AV
Ankit Verma
University of Cambridge, Institute of Genetics and Biophysics, All India Institute of Medical Sciences, University of Delhi, CNR-Institute of Genetics and Biophysics, Rajkiya Pratibha Vikas Vidyalaya
Employment
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University of Cambridge Bioinformatician2022 - Present
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Institute of Genetics and Biophysics Postdoctoral Research Fellow2021 - 2022
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CNR-Institute of Genetics and Biophysics PhD2017 - 2021
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CSIR-Institute of Genomics and Integrative Biology Senior Project Fellow2017 - 2017
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CSIR-Insititute of Genomics and Integrative Biology Project fellow2013 - 2017
Education
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All India Institute of Medical Sciences Master of Science (MSc)2011 - 2013
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University of Delhi Bachelor of Science (B.Sc)2008 - 2011
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Rajkiya Pratibha Vikas Vidyalaya Senior Secondary (12th)2007 - 2008
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Sarvodaya Vidyalaya Higher Secondary (10th)2005 - 2006
Projects & Funding
Projects & funding information is unavailable.
Publications (37)
- Poldip2 promotes mtDNA elimination during Drosophila spermatogenesis to ensure maternal inheritance Save
- Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality. Save
- ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming Save
- Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs Save
- A Temporal Map of Gene Expression Pattern during Zebrafish Liver Regeneration Save
- Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance Save
- Saliva microbiome in primary Sjögren’s syndrome reveals distinct set of disease-associated microbes Save
- A temporal map of gene expression pattern during zebrafish liver regeneration Save
- Organellar transcriptome sequencing reveals mitochondrial localization of nuclear encoded transcripts Save
- Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy Save