresan, Periasamy, Sauvé, Yves, Koenekoop, Robert K, Berry, Fred B, Allison, W Ted, Waskiewicz, Andrew J, Lehmann, Ordan J
Published in Human molecular genetics (01.04.2013)
Published in Human molecular genetics (01.04.2013)
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Journal Article
Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population
Di, Yanan, Huang, Lulin, Sundaresan, Periasamy, Li, Shujin, Kim, Ramasamy, Ballav Saikia, Bibhuti, Qu, Chao, Zhu, Xiong, Zhou, Yu, Jiang, Zhilin, Zhang, Lin, Lin, Ying, Zhang, Dingding, Li, Yuanfen, Zhang, Houbin, Yin, Yibing, Lu, Fang, Zhu, Xianjun, Yang, Zhenglin
Published in Scientific reports (20.01.2016)
Published in Scientific reports (20.01.2016)
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Journal Article
Whole-exome sequencing identifies multiple pathogenic variants in a large South Indian family with primary open-angle glaucoma
Shah, Mohd, Kumaran, Manojkumar, Chermakani, Prakash, Kader, Mohideen, Ramakrishnan, R, Krishnadas, Subbiah, Devarajan, Bharanidharan, Sundaresan, Periasamy
Published in Indian journal of ophthalmology (01.09.2021)
Published in Indian journal of ophthalmology (01.09.2021)
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Journal Article
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
Vithana, Eranga N, Morgan, Patricio, Sundaresan, Periasamy, Ebenezer, Neil D, Tan, Donald T H, Mohamed, Moin D, Anand, Seema, Khine, Khin O, Venkataraman, Divya, Yong, Victor H K, Salto-Tellez, Manuel, Venkatraman, Anandalakshmi, Guo, Ke, Hemadevi, Boomiraj, Srinivasan, Muthiah, Prajna, Venkatesh, Khine, Myint, Casey, Joseph R, Inglehearn, Chris F, Aung, Tin
Published in Nature genetics (01.07.2006)
Published in Nature genetics (01.07.2006)
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Journal Article
Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa
Li, Shujin, Yang, Mu, Liu, Wenjing, Liu, Yuqing, Zhang, Lin, Yang, Yeming, Sundaresan, Periasamy, Yang, Zhenglin, Zhu, Xianjun
Published in Genetic testing and molecular biomarkers (01.02.2018)
Published in Genetic testing and molecular biomarkers (01.02.2018)
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Journal Article
EPHA2 polymorphisms and age-related cataract in India
Sundaresan, Periasamy, Ravindran, Ravilla D, Vashist, Praveen, Shanker, Ashwini, Nitsch, Dorothea, Talwar, Badrinath, Maraini, Giovanni, Camparini, Monica, Nonyane, Bareng Aletta S, Smeeth, Liam, Chakravarthy, Usha, Hejtmancik, James F, Fletcher, Astrid E
Published in PloS one (08.03.2012)
Published in PloS one (08.03.2012)
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Journal Article
Polymorphisms in ARMS2/HTRA1 and complement genes and age-related macular degeneration in India: findings from the INDEYE study
Sundaresan, Periasamy, Vashist, Praveen, Ravindran, Ravilla D, Shanker, Ashwini, Nitsch, Dorothea, Nonyane, Bareng A S, Smeeth, Liam, Chakravarthy, Usha, Fletcher, Astrid E
Published in Investigative ophthalmology & visual science (01.11.2012)
Published in Investigative ophthalmology & visual science (01.11.2012)
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Journal Article
Genetic characterization of Stargardt clinical phenotype in South Indian patients using sanger and targeted sequencing
Raj, Rajendran Kadarkarai, Dhoble, Pankaja, Anjanamurthy, Rupa, Chermakani, Prakash, Kumaran, Manojkumar, Devarajan, Bharanidharan, Sundaresan, Periasamy
Published in Eye and vision (Novato, Calif.) (09.01.2020)
Published in Eye and vision (Novato, Calif.) (09.01.2020)
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Journal Article
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
Shah, Mohd Hussain, Tabanera, Noemi, Krishnadas, Subbaiah Ramasamy, Pillai, Manju R., Bovolenta, Paola, Sundaresan, Periasamy
Published in Molecular genetics & genomic medicine (01.07.2017)
Published in Molecular genetics & genomic medicine (01.07.2017)
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