Author

George C Murray

Jackson Laboratory

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

Biology Disciplines

Click to filter author papers

Genetics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Robert W. BurgessiD· 2 shared Abby LD Tadenev· 1 shared Abigail L. D. TadeneviD· 1 shared Belinda S. HarrisiD· 1 shared Chew Yee NganiD· 1 shared Courtany Hanley· 1 shared Harianto TjongiD· 1 shared Isaac R. L. XuiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Robert W. BurgessORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Testing SIPA1L2 as a modifier of CMT1A using mouse models

George C Murray, Timothy J. Hines, Abigail L. D. Tadenev, Isaac R. L. Xu, Stephan L. Zuchner, Robert W. Burgess

The paper tests SIPA1L2 as a modifier of CMT1A using mouse models and identifies some genetic interactions but finds a small overall effect on neuropathy.

Journal of Neuropathology & Experimental Neurology · Feb 20, 2024Peer-reviewedGenetics

An allelic series of spontaneous mutations in Rorb cause a gait phenotype, retinal abnormalities, and transcriptomic changes relevant to human neurodevelopmental conditions

George C Murray, Jason A. Bubier, Oraya J. Zinder, Belinda S. Harris, James Clark, Mia-Cara Christopher, Courtany Hanley, Harianto Tjong, Meihong Li, Chew Yee Ngan, Laura G. Reinholdt, Robert W. Burgess, Abby LD Tadenev

The paper describes five Rorb mutant mouse strains with gait and retinal abnormalities, showing transcriptomic changes linked to neurodevelopmental disorders.

bioRxiv · Nov 23, 2021 · PreprintGenetics