1. A novel 5 bp homozygous deletion mutation in ASPH gene associates with Traboulsi syndrome. (4th March 2019) Authors: Chandran, Premanand; Chermakani, Prakash; Venkataraman, Prasanna; Thilagar, Siva Prasanna; Raman, Ganesh V; Sundaresan, Periasamy Journal: Ophthalmic genetics Issue: Volume 40:Number 2(2019) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical reassessments and whole-exome sequencing uncover novel BEST1 mutation associated with bestrophinopathy phenotype. (4th March 2022) Authors: Chowdhury, Susmita; Duvesh, Roopam; Kumaran, Manojkumar; Anjanamurthy, Rupa; Kumar, Jayant; Vanniarajan, Ayyasamy; Devarajan, Bharanidharan; Sundaresan, Periasamy Journal: Ophthalmic genetics Issue: Volume 43:Number 2(2022) Page Start: 191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Evaluation of Genetic Polymorphisms in Clusterin and Tumor Necrosis Factor-Alpha Genes in South Indian Individuals with Pseudoexfoliation Syndrome. (2nd December 2015) Authors: Dubey, Sushil K.; Hejtmancik, James F.; Krishnadas, Subbaiah R.; Sharmila, Rajendrababu; Haripriya, Aravind; Sundaresan, Periasamy Journal: Current eye research Issue: Volume 40:Number 12(2015:Dec.) Page Start: 1218 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic risk factors for late age-related macular degeneration in India. Issue 9 (19th December 2017) Authors: Rajendran, Anand; Dhoble, Pankaja; Sundaresan, Periasamy; Saravanan, Vijayan; Vashist, Praveen; Nitsch, Dorothea; Smeeth, Liam; Chakravarthy, Usha; Ravindran, Ravilla D; Fletcher, Astrid E Journal: British journal of ophthalmology Issue: Volume 102:Issue 9(2018) Page Start: 1213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic variants in a sodium-dependent vitamin C transporter gene and age-related cataract. Issue 9 (15th November 2018) Authors: Ravindran, Ravilla D; Sundaresan, Periasamy; Krishnan, Tiruvengada; Vashist, Praveen; Maraini, Giovanni; Saravanan, Vijayan; Chakravarthy, Usha; Smeeth, Liam; Nitsch, Dorothea; Young, Ian S; Fletcher, Astrid E Journal: British journal of ophthalmology Issue: Volume 103:Issue 9(2019) Page Start: 1223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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. Issue 4 (27th April 2017) Authors: Shah, Mohd Hussain; Tabanera, Noemi; Krishnadas, Subbaiah Ramasamy; Pillai, Manju R.; Bovolenta, Paola; Sundaresan, Periasamy Journal: Molecular genetics & genomic medicine Issue: Volume 5:Issue 4(2017) Page Start: 323 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Multiplex Cytokine Analysis of Aqueous Humor from the Patients with Chronic Primary Angle Closure Glaucoma. (2nd December 2017) Authors: Duvesh, Roopam; Puthuran, George; Srinivasan, Kavitha; Rengaraj, Venkatesh; Krishnadas, SR; Rajendrababu, Sharmila; Balakrishnan, Vijayakumar; Ramulu, Pradeep; Sundaresan, Periasamy Journal: Current eye research Issue: Volume 42:Number 12(2017) Page Start: 1608 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome. (15th April 2019) Authors: Berner, Daniel; Hoja, Ursula; Zenkel, Matthias; Ross, James Julian; Uebe, Steffen; Paoli, Daniela; Frezzotti, Paolo; Rautenbach, Robyn M; Ziskind, Ari; Williams, Susan E; Carmichael, Trevor R; Ramsay, Michele; Topouzis, Fotis; Chatzikyriakidou, Anthi; Lambropoulos, Alexandros; Sundaresan, Periasa... Journal: Human molecular genetics Issue: Volume 28:Number 15(2019) Page Start: 2531 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathy. (June 2022) Authors: Li, Shujin; Yang, Mu; He, Yunqi; Jiang, Xiaoyan; Zhao, Rulian; Liu, Wenjing; Huang, Lulin; Shi, Yi; Li, Xiao; Sun, Kuanxiang; Yang, Yeming; Sundaresan, Periasamy; Zhao, Peiquan; Yang, Zhenglin; Zhu, Xianjun Journal: Journal of genetics and genomics Issue: Volume 49:Number 6(2022) Page Start: 590 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