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Jharna Ray - Publications

Affiliations: 
Cornell University, Ithaca, NY, United States 
Area:
Genetics, Molecular Biology, Veterinary Science Biology
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Ganaie HA, Biswas A, Bhattacharya AP, Pal S, Ray J, Das SK. Association of Gene Polymorphism with Stroke Patients from Rural Eastern India. Annals of Indian Academy of Neurology. 23: 504-509. PMID 33223668 DOI: 10.4103/Aian.Aian_45_19  0.324
2020 Sadhukhan D, Biswas A, Bhaduri A, Sarkar N, Biswas A, Das SK, Banerjee TK, Ray K, Ray J. Role of variant p.Gly2019Ser in patients with Parkinsonism. The Indian Journal of Medical Research. 151: 592-597. PMID 32719233 DOI: 10.4103/Ijmr.Ijmr_25_18  0.342
2020 Giri S, Ghosh A, Roy S, Sankhla CS, Das SK, Ray K, Ray J. Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India. Journal of Molecular Neuroscience : Mn. PMID 32662044 DOI: 10.1007/S12031-020-01653-1  0.345
2019 Roy S, Ghosh S, Bhattacharya S, Saha A, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients. The Journal of Gene Medicine. e3109. PMID 31265749 DOI: 10.1002/Jgm.3109  0.311
2019 Pal P, Sadhukhan T, Chakraborty S, Sadhukhan S, Biswas A, Das SK, Ray K, Ray J. Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson's Disease: A Study from Eastern India. Neuromolecular Medicine. PMID 31134487 DOI: 10.1007/S12017-019-08548-4  0.379
2019 Ghosh A, Sadhukhan T, Giri S, Biswas A, Das SK, Ray K, Ray J. Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India. Neuroscience Letters. PMID 31082450 DOI: 10.1016/J.Neulet.2019.05.015  0.347
2019 Giri S, Naiya T, Roy S, Das G, Wali GM, Das SK, Ray K, Ray J. A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia. Journal of Molecular Neuroscience : Mn. PMID 30911941 DOI: 10.1007/S12031-019-01301-3  0.341
2018 Roy S, Pal P, Ghosh S, Bhattacharya S, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. 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. Neuromolecular Medicine. PMID 29992511 DOI: 10.1007/S12017-018-8501-2  0.391
2018 Sadhukhan D, Das G, Biswas A, Ghosh S, Das SK, Ray K, Ray J. Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern Indians. Neuroscience Letters. PMID 29604408 DOI: 10.1016/J.Neulet.2018.03.059  0.332
2017 Roy S, Ganguly K, Pal P, Ghosh S, Das SK, Gangopadhyay PK, Bavdekar A, Ray K, Sengupta M, Ray J. Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease. Annals of Human Genetics. PMID 29059476 DOI: 10.1111/Ahg.12223  0.387
2016 Giri S, Naiya T, Equbal Z, Sankhla CS, Das SK, Ray K, Ray J. Genetic Screening of THAP1 in Primary Dystonia Patients of India. Neuroscience Letters. PMID 27913194 DOI: 10.1016/J.Neulet.2016.11.060  0.318
2016 Vishal M, Sharma A, Kaurani L, Alfano G, Mookherjee S, Narta K, Agrawal J, Bhattacharya I, Roychoudhury S, Ray J, Waseem NH, Bhattacharya SS, Basu A, Sen A, Ray K, et al. Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma. Bmc Medical Genomics. 9: 15. PMID 27001270 DOI: 10.1186/S12920-016-0177-6  0.348
2014 Vishal M, Sharma A, Kaurani L, Chakraborty S, Ray J, Sen A, Mukhopadhyay A, Ray K. Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. Scientific Reports. 4: 5115. PMID 24875940 DOI: 10.1038/Srep05115  0.339
2014 Kaurani L, Vishal M, Kumar D, Sharma A, Mehani B, Sharma C, Chakraborty S, Jha P, Ray J, Sen A, Dash D, Ray K, Mukhopadhyay A. Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins. Investigative Ophthalmology & Visual Science. 55: 3258-64. PMID 24764060 DOI: 10.1167/Iovs.14-14339  0.321
2014 Ghosh A, Biswas A, Sadhukhan T, Das SK, Ray J. Role of Dopamine β Hydroxylase (DBH) in Parkinson's disease patients of Indian population Molecular Cytogenetics. 7: P122. DOI: 10.1186/1755-8166-7-S1-P122  0.325
2012 Sadhukhan T, Biswas A, Das SK, Ray K, Ray J. DJ-1 variants in Indian Parkinson's disease patients. Disease Markers. 33: 127-35. PMID 22960331 DOI: 10.1155/2012/467085  0.376
2012 Sadhukhan T, Vishal M, Das G, Sharma A, Mukhopadhyay A, Das SK, Ray K, Ray J. Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohort. Disease Markers. 32: 355-62. PMID 22684232 DOI: 10.3233/Dma-2012-0898  0.396
2012 Naiya T, Misra AK, Biswas A, Das SK, Ray K, Ray J. Occurrence of GCH1 gene mutations in a group of Indian dystonia patients. Journal of Neural Transmission (Vienna, Austria : 1996). 119: 1343-50. PMID 22373569 DOI: 10.1007/S00702-012-0777-Z  0.379
