Author

Julie Ruston

Hospital for Sick Children

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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Genetics· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Approach:statistical model· 1

Frequent Co-Authors

Christine Taylor· 3 shared Monica J. JusticeiD· 3 shared Rebekah TillotsoniD· 2 shared Adebola EnikanolaiyeiD· 1 shared Alex CórdovaiD· 1 shared Brian J. NiemaniD· 1 shared Christian BabbsiD· 1 shared Christie M. BuchoveckyiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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3 shared papersGenetics

Christine Taylor

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Visible traits demonstrate that crispant founder mice can be used for phenotypic assessment

Rebekah Tillotson, Marina Gertsenstein, Li‐Hsin Chang, Julie Ruston, Fernando Bellido Molías, Lauri G. Lintott, Christine Taylor, Philippe Emmanuel Gautier, Lauryl M. J. Nutter, Monica J. Justice

This study shows that crispant founder mice can be used for phenotypic assessment despite genetic mosaicism, as observed null phenotypes were present in up to 100% of founders.

bioRxiv · Jun 27, 2025 · PreprintGenetics

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

Suppressor mutations in Mecp2-null mice reveal that the DNA damage response is key to Rett syndrome pathology

Adebola Enikanolaiye, Julie Ruston, Rong Zeng, Christine Taylor, Marijke Schrock, Christie M. Buchovecky, Jay Shendure, Elif Fidan Acar, Monica J. Justice

The paper identifies suