| Mechanistic basis of abnormal neurogenesis due to HSAN1Eassociated DNA methyltransferase 1 (Dnmt1) mutation and pharmacological intervention for phenotypic correction | | 2017 | 2020 |
| Molecular Characterization of Organic Acidurias using Targeted Next Generation Sequencing | | 2015 | 2018 |
| Molecular characterization of undiagnosed cases of congenital hemolytic anemia using a multigene next generation sequencing panel | | 2017 | 2020 |
| Relevance of telomere biology in the pathogenesis and treatment outcome of patients with bone marrow failure disorders | | 2017 | 2020 |
| Study the role of T cell Receptor Excision Circle (TREC) assay in diagnosis of various combined immunodeficiency disorders. | | 2018 | 2021 |
| The clinical, enzymological and molecular study of children with Gaucher disease (GD): Identification of demographical loci on GD phenotype. | | 2016 | 2019 |
| The human gut and eye microbiome: An insight into eye infections | | 2017 | 2019 |
| Tumour genome profiling and minimal residual disease estimation in acute haematological malignancies using single-platform next generation sequencing strategies | | 2017 | 2022 |
| Whole exome sequencing in Leber congenital amarousis (LCA) to identify novel gene(s) | | 2015 | 2018 |
| A “bench to bedside” model for clinical and translational science between academic research institutes and hospitals focused on fetal growth restriction and preterm birth. | | 2018 | 2023 |