| Establishment of a biorepository of epilepsy and investigating the relation of multidrug transporter polymorphism with fetal malformations based on the repository | | 2017 | 2020 |
| Evaluating WISP3 (Wnt Induced Secreted Protein 3) and promoting societal benefit in the context of PPRD (Progressive Pseudo Rheumatoid Dysplasia), a debilitating genetic disorder | | 2018 | 2021 |
| Genetic And Clinical Factors Associated With Aspirin Resistance In Indian Population With Ischemic Stroke | | 2017 | 2020 |
| Genetic and Hormonal determinants of obstructive sleep apnea syndrome in obese children from north India | | 2014 | 2019 |
| Genetics of Dilatedcardiomyopathy | | 2018 | 2021 |
| Genome-wide association study of phenotypic extremes in primary angle closure glaucoma | | 2016 | 2019 |
| Genotype-phenotype relationship in rare genetic disorders: Physicochemical analysis of mutations in GNE myopathy and phenotypic modulation by small molecule effectors | | 2018 | 2021 |
| Identification, cloning, expression, purification and characterization of DNA demethylase enzyme activity: Investigation of the mechanism of demethylation of cytosine-5carbon methylated-DNA keeping the DNA strand intact | | 2017 | 2020 |
| How Lysophospholipids (lysophosphatidic acid and sphingosine-1phosphate) metabolic pathways regulate placental development during pregnancy maintenance | | 2017 | 2020 |
| Identification of transcription factors perturbed at early stages of heart development during pregestational diabetes. | | 2017 | 2019 |