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Narayanan, Ranjit, Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, Ankit Verma, Vishal Dixit, Vinod Scaria, a Sridhar Sivasubbu. "Case Report: Application of Whole Exome Sequencing for Accurate Diagnosis of Rare Syndromes of Mineralocorticoid Excess." F1000Res 2017.

Narayanan, Ranjit, et al. "Case Report: Application of Whole Exome Sequencing for Accurate Diagnosis of Rare Syndromes of Mineralocorticoid Excess." F1000Res 2017.