Author

Ronan Challinge

Memorial Sloan Kettering Cancer Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genomics· 1

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:spatial transcriptomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

Agnel J. SfeiriD· 1 shared Alexander van OudenaardeniD· 1 shared Amir GiladiiD· 1 shared Chih-Yao ChungiD· 1 shared Craig B. ThompsoniD· 1 shared Ed ReznikiD· 1 shared Emily DeBitetto· 1 shared Josephine AdamsiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Agnel J. SfeirORCID

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1 paper

Recent·Most cited

Random mtDNA mutagenesis maps genotype-phenotype associations across metabolic contexts and lineages

Amir Giladi, Ron Baik, Chih-Yao Chung, Minsoo Kim, Josephine Adams, Rahul Saha, Max Land, Ruobing Cui, Emily DeBitetto, Megan E. Kelley, Craig B. Thompson, Ed Reznik, Roshan Sharma, Ronan Challinge, R. Stefan Isaac, , Agnel J. Sfeir

The paper introduces mtDIVE, a random mtDNA mutagenesis platform, to study genotype-phenotype associations in metabolic contexts and lineages, revealing lineage-specific effects and mutation-specific impacts.

bioRxiv · Oct 9, 2026 · PreprintGenomics