TitleAuthorPublication DatePublisherType
    Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach.  Sneha, P; Zenith, Tanzila U; Abu Habib, Ummay Salma; Evangeline, Judith; Thirumal Kumar, D; George Priya Doss, C; Siva, R; Zayed, Hatem2018Springer USArticle
    Molecular insights of the G2019S substitution in LRRK2 kinase domain associated with Parkinson's disease: A molecular dynamics simulation approach.  Agrahari, Ashish Kumar; Doss, George Priya C; Siva, R; Magesh, R; Zayed, Hatem2019ElsevierArticle
    A profound computational study to prioritize the disease-causing mutations in PRPS1 gene.  Agrahari, Ashish Kumar; Sneha, P; George Priya Doss, C; Siva, R; Zayed, Hatem2017Springer VerlagArticle
    A profound computational study to prioritize the disease-causing mutations in PRPS1 gene.  Agrahari, Ashish Kumar; Sneha, P; George Priya Doss, C; Siva, R; Zayed, Hatem2017Springer VerlagArticle
    Understanding the structure-function relationship of HPRT1 missense mutations in association with Lesch-Nyhan disease and HPRT1-related gout by in silico mutational analysis.  Agrahari, Ashish Kumar; Krishna Priya, M; Praveen Kumar, Medapalli; Tayubi, Iftikhar Aslam; Siva, R; Prabhu Christopher, B; George Priya Doss, C; Zayed, Hatem2019ElsevierArticle