Author

Maylin L. Fu

Stanford UniversityORCID 0000-0003-3749-5003Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:mouse· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:electronic health records· 1

Frequent Co-Authors

Lei S. QiiD· 2 shared Mengting HaniD· 2 shared Alexander A. ChoiiD· 1 shared Boxiong Deng· 1 shared Edward H. KooiD· 1 shared Emmy LiiD· 1 shared Gautam Narayan· 1 shared Jill K. LeutgebiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersBioengineering

Lei S. QiORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioengineeringNature Cell BiologyPeer-reviewedApr 1, 2026

Programmable macromolecule delivery via engineered trogocytosis

Xinyi Chen, Yinglin Situ, Yuexuan Yang…·Lei S. Qi

This study demonstrates a programmable macromolecule delivery system using engineered trogocytosis to transfer proteins between cells, enabling genome editing and targeted cell ablation.

4 citationstop 4%

experimental assaydrug response / drug discovery

𝕏 PostBluesky

BioengineeringbioRxivPreprintApr 5, 2025

Perturbing RNA localization for functional study in neurons

Mengting Han, Maylin L. Fu, Yanyu Zhu…·Lei S. Qi

This study introduces CRISPR-TO to manipulate RNA localization in neurons, showing it affects neurite outgrowth and axonal regeneration.

DOI 10.1101/2025.04.05.646707

mousescRNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintOct 24, 2022

Localized APP pathology in the hippocampus is sufficient to result in progressive disorganization of the timing of neuronal firing patterns

Silvia Viana da Silva, Matthias Georg Haberl, Kshitij Gaur…·Stefan Leutgeb

This study shows that localized APP pathology in hippocampal CA3 cells leads to altered neuronal firing patterns in connected regions, suggesting disease progression can occur through physiological dysfunction rather than just spreading pathology.

DOI 10.1101/2022.10.24.513188

mouseelectronic health records

𝕏 PostBluesky