Author

Carmen Glaze

Broad Institute

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· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Anne O’Donnell‐LuriaiD· 2 shared Emily GroopmaniD· 2 shared Heidi L. RehmiD· 2 shared Kathryn Russell· 2 shared Moriel Singer‐BerkiD· 2 shared Samantha M. BaxteriD· 2 shared A. D. Neale· 1 shared Alba Sanchis‐JuaniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anne O’Donnell‐LuriaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genomic Research as a Critical Pathway to Diagnosis for Individuals with Rare Disease

Anne O’Donnell‐Luria, Stephanie P. DiTroia, Melanie O’Leary, Lynn S. Pais, Vijay S Ganesh, Gabrielle Lemire, Emily O’Heir, A. D. Neale, Alicia Pham, Grace E. VanNoy, Brian E. Mangilog, Moriel Singer‐Berk, Alba Sanchis‐Juan, Hana Snow, Siwaar Abouhala, , Heidi L. Rehm

The Rare Genomes Project provides remote genomic sequencing to rare disease families, achieving a 23.3% diagnostic solve rate and highlighting the role of research in overcoming clinical diagnostic barriers.

medRxiv · Sep 20, 2026 · PreprintGenetic & Genomic Medicine

The Power of Partnership: Democratizing Genetic Prevalence to Empower Patient Advocacy

Samantha M. Baxter, Moriel Singer‐Berk, Carmen Glaze, Kathryn Russell, Riley H. Grant, Emily Groopman, J. H. Lee, Nick Watts, Jordan C. Wood, Michael Wilson, Rare As One Network, Heidi L. Rehm, Anne O’Donnell‐Luria

The paper estimates genetic prevalence for 22 autosomal recessive conditions using gnomAD data and develops a tool to democratize these calculations, highlighting the dynamic nature of prevalence estimates.

medRxiv · Mar 31, 2026 · PreprintGenetic & Genomic Medicine