Author

Keqin Yan

Ottawa Hospital Research Institute

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

Brian J. NiemaniD· 2 shared David J. PickettsiD· 2 shared Yohan YeeiD· 2 shared Alana Iaboni· 1 shared Alea A. MillsiD· 1 shared Alessandro GozziiD· 1 shared Alex CórdovaiD· 1 shared Alex P. A. DonovaniD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersNeuroscience

Brian J. NiemanORCID

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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

A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects

Rebekah Tillotson, Keqin Yan, Julie Ruston, Taylor DeYoung, Alex Córdova, Valérie Turcotte-Cardin, Yohan Yee, Christine Taylor, Shagana Visuvanathan, Christian Babbs, Evgueni A. Ivakine, John G. Sled, Brian J. Nieman, David J. Picketts, Monica J. Justice

This paper introduces a knock-in mouse model of ATR-X syndrome carrying a common patient mutation, showing craniofacial defects, microcephaly, and impaired neurological function.

Human Molecular Genetics · May 12, 2023Peer-reviewedNeuroscience