Jonasz Jeremiasz Weber
11PUBLICATIONS
87CO-AUTHORS
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Publications (11)
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|Feb 25, 2026
The DNA/RNA autophagy protein SIDT2 as a novel neuropathological hallmark in Huntington disease.Sanaz Gabery, Sofia Bergh, Chrisovalantou Huridou
|Feb 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.Benita Menden, Rana D Incebacak Eltemur, German Demidov
|Aug 01, 2024
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy.Jonasz J Weber, Leah Czisch, Priscila Pereira Sena
|Dec 11, 2022
Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease Animals.Libo Yu-Taeger, Arianna Novati, Jonasz Jeremiasz Weber
|Jul 06, 2022
KPNB1 modulates the Machado-Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP.Mahkameh Abeditashi, Jonasz Jeremiasz Weber, Priscila Pereira Sena
|Jun 10, 2022
Mitochondrial Dysfunction in Spinocerebellar Ataxia Type 3 Is Linked to VDAC1 Deubiquitination.Tina Harmuth, Jonasz J Weber, Anna J Zimmer
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Frequent Collaborators
7 joint publications
Priscila Pereira Sena
5 joint publications
Huu Phuc Nguyen
5 joint publications
Olaf Riess
4 joint publications
Chrisovalantou Huridou
4 joint publications
Rana Dilara Incebacak Eltemur
4 joint publications
Jeannette Hübener-Schmid
3 joint publications
Thorsten Schmidt
2 joint publications
Elisabeth Singer-Mikosch
2 joint publications
Florian Fath
2 joint publications
Stefan Hauser
