Publications by authors named "Kunal Ray"

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A Perspective on Evaluating Life Stage Differences in Drug Dosages for Drug Labeling and Instructions.
Tianshu Gu, Guiying Wang, Edwin J C van den Oord, Emanuel Goldman, Chengyuan Yang, Kunal Ray

AAPS J· August 2024

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Identifying genetic defects in oculocutaneous albinism patients of West Bengal, Eastern India.
Tithi Dutta, Kausik Ganguly, Arpan Saha, Asim Sil, Kunal Ray

Mol Biol Rep· July 2024

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Time to establish an international vaccine candidate pool for potential highly infectious respiratory disease: a community's view.
Lan Yao, Hiam Chemaitelly, Emanuel Goldman, Esayas Kebede Gudina, Asma Khalil, Kunal Ray

EClinicalMedicine· October 2023

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Missing heritability of Wilson disease: a search for the uncharacterized mutations.
Shubhrajit Roy, Sampurna Ghosh, Jharna Ray, Kunal Ray, Mainak Sengupta

Mamm Genome· March 2023

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Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration.
Kiran Narta, Manoj Ramesh Teltumbade, Mansi Vishal, Samreen Sadaf, Mohd Faruq, Kunal Ray

Genes (Basel)· February 2023

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Parkinson's disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expression.
Prosenjit Pal, Shubhrajit Roy, Abhishek Chowdhury, Raghunath Chatterjee, Kunal Ray, Jharna Ray

Neurosci Lett· January 2023

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Genetic Polymorphisms in and Risk for Parkinson's Disease Among Eastern Indians.
Sadhukhan Dipanwita, Biswas Arindam, Biswas Atanu, Ray Kunal, Ray Jharna

Neurol India· May 2022

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Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian Population.
Tania Saha, Somrita Roy, Rajashree Chakraborty, Arindam Biswas, Shyamal K Das, Kunal Ray, Jharna Ray

Neurol India· June 2021

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A cost-effective plan for global testing - an infection rate stratified, algorithm guided, multiple-level, continuously pooled testing strategy.
Tianshu Gu, Lan Yao, Xia Meng, J Carolyn Graff, Donald Thomason, Kunal Ray

Sci Total Environ· April 2021

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Identification of GBA mutations among neurodegenerative disease patients from eastern India.
Arindam Biswas, Dipanwita Sadhukhan, Atanu Biswas, Shyamal K Das, Tapas K Banerjee, Kunal Ray, Jharna Ray

Neurosci Lett· April 2021

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Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.
Subhajit Giri, Arunibha Ghosh, Shubhrajit Roy, Charulata Savant Sankhla, Shyamal Kumar Das, Kunal Ray, Jharna Ray

J Mol Neurosci· February 2021

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COVID-19 vaccine: Call for employees in international transportation industries and international travelers as the first priority in global distribution.
Zhuo Yu, Gang Wang, Emanuel Goldman, Barbara Zangerl, Ning Xie, Kunal Ray

Open Med (Wars)· January 2021

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Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties.
Shubhrajit Roy, Courtney J McCann, Martina Ralle, Kunal Ray, Jharna Ray

Sci Rep· August 2020

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Role of variant p.Gly2019Ser in patients with Parkinsonism.
Dipanwita Sadhukhan, Arindam Biswas, Arunima Bhaduri, Neelanjana Sarkar, Atanu Biswas, Kunal Ray, Jharna Ray

Indian J Med Res· June 2020

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Mapping the TYR gene reveals novel and previously reported variants in Eastern Indian patients highlighting preponderance of the same changes in multiple unrelated ethnicities.
Kausik Ganguly, Tithi Dutta, Arpan Saha, Devroop Sarkar, Asim Sil, Kunal Ray

Ann Hum Genet· May 2020

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Primary generalized dystonia due to TOR1A ΔGAG mutation in an Indian family with intrafamilial clinical heterogeneity.
Subhajit Giri, Arindam Biswas, Shyamal Kumar Das, Kunal Ray, Jharna Ray

Neurol India· March 2020

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Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern India.
Prosenjit Pal, Tamal Sadhukhan, Subhadip Chakraborty, Sriparna Sadhukhan, Arindam Biswas, Kunal Ray, Jharna Ray

Neuromolecular Med· September 2019

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Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients.
Shubhrajit Roy, Sampurna Ghosh, Sreyashi Bhattacharya, Arpan Saha, Shyamal Kumar Das, Kunal Ray, Jharna Ray

J Gene Med· September 2019

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Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India.
Arunibha Ghosh, Tamal Sadhukhan, Subhajit Giri, Arindam Biswas, Shyamal Kumar Das, Kunal Ray, Jharna Ray

Neurosci Lett· July 2019

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A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia.
Subhajit Giri, Tufan Naiya, Shubhrajit Roy, Gautami Das, Gurusidheshwar M Wali, Kunal Ray, Jharna Ray

J Mol Neurosci· June 2019

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Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson's Disease.
Shubhrajit Roy, Prosenjit Pal, Sampurna Ghosh, Sreyashi Bhattacharya, Shyamal Kumar Das, Kunal Ray, Jharna Ray

Neuromolecular Med· September 2018

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Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern Indians.
Dipanwita Sadhukhan, Gautami Das, Arindam Biswas, Soumitra Ghosh, Shyamal K Das, Kunal Ray, Jharna Ray

Neurosci Lett· May 2018

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Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease.
Shubhrajit Roy, Kausik Ganguly, Prosenjit Pal, Sampurna Ghosh, Shyamal K Das, Kunal Ray, Jharna Ray

Ann Hum Genet· March 2018

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A glimpse into the regulation of the Wilson disease protein, ATP7B, sheds light on the complexity of mammalian apical trafficking pathways.
Arnab Gupta, Santanu Das, Kunal Ray

Metallomics· March 2018

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Genetic screening of THAP1 in primary dystonia patients of India.
Subhajit Giri, Tufan Naiya, Zaffar Equbal, Charulata Savant Sankhla, Shyamal Kumar Das, Kunal Ray, Jharna Ray

Neurosci Lett· January 2017

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