2012 Biswas A, Sadhukhan T, Bose K, Ghosh P, Giri AK, Das SK, Ray K, Ray J. Role of glutathione S-transferase T1, M1 and P1 polymorphisms in Indian Parkinson's disease patients. Parkinsonism & Related Disorders. 18: 664-5. PMID 21993019 DOI: 10.1016/J.Parkreldis.2011.09.019  0.307
2012 Das G, Misra AK, Das SK, Ray K, Ray J. Role of tau kinases (CDK5R1 and GSK3B) in Parkinson's disease: a study from India. Neurobiology of Aging. 33: 1485.e9-15. PMID 21130530 DOI: 10.1016/J.Neurobiolaging.2010.10.016  0.325
2012 Ray J, Biswas A, Das G, Sadhukhan T, Das S, Ray K. 3.008 GENETIC SUSCEPTIBILITY OF EASTERN INDIANS TOWARDS PARKINSON'S DISEASE Parkinsonism & Related Disorders. 18: S171. DOI: 10.1016/S1353-8020(11)70744-1  0.317
2010 Biswas A, Sadhukhan T, Majumder S, Misra AK, Das SK, Variation Consortium IG, Ray K, Ray J. Evaluation of PINK1 variants in Indian Parkinson's disease patients. Parkinsonism & Related Disorders. 16: 167-71. PMID 19889566 DOI: 10.1016/J.Parkreldis.2009.10.005  0.411
2009 Das G, Misra AK, Das SK, Ray K, Ray J. Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians. Neuroscience Letters. 460: 16-20. PMID 19450659 DOI: 10.1016/J.Neulet.2009.05.031  0.325
2007 Biswas A, Maulik M, Das SK, Ray K, Ray J. Parkin polymorphisms: Risk for Parkinson's disease in Indian population [1] Clinical Genetics. 72: 484-486. PMID 17935510 DOI: 10.1111/J.1399-0004.2007.00878.X  0.315
2006 Naiya T, Biswas A, Neogi R, Datta S, Misra AK, Das SK, Ray K, Ray J. Clinical characterization and evaluation of DYT1 gene in Indian primary dystonia patients. Acta Neurologica Scandinavica. 114: 210-215. PMID 16911351 DOI: 10.1111/J.1600-0404.2006.00663.X  0.406
2006 Biswas A, Gupta A, Naiya T, Das G, Neogi R, Datta S, Mukherjee S, Das SK, Ray K, Ray J. Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients. Parkinsonism & Related Disorders. 12: 420-6. PMID 16793319 DOI: 10.1016/J.Parkreldis.2006.04.005  0.379
2005 Gupta A, Aikath D, Neogi R, Datta S, Basu K, Maity B, Trivedi R, Ray J, Das SK, Gangopadhyay PK, Ray K. Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients. Human Genetics. 118: 49-57. PMID 16133174 DOI: 10.1007/S00439-005-0007-Y  0.388
2005 Brooks MB, Barnas JL, Fremont J, Ray J. Cosegregation of a factor VIII microsatellite marker with mild hemophilia A in Golden Retriever dogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 19: 205-10. PMID 15822565 DOI: 10.1111/J.1939-1676.2005.Tb02683.X  0.311
2002 Pellegrini B, Acland GM, Ray J. Cloning and characterization of opticin cDNA: evaluation as a candidate for canine oculo-skeletal dysplasia. Gene. 282: 121-31. PMID 11814684 DOI: 10.1016/S0378-1119(01)00842-3  0.358
2001 Acland GM, Aguirre GD, Ray J, Zhang Q, Aleman TS, Cideciyan AV, Pearce-Kelling SE, Anand V, Zeng Y, Maguire AM, Jacobson SG, Hauswirth WW, Bennett J. Gene therapy restores vision in a canine model of childhood blindness. Nature Genetics. 28: 92-5. PMID 11326284 DOI: 10.1038/Ng0501-92  0.339
2000 Du F, Acland GM, Ray J. Cloning and expression of type II collagen mRNA: evaluation as a candidate for canine oculo-skeletal dysplasia. Gene. 255: 307-16. PMID 11024291 DOI: 10.1016/S0378-1119(00)00324-3  0.65
1999 Ray J, Scarpino V, Laing C, Haskins ME. Biochemical basis of the β-glucuronidase gene defect causing canine mucopolysaccharidosis VII Journal of Heredity. 90: 119-123. PMID 9987917 DOI: 10.1093/Jhered/90.1.119  0.307
1999 Gu W, Catalfamo J, Ray J, Ray K, Brooks M. Two Distinct Mutations Cause Severe Hemophilia B in Two Unrelated Canine Pedigrees Thrombosis and Haemostasis. 82: 1270-1275. DOI: 10.1055/S-0037-1614374  0.351
1998 Du F, Acland GM, Ray J. A highly polymorphic PCR/RFLP marker in the canine type II collagen gene (COL2A1). Animal Genetics. 29: 407-8. PMID 9800341  0.621
1998 Du F, Ray J. A tetranucleotide polymorphism in the canine type II collagen gene (COL2A1) Animal Genetics. 29: 400. PMID 9800332  0.617
1998 Du F, Acland GM, Ray J. Differential splicing of type II procollagen mRNA in canine retina. Animal Biotechnology. 9: 15-20. PMID 9676231 DOI: 10.1080/10495399809525888  0.604
1998 Ray J, Bouvet A, DeSanto C, Fyfe JC, Xu D, Wolfe JH, Aguirre GD, Patterson DF, Haskins ME, Henthorn PS. Cloning of the canine beta-glucuronidase cDNA, mutation identification in canine MPS VII, and retroviral vector-mediated correction of MPS VII cells. Genomics. 48: 248-53. PMID 9521879 DOI: 10.1006/Geno.1997.5189  0.318
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