Author

Scott A. LeMaire

Baylor College of MedicineORCID 0000-0002-8736-4266Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

Alan DaughertyiD· 3 shared Yanming LiiD· 3 shared Ying H. SheniD· 3 shared Chen ZhangiD· 2 shared Hisashi SawadaiD· 2 shared Hong S. LuiD· 2 shared Abhijit ChakrabortyiD· 1 shared Alexander H. LiiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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3 shared papersImmunology

Alan DaughertyORCID

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3 papers

Recent·Most cited

ImmunologybioRxivPreprintJan 25, 2026

Epigenetic Programming of Macrophage Phenotypes by STING-IRF3 Drives Inflammation in Ascending Thoracic Aortic Dissection

Bowen Li, Chen Zhang, Samantha Xu…·Ying H. Shen

This study identifies STING-IRF3-mediated epigenetic programming of macrophages as a driver of inflammation in aortic dissection, showing its role in pro-inflammatory bias and therapeutic potential.

2 citations

humanmouse

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PathologybioRxivPreprintJan 23, 2025

Smooth Muscle Cells and Fibroblasts in the Proximal Thoracic Aorta Exhibit Minor Differences Between Embryonic Origins in Angiotensin II-driven Transcriptional Alterations

Sohei Ito, David B Graf, Yuriko Katsumata…·Hisashi Sawada

The paper examines transcriptomic changes in smooth muscle cells and fibroblasts from different embryonic origins in the proximal thoracic aorta under AngII infusion, finding modest differences between origins.

1 citation

mousescRNA-seq

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GenomicsNature MedicinePeer-reviewedJan 1, 2021

Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes

Joseph Park, Anastasia Lucas, Xinyuan Zhang…·Daniel James Rader

This study identifies robust gene-phenotype associations by analyzing rare loss-of-function variants in exome-wide data linked to electronic health records.

58 citationstop 2%

humanwhole-exome sequencing

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