Author

Maia Lee

Massachusetts Institute of TechnologyORCID 0000-0002-5992-9477Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1

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Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1

Frequent Co-Authors

Carol L. WilkinsoniD· 1 shared Çiğdem Gelegen· 1 shared Craig A. EricksoniD· 1 shared Francesca A. ChaloneriD· 1 shared Jordan E. NorrisiD· 1 shared Lauren E. EthridgeiD· 1 shared Lauren SchmittiD· 1 shared Mark F. BeariD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Carol L. WilkinsonORCID

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1 paper

Recent·Most cited

A human electrophysiological biomarker of Fragile X Syndrome is shared in V1 of Fmr1 KO mice and caused by loss of FMRP in cortical excitatory neurons

Sara S. Kornfeld-Sylla, Çiğdem Gelegen, Jordan E. Norris, Francesca A. Chaloner, Maia Lee, Michael Khela, Maxwell J. Heinrich, Peter S.B. Finnie, Lauren E. Ethridge, Craig A. Erickson, Lauren Schmitt, Samuel F. Cooke, Carol L. Wilkinson, Mark F. Bear

The paper identifies a shared electrophysiological biomarker of Fragile X Syndrome in human and mouse models, showing slowed alpha oscillations linked to FMRP loss in excitatory neurons.

bioRxiv · Mar 19, 2025 · PreprintNeuroscience