Emil K. Gustavsson
UCL Queen Square Institute Of Neurology
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 51 publications
Population-scale interpretation of RNA isoform diversity enabled by Isopedia.
Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026
ORFannotate: reproducible coding sequence annotation of transcriptome assemblies.
Journal: Bioinformatics (Oxford, England)
Published: August 12, 2025
Astrocytic RNA editing regulates the host immune response to alpha-synuclein.
Journal: Science advances
Published: April 11, 2025
PSQAN: a pipeline to prioritize novel and biologically relevant transcripts from long-read RNA sequencing.
Journal: Bioinformatics advances
Published: April 03, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1.
Journal: medRxiv : the preprint server for health sciences
Published: January 13, 2025
Ancestry-specific gene expression in peripheral monocytes mediates risk of neurodegenerative disease.
Journal: bioRxiv : the preprint server for biology
Published: January 13, 2025
RNApysoforms: fast rendering interactive visualization of RNA isoform structure and expression in Python.
Journal: Bioinformatics advances
Published: December 11, 2024
RNApysoforms: Fast rendering interactive visualization of RNA isoform structure and expression in Python.
Journal: bioRxiv : the preprint server for biology
Published: November 22, 2024
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.
Journal: Brain : a journal of neurology
Published: November 20, 2024
Editorial on: Confirmation of RAB32 Ser71Arg involvement in Parkinson's disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 19, 2024
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?
Journal: Brain : a journal of neurology
Published: November 13, 2024
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 07, 2024
Last Updated: 09/26/2026