Author

Gavin S. McNee

University of BirminghamORCID 0000-0003-4504-0404Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:spatial domain detection· 1 Approach:statistical model· 1

Frequent Co-Authors

Grant S. StewartiD· 2 shared Abolfazl RadiD· 1 shared Agnese LodaiD· 1 shared Amélie PitoniD· 1 shared Andrew P. JacksoniD· 1 shared Bader AlhaddadiD· 1 shared Benjamin CognéiD· 1 shared Bertrand IsidoriD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Grant S. StewartORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 20, 2025

CIZ1-LOSS CAUSES FEMALE-SPECIFIC AUTOSOMAL NEURODEVELOPMENTAL DISORDER THROUGH DEFECTIVE X-INACTIVATION MAINTENANCE

Thomas Besnard, Agnese Loda, Emma Kneuss…·Bertrand Isidor

The paper identifies a female-specific neurodevelopmental disorder caused by biallelic CIZ1 loss-of-function variants, which disrupt X-chromosome inactivation maintenance.

1 citation

humanexperimental assay

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Molecular BiologyNature CommunicationsPeer-reviewedAug 7, 2020

DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain

Jing Zhang, Marina A. Bellani, Ryan C. James…·Michael M. Seidman

The paper identifies two distinct replisomes, one associated with DONSON in early S phase and euchromatin, and another with FANCM in late S phase and heterochromatin.

42 citations

humanChIP-seq

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