Author

Elisa Majounie

Illumina (United States)

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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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:DNA methylation· 1 Research Focus:imputation· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrew SingletoniD· 1 shared Anita PottekatiD· 1 shared Armando Reyes‐PalomaresiD· 1 shared Bret Barnes· 1 shared Bryan J. TraynoriD· 1 shared Cameron Cloud· 1 shared Christine KleiniD· 1 shared Christine Tran· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrew SingletonORCID

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2 papers

Recent·Most cited

Scalable Screening of Ternary-Code DNA methylation Dynamics Associated with Human Traits.

David C. Goldberg, Cameron Cloud, Sol Moe Lee, Bret Barnes, Steven Gruber, Elliot Kim, Anita Pottekat, Maximillian S. Westphal, Luana McAuliffe, Elisa Majounie, Manesh Kalayil Manian, Qingdi Zhu, Christine Tran, Mark S. T. Hansen, Jelena Stojakovic, , Wanding Zhou

The paper introduces MSA, a new epigenotyping platform for analyzing ternary-code DNA methylation, and applies it to uncover aging dynamics and trait associations involving 5hmC and 5mC.

Cell Genomics · Jul 3, 2025Peer-reviewedGenomics

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