Author

Neha Verma

Institute of Medical SciencesORCID 0000-0002-6393-0323Unclaimed ORCID profile · follow to get notified of new preprints

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Neha Verma1 paper · Institute of Microbial Technology

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

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Chandra DeviiD· 1 shared Parimal Kumar DasiD· 1 shared Prashant RanjaniD· 1 shared Rajesh Bansal· 1 shared Rimjhim Kumari· 1 shared Vinay KumariD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Chandra DeviORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineGenePeer-reviewedJun 23, 2026

Whole Exome Sequencing Uncovers Key Genetic Variants in Congenital Tooth Agenesis: An Integrative Omics Approach

Prashant Ranjan, Chandra Devi, Neha Verma…·Parimal Kumar Das

This study uses whole exome sequencing and multi-omics integration to identify genetic variants associated with congenital tooth agenesis, revealing potential biomarkers and therapeutic targets.

4 citations

humanwhole-exome sequencing

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