Author

Martha Pace

Upper Iowa University

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

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Neuroscience· 2

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Aislinn Joanmarie WilliamsiD· 2 shared Annette KlompiD· 2 shared Cessily Hayes· 2 shared Anthony Fleck· 1 shared Asriya Karki· 1 shared Binh Doan· 1 shared Hsiang Wen· 1 shared Hunter E. Halverson· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersNeuroscience

Aislinn Joanmarie WilliamsORCID

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2 papers

Recent·Most cited

Deletion of the voltage-gated calcium channel gene, CaV1.3, reduces Purkinje cell dendritic complexity without altering cerebellar-mediated eyeblink conditioning

Annette Klomp, Martha Pace, Jacqueline B. Mehr, Maria Fernanda Hermosillo Arrieta, Cessily Hayes, Anthony Fleck, Shane A. Heiney, Aislinn Joanmarie Williams

This study shows that deleting the CaV1.3 gene in mice reduces Purkinje cell dendritic complexity but does not affect cerebellar-mediated eyeblink conditioning or MLI numbers.

The Cerebellum · Oct 11, 2025Peer-reviewedNeuroscience

16p11.2 Microduplication is Associated with Lobule-Specific Abnormalities in Cerebellar Structure and Function

Cessily Hayes, Hunter E. Halverson, Krisha Keeran, Krislen Tison, Kamilla Jacobo, Asriya Karki, Isaias Herring, Swetha Tunuguntla, Martha Pace, Binh Doan, Hsiang Wen, Annette Klomp, Marisol Carmela Lauffer, Marie E. Gaine, Krystal Lynn Parker, Aislinn Joanmarie Williams

This study identifies lobule VI-specific structural and functional cerebellar abnormalities in 16p11.2 microduplication mice, linking them to learning impairments and neuropsychiatric disorder symptoms.

bioRxiv · Nov 20, 2023 · PreprintNeuroscience