Author

Amit Singh

University of DaytonORCID 0000-0002-2962-2255Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Amit Singh5 papers · University of Oklahoma

Biology Disciplines

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Developmental Biology· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:Drosophila· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Organism:human· 1

Frequent Co-Authors

Anuradha Venkatakrishnan ChimataiD· 2 shared Abijeet Singh MehtaiD· 1 shared Afif Ben‐MahmoudiD· 1 shared Alain VerloèsiD· 1 shared Anita M. RauchiD· 1 shared Anne M. ComiiD· 1 shared Annette E. BleyiD· 1 shared Arushi RaiiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anuradha Venkatakrishnan ChimataORCID

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3 papers

Recent·Most cited

A Genetic Mechanism Linking Hippo Signaling to Dorsoventral Patterning for Control of Head and Eye Development

Basavanahalli Nanjundaiah Rohith, Neha Gogia, Arushi Rai, Amit Singh, Madhuri Kango‐Singh

This study identifies a genetic mechanism linking Hippo signaling to dorsoventral patterning in Drosophila eye development, showing how Yki and Dve coordinate growth and head cuticle domain regulation.

bioRxiv · Jan 25, 2026 · PreprintDevelopmental Biology

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

Eric Nathaniel Anderson, Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Soundara Rajan, Senta Schönnagel, Karen Lucy Stals, Deirdre E. Donnelly, Siobhan O’Sullivan, John F. Mantovani, Tiong Yang Tan, Zornitza Stark, Pia Zacher, Nicolas Chatron, Pauline Monin, , Konrad Platzer

This study identifies de novo KDM2A variants as a cause of a syndromic neurodevelopmental disorder with specific clinical features and functional consequences.

medRxiv · Mar 31, 2025 · PreprintGenetic & Genomic Medicine

Novel newt regeneration genes regulate Wingless signaling to restore patterning in Drosophila eye

Abijeet Singh Mehta, Prajakta Deshpande, Anuradha Venkatakrishnan Chimata, Panagiotis A. Tsonis, Amit Singh

The paper shows that newt regeneration genes can rescue Drosophila eye mutant phenotypes by modulating Wingless signaling.

iScience · Sep 24, 2021Peer-reviewedDevelopmental Biology