Author

Nycole A. Copping

University of California Davis Medical Center

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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Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

Alex S. NordiD· 2 shared César P. CanalesiD· 2 shared Jill L. SilvermaniD· 2 shared A. Ayanna WadeiD· 1 shared Alana Iaboni· 1 shared Alea A. MillsiD· 1 shared Alessandro GozziiD· 1 shared Alex P. A. DonovaniD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersNeuroscience

Alex S. NordORCID

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Author profile →

2 papers

Recent·Most cited

Assigning Targetable Pathways to Transdiagnostic Subgroups Across Neurodevelopmental Disorders

Jacob Ellegood, Antoine Beauchamp, Yohan Yee, Gabe Devenyi, Justine Ziolkowski, Lily R. Qiu, Rand Askalan, Muhammad Ayub, Philipp Suetterlin, Alex P. A. Donovan, M. Albert Basson, Katherine Quesnel, Nathalie G. Bérubé, Taeseon Woo, David Quentin Beversdorf, , Jill L. Silverman

The paper identifies molecular pathways associated with neurodevelopmental disorder subgroups using neuroimaging data from mice and humans.

bioRxiv · Mar 4, 2025 · PreprintNeuroscience

Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice

Jess Haigh, Anna Adhikari, Nycole A. Copping, Tyler W. Stradleigh, A. Ayanna Wade, Rinaldo Catta-Preta, Linda Su-Feher, Iva Zdilar, Sarah J. Morse, Timothy A. Fenton, Anh Nguyen, Diana Quintero, Samrawit Agezew, Michael Sramek, Ellie J. Kreun, , Alex S. Nord

This study shows that deleting a non-canonical regulatory region of Scn1a in mice leads to reduced Scn1a expression and epileptic symptoms.

Genome Medicine · Apr 26, 2021Peer-reviewedNeuroscience