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Hannah Macpherson

Showing results (1-10 of 9) with videos related to

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Bioinformatics (Oxford, England)|February 17, 2026
ORFannotate: reproducible coding sequence annotation of transcriptome assembliesSonia García-Ruiz, Hannah Macpherson, Laura Caton, et al.
Brain : a Journal of Neurology|May 16, 2025
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?Joshua Laß, Mirja Thomsen, Max Borsche, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2024
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderZhongbo Chen, Pilar Alvarez Jerez, Claire Anderson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 10, 2024
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4Zhongbo Chen, Emil K Gustavsson, Hannah Macpherson, et al.
Nature Medicine|January 16, 2026
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapySarah Buddle, Li-An K Brown, Sofia Morfopoulou, et al.
Acta Neuropathologica Communications|January 3, 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)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, et al.
Science Advances|June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
Brain : a Journal of Neurology|July 14, 2023
Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosisNatalia Dominik, Stefania Magri, Riccardo Currò, et al.
Nature|March 30, 2023
Genomic investigations of unexplained acute hepatitis in childrenSofia Morfopoulou, Sarah Buddle, Oscar Enrique Torres Montaguth, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|February 17, 2026
ORFannotate: reproducible coding sequence annotation of transcriptome assembliesSonia García-Ruiz, Hannah Macpherson, Laura Caton, et al.
Brain : a Journal of Neurology|May 16, 2025
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?Joshua Laß, Mirja Thomsen, Max Borsche, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2024
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderZhongbo Chen, Pilar Alvarez Jerez, Claire Anderson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 10, 2024
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4Zhongbo Chen, Emil K Gustavsson, Hannah Macpherson, et al.
Nature Medicine|January 16, 2026
Contaminating plasmid sequences and disrupted vector genomes in the liver following adeno-associated virus gene therapySarah Buddle, Li-An K Brown, Sofia Morfopoulou, et al.
Acta Neuropathologica Communications|January 3, 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)Huihui Luo, Emil K Gustavsson, Hannah Macpherson, et al.
Science Advances|June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
Brain : a Journal of Neurology|July 14, 2023
Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosisNatalia Dominik, Stefania Magri, Riccardo Currò, et al.
Nature|March 30, 2023
Genomic investigations of unexplained acute hepatitis in childrenSofia Morfopoulou, Sarah Buddle, Oscar Enrique Torres Montaguth, et al.
Pageof 1