Author

Katelyn Dunn

Cincinnati Children's Hospital Medical Center

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

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1

Frequent Co-Authors

Leah Claire KottyaniD· 2 shared Marissa GranittoiD· 2 shared Matthew T. WeirauchiD· 2 shared Omer A. DonmeziD· 2 shared Xiaoting CheniD· 2 shared Adam Z. MagieriD· 1 shared Adriana Barreiro-Rosario· 1 shared Alejandro Rivera-MaderaiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenomics

Leah Claire KottyanORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Global Evaluation of Congenital Heart Disease-Associated Non-Coding Variants

Edwin G. Peña-Martínez, Edwin Peña-Martínez, Shreya Sharma, Joshua Medina-Feliciano, Elise Root, Lois Parks, Marissa Granitto, Diego Pomales-Matos, Jean Messon- Bird, Adriana Barreiro-Rosario, Leandro Sanabria-Alberto, Alejandro Rivera-Madera, Jessica Rodríguez-Ríos, Rosalba Velázquez-Roig, Juan Figueroa- Rosado, , Devesh Bhimsaria

This study evaluates over 3,000 congenital heart disease-risk variants using SNP Bind-n-Seq and MPRA to identify variants with allelic TF binding and regulatory activity.

bioRxiv · Dec 10, 2025 · PreprintGenomics

Epigenetic and Transcriptional Dysregulation in CD4+ T cells of Patients with Atopic Dermatitis

Amy Eapen, Sreeja Parameswaran, Carmy R. Forney, Lee Edsall, Daniel Miller, Omer A. Donmez, Katelyn Dunn, Xiaoming Lu, Marissa Granitto, Hope Rowden, Adam Z. Magier, Mario Andres Pujato, Xiaoting Chen, Kenneth M. Kaufman, David I Bernstein, , Leah Claire Kottyan

This study identifies epigenetic and transcriptional dysregulation in CD4+ T cells of atopic dermatitis patients, linking genetic risk variants to altered chromatin accessibility and NFKB1 binding.

Journal of Allergy and Clinical Immunology · Feb 1, 2022Peer-reviewedGenomics