Author

Ronald L. Walton

Mayo Clinic

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 2 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alexandra I. Soto‐BeasleyiD· 2 shared Owen A. RossiD· 2 shared Afina Willemina LemstraiD· 1 shared Alexis BriceiD· 1 shared Andrea CalvoiD· 1 shared Anni K. MooreiD· 1 shared Antonio CanosaiD· 1 shared Bension Shlomo Tilley· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersNeuroscience

Alexandra I. Soto‐BeasleyORCID

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Author profile →

3 papers

Recent·Most cited

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

Rebecca R. Valentino, Nikoleta Tamvaka, Michael G. Heckman, Patrick W. Johnson, Alexandra I. Soto‐Beasley, Ronald L. Walton, Shunsuke Koga, Ryan J. Uitti, Zbigniew K. Wszołek, Dennis W. Dickson, 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.

Acta Neuropathologica Communications · Sep 17, 2020Peer-reviewedNeuroscience

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Regina Hertfelder Reynolds, Emil Karl Gustavsson, Ronald L. Walton, Sarah Ahmed, Coralie Viollet, Jinhui Ding, Mary B. Makarious, Mónica Díez-Fairén, Makayla K. Portley, Zalak Shah, Yevgeniya A. Abramzon, , Thomas G. Beach

This paper identifies five new genetic risk loci for Lewy body dementia through whole-genome sequencing and shows shared risk profiles with Alzheimer’s and Parkinson’s disease.

bioRxiv · Jul 6, 2020 · PreprintGenomics

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

Oswaldo Lorenzo‐Betancor, Patrick R. Blackburn, Luca P. Farrugia, Alexandra I. Soto‐Beasley, Ronald L. Walton, Emily Edwards, Rabih G. Tawk, Eric W. Klee, William David Freeman, David W. Miller, James Frederick Meschia, 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.

bioRxiv · Mar 31, 2020 · PreprintNeuroscience