Author

Steven E. Pierce

Van Andel InstituteORCID 0000-0002-7417-2302Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 3 Research Focus:differential expression· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Approach:experimental assay· 1

Frequent Co-Authors

Gerhard A. CoetzeeiD· 3 shared Edwin J. C. Van der Schans· 2 shared Alix BoomsiD· 1 shared Elizabeth EnsinkiD· 1 shared Jordan D PrahliD· 1 shared Trevor Tyson· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 9 mutual co-author links

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3 shared papersNeuroscience

Gerhard A. CoetzeeORCID

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3 papers

Recent·Most cited

Gene expression asymmetry in Parkinson's Disease; variation of CCT and BEX gene expression levels are correlated with hemisphere specific severity

Steven E. Pierce, Edwin J. C. Van der Schans, Elizabeth Ensink, Gerhard A. Coetzee

The paper examines gene expression asymmetry in Parkinson's Disease, finding that CCT and BEX gene expression levels vary between hemispheres and correlate with symptom onset side.

bioRxiv · Jul 2, 2024 · PreprintNeuroscience

GLOBAL EFFECTS OF A PD RISK-SNP AT THE ALPHA-SYNUCLEIN LOCUS

Jordan D Prahl, Steven E. Pierce, Edwin J. C. Van der Schans, Gerhard A. Coetzee, Trevor Tyson

This study investigates the risk mechanism of rs356182, a PD risk SNP near SNCA, by generating CRISPR-Cas9 lesions in LUHMES cells and observing effects on neuronal differentiation and axonogenesis.

bioRxiv · Jul 6, 2021 · PreprintNeuroscience

Parkinsons Disease Genetic Risk Evaluation in Microglia Highlights Autophagy and Lysosomal Genes

Alix Booms, Steven E. Pierce, Gerhard A. Coetzee

The paper identifies functional SNPs in microglia associated with Parkinson's disease risk, highlighting autophagy and lysosomal genes as key candidates for further study.

bioRxiv · Aug 17, 2020 · PreprintNeuroscience