| العنوان | المؤلف | تاريخ النشر | الناشر | النوع |
| Computational approach to unravel the impact of missense mutations of proteins (D2HGDH and IDH2) causing D-2-hydroxyglutaric aciduria 2. | Thirumal Kumar, D; Jerushah Emerald, L; George Priya Doss, C; Sneha, P; Siva, R; Charles Emmanuel Jebaraj, W; Zayed, Hatem... more authors ... less authors | 2018 | Springer US | Article |
| Computational modelling approaches as a potential platform to understand the molecular genetics association between Parkinson's and Gaucher diseases. | Thirumal Kumar, D; Eldous, Hend Ghasan; Mahgoub, Zainab Alaa; George Priya Doss, C; Zayed, Hatem | 2018 | Springer | Article |
| A computational method to characterize the missense mutations in the catalytic domain of GAA protein causing Pompe disease. | Thirumal Kumar, D; Umer Niazullah, Maryam; Tasneem, Sadia; Judith, E; Susmita, B; George Priya Doss, C; Selvarajan, E; Zayed, Hatem... more authors ... less authors | 2019 | Wiley | Article |
| 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, Hatem... more authors ... less authors | 2018 | Springer US | Article |
| A computational model to predict the structural and functional consequences of missense mutations in O-methylguanine DNA methyltransferase. | Thirumal Kumar, D; Mendonca, Enid; Priyadharshini Christy, J; George Priya Doss, C; Zayed, Hatem | 2019 | Elsevier | Article |
| Elucidating the role of interacting residues of the MSH2-MSH6 complex in DNA repair mechanism: A computational approach. | Thirumal Kumar, D; Susmita, B; Judith, E; Priyadharshini Christy, J; George Priya Doss, C; Zayed, Hatem... more authors ... less authors | 2019 | Elsevier | Article |
| A computational approach for investigating the mutational landscape of RAC-alpha serine/threonine-protein kinase (AKT1) and screening inhibitors against the oncogenic E17K mutation causing breast cancer. | Thirumal Kumar, D; Jain, Nikita; Evangeline, Judith; Kamaraj, Balu; Siva, R; Zayed, Hatem; George Priya Doss, C... more authors ... less authors | 2019 | Elsevier | Article |
| Computational model to analyze and characterize the functional mutations of NOD2 protein causing inflammatory disorder - Blau syndrome. | Thirumal Kumar, D; Udhaya Kumar, S; Nishaat Laeeque, Ahmed Shaikh; Apurva Abhay, Shivalkar; Bithia, R; Magesh, R; Kumar, Maignana; Zayed, Hatem; George Priya Doss, C... more authors ... less authors | 2020 | Elsevier | Article |
| Comprehensive in silico screening and molecular dynamics studies of missense mutations in Sjogren-Larsson syndrome associated with the ALDH3A2 gene. | Udhaya Kumar, S; Thirumal Kumar, D; Mandal, Pinky D; Sankar, Srivarshini; Haldar, Rishin; Kamaraj, Balu; Walter, Charles Emmanuel Jebaraj; Siva, R; George Priya Doss, C; Zayed, Hatem... more authors ... less authors | 2020 | Elsevier | Article |
| Molecular dynamics simulations to decipher the structural and functional consequences of pathogenic missense mutations in the galactosylceramidase (GALC) protein causing Krabbe's disease. | Thirumal Kumar, D; Jain, Nikita; Udhaya Kumar, S; Jena, Prangya Paramita; Ramamoorthy, Siva; George Priya Doss, C; Zayed, Hatem... more authors ... less authors | 2020 | Taylor & Francis | Article |
