Author

Martín F. Pera

Jackson LaboratoryORCID 0000-0001-6239-0428Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:mouse· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Research Focus:benchmarking· 1 Approach:diffusion model· 1

Frequent Co-Authors

Laura G. ReinholdtiD· 2 shared Selcan C. AydiniD· 2 shared Steven C. MungeriD· 2 shared Agnieszka D’Antonio‐ChronowskaiD· 1 shared Alexander R. StantoniD· 1 shared Alyssa EdwardsiD· 1 shared André Ducati LuchessiiD· 1 shared Angelo D. Arias· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenetics

Laura G. ReinholdtORCID

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3 papers

Recent·Most cited

GeneticsStem Cell ReportsPeer-reviewedJun 9, 2026

Chromosome X Dosage Modulates Development of Aneuploidy in Genetically Diverse Mouse Embryonic Stem Cells

Alexander R. Stanton, Selcan C. Aydin, Daniel A. Skelly…·Martín F. Pera

The paper identifies that X chromosome dosage influences aneuploidy development in mouse embryonic stem cells, with XO and XY lines showing higher aneuploidy rates than XX lines.

2 citations

mousebulk RNA-seq

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GenomicsNature CommunicationsPeer-reviewedFeb 23, 2024

Analysis of regulatory network modules in hundreds of human stem cell lines reveals complex epigenetic and genetic factors contribute to pluripotency state differences between subpopulations

Timothy D. Arthur, Jennifer Nguyen, Agnieszka D’Antonio‐Chronowska…·Kelly A. Frazer

The paper identifies regulatory network modules in human stem cells, showing epigenetic and genetic factors influence pluripotency state differences.

30 citationstop 4%

humanATAC-seq

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NeurosciencebioRxivPreprintJan 21, 2022

An in vitro neurogenetics platform for precision disease modeling in the mouse

Daniel Cortés, Mélanie Escudero, Austin C. Korgan…·Martín F. Pera

This paper develops a cross-species platform to model human disease using genetically diverse mouse and human stem cells, showing that DYRK1A loss of function effects vary with genetic background.

DOI 10.1101/2022.01.21.477242

mousebulk RNA-seq

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