Author

Natasha Y. Frank

Brigham and Women's HospitalORCID 0000-0001-8196-0449Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aaron J. GoldmaniD· 1 shared Ágnes Tóth-PetróczyiD· 1 shared Alexis H. BennettiD· 1 shared Basil T. DarrasiD· 1 shared Brigham Genomic Medicine· 1 shared Claire A GrosgogeatiD· 1 shared Elicia A. EstrellaiD· 1 shared Gabriel Gonzalez· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperCancer Biology

Aaron J. GoldmanORCID

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2 papers

Recent·Most cited

Cancer BiologyWorld Journal of GastroenterologyPeer-reviewedApr 3, 2026

Optimal Cannabinoid-Terpene Combination Ratios Suppress Mutagenicity of Gastric Reflux in Normal and Metaplastic Esophageal Cells

Aaron J. Goldman, Gabriel Gonzalez, Svetlana A. Karpova…·Natasha Y. Frank

The paper identifies an optimal cannabinoid-terpene ratio that reduces DCA-induced DNA damage and mutagenicity in esophageal cells and correlates ECS receptor expression with EAC progression.

DOI 10.3748/wjg.v32.i14.111455

humanbulk RNA-seq

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GeneticsNeurology GeneticsPeer-reviewedMar 7, 2019

Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis

J. Velilla, Michael Mario Marchetti, Ágnes Tóth-Petróczy…·Vandana Gupta

This study identifies a homozygous TRPV4 mutation as a cause of congenital spinal muscular atrophy and arthrogryposis through whole exome sequencing and functional analysis.

25 citations

humanwhole-exome sequencing

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