Author

Nicholas J. Murray

Victor Chang Cardiac Research Institute

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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Developmental Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Assay:imaging· 1 Organism:mouse· 1

Frequent Co-Authors

Richard Paul HarveyiD· 2 shared Alex J. McCanniD· 1 shared Alexander O. WardiD· 1 shared Anai Gonzalez-CorderoiD· 1 shared Chris G. ThekkedamiD· 1 shared Dimuthu AlankarageiD· 1 shared Frédéric A. MeunieriD· 1 shared Fujian WuiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersDevelopmental Biology

Richard Paul HarveyORCID

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2 papers

Recent·Most cited

OpenEMMU: a versatile, open-source EdU multiplexing methodology for studying DNA replication and cell cycle dynamics

Osvaldo Contreras, Chris G. Thekkedam, John James Zaunders, Ismael Aguirre-MacLennan, Nicholas J. Murray, Anai Gonzalez-Cordero, Richard Paul Harvey

OpenEMMU improves EdU staining efficiency, brightness, and multiplexing for DNA replication and cell cycle analysis using affordable, open-source reagents.

iScience · Aug 18, 2025Peer-reviewedDevelopmental Biology

NKX2-5 congenital heart disease mutations show diverse loss and gain of epigenomic, biochemical and chromatin search functions underpinning pathogenicity

Alexander O. Ward, Nicole Schönrock, Alex J. McCann, Sabrina K. Phanor, Kian Hong Kock, Jesse V. Kurland, Fujian Wu, Nicholas J. Murray, James L. Walshe, Dimuthu Alankarage, Sally L. Dunwoodie, Frédéric A. Meunier, Mathias François, Martha L. Bulyk, Mirana Ramialison, Richard Paul Harvey

The paper investigates NKX2-5 mutations in congenital heart disease by analyzing their epigenomic, biochemical, and chromatin search functions in cardiomyocytes, revealing diverse loss and gain-of-function defects.

bioRxiv · Jun 20, 2025 · PreprintGenomics