Kunal Ray

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2014-2023
Publications (10 Years): 6

Top Topics

Extracellular Matrix

Top Venues

Metallomics : integrated biometal science

BioMed research international

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohammed Faruq, Hodan Jama, Naushin Waseem, Aparna Rao, Abhijit Sen, Kunal Ray, Arijit Mukhopadhyay
Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration. Genes 14 (2) (2023)
Kausik Ganguly, Tithi Dutta, Arpan Saha, Devroop Sarkar, Asim Sil, Kunal Ray, Mainak Sengupta
Mapping the TYR gene reveals novel and previously reported variants in Eastern Indian patients highlighting preponderance of the same changes in multiple unrelated ethnicities. Annals of human genetics 84 (3) (2020)
Subhajit Giri, Arunibha Ghosh, Shubhrajit Roy, Charulata Savant Sankhla, Shyamal Kumar Das, Kunal Ray, Jharna Ray
Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India. Journal of molecular neuroscience : MN 71 (2) (2020)
Arnab Gupta, Santanu Das, Kunal Ray
A glimpse into the regulation of the Wilson disease protein, ATP7B, sheds light on the complexity of mammalian apical trafficking pathways. Metallomics : integrated biometal science 10 (3) (2018)
Devroop Sarkar, Kunal Ray, Mainak Sengupta
Structure-function correlation analysis of connexin50 missense mutations causing congenital cataract: electrostatic potential alteration could determine intracellular trafficking fate of mutants. BioMed research international 2014 (2014)