Publications and communications of Giri, Subhajit

Giri, S., & Malgrange, B. (2022). Application of CRISPR/Cas system in iPSC-based disease model of hereditary deafness 9. In A. Birbrair, iPSCs - State of the Science. academic press. doi:10.1016/B978-0-323-85767-3.00009-8

Giri, S., Ghosh, A., Roy, S., Savant Sankhla, C., Das, S. K., Ray, K., & Ray, J. (2020). Association of TOR1A & GCH1 polymorphisms with isolated dystonia in India. Journal of Molecular Neuroscience. doi:10.1007/s12031-020-01653-1

Ghosh, A., Sadhukhan, T., Giri, S., Biswas, A., Das, S. K., Ray, K., & Ray, J. (2019). Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India. Neuroscience Letters, 706, 75-80. doi:10.1016/j.neulet.2019.05.015

Giri, S., Biswas, A., Das, S. K., Ray, K., & Ray, J. (2019). Primary generalized dystonia due to TOR1A ΔGAG mutation in an Indian family with intrafamilial clinical heterogeneity. Neurology India, 67 (3), 872-875. doi:10.4103/0028-3886.263172

Giri, S., Naiya, T., Roy, S., Das, G., Wali, G. M., Das, S. K., Ray, K., & Ray, J. (2019). A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia. Journal of molecular neuroscience : MN, 68 (2), 214-220. doi:10.1007/s12031-019-01301-3

Giri, S., Purushottam, M., Viswanath, B., & Muddashetty, R. S. (2019). Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing. Stem Cell Research, 39, 101494. doi:10.1016/j.scr.2019.101494

Giri, S. (2018). MOLECULAR BASIS OF PATHOGENESIS OF DYSTONIA AMONG INDIAN PATIENTS. Unpublished doctoral thesis, University of Calcutta, Kolkata, India.
Jury: Ray, J. (Promotor).

Giri, S., Naiya, T., Equbal, Z., Sankhla, C. S., Das, S. K., Ray, K., & Ray, J. (2017). Genetic screening of THAP1 in primary dystonia patients of India. Neuroscience Letters, 637, 31-37. doi:10.1016/j.neulet.2016.11.060

Giri, S., Biswas, A., Das, S. K., Ray, K., & Ray, J. (21 January 2014). Molecular basis of DYT1 and DYT6 primary dystonia in Indian patients. Molecular Cytogenetics, 7 (Supplement 1), 121. doi:10.1186/1755-8166-7-S1-P121

Giri, S., Naiya, T., Das, S. K., Savant Sankhla, C., Ray, K., & Ray, J. (2014). Genetic analysis of TOR1A & THAP1 genes in Indian primary dystonia patients. Movement Disorders, 29 (Supplement 2), 71.

Mukherjee, K., Tribedi, P., Chowdhury, A., Ray, T., Joardar, A., Giri, S., & Sil, A. K. (2011). Isolation of a Pseudomonas aeruginosa strain from soil that can degrade polyurethane diol. Biodegradation, 22 (2), 377-88. doi:10.1007/s10532-010-9409-1