Author

Engela Magdalena Honey

University of PretoriaORCID 0000-0002-4587-2844Unclaimed 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 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1

Frequent Co-Authors

Aimé Zola LumakaiD· 1 shared Amanda KrauseiD· 1 shared Ana Tangari Saredo· 1 shared Barry ShingwenyanaiD· 1 shared Benjamin Bunce· 1 shared Daphne YauiD· 1 shared Dinesh GiriiD· 1 shared Gerrye Lumbono MubunguiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aimé Zola LumakaORCID

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2 papers

Recent·Most cited

Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders, the DDD-Africa study

Nadja Louw, Prince Bamba Makay, Phelelani Thokozani Mpangase, Barry Shingwenyana, Zandisiwe Goliath, Thirona Naicker, Laura M. Yates, Engela Magdalena Honey, Gerrye Lumbono Mubungu, Kris Van Den Bogaert, Helen V. Firth, Matthew E. Hurles, Prosper Lukusa-Tshilobo, Koenraad Devriendt, Amanda Krause, , Zané Lombard

The paper demonstrates that integrating CNV detection into exome sequencing analysis improves diagnostic yield for developmental disorders in the DDD-Africa cohort by 8.3% without additional costs.

European Journal of Human Genetics · Jul 9, 2026Peer-reviewedGenetic & Genomic Medicine

Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the likely disruption of FOXA2

Thomas William Laver, Matthew Neil Wakeling, Richard C. Caswell, Benjamin Bunce, Daphne Yau, Jonna M. E. Männistö, Jayne Houghton, Jasmin J. Hopkins, Michael N. Weedon, Vrinda Saraff, Melanie Kershaw, Engela Magdalena Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, , Sarah Elizabeth Flanagan

The paper identifies chromosome 20p11.2 deletions as a cause of congenital hyperinsulinism by disrupting FOXA2 expression in pancreatic beta-cells.

European Journal of Human Genetics · Apr 11, 2024Peer-reviewedGenetic & Genomic Medicine