Author

Jeya Natarajan

Royal Glamorgan Hospital

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

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Adam T. HigginsiD· 1 shared Ann J. Johnston· 1 shared Fiona Wang· 1 shared Johann te Water Naudé· 1 shared Khalid HamandiiD· 1 shared Mark I. ReesiD· 1 shared Mary ChebibiD· 1 shared Phil E M SmithiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam T. HigginsORCID

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1 paper

Recent·Most cited

A synonymous SLC2A1 variant causes familial epilepsy and paroxysmal exercise-induced dyskinesia by creating aberrant mosaic splicing patterns

Adam T. Higgins, Fiona Wang, William Owen Pickrell, Ann J. Johnston, Jeya Natarajan, Khalid Hamandi, Johann te Water Naudé, Mary Chebib, Mark I. Rees, Phil E M Smith, Seo‐Kyung Chung

This paper identifies a synonymous SLC2A1 variant causing GLUT1-DS through mosaic splicing, leading to variable haploinsufficiency and phenotypic diversity.

medRxiv · Apr 5, 2025 · PreprintGenetic & Genomic Medicine