Author

James E. Faber

University of North Carolina at Chapel HillORCID 0000-0002-0377-6993Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 3 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Fernando Pardo‐Manuel de VillenaiD· 2 shared Martin T. FerrisiD· 2 shared Pablo Hock· 2 shared Timothy A. BelliD· 2 shared A. Wesley BurksiD· 1 shared Abraham A. PalmeriD· 1 shared Alessandra Livraghi-ButricoiD· 1 shared Allison R. RogalaiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Fernando Pardo‐Manuel de VillenaORCID

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3 papers

Recent·Most cited

NeuroscienceTheranosticsPeer-reviewedDec 2, 2024

Inhibition of nitric oxide synthase transforms carotid occlusion-mediated benign oligemia into de novo large cerebral infarction

H.-Y. Kim, Jinyong Chung, Jeong Wook Kang…·Dong‐Eog Kim

The paper investigates how NOS inhibition transforms benign oligemia into large cerebral infarction in mice and links SDMA levels to ischemic stroke risk in humans.

4 citations

mousestatistical model

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GeneticsJournal of Cerebral Blood Flow & MetabolismPeer-reviewedAug 12, 2023

Large differences in collateral blood vessel abundance among individuals arise from multiple genetic variants

James E. Faber, Hua Zhang, James G. Xenakis…·Wojciech Rzechorzek

The paper identifies genetic variants associated with collateral blood vessel abundance in mice, linking them to potential human disease mechanisms.

12 citations

mousestatistical model

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GeneticsGeneticsPeer-reviewedOct 17, 2020

Content and performance of the MiniMUGA genotyping array, a new tool to improve rigor and reproducibility in mouse research

John Sebastian Sigmon, Matthew W Blanchard, Ralph Steven Baric…·Fernando Pardo‐Manuel de Villena

The paper introduces MiniMUGA, a genotyping array for mouse genetic QC, showing it effectively discriminates strains, detects genetic constructs, and identifies sex chromosome abnormalities.

93 citationstop 2%

mouseexperimental assay

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