Kiran Narta

发表

Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma.

Richard A. Moore, S. Scherer, M. Marra, 2019, Cancer research.

Subclonal architecture, evolutionary trajectories and patterns of inheritance of germline variants in pediatric glioblastoma

Richard A. Moore, Trevor J Pugh, M. Marra, 2018, bioRxiv.

Whole exome-sequencing of vitiligo lesions indicate lower burden of somatic variations: implications in risk for non-melanoma skin cancers

Vivek T. Natarajan, D. Dash, M. Mukerji, 2022, bioRxiv.

Myg1 exonuclease couples the nuclear and mitochondrial translational programs through RNA processing

Vivek T. Natarajan, K. Natarajan, S. Roy, 2019, Nucleic acids research.

Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration

A. Rao, K. Ray, N. Waseem, 2023, Genes.

Fusion transcripts in normal human cortex increase with age and show distinct genomic features for single cells and tissues

C. Sarkar, D. Dash, Deepak Kumar, 2020, Scientific Reports.

Next-Generation Sequencing: Technology, Advancements, and Applications

Gourja Bansal, Kiran Narta, Manoj Ramesh Teltumbade, 2018 .

Novel internal regulators and candidate miRNAs within miR-379/miR-656 miRNA cluster can alter cellular phenotype of human glioblastoma

C. Sarkar, Prajakta Bajad, Anupam Kumar, 2018, Scientific Reports.

Novel internal regulators and candidate miRNAs within miR-379/miR-656 miRNA cluster can alter cellular phenotype of human glioblastoma

C. Sarkar, Prajakta Bajad, Anupam Kumar, 2018, Scientific reports.

Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma

Arijit Mukhopadhyay, Kunal Ray, Shomi S. Bhattacharya, 2016, BMC Medical Genomics.

Fusion transcripts in normal human cortex increase with age and show distinct genomic features for single cells and tissues

C. Sarkar, D. Dash, Deepak Kumar, 2020, Scientific Reports.