FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Kunal Ray

Research Profile

Geographic Areas

India

Anatomy

Oculocutaneous Albinism

Disorders

Chemicals & Drugs

Physiology

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Living Beings

Heterozygote

Procedures

Co-author Network

Publications

TOP 3
M Mondal; S Samanta; Mainak Sengupta; A Sil; Kunal Ray
Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.
Suddhasil Mookherjee; Moulinath Acharya; Deblina Banerjee; Ashima Bhattacharjee; Kunal Ray
Molecular basis for involvement of CYP1B1 in MYOC upregulation and its potential implication in glaucoma pathogenesis.
Suddhasil Mookherjee; Deblina Banerjee; Subhadip Chakraborty; Abhijit Sen; Mansi Vishal; Kunal Ray
WDR36 variants in East Indian primary open-angle glaucoma patients.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Kunal Ray (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: M Mondal; S Samanta; Mainak Sengupta; A Sil; Kunal Ray
Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.
Gene 2012;511(2):470-4.
2012: Suddhasil Mookherjee; Moulinath Acharya; Deblina Banerjee; Ashima Bhattacharjee; Kunal Ray
Molecular basis for involvement of CYP1B1 in MYOC upregulation and its potential implication in glaucoma pathogenesis.
PloS one 2012;7(9):e45077.
2011: Suddhasil Mookherjee; Deblina Banerjee; Subhadip Chakraborty; Abhijit Sen; Mansi Vishal; Kunal Ray
WDR36 variants in East Indian primary open-angle glaucoma patients.
Molecular vision 2011;17():2618-27.
2011: Sanchari Pradhan; Mainak Sengupta; Anirban Dutta; Kausik Bhattacharyya; Sumit K Bag; Chitra Dutta; Kunal Ray
Indian genetic disease database.
Nucleic acids research 2011;39(Database issue):D933-8.
2010: Mainak Sengupta; M Mondal; P Jaiswal; S Sinha; Moumita Chaki; S Samanta; Kunal Ray
Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene.
The British journal of dermatology 2010;163(3):487-94.
2010: Mainak Sengupta; Amrita Chakraborty; Kunal Ray
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of India.
Journal of genetics 2010;89(2):247-51.
2010: Kunal Ray; Mainak Sengupta
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Human genetics 2010;127(4):487-8.
2010: Kunal Ray; Mainak Sengupta
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Human genetics 2010;127(4):487.
2010: Suddhasil Mookherjee; Deblina Banerjee; Subhadip Chakraborty; Antara Banerjee; Indranil Mukhopadhyay; Abhijit Sen; Kunal Ray
Association of IL1A and IL1B loci with primary open angle glaucoma.
BMC medical genetics 2010;11():99.
2010: Arnab Gupta; Ishita Chattopadhyay; Shashwata Mukherjee; Mainak Sengupta; Shyamal K Das; Kunal Ray
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient.
Behavioral and brain functions : BBF 2010;6():33.
2009: Kunal Ray; Suddhasil Mookherjee
Molecular complexity of primary open angle glaucoma: current concepts.
Journal of genetics 2009;88(4):451-67.
2008: Moulinath Acharya; Arijit Mukhopadhyay; Ashima Bhattacharjee; Sanjay Thakur; Arun K Bandyopadhyay; Kunal Ray
Complex genetics of glaucoma: defects in CYP1B1, and not MYOC, cause pathogenesis in an early-onset POAG patient with double variants at both loci.
Journal of genetics 2008;87(3):265-9.
2008: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2008;124(3):297.
2008: Pritha Ghosh; Mayukh Banerjee; Ashok K Giri; Kunal Ray
Toxicogenomics of arsenic: classical ideas and recent advances.
Mutation research 2008;659(3):293-301.
2008: S Mukherjee; A Saha; P Biswas; C Mandal; Kunal Ray
Structural analysis of factor IX protein variants to predict functional aberration causing haemophilia B.
Haemophilia : the official journal of the World Federation of Hemophilia 2008;14(5):1076-81.
2008: Mainak Sengupta; Ananya Ray; Moumita Chaki; Mahua Maulik; Kunal Ray
SNPs in genes with copy number variation: a question of specificity.
Journal of genetics 2008;87(1):95-7.
2008: Sujata De Chaudhuri; Pritha Ghosh; nilendu sarma; Papiya Majumdar; Tanmoy Jyoti Sau; Santanu Basu; Susanta Roychoudhury; Kunal Ray; Ashok K Giri
Genetic variants associated with arsenic susceptibility: study of purine nucleoside phosphorylase, arsenic (+3) methyltransferase, and glutathione S-transferase omega genes.
