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| 36764301 | Large-scale differentiation of iPSC-derived motor neurons from ALS and control subjects. | Neuron | 2023 |
| 36712069 | Frontotemporal Dementia Patient Neurons With Progranulin Deficiency Display Protein Dyshomeostasis. | bioRxiv | 2023 |
| 36764301 | Large-scale differentiation of iPSC-derived motor neurons from ALS and control subjects. | Neuron | 2023 |
| 36950378 | The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism. | Cell Genom | 2023 |
| 36603024 | Nuclear accumulation of host transcripts during Zika Virus Infection. | PLoS Pathog | 2023 |
| 36950378 | The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism. | Cell Genom | 2023 |
| 36712069 | Frontotemporal Dementia Patient Neurons With Progranulin Deficiency Display Protein Dyshomeostasis. | bioRxiv | 2023 |
| 36603024 | Nuclear accumulation of host transcripts during Zika Virus Infection. | PLoS Pathog | 2023 |
| 35266954 | The E3 ligase TRIM1 ubiquitinates LRRK2 and controls its localization, degradation, and toxicity. | J Cell Biol | 2022 |
| 36093369 | Fluorescently labeled nuclear morphology is highly informative of neurotoxicity. | Front Toxicol | 2022 |
| 35378365 | Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson's disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004). | Stem Cell Res | 2022 |
| 35865413 | Huntington's disease iPSC models-using human patient cells to understand the pathology caused by expanded CAG repeats. | Fac Rev | 2022 |
| 34981791 | Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. | J Clin Invest | 2022 |
| 35266954 | The E3 ligase TRIM1 ubiquitinates LRRK2 and controls its localization, degradation, and toxicity. | J Cell Biol | 2022 |
| 35115730 | Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines. | Nat Neurosci | 2022 |
| 35378365 | Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson's disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004). | Stem Cell Res | 2022 |
| 35865413 | Huntington's disease iPSC models-using human patient cells to understand the pathology caused by expanded CAG repeats. | Fac Rev | 2022 |
| 36093369 | Fluorescently labeled nuclear morphology is highly informative of neurotoxicity. | Front Toxicol | 2022 |
| 34981791 | Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. | J Clin Invest | 2022 |
| 35115730 | Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines. | Nat Neurosci | 2022 |
| 34362731 | Longitudinal tracking of neuronal mitochondria delineates PINK1/Parkin-dependent mechanisms of mitochondrial recycling and degradation. | Sci Adv | 2021 |
| 33792567 | ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects. | J Clin Invest | 2021 |
| 34746930 | Huntington's disease mouse models: unraveling the pathology caused by CAG repeat expansion. | Fac Rev | 2021 |
| 34626895 | Transcriptional signatures in iPSC-derived neurons are reproducible across labs when differentiation protocols are closely matched. | Stem Cell Res | 2021 |
| 34736041 | Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson's patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006). | Stem Cell Res | 2021 |
| 34496257 | Persistent mRNA localization defects and cell death in ALS neurons caused by transient cellular stress. | Cell Rep | 2021 |
| 34489414 | Genetically encoded cell-death indicators (GEDI) to detect an early irreversible commitment to neurodegeneration. | Nat Commun | 2021 |
| 34826737 | Generation of two human induced pluripotent stem cell lines (iPSCs) with mutations of the α-synuclein (SNCA) gene associated with Parkinson's disease; the A53T mutation (LCSBi003) and a triplication of the SNCA gene (LCSBi007). | Stem Cell Res | 2021 |
| 34878844 | Superhuman cell death detection with biomarker-optimized neural networks. | Sci Adv | 2021 |
| 34362731 | Longitudinal tracking of neuronal mitochondria delineates PINK1/Parkin-dependent mechanisms of mitochondrial recycling and degradation. | Sci Adv | 2021 |
| 33792567 | ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects. | J Clin Invest | 2021 |
| 34878844 | Superhuman cell death detection with biomarker-optimized neural networks. | Sci Adv | 2021 |
| 34736041 | Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson's patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006). | Stem Cell Res | 2021 |
| 34496257 | Persistent mRNA localization defects and cell death in ALS neurons caused by transient cellular stress. | Cell Rep | 2021 |
| 34489414 | Genetically encoded cell-death indicators (GEDI) to detect an early irreversible commitment to neurodegeneration. | Nat Commun | 2021 |
| 34746930 | Huntington's disease mouse models: unraveling the pathology caused by CAG repeat expansion. | Fac Rev | 2021 |
| 34626895 | Transcriptional signatures in iPSC-derived neurons are reproducible across labs when differentiation protocols are closely matched. | Stem Cell Res | 2021 |
| 34826737 | Generation of two human induced pluripotent stem cell lines (iPSCs) with mutations of the α-synuclein (SNCA) gene associated with Parkinson's disease; the A53T mutation (LCSBi003) and a triplication of the SNCA gene (LCSBi007). | Stem Cell Res | 2021 |
| 30936119 | The Autophagy Lysosomal Pathway and Neurodegeneration. | Cold Spring Harb Perspect Biol | 2020 |
| 32081961 | Author Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington's disease. | Nat Commun | 2020 |
| 31962288 | Approaches to develop therapeutics to treat frontotemporal dementia. | Neuropharmacology | 2020 |
| 32382035 | Publisher Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington's disease. | Nat Commun | 2020 |
| 32977020 | Functional genomics, genetic risk profiling and cell phenotypes in neurodegenerative disease. | Neurobiol Dis | 2020 |
| 30936119 | The Autophagy Lysosomal Pathway and Neurodegeneration. | Cold Spring Harb Perspect Biol | 2020 |
| 32081961 | Author Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington's disease. | Nat Commun | 2020 |
| 31962288 | Approaches to develop therapeutics to treat frontotemporal dementia. | Neuropharmacology | 2020 |
| 32977020 | Functional genomics, genetic risk profiling and cell phenotypes in neurodegenerative disease. | Neurobiol Dis | 2020 |
| 32382035 | Publisher Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington's disease. | Nat Commun | 2020 |
| 30696728 | Genetic Regulation of Neuronal Progranulin Reveals a Critical Role for the Autophagy-Lysosome Pathway. | J Neurosci | 2019 |
| 31179783 | Cell death assays for neurodegenerative disease drug discovery. | Expert Opin Drug Discov | 2019 |