Author

Ivy Evergreen

Stanford UniversityORCID 0009-0004-6737-889XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Anshul Bharat KundajeiD· 3 shared J EngreitziD· 2 shared Salil DeshpandeiD· 2 shared Soumya KunduiD· 2 shared Stephen B. MontgomeryiD· 2 shared Alexandr BoytsoviD· 1 shared Alkes L. PriceiD· 1 shared Anca M. PașcaiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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3 shared papersGenetics

Anshul Bharat KundajeORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintOct 15, 2025

Decoding Chromatin Dynamics in Cardiac Organoids Reveals Genetic Drivers of Human Heart Development and Disease

Eyal Metzl-Raz, Ryan Zhao, Salil Deshpande…·Casey A. Gifford

The paper uses a single-cell multi-omic atlas and deep learning to identify cis-regulatory elements and genetic drivers of heart development and disease.

4 citations

humanscRNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineCellPeer-reviewedMar 5, 2025

CXCL12 drives natural variation in coronary artery anatomy in diverse populations

Pamela E. Rios Coronado, Jiayan Zhou, Xiaochen Fan…·Themistocles L. Assimes

The paper identifies CXCL12 as a genetic driver of coronary artery anatomy variation through GWAS and mouse models, showing its role in fetal coronary development.

15 citationstop 1%

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsbioRxivPreprintNov 7, 2024

A consensus variant-to-function score to functionally prioritize variants for disease

Tabassum Fabiha, Ivy Evergreen, Soumya Kundu…·Kushal K. Dey

This paper introduces a consensus variant-to-function score to prioritize disease-causing variants, showing improved performance in heritability enrichment and fine-mapping.

10 citations

humanwhole-genome sequencing

𝕏 PostBluesky