Author

Ronya Strom

Brigham and Women's Hospital

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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Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Research Focus:gene regulatory network inference· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Autumn Rose MorrowiD· 3 shared Dylan RitteriD· 3 shared Lorenz StuderiD· 3 shared Shamil R. SunyaeviD· 3 shared Sumaiya NazeeniD· 3 shared Vikram KhuranaiD· 3 shared Xinyuan WangiD· 3 shared Elizabeth Ethier· 2 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Autumn Rose MorrowORCID

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3 papers

Recent·Most cited

NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's disease

Sumaiya Nazeen, Xinyuan Wang, Autumn Rose Morrow, Ronya Strom, Elizabeth Ethier, Dylan Ritter, Alexander B.H. Henderson, Jalwa Afroz, Christopher A. Cassa, Nathan O. Stitziel, Rajat M. Gupta, Kelvin C. Luk, Lorenz Studer, Vikram Khurana, Shamil R. Sunyaev

NERINE tests gene network hypotheses with rare variant associations, identifying a subnetwork linked to Parkinson's disease.

Cell Genomics · Jun 22, 2026Peer-reviewedGenetics

A single-cell genetic colocalization test improves power and resolves disease-mediating cell types

Jonathan Mitchel, Sumaiya Nazeen, Xinyuan Wang, Praveen K. Patnaik, Autumn Rose Morrow, Habib Nasir, Ronya Strom, Dylan Ritter, Lorenz Studer, Sung Chun, Chris J. Cotsapas, Vikram Khurana, Peter V. Kharchenko, Shamil R. Sunyaev

The paper introduces scJLIM, a cluster-free method for single-cell colocalization testing, improving power to link GWAS loci with gene expression changes in specific cell types.

bioRxiv · Oct 10, 2025 · PreprintGenomics

Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies

Sumaiya Nazeen, Xinyuan Wang, Dina Zielinski, Isabel Lam, Erinc Hallacli, Ping Xu, Elizabeth Ethier, Ronya Strom, Camila A. Zanella, Vanitha Nithianandam, Dylan Ritter, Alexander Henderson, Nathalie G. Saurat, Jalwa Afroz, Andrew Nutter-Upham, , Vikram Khurana

The paper identifies a shared genetic risk module involving PSEN2 and actin regulation across alpha-synucleinopathies, linking them to Alzheimer's disease mechanisms.

bioRxiv · Mar 3, 2024 · PreprintGenomics