Environmental health perspectives 2008;116(4):501-5.
2008: Ashima Bhattacharjee; Deblina Banerjee; Suddhasil Mookherjee; Moulinath Acharya; Antara Banerjee; Ananya Ray; Abhijit Sen; Kunal Ray
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma.
Molecular vision 2008;14():841-50.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Human genetics 2007;122(5):556.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Human genetics 2007;122(5):556.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Human genetics 2007;122(5):555.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1.
Human genetics 2007;122(5):555.
2007: Atreyee Saha; Saibal Mukherjee; Mahua Maulik; Giriraj R Chandak; Kunal Ray
Evaluation of genetic markers linked to hemophilia A locus: an Indian experience.
Haematologica 2007;92(12):1725-6.
2007: Arnab Gupta; Ishita Chattopadhyay; Sumit Dey; Poonam Nasipuri; Shyamal K Das; Prasanta K Gangopadhyay; Kunal Ray
Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis.
Cellular and molecular neurobiology 2007;27(8):1023-33.
2007: Arnab Gupta; Mahua Maulik; Poonam Nasipuri; Ishita Chattopadhyay; Shyamal K Das; Prasanta K Gangopadhyay; Kunal Ray
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.
Clinical chemistry 2007;53(9):1601-8.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Tyrosinase and ocular diseases: some novel thoughts on the molecular basis of oculocutaneous albinism type 1.
Progress in retinal and eye research 2007;26(4):323-58.
2007: Ashima Bhattacharjee; Moulinath Acharya; Arijit Mukhopadhyay; Suddhasil Mookherjee; Deblina Banerjee; Arun K Bandopadhyay; Sanjay Thakur; Abhijit Sen; Kunal Ray
Myocilin variants in Indian patients with open-angle glaucoma.
Archives of ophthalmology 2007;125(6):823-9.
2007: Pritha Ghosh; Mayukh Banerjee; Sujata De Chaudhuri; Rajdeep Chowdhury; Jayanta K Das; Angshuman Mukherjee; Ajoy K Sarkar; Lakshmikanta Mondal; Krishnapada Baidya; Tanmoy Jyoti Sau; Apurba Banerjee; Arindam Basu; Keya Chaudhuri; Kunal Ray; Ashok K Giri
Comparison of health effects between individuals with and without skin lesions in the population exposed to arsenic through drinking water in West Bengal, India.
Journal of exposure science & environmental epidemiology 2007;17(3):215-23.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Gene symbol: SLC45A2.
Human genetics 2007;121(2):295.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Gene symbol: SLC45A2.
Human genetics 2007;121(2):295.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Gene symbol: SLC45A2.
Human genetics 2007;121(2):294.
2007: Kunal Ray; Moulinath Acharya; Suddhasil Mookherjee
Gene symbol: CYP1B1.
Human genetics 2007;121(2):292.
2007: Kunal Ray; Moulinath Acharya; Suddhasil Mookherjee
Gene symbol: CYP1B1.
Human genetics 2007;121(2):291.
2007: Kunal Ray; Moulinath Acharya; Suddhasil Mookherjee
Gene symbol: CYP1B1.
Human genetics 2007;121(2):291.
2007: Kunal Ray; Ashima Bhattacharjee
Gene symbol: MYOC.
Human genetics 2007;121(2):290.
2007: Kunal Ray; Moumita Chaki; Mainak Sengupta
Gene symbol: SLC45A2.
Human genetics 2007;121(2):294.
2007: Kunal Ray; Moulinath Acharya
Gene symbol: CYP1B1.
Human genetics 2007;121(2):291.
2007: Kunal Ray; Arijit Mukhopadhyay; Moulinath Acharya
Gene symbol: MYOC.
Human genetics 2007;121(2):290-1.
2007: Mainak Sengupta; Moumita Chaki; N Arti; Kunal Ray
SLC45A2 variations in Indian oculocutaneous albinism patients.
Molecular vision 2007;13():1406-11.
2007: Moulinath Acharya; Suddhasil Mookherjee; Ashima Bhattacharjee; Sanjay Thakur; Arun K Bandyopadhyay; Abhijit Sen; Subhabrata Chakrabarti; Kunal Ray
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change.
BMC molecular biology 2007;8():21.
2006: D Aikath; Arnab Gupta; Ishita Chattopadhyay; M A Hashmi; Prasanta K Gangopadhyay; Shyamal Kumar Das; Kunal Ray
Subcortical white matter abnormalities related to drug resistance in Wilson disease.
Neurology 2006;67(5):878-80.
2006: Moumita Chaki; Mainak Sengupta; Arijit Mukhopadhyay; I Subba Rao; Partha P Majumder; Madhusudan Das; S Samanta; Kunal Ray
OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.
Annals of human genetics 2006;70(Pt 5):623-30.
