Hannah L. Macpherson

Queen Square Institute Of Neurology
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association study.

Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association study.

Journal: medRxiv : the preprint server for health sciences

Published: January 02, 2026

ORFannotate: reproducible coding sequence annotation of transcriptome assemblies.

ORFannotate: reproducible coding sequence annotation of transcriptome assemblies.

Journal: Bioinformatics (Oxford, England)

Published: August 12, 2025

Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy.

Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapy.

Journal: Nature medicine

Published: January 07, 2025

FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?

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.

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

The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1.

The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1.

Journal: Science advances

Published: June 26, 2024

Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022).

Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022).

Journal: Acta neuropathologica communications

Published: November 20, 2023

Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.

Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: November 03, 2023

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study.

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study.

Journal: The Lancet. Neurology

Published: July 04, 2023

Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.

Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.

Journal: medRxiv : the preprint server for health sciences

Published: May 10, 2023

Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis.

Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis.

Journal: Brain : a journal of neurology

Published: March 27, 2023

Genomic investigations of unexplained acute hepatitis in children.

Genomic investigations of unexplained acute hepatitis in children.

Journal: Nature

Published: July 25, 2022

Showing 1-12 of 16

Last Updated: 09/26/2026