Parimal Das

Baylor College of Medicine, Houston, TX 
"Parimal Das"
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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
Pemberton TJ, Das P, Patel PI. (2005) Hypodontia: genetics and future Hypodontia: genetics and future perspectives Brazilian Journal of Oral Sciences. 4: 695-706
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