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TDP-43 is intercellularly transmitted across axon terminals

The Journal of cell biology, 2015-11, Vol.211 (4), p.897-911

2015

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Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation

Nature communications, 2018-01, Vol.9 (1), p.335-17, Article 335

2018

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Downstream Effects of Mutations in SOD1 and TARDBP Converge on Gene Expression Impairment in Patient-Derived Motor Neurons

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9652

2022

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De novo mutations in SOD1 are a cause of ALS

Journal of neurology, neurosurgery and psychiatry, 2022-02, Vol.93 (2), p.201-206

2022

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Peripheral monocytes are functionally altered and invade the CNS in ALS patients

Acta neuropathologica, 2016-09, Vol.132 (3), p.391-411

2016

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Retinoic acid worsens ATG10-dependent autophagy impairment in TBK1-mutant hiPSC-derived motoneurons through SQSTM1/p62 accumulation

Autophagy, 2019-10, Vol.15 (10), p.1719-1737

2019

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Update on genetics of amyotrophic lateral sclerosis

Current opinion in neurology, 2022-10, Vol.35 (5), p.672-677

2022

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Heterozygous Tbk1 loss has opposing effects in early and late stages of ALS in mice

The Journal of experimental medicine, 2019-02, Vol.216 (2), p.267-278

2019

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Restoring expression of Stathmin-2: a novel strategy to treat TDP-43 proteinopathies

Signal transduction and targeted therapy, 2023-07, Vol.8 (1), p.266-266, Article 266

2023

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Nature communications, 2023-01, Vol.14 (1), p.342-342, Article 342

2023

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Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Acta neuropathologica communications, 2013-07, Vol.1 (1), p.42-42, Article 42

2013

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Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Nature communications, 2023-12, Vol.14 (1), p.8026-8026, Article 8026

2023

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CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency

Human molecular genetics, 2018-02, Vol.27 (4), p.706-715

2018

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FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees

Neurogenetics, 2022-01, Vol.23 (1), p.59-65

2022

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Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activity

Frontiers in neuroscience, 2020-09, Vol.14, p.551006-551006

2020

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A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations

Translational neurodegeneration, 2021-10, Vol.10 (1), p.42-3, Article 42

2021

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Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease Serum

Cells (Basel, Switzerland), 2021-04, Vol.10 (4), p.791

2021

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Cryptic exon inclusion in TDP-43 proteinopathies: opportunities and challenges

Neural regeneration research, 2025-07, Vol.20 (7), p.2003-2004

2025

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An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neurons

Human molecular genetics, 2024-07, Vol.33 (15), p.1300-1314

2024

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Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

JAMA neurology, 2017-01, Vol.74 (1), p.110

2017

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The Fragile X Protein Family in Amyotrophic Lateral Sclerosis

Molecular neurobiology, 2023-07, Vol.60 (7), p.3898-3910

2023

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Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes

Acta neuropathologica, 2016-03, Vol.131 (3), p.379-391

2016

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Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43 transgenic mice

Experimental neurology, 2021-01, Vol.335, p.113496, Article 113496

2021

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TDP-43 is intercellularly transmitted across axon terminals

Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation

Downstream Effects of Mutations in SOD1 and TARDBP Converge on Gene Expression Impairment in Patient-Derived Motor Neurons

De novo mutations in SOD1 are a cause of ALS

Peripheral monocytes are functionally altered and invade the CNS in ALS patients

Retinoic acid worsens ATG10-dependent autophagy impairment in TBK1-mutant hiPSC-derived motoneurons through SQSTM1/p62 accumulation

Update on genetics of amyotrophic lateral sclerosis

Heterozygous Tbk1 loss has opposing effects in early and late stages of ALS in mice

Restoring expression of Stathmin-2: a novel strategy to treat TDP-43 proteinopathies

Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency

FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees

Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activity

A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations

Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease Serum

Cryptic exon inclusion in TDP-43 proteinopathies: opportunities and challenges

An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neurons

Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

The Fragile X Protein Family in Amyotrophic Lateral Sclerosis

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes

Hot-spot KIF5A mutations cause familial ALS

Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43 transgenic mice

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