Souradip Chatterjee

TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study

A. Mukherjee, M. Mutsuddi, Shashank Gupta, 2018, Ophthalmic genetics.

Whole exome sequencing identifies a novel splice-site mutation in IMPG2 gene causing Stargardt-like juvenile macular dystrophy in a north Indian family

A. Mukherjee, M. Mutsuddi, Souradip Chatterjee, 2022, Gene.

Whole exome sequencing: Uncovering causal genetic variants for ocular diseases

Shashank Gupta, A. Mukherjee, M. Mutsuddi, 2017, Experimental eye research.

Modeling of Human Parkinson’s Disease in Fly

A. Mukherjee, P. K. Bhaskar, M. Mutsuddi, 2019, Insights into Human Neurodegeneration: Lessons Learnt from Drosophila.

Identification and molecular characterization of two recurrent missense mutations in RS1 gene in two families with X-linked retinoschisis from North India.

A. Mukherjee, M. Mutsuddi, Souradip Chatterjee, 2023, American journal of medical genetics. Part A.