040-2721-6211

Mr. Jibin John

Manager (Computational)

Qualification

Ph.D (Genetics) University of Delhi, New Delhi, India
MSc (Biotechnology) University of Madras
BSc (Biotechnology) Bharathidasan University


Experience
  • Working as Computational Laboratory Manager, NGC, CDFD
  • McGill University Montreal, Quebec, Canada:2019-2021
  • Montreal University Institute of Mental Health : 2018-2019
  • University of Delhi, South campus, New Delhi, India: 2017-2018
  • University of Pittsburgh, Pittsburgh, Pennsylvania, USA: 2012
Publications
  • John J, Kukshal P, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia. Schizophr Res. 2019 Aug;210:296-298.
  • John J, Bhattacharyya U, Yadav N, Kukshal P, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance. Schizophr Res. 2020 Feb;216:288-294.
  • John J, Sharma A, Kukshal P, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis. Schizophr Bull. 2019 Jan 1;45(1):256-263.
  • John J, Bhatia T, Kukshal P, Chandna P, Nimgaonkar VL, Deshpande SN, Thelma BK. Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition. Schizophr Res. 2016 Jul;174(1-3):29-34.
  • John J, Kukshal P, Sharma A, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study. Schizophr Res. 2019 Apr;206:75-81.
  • Chaudhuri Z, John J, Aneja S, Thelma BK. Pedigree Analysis of Familial Primary Concomitant Horizontal Strabismus in Northern India. Strabismus. 2017 Dec;25(4):200-213.
  • John J, Kukshal P, Bhatia T, Chowdari KV, Nimgaonkar VL, Deshpande SN, Thelma BK. Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia. Schizophr Res. 2017 Nov;189:190-195.
  • John J, Kukshal P, Bhatia T,Harripaul R, Nimgaonkar VL, Deshpande SN, Thelma BK. Oligogenic rare variant contributions in schizophrenia and their convergence with genes harbouring de novo mutations in schizophrenia, autism and intellectual disability: Evidence from multiplex families. bioRxiv; doi: https://doi.org/10.1101/829101