Author

Savannah Kilpatrick

University Health Network

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Organism:mouse· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

Chad O. Brown· 2 shared Jennifer Howe· 2 shared Karun Kar SinghiD· 2 shared Nadeem MurtazaiD· 2 shared Sansi Xing· 2 shared Stephen W. SchereriD· 2 shared Yu Lu· 2 shared Alain VerloèsiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersNeuroscience

Chad O. Brown

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Disruption of the autism-associated gene SCN2A alters synaptic development and neuronal signaling in patient iPSC-glutamatergic neurons

Chad O. Brown, Jarryll A. Uy, Nadeem Murtaza, Elyse Rosa, Alexandria Alfonso, Sansi Xing, Biren M. Dave, Savannah Kilpatrick, Annie A. Cheng, Sean H. White, Jennifer Howe, Stephen W. Scherer, Yu Lu, Karun Kar Singh

This study examines how different SCN2A de novo variants affect human neuron development and function using patient-derived iPSCs.

Frontiers in Cellular Neuroscience · Jan 15, 2024Peer-reviewedNeuroscience

Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome

Brianna K. Unda, Leon Chalil, Sehyoun Yoon, Savannah Kilpatrick, Courtney L. Irwin, Sansi Xing, Nadeem Murtaza, Anran Cheng, Chad O. Brown, Alexandria Afonso, Elizabeth McCready, Gabriel M. Ronen, Jennifer Howe, Aurélie Caye‐Eude, Alain Verloès, , Karun Kar Singh

This study identifies impaired OTUD7A-Ankyrin regulation as a mechanism underlying neuronal dysfunction in 15q13.3 microdeletion syndrome using mouse and human models.

Molecular Psychiatry · Jan 5, 2023Peer-reviewedNeuroscience