Author

Daniel N. Hupalo

Henry M. Jackson FoundationORCID 0000-0001-7816-2948Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:host-pathogen & immune response· 1 Organism:plant (other)· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

Clifton L. DalgardiD· 3 shared Camille AlbaiD· 2 shared Amy E. RobertsiD· 1 shared Andrew F. TeichiD· 1 shared April E. WilliamsiD· 1 shared Badri Narayan VardarajaniD· 1 shared Barbara R. PoberiD· 1 shared Belinda J. Morahan· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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3 shared papersMicrobiology

Clifton L. DalgardORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

MicrobiologyNature CommunicationsPeer-reviewedJan 17, 2026

A single valine to leucine switch disrupts Plasmodium falciparum AP2-G DNA binding and reveals the role of GDV1 in ap2-g activation.

Surendra K. Prajapati, J Dong, Belinda J. Morahan…·Kim C. Williamson

This study identifies a valine-to-leucine mutation in AP2-G that disrupts DNA binding and sexual differentiation in Plasmodium falciparum, revealing GDV1's role in ap2-g activation.

1 citation

plant (other)experimental assay

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GeneticsActa NeuropathologicaPeer-reviewedApr 10, 2024

Rare genetic variation in Fibronectin 1 (FN1) protects against APOEe4 in Alzheimer's disease

Prabesh Bhattarai, Tamil Iniyan Gunasekaran, Michaël E. Belloy…·Badri Narayan Vardarajan

The paper identifies rare FN1 variants that protect APOEε4 carriers from Alzheimer's disease by modulating extracellular matrix deposition and gliosis.

59 citationstop 1%

humanzebrafish

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Genetic & Genomic MedicinemedRxivPreprintSep 21, 2022

Pathway analysis identifies novel non-synonymous variants contributing to extreme vascular outcomes in Williams-Beuren syndrome

D. Liu, Charles John Billington, N. Raja…·Beth A. Kozel

The paper identifies novel non-synonymous variants associated with extreme vascular outcomes in Williams-Beuren syndrome through whole-genome sequencing and pathway analysis.

DOI 10.1101/2022.09.21.22280107

humanwhole-genome sequencing

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