Indraprastha Institute of Information Technology Delhi,
Institute of Genomics and Integrative Biology, Academy of Scientific and Innovative Research
Doctoral advisor
Samir K. Brahmachari
Website
vinodscaria.rnabiology.org
Dr Vinod Scaria FRSB, FRSPH (born 9 March 1981) is an Indian biologist, medical researcher pioneering in Precision Medicine and Clinical Genomics in India. He is best known for sequencing the first Indian genome.[1][2][3] He was also instrumental in the sequencing of The first Sri Lankan Genome, analysis of the first Malaysian Genome[4] sequencing and analysis of the Wild-type strain of Zebrafish[5] and the IndiGen programme on Genomics for Public Health in India.[6][7][8]
He is presently a senior consultant to Vishwanath Cancer Care Foundation, an Adjunct Professor at the IIT Kanpur.[9] He was previously a senior scientist at CSIR Institute of Genomics and Integrative Biology and an adjunct faculty at Indraprastha Institute of Information Technology, Delhi.[10]
He along with his colleague and collaborator Sridhar Sivasuubu are widely regarded as the pioneers in the area of clinical genomics in India. They are also the co-founders of the Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN) a large clinical network working in the area of Rare Disease Genomics in India. They were also instrumental in setting up a comprehensive fellowship programme in genomics for clinicians[11]
His research has also contributed to a number of commercially viable technologies for healthcare and public health applications.[12] This includes one of the methods for fast and accurate diagnosis and screening of mitochondrial genetic diseases.[13]
^Manoj CG (10 December 2009). "After human genome sequence, the scientist duo look ahead". The Indian Express. Retrieved 10 February 2013.
^Prasanth GN (10 December 2009). "Genome sequencing can be applied in clinical setting". The Times of India. Archived from the original on 28 September 2013. Retrieved 10 February 2013.
^Jingjing H (9 December 2009). "Scientists decode human genome for the first time in India". China News. Archived from the original on 13 December 2009. Retrieved 10 February 2013.
^Salleh MZ, Teh LK, Lee LS, Ismet RI, Patowary A, Joshi K, et al. (2013). "Systematic pharmacogenomics analysis of a Malay whole genome: proof of concept for personalized medicine". PLOS ONE. 8 (8): e71554. Bibcode:2013PLoSO...871554S. doi:10.1371/journal.pone.0071554. PMC 3751891. PMID 24009664.
^Patowary A, Purkanti R, Singh M, Chauhan R, Singh AR, Swarnkar M, et al. (March 2013). "A sequence-based variation map of zebrafish". Zebrafish. 10 (1): 15–20. doi:10.1089/zeb.2012.0848. PMC 3629779. PMID 23590399.
^"The Gene Business- Business News". businesstoday.in. 18 February 2020. Retrieved 22 June 2020.
^Koshy, Jacob (25 October 2019). "CSIR offers free mapping of Indian genomes". The Hindu. ISSN 0971-751X. Retrieved 22 June 2020.
^"Genomics for Public Health". sites.google.com. Retrieved 22 June 2020.
^"Adjunct Faculty". www.iitk.ac.in. Retrieved 11 November 2023.
^"Visiting and Adjunct Faculty at IIIT-D".
^"Genomics training for clinicians - CSIR-IGIB Sanofi Genzyme fellowship: From labs to patients". Genomics training for clinicians - CSIR-IGIB Sanofi Genzyme fellowship. Retrieved 14 March 2020.
^"The Gene Business- Business News". businesstoday.in. 18 February 2020. Retrieved 14 March 2020.
^Prasad, R. (10 July 2016). "Screening for rare genetic disorders at a point-of-click". The Hindu. ISSN 0971-751X. Retrieved 14 March 2020.
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