Author

Adam T. Higgins

Observed names: Adam T. Higgins, Adam T Higgins, Higgins, Adam T.

Institution: Swansea University

Observed institutions: Swansea University, Cardiff University

ORCID: 0000-0002-2906-8151

Observed ORCID: 0000-0002-2906-8151

OpenAlex ID: A5088784607

Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy

2020 · Andrew E. Fry, Christopher Marra, et al. · The American Journal of Human Genetics · 43

Enhanced bacterial cancer therapy delivering therapeutic RNA interference of c-Myc

2024 · Jason S. Williams, Adam T. Higgins, et al. · Cell & Bioscience · 9

Modification of Diet to Reduce the Stemness and Tumorigenicity of Murine and Human Intestinal Cells

2022 · Stephanie May, Kirsty R. Greenow, et al. · Molecular Nutrition & Food Research · 6

Multiple and novel molecular mechanisms in TUBA1A-related tubulinopathy: insights from deep clinical and neuroradiological phenotyping.

2025 · James Fasham, Rucha Pandit, et al. · medRxiv · 2

Conditional in vivo deletion of LYN kinase has little effect on a BRCA1 loss-of-function-associated mammary tumour model

2023 · Giusy Tornillo, Lauren Warrington, et al. · Disease Models & Mechanisms · 2

Back Cover: Modification of Diet to Reduce the Stemness and Tumorigenicity of Murine and Human Intestinal Cells

2022 · Stephanie May, Kirsty R. Greenow, et al. · Molecular Nutrition & Food Research · 1

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

2026 · Adam T. Higgins, Fiona Wang, et al. · Neurobiology of Disease

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

2025 · Adam T Higgins, Fiona Wang, et al. · medRxiv

Pathogenic ultra-rare variants in SLC6A1, SLC6A11, GAD1 and GAD2 are new & recurrent GABAergic loci for GGE syndromes

2025 · Seo-Kyung Chung, Kate V. Everett, et al. · medRxiv

Pathogenic Ultra-Rare Variants in SLC6A1, SLC6A11, GAD1 and GAD2 are New & Recurrent GABAergic Loci for Genetic Generalised Epilepsy

2025 · Seo-Kyung Chung, Kate V. Everett, et al. · SSRN Electronic Journal

Conditional in vivo deletion of LYN kinase has little effect on a BRCA1 loss-of-function-associated mammary tumour model

2023 · Giusy Tornillo, Lauren Warrington, et al. · bioRxiv (Cold Spring Harbor Laboratory)

Analysis of Potential mRNA Splice-Affecting Gene Variants Identified in Epilepsy Families and Cases

2018 · Adam T Higgins

Works count: 14

Citation count: 63

H-index: 3

I10-index: 1