2006: Kunal Ray; Moumita Chaki; Mainak Sengupta
Gene symbol: TYR. Disease: albinism, oculocutaneous 1.
Human genetics 2006;119(6):675.
2006: Kunal Ray; Mainak Sengupta
TRendys meeting report 2005.
Indian journal of biochemistry & biophysics 2006;43(3):190-3.
2006: Pritha Ghosh; Anamika Basu; Julie Mahata; Sreemanti Basu; Mainak Sengupta; Jayanta K Das; Angshuman Mukherjee; Ajoy K Sarkar; Lakshmikanta Mondal; Kunal Ray; Ashok K Giri
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water.
International journal of cancer. Journal international du cancer 2006;118(10):2470-8.
2006: S Mukherjee; A Saha; SENTHIL KUMAR PAZHANISAMY; Giriraj R Chandak; Partha P Majumder; Kunal Ray
Remarkable variation in the informativeness of RFLP markers linked to hemophilia B locus in Indian population groups: implication in the strategy for carrier detection.
Disease markers 2006;22(5-6):327-34.
2006: Moulinath Acharya; Suddhasil Mookherjee; Ashima Bhattacharjee; Arun Kumar Bandyopadhyay; Sanjay Kumar Daulat Thakur; Gautam Bhaduri; Abhijit Sen; Kunal Ray
Primary role of CYP1B1 in Indian juvenile-onset POAG patients.
Molecular vision 2006;12():399-404.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson's disease.
Human genetics 2005;118(3-4):541.
2005: Arnab Gupta; D Aikath; Rajarshi Neogi; S Datta; K Basu; Bibekananda Maity; Rajni Trivedi; J Ray; Shyamal Kumar Das; Prasanta K Gangopadhyay; Kunal Ray
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients.
Human genetics 2005;118(1):49-57.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2005;117(2-3):299.
2005: Kunal Ray; Moumita Chaki; Arijit Mukhopadhyay
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Human genetics 2005;117(2-3):299.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2005;117(2-3):296.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2005;117(2-3):295.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2005;117(2-3):294.
2005: Kunal Ray; Arnab Gupta
Gene symbol: ATP7B. Disease: Wilson disease.
Human genetics 2005;117(2-3):294.
2005: Moumita Chaki; Arijit Mukhopadhyay; Kunal Ray
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification.
Human mutation 2005;26(1):53-8.
2005: Madhubanti Sarkar; Soumita Das; Arunava Bandyopadhaya; Kunal Ray; Keya Chaudhuri
Upregulation of human mitochondrial NADH dehydrogenase subunit 5 in intestinal epithelial cells is modulated by Vibrio cholerae pathogenesis.
FEBS letters 2005;579(16):3449-60.
2005: Kunal Ray; Moumita Chaki; Arijit Mukhopadhyay
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Human genetics 2005;116(6):545.
2005: Kunal Ray; Moumita Chaki; Arijit Mukhopadhyay
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Human genetics 2005;116(6):544.
2005: Kunal Ray; Moumita Chaki; Arijit Mukhopadhyay
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Human genetics 2005;116(6):544.
2005: Kunal Ray; Moumita Chaki; Arijit Mukhopadhyay
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Human genetics 2005;116(6):533.
2005: Subhabrata Chakrabarti; Kiranpreet Kaur; Sreelatha Komatireddy; Moulinath Acharya; Koilkonda R Devi; Arijit Mukhopadhyay; Anil K Mandal; Seyed E Hasnain; Garudadri Chandrasekhar; Ravi Thomas; Kunal Ray
Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India.
Molecular vision 2005;11():111-3.
2005: Arijit Mukhopadhyay; Sreelatha Komatireddy; Moulinath Acharya; Ashima Bhattacharjee; Anil K Mandal; Sanjay Thakur; Garudadri Chandrasekhar; Arun Banerjee; Ravi Thomas; Subhabrata Chakrabarti; Kunal Ray
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma.
Molecular vision 2005;11():792-7.
2005: Moumita Chaki; Arijit Mukhopadhyay; Shamba Chatterjee; Madhusudan Das; Swapan Samanta; Kunal Ray
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase gene.
Molecular vision 2005;11():531-4.
2004: Kunal Ray; Sanjay Thakur; Arun Kumar Banerjee; Arijit Mukhopadhyay; Moulinath Acharya; Ashima Bhattacharjee; Abhijit Sen; Gautam Bhaduri
Genetics and bioinformatics of primary open angle glaucoma: an Indian perspective.
Journal of the Indian Medical Association 2004;102(12):708, 710, 712 passim.
2004: Anamika Basu; Pritha Ghosh; Jayanta K Das; Apurba Banerjee; Kunal Ray; Ashok K Giri
