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K Gustavsson

Showing results (61-70 of 83) with videos related to

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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.
Parkinsonism & Related Disorders|May 3, 2016
DCTN1 p.K56R in progressive supranuclear palsyEmil K Gustavsson, Joanne Trinh, Ilaria Guella, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2023
Splicing accuracy varies across human introns, tissues and ageS García-Ruiz, D Zhang, E K Gustavsson, et al.
Nature Communications|January 27, 2025
Splicing accuracy varies across human introns, tissues, age and diseaseS García-Ruiz, D Zhang, E K Gustavsson, et al.
Brain : a Journal of Neurology|January 9, 2023
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxiaZhongbo Chen, Arianna Tucci, Valentina Cipriani, 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.
European Journal of Neurology|November 21, 2020
Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathiesZhongbo Chen, Reza Maroofian, A Nazlı Başak, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
Neurobiology of Disease|March 16, 2023
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseasesZhongbo Chen, Regina H Reynolds, Antonio F Pardiñas, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
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.
Parkinsonism & Related Disorders|May 3, 2016
DCTN1 p.K56R in progressive supranuclear palsyEmil K Gustavsson, Joanne Trinh, Ilaria Guella, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2023
Splicing accuracy varies across human introns, tissues and ageS García-Ruiz, D Zhang, E K Gustavsson, et al.
Nature Communications|January 27, 2025
Splicing accuracy varies across human introns, tissues, age and diseaseS García-Ruiz, D Zhang, E K Gustavsson, et al.
Brain : a Journal of Neurology|January 9, 2023
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxiaZhongbo Chen, Arianna Tucci, Valentina Cipriani, 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.
European Journal of Neurology|November 21, 2020
Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathiesZhongbo Chen, Reza Maroofian, A Nazlı Başak, et al.
The Lancet. Neurology|October 4, 2016
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association studyJoanne Trinh, Emil K Gustavsson, Carles Vilariño-Güell, et al.
Neurobiology of Disease|March 16, 2023
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseasesZhongbo Chen, Regina H Reynolds, Antonio F Pardiñas, et al.
Pageof 9