Author

Inshya Desai

Pennsylvania State University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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Organism:Drosophila· 2 Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Emily HuberiD· 2 shared Janani S. IyeriD· 2 shared Laura Anne LoweryiD· 2 shared Lucilla PizzoiD· 2 shared Matthew JenseniD· 2 shared Mayanglambam Dhruba SinghiD· 2 shared Micaela C. LasseriD· 2 shared Santhosh GirirajaniD· 2 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Emily HuberORCID

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2 papers

Recent·Most cited

Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis

Lucilla Pizzo, Micaela C. Lasser, Tanzeen Yusuff, Matthew Jensen, Phoebe Ingraham, Emily Huber, Mayanglambam Dhruba Singh, Connor Monahan, Janani S. Iyer, Inshya Desai, Siddharth Karthikeyan, Dagny J. Gould, Sneha Yennawar, Alexis T. Weiner, Vijay Kumar Pounraja, , Santhosh Girirajan

The paper tests a 'two-hit' model for neurodevelopmental defects by examining interactions between 16p12.1 homologs and 'second-hit' genes in Drosophila and Xenopus laevis, finding genetic interactions in 63% of tested pairs.

PLoS Genetics · Apr 5, 2021Peer-reviewedGenomics

NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and X. laevis models

Mayanglambam Dhruba Singh, Matthew Jensen, Micaela C. Lasser, Emily Huber, Tanzeen Yusuff, Lucilla Pizzo, Brian Lifschutz, Inshya Desai, Alexis Kubina, Sneha Yennawar, Sydney Kim, Janani S. Iyer, Diego E. Rincón-Limas, Laura Anne Lowery, Santhosh Girirajan

This study identifies NCBP2 as a key modifier gene in the 3q29 deletion, showing it enhances developmental defects through disrupted apoptosis and cell cycle mechanisms in Drosophila and Xenopus models.

bioRxiv · Dec 4, 2019 · PreprintGenomics