Author

Danielle Carpenter

Saint Louis 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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Genetics· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Ameya Padakanti· 1 shared Anna FärnertiD· 1 shared Anutosh ChakrabortyiD· 1 shared Billy NgasalaiD· 1 shared Brent A Neuschwander-Tetri· 1 shared Craig W. Vander KooiiD· 1 shared Edward J. HolloxiD· 1 shared Fengtang YangiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperPhysiology

Ameya Padakanti

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2 papers

Recent·Most cited

Hepatocyte UBE4A protects against MASLD/MASH by maintaining ER homeostasis via UBXN4 interaction

Naga Lakshmi Challa, Vineet Babu, Molee Chakraborty, Matthew Hayes, Gaurav Kumar, Kyle S. McCommis, Craig W. Vander Kooi, Danielle Carpenter, Isabela Ramos, Shivankitha Kattekola, Ameya Padakanti, Shikara Patel, Kaitlyn Mills, Sanchita Gupta, Louise Lantier, , Anutosh Chakraborty

This study identifies Ube4A's role in protecting against MASLD/MASH by maintaining ER homeostasis through its interaction with UBXN4, highlighting potential therapeutic targets.

bioRxiv · Oct 13, 2026 · PreprintPhysiology

The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels

Walid Algady, Sandra Louzada, Danielle Carpenter, Paulina Brajer, Anna Färnert, Ingegerd Rooth, Billy Ngasala, Fengtang Yang, Marie‐Anne Shaw, Edward J. Hollox

The paper identifies DUP4, a structural variant associated with reduced malaria risk and higher hemoglobin levels in a Tanzanian population.

The American Journal of Human Genetics · Nov 1, 2018Peer-reviewedGenetics