Author

Lily C. Wong‐Kisiel

Mayo ClinicORCID 0000-0002-5306-0862Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1

Frequent Co-Authors

Abigail TurnwaldiD· 1 shared Adeline JacquinetiD· 1 shared Alexia BourgoisiD· 1 shared Amanda Carnevale· 1 shared Amber Hogart BegtrupiD· 1 shared Amélie PitoniD· 1 shared Amelle ShillingtoniD· 1 shared Angelika Rieß· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abigail TurnwaldORCID

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2 papers

Recent·Most cited

Functional Mapping of Movement and Speech Using Task-Based Electrophysiological Changes in Stereoelectroencephalography

Michael A. Jensen, Anthony L. Fine, Panagiotis Kerezoudis, Lily C. Wong‐Kisiel, Eva Alden, Dora Hermes, Kai Joshua Miller

This study develops a functional brain mapping technique using task-based electrophysiological changes in sEEG to identify movement and speech areas in epilepsy patients.

Journal of neurosurgery · Aug 30, 2024Peer-reviewedNeuroscience

Adaptor protein 2 sigma subunit (AP2S1) variants associated with neurodevelopmental disorders

Mark Stevenson, Asha L. Bayliss, Victoria J. Stokes, Katherine A. English, Kreepa G. Kooblall, Roman Fischer, Raphael Heilig, Iolanda Vendrell, Maria E. W. A. Albers, Meghan N. Bartos, Amber Hogart Begtrup, Alexia Bourgois, Rebecca Buchert, David J. Carey, Deanna Alexis Carere, , Rajesh V. Thakker

The paper identifies AP2S1 variants linked to neurodevelopmental disorders by showing they impair clathrin-mediated endocytosis and disrupt protein interactions.

medRxiv · Jul 22, 2024 · PreprintGenetic & Genomic Medicine