I am Jibin John, a human geneticist and bioinformatician with over eight years of experience. I specialize in analyzing Next Generation Sequencing (NGS) and SNP microarray data to uncover the genetic basis of diseases. My expertise lies in building and managing automated data analysis pipelines, and I use statistical analysis to connect genetic variants and genes to disease biology.
Large-scale 2-sample mendelian randomization (MR) can examine the potentially causal impact of circulating proteins on neuropsychiatric phenotypes without these confounds.
Given the increasingly large number of loci discovered by psychiatric genome-wide association studies (GWASs), specification of the key biological pathways that underlie these loci has become a priority for the field.
WES in multiplex families may be an insightful strategy for the identification of highly penetrant rare variants in SZ and possibly enhance our understanding of disease biology.
Council for Scientific and Industrial Research (CSIR), New Delhi, India, 2011
University Grants Commission (UGC), New Delhi, India, 2011
Fogarty International Center, National Institutes of Health (NIH), USA, 2012
Council for Scientific and Industrial Research (CSIR), New Delhi, India, 2012–2014
International Conference of Human Genetics & 39th Annual Meeting of the Indian Society of Human Genetics, Ahmedabad, India, 2014
Indian Council of Medical Research (ICMR), New Delhi, India, to attend the World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, 2015
Council for Scientific and Industrial Research (CSIR), Delhi, India, 2015
Healthy Brains for Healthy Lives (HBHL) initiative, McGill University, Montreal, Canada, 2019; CAD 125,000