Micronuclei as biomarkers of carcinogen exposure in populations exposed to arsenic through drinking water in West Bengal, India: a comparative study in three cell types.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2004;13(5):820-7.
2004: Julie Mahata; Pritha Ghosh; Jyotirmoy Sarkar; Kunal Ray; Adayapalam T Natarajan; Ashok K Giri
Effect of sodium arsenite on peripheral lymphocytes in vitro: individual susceptibility among a population exposed to arsenic through the drinking water.
Mutagenesis 2004;19(3):223-9.
2004: S Mukherjee; A Mukhopadhyay; D Banerjee; Giriraj R Chandak; Kunal Ray
Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.
Haemophilia : the official journal of the World Federation of Hemophilia 2004;10(3):259-63.
2004: Arijit Mukhopadhyay; Sangita Talukdar; Ashima Bhattacharjee; Kunal Ray
Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders.
Molecular vision 2004;10():304-14.
2004: Julie Mahata; Moumita Chaki; Pritha Ghosh; Lopamudra Das; Krishnapada Baidya; Kunal Ray; Adayapalam T Natarajan; Ashok K Giri
Chromosomal aberrations in arsenic-exposed human populations: a review with special reference to a comprehensive study in West Bengal, India.
Cytogenetic and genome research 2004;104(1-4):359-64.
2003: Arnab Gupta; Rajarshi Neogi; M Mukherjea; A Mukhopadhyay; Susanta Roychoudhury; A Senapati; Prasanta K Gangopadhyay; Kunal Ray
DNA linkage based diagnosis of Wilson disease in asymptomatic siblings.
The Indian journal of medical research 2003;118():208-14.
2003: Kunal Ray; Arijit Mukhopadhyay; Moulinath Acharya
Recent advances in molecular genetics of glaucoma.
Molecular and cellular biochemistry 2003;253(1-2):223-31.
2003: Arijit Mukhopadhyay; Moulinath Acharya; Jharna Ray; Mita Khan; Krishnendu Sarkar; Asit Ranjan Banerjee; Kunal Ray
Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucoma.
Indian journal of ophthalmology 2003;51(3):279-81.
2003: S Mukherjee; A Mukhopadhyay; Keya Chaudhuri; Kunal Ray
Analysis of haemophilia B database and strategies for identification of common point mutations in the factor IX gene.
Haemophilia : the official journal of the World Federation of Hemophilia 2003;9(2):187-92.
2003: Julie Mahata; Anamika Basu; S Ghoshal; Jyotirmoy Sarkar; A K Roy; G Poddar; AK Nandy; Apurba Banerjee; Kunal Ray; Adayapalam T Natarajan; R Nilsson; Ashok K Giri
Chromosomal aberrations and sister chromatid exchanges in individuals exposed to arsenic through drinking water in West Bengal, India.
Mutation research 2003;534(1-2):133-43.
2003: S Mitra; S Chatterjee; Chinmay Kumar Panda; Keya Chaudhuri; Kunal Ray; Nitai P Bhattacharyya; A Sengupta; Susanta Roychoudhury
Haplotype structure of TP53 locus in Indian population and possible association with head and neck cancer.
Annals of human genetics 2003;67(Pt 1):26-34.
2002: Arijit Mukhopadhyay; Moulinath Acharya; Saibal Mukherjee; Jharna Ray; Sumit Choudhury; Mita Khan; Kunal Ray
Mutations in MYOC gene of Indian primary open angle glaucoma patients.
Molecular vision 2002;8():442-8.
2002: Moulinath Acharya; Sayan Mitra; Arijit Mukhopadhyay; Mita Khan; Susanta Roychoudhury; Kunal Ray
Distribution of p53 codon 72 polymorphism in Indian primary open angle glaucoma patients.
Molecular vision 2002;8():367-71.
2002: Arijit Mukhopadhyay; Arnab Gupta; Saibal Mukherjee; Keya Chaudhuri; Kunal Ray
Did myocilin evolve from two different primordial proteins?
Molecular vision 2002;8():271-9.
2002: Anamika Basu; Julie Mahata; A K Roy; Jyotirmoy Sarkar; G Poddar; AK Nandy; P K Sarkar; Pradeep K Dutta; Apurba Banerjee; M Das; Kunal Ray; S Roychaudhury; Adayapalam T Natarajan; R Nilsson; Ashok K Giri
Enhanced frequency of micronuclei in individuals exposed to arsenic through drinking water in West Bengal, India.
Mutation research 2002;516(1-2):29-40.
2001: S Chakrabarti; S Dasgupta; S Roy; A Bhar; A Sengupta; A Roy; Kunal Ray; Nitai P Bhattacharyya; Bidyut Roy; Chinmay Kumar Panda; Susanta Roychoudhury
Microsatellite instability in squamous cell carcinoma of head and neck from the Indian patient population.
International journal of cancer. Journal international du cancer 2001;92(4):555-61.