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Annals of Human Genetics|October 24, 2017
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson diseaseShubhrajit Roy, Kausik Ganguly, Prosenjit Pal, et al.
Genes|February 25, 2023
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous NeurodegenerationKiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, et al.
Neuroscience Letters|March 12, 2021
Identification of GBA mutations among neurodegenerative disease patients from eastern IndiaArindam Biswas, Dipanwita Sadhukhan, Atanu Biswas, et al.
Parkinsonism & Related Disorders|October 8, 2013
Genetic defects in Indian Wilson disease patients and genotype-phenotype correlationShashwata Mukherjee, Shruti Dutta, Sulagna Majumdar, et al.
Molecular Vision|February 22, 2005
Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in IndiaSubhabrata Chakrabarti, Kiranpreet Kaur, Sreelatha Komatireddy, et al.
International Journal of Cancer|December 15, 2005
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking waterPritha Ghosh, Anamika Basu, Julie Mahata, et al.
Molecular Vision|October 6, 2005
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucomaArijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya, et al.
Scientific Reports|August 8, 2014
Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complicationsMayumi Ueta, Chitra Kannabiran, Tais Hitomi Wakamatsu, et al.
American Journal of Human Genetics|December 23, 2006
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degenerationJames S Friedman, Bo Chang, Chitra Kannabiran, et al.
Investigative Ophthalmology & Visual Science|April 26, 2014
Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian originsLalit Kaurani, Mansi Vishal, Dhirendra Kumar, et al.
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