Author

Charlotte M. Fare

University of PennsylvaniaORCID 0000-0003-0394-6435Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cell-cell communication· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:mouse· 1 Assay:protein structure· 1

Frequent Co-Authors

Alice Flynn Ford· 2 shared Hong Joo KimiD· 2 shared J. Paul TayloriD· 2 shared James ShorteriD· 2 shared Lin E. GuoiD· 2 shared Adnan Yousaf Manzur· 1 shared Aileen Reghan FoleyiD· 1 shared Aki Sato· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alice Flynn Ford

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3 papers

Recent·Most cited

NeuroscienceActa Neuropathologica CommunicationsPeer-reviewedAug 9, 2025

Divergent and Convergent TMEM106B Pathology in Murine Models of Neurodegeneration and Human Disease

Muzi Du, Suleyman C. Akerman, Charlotte M. Fare…·Jeffrey D. Rothstein

The paper compares TMEM106B pathology in murine models of neurodegenerative diseases to human postmortem tissue, identifying differences and convergent links to TDP-43 and Tau pathology.

4 citations

mousehuman

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Genetic & Genomic MedicineNature CommunicationsPeer-reviewedApr 28, 2022

Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

Hong Joo Kim, Payam Mohassel, Sandra C. Donkervoort…·J. Paul Taylor

The paper identifies heterozygous frameshift variants in hnRNPA2B1 causing early-onset oculopharyngeal muscular dystrophy by altering nucleocytoplasmic transport.

44 citations

humanexperimental assay

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Genetic & Genomic MedicineJCI InsightPeer-reviewedJul 21, 2021

DEFINING THE DIVERSITY OF HNRNPA1 MUTATIONS IN CLINICAL PHENOTYPE AND PATHOMECHANISM

Danique Beijer, Hong Joo Kim, Lin E. Guo…·Jonathan Baets

The paper characterizes HNRNPA1 mutations in patients with neurodegenerative diseases, showing varied effects on fibrillization, phase separation, and stress granule dynamics.

72 citationstop 3%

humanproteomics

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