Author

Sonya B. Dumanis

Aligning Science Across Parkinson'sORCID 0000-0002-3345-9497Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Scientific Communication & Education· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Research Focus:imputation· 1 Research Focus:software / tool· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ekemini A. U. RileyiD· 2 shared Andrew SingletoniD· 1 shared Armando Reyes‐PalomaresiD· 1 shared Barbara MarebwaiD· 1 shared Bryan J. TraynoriD· 1 shared Christine KleiniD· 1 shared Claudia SchulteiD· 1 shared Cornelis BlauwendraatiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersScientific Communication & Education

Ekemini A. U. RileyORCID

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2 papers

Recent·Most cited

Investing in Open Science: Key Considerations for Funders

Dana E. Cobb-Lewis, Devin E. Snyder, Sonya B. Dumanis, Robert T. Thibault, Barbara Marebwa, Elisia Clark, Lara St. Clair, Leslie Kirsch, Michelle Durborow, Ekemini A. U. Riley

This paper outlines the costs and logistical challenges of implementing open science policies in biomedical research, using the ASAP initiative as a case study.

bioRxiv · Dec 9, 2024 · PreprintScientific Communication & Education

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Sara Bandrés‐Ciga, Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin S. Levine, Hampton L. Leonard, Mary B. Makarious, Hirotaka Iwaki, Peter Wild Crea, Dena G. Hernandez, Sampath Arepalli, Kimberley J. Billingsley, Katja Lohmann, Christine Klein, , Dan Vitale

The paper introduces the NeuroBooster Array, a genome-wide genotyping platform designed to study neurological disorders across diverse populations by capturing genetic variation and enabling imputation of disease-related variants.

Movement Disorders · Sep 16, 2024Peer-reviewedGenetic & Genomic Medicine