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| Banerjee S, Zhao Q, Wang B, et al. (2024) A novel in-frame deletion in KIF5C gene causes infantile onset epilepsy and psychomotor retardation. Medcomm. 5: e469 |
| Ranjan P, Das P. (2023) An inclusive study of deleterious missense PAX9 variants using user-friendly tools reveals structural, functional alterations, as well as potential therapeutic targets. International Journal of Biological Macromolecules. 123375 |
| Sarkar T, Ranjan P, Kanathur S, et al. (2022) An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis. Molecular Genetics and Genomics : Mgg |
| Ranjan P, Das P. (2021) Understanding the impact of missense mutations on the structure and function of the EDA gene in X-linked hypohidrotic ectodermal dysplasia: A bioinformatics approach. Journal of Cellular Biochemistry |
| Raj S, Singh RG, Das P. (2020) Mutational screening of PKD1 and PKD2 in Indian ADPKD patients identified 95 genetic variants. Mutation Research. 821: 111718 |
| Sarkar T, Bansal R, Das P. (2017) A novel G to A transition at initiation codon and exon-intron boundary of PAX9 identified in association with familial isolated oligodontia. Gene |
| Sarkar T, Bansal R, Das P. (2014) Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis. Plos One. 9: e106811 |
| Das P, Kotilingam D, Korchin B, et al. (2007) High prevalence of p53 exon 4 mutations in soft tissue sarcoma. Cancer. 109: 2323-33 |
| Tarpey P, Pemberton TJ, Stockton DW, et al. (2007) A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia. American Journal of Medical Genetics Part A. 143: 390-394 |
| Rosenberg NA, Mahajan S, Gonzalez-Quevedo C, et al. (2006) Low levels of genetic divergence across geographically and linguistically diverse populations from India. Plos Genetics. 2: e215 |