Sanish Sathyan
Affiliations: | 2009-2015 | Medical School | Albert Einstein College of Medicine, New York, New York, United States |
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"Sanish Sathyan"
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| Sood A, Cherian LM, Heera R, et al. (2022) Association between matrix metalloproteinases-2 and -9 gene polymorphism with basement membrane disruption in oral lichen planus: A case-control pilot study. Journal of Oral Biology and Craniofacial Research. 12: 258-262 |
| Shafeeque CM, Sathyan S, Saradalekshmi KR, et al. (2020) Methylation map genes can be critical in determining the methylome of intracranial aneurysm patients. Epigenomics |
| Aloka D, Padmakumar SK, Sathyan S, et al. (2019) Association of matrix metalloproteinase 2 and matrix metalloproteinase 9 gene polymorphism in aggressive and nonaggressive odontogenic lesions: A pilot study. Journal of Oral and Maxillofacial Pathology : Jomfp. 23: 158 |
| Sathyan S, Barzilai N, Atzmon G, et al. (2017) Association of anti-inflammatory cytokine IL10 polymorphisms with motoric cognitive risk syndrome in an Ashkenazi Jewish population. Neurobiology of Aging |
| Chauhan I, Sugirtharaj G, Sathyan S, et al. (2016) Evaluation of salivary DNA obtained from dental prosthesis and its applicability in forensic investigations. Journal of Forensic and Legal Medicine. 42: 100-105 |
| Sathyan S, Koshy LV, Srinivas L, et al. (2015) Erratum to: Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors. Journal of Neuroinflammation. 12: 164 |
| Sathyan S, Koshy LV, Srinivas L, et al. (2015) Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors. Journal of Neuroinflammation. 12: 135 |
| Sathyan S, Koshy LV, Balan S, et al. (2014) Association of Versican (VCAN) gene polymorphisms rs251124 and rs2287926 (G428D), with intracranial aneurysm. Meta Gene. 2: 651-60 |
| Saradalekshmi KR, Neetha NV, Sathyan S, et al. (2014) DNA methyl transferase (DNMT) gene polymorphisms could be a primary event in epigenetic susceptibility to schizophrenia. Plos One. 9: e98182 |
| Balan S, Bharathan SP, Vellichiramal NN, et al. (2014) Genetic association analysis of ATP binding cassette protein family reveals a novel association of ABCB1 genetic variants with epilepsy risk, but not with drug-resistance. Plos One. 9: e89253 |