Author

Venkata Hemanjani Bhavana

Baylor College of MedicineORCID 0009-0008-0113-5325Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Organism:Drosophila· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alfredo BruscoiD· 1 shared Amanda GerardiD· 1 shared Anisha Prabhu· 1 shared Annalisa VetroiD· 1 shared Belinda M. GiardineiD· 1 shared Boris KereniD· 1 shared Brooke HulliD· 1 shared Catherine A. BrownsteiniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Alfredo BruscoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 22, 2025

An integrated framework for functional dissection of variable expressivity in genetic disorders

Jiawan Sun, Serena Noss, Deepro Banerjee…·Santhosh Girirajan

The paper develops a framework to study variable expressivity in genetic disorders using 16p12.1 deletion models, showing how genetic background and secondary variants influence gene expression and phenotypes.

2 citations

humanATAC-seq

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GeneticsCell ReportsPeer-reviewedMar 1, 2022

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews…·Shinya Yamamoto

The paper functionally tests ASD missense variants in Drosophila, finding 38% caused functional alterations and identifying GLRA2 as a cause of neurodevelopmental phenotypes.

62 citationstop 2%

Drosophilaexperimental assay

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