Accessibility Skip to Global Navigation Skip to Local Navigation Skip to Content Skip to Search Skip to Site Map Menu

DSM staff profile

Sarada Ketharnathan

PositionPhD Student
DepartmentDepartment of Pathology (Dunedin)
QualificationsBTech MSc
Research summaryMy research involves assigning functional significance to genetic variations in gout.

Publications

Ketharnathan, S., Leask, M., Boocock, J., Phipps-Green, A. J., Antony, J., O'Sullivan, J. M., Merriman, T. R., & Horsfield, J. A. (2018). A non-coding genetic variant maximally associated with serum urate levels is functionally linked to HNF4A-dependent PDZK1 expression. Human Molecular Genetics, 27(22), 3964-3973. doi: 10.1093/hmg/ddy295

Chung, I.-M., Ketharnathan, S., Kim, S.-H., Thiruvengadam, M., Rani, M. K., & Rajakumar, G. (2016). Making sense of the tangle: Insights into chromatin folding and gene regulation. Genes, 7(10), 71. doi: 10.3390/genes7100071

Chung, I.-M., Ketharnathan, S., Thiruvengadam, M., & Rajakumar, G. (2016). Rheumatoid arthritis: The stride from research to clinical practice. International Journal of Molecular Sciences, 17(6), 900. doi: 10.3390/ijms17060900

Ketharnathan, S., Koshy, T., Sethuratnam, R., Paul, S., & Venkatesan, V. (2015). Investigation of NKX2.5 gene mutations in congenital heart defects in an Indian population. Genetic Testing & Molecular Biomarkers, 19(10), 579-583. doi: 10.1089/gtmb.2015.0112

Journal - Research Article

Ketharnathan, S., Leask, M., Boocock, J., Phipps-Green, A. J., Antony, J., O'Sullivan, J. M., Merriman, T. R., & Horsfield, J. A. (2018). A non-coding genetic variant maximally associated with serum urate levels is functionally linked to HNF4A-dependent PDZK1 expression. Human Molecular Genetics, 27(22), 3964-3973. doi: 10.1093/hmg/ddy295

Chung, I.-M., Ketharnathan, S., Kim, S.-H., Thiruvengadam, M., Rani, M. K., & Rajakumar, G. (2016). Making sense of the tangle: Insights into chromatin folding and gene regulation. Genes, 7(10), 71. doi: 10.3390/genes7100071

Chung, I.-M., Ketharnathan, S., Thiruvengadam, M., & Rajakumar, G. (2016). Rheumatoid arthritis: The stride from research to clinical practice. International Journal of Molecular Sciences, 17(6), 900. doi: 10.3390/ijms17060900

Ketharnathan, S., Koshy, T., Sethuratnam, R., Paul, S., & Venkatesan, V. (2015). Investigation of NKX2.5 gene mutations in congenital heart defects in an Indian population. Genetic Testing & Molecular Biomarkers, 19(10), 579-583. doi: 10.1089/gtmb.2015.0112

More publications...