Author

Rebecca R. Valentino

Mayo ClinicORCID 0000-0001-7253-961XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Dennis W. DicksoniD· 3 shared Owen A. RossiD· 3 shared Christopher KobyleckiiD· 2 shared Huw R. MorrisiD· 2 shared James Benedict RoweiD· 2 shared John HardyiD· 2 shared Kin Ying MokiD· 2 shared Maryam ShoaiiD· 2 shared

Activity by Year

2020-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Dennis W. DicksonORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 27, 2025

Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association study.

William J. Scotton, Rebecca R. Valentino, Alejandro Martínez-Carrasco…·Maryam Shoai

This study conducts a GWAS on Pick's disease and identifies two SNPs associated with risk, though not at genome-wide significance, suggesting potential genetic factors beyond MAPT mutations.

DOI 10.64898/2025.12.21.25342758

humanGWAS summary statistics

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

GeneticsbioRxivPreprintFeb 4, 2020

Common variation at the LRRK2 locus is associated with survival in the primary tauopathy progressive supranuclear palsy

Edwin Jabbari, Manuela M. X. Tan, Regina Hertfelder Reynolds…·Huw R. Morris

The paper identifies common LRRK2 locus variation associated with survival in progressive supranuclear palsy, linking it to gene expression regulation and suggesting therapeutic implications for tauopathies.

4 citations

humanGWAS summary statistics