Author

Alexandra I. Soto‐Beasley

Mayo ClinicORCID 0000-0002-0153-1917Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Owen A. RossiD· 3 shared Michael G. HeckmaniD· 2 shared Ronald L. Walton· 2 shared Zbigniew K. WszołekiD· 2 shared Aditya Vijay BhagwateiD· 1 shared Andrew C. Osborne· 1 shared Briana N Markham· 1 shared Chen WangiD· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersNeuroscience

Owen A. RossORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintJan 17, 2024

miRNA family miR-29 inhibits PINK1-PRKN dependent mitophagy via ATG9A

Briana N Markham, Chloe Ramnarine, Songeun Kim…·Fabienne C. Fiesel

The paper identifies miR-29 and ATG9A as regulators of mitophagy and discovers EOPD-linked variants in ATG9A.

7 citations

humanbulk RNA-seq

NeuroscienceActa Neuropathologica CommunicationsPeer-reviewedSep 17, 2020

Associations of Mitochondrial Genomic Variation with Corticobasal Degeneration, Progressive Supranuclear Palsy, and Neuropathological Tau Measures

Rebecca R. Valentino, Nikoleta Tamvaka, Michael G. Heckman…·Owen A. Ross

This study investigates associations between mitochondrial genomic variation and risk of Corticobasal Degeneration (CBD) and Progressive Supranuclear Palsy (PSP), as well as tau pathology measures in PSP.

13 citations

humanDNA methylation

NeurosciencebioRxivPreprintMar 31, 2020

RNF213 variation, a broader role in neurovascular disease in Caucasian and Japanese populations

Oswaldo Lorenzo‐Betancor, Patrick R. Blackburn, Luca P. Farrugia…·Owen A. Ross

The paper investigates RNF213 variation's role in neurovascular diseases across Caucasian and Japanese populations, finding linkage disequilibrium between SLC26A11 and RNF213 variants associated with ischemic stroke and aneurysms.

1 citation

humanGWAS summary statistics