Author

Jessica R. Hopkinson

University of ExeterORCID 0000-0001-7870-265XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Andrew Tym HattersleyiD· 2 shared Jasmin J. BennettiD· 2 shared Jayne HoughtoniD· 2 shared Kristen A. NevilleiD· 2 shared Matthew B. JohnsoniD· 2 shared Matthew Neil WakelingiD· 2 shared Nick D. L. OwensiD· 2 shared Sarah Elizabeth FlanaganiD· 2 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew Tym HattersleyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 18, 2025

A 94-bp Deletion in the Promoter of the Beta-Cell Disallowed gene SLC16A1 causing Adult-onset Hyperinsulinism

Jasmin J. Bennett, Hazem Ibrahim, Jonna M. E. Männistö…·Sarah Elizabeth Flanagan

This study identifies a 94-bp deletion in the SLC16A1 promoter causing hyperinsulinism by increasing MCT1 expression and triggering inappropriate insulin secretion during physical activity.

DOI 10.64898/2025.12.16.25342131

humanexperimental assay

𝕏 PostBluesky

Genetic & Genomic MedicineNature GeneticsPeer-reviewedNov 1, 2022

A novel disease mechanism leading to the expression of a disallowed gene in the pancreatic beta-cell identified by non-coding, regulatory mutations controlling HK1

Matthew Neil Wakeling, Nick D. L. Owens, Jessica R. Hopkinson…·Sarah Elizabeth Flanagan

The paper identifies non-coding mutations in a regulatory element of HK1 that lead to inappropriate expression in pancreatic beta-cells and cause congenital hyperinsulinism.

66 citationstop 1%

humanbulk RNA-seq

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