Author

Dale Bryant

University College LondonORCID 0000-0002-4783-4796Unclaimed 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· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Dagan JenkinsiD· 2 shared Gudrun E. MooreiD· 2 shared Philip StanieriD· 2 shared Aguilera Paula· 1 shared Alan Michael PittmaniD· 1 shared Anna C. ThomasiD· 1 shared Catherine A HarwoodiD· 1 shared Charalambos DemetriouiD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Dagan JenkinsORCID

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2 papers

Recent·Most cited

Inherited duplications of PPP2R3B promote naevi and melanoma via a novel C21orf91-driven proliferative phenotype

Satyamaanasa Polubothu, Lara Al-Olabi, Daniël A. Lionarons, Mark Harland, Anna C. Thomas, Stuart D. Horswell, Lilian Hunt, Nathan Wlodarchak, Aguilera Paula, Sarah Brand, Dale Bryant, Philip L. Beales, Cristina Carrera, Hui Chen, Greg S Elgar, , Veronica A. Kinsler

This study identifies inherited PPP2R3B duplications as a melanoma predisposing factor, revealing a C21orf91-driven proliferative phenotype in melanocytes.

Genetics in Medicine · Jun 18, 2021Peer-reviewedGenomics

Diverse Species-Specific Phenotypic Consequences of Loss of Function Sorting Nexin 14 Mutations

Dale Bryant, Marian Seda, Emma Peskett, Constance Maurer, Gideon Pomeranz, Marcus Ghosh, Thomas A. Hawkins, James Cleak, Sanchari Datta, Hanaa H. Hariri, Kaitlyn M. Eckert, Daniyal J. Jafree, Claire Walsh, Charalambos Demetriou, Miho Ishida, , Philip Stanier

This study examines the phenotypic effects of SNX14 loss-of-function mutations in mice and zebrafish, revealing species-specific consequences despite conserved biochemical roles.

Scientific Reports · Aug 13, 2020Peer-reviewedDevelopmental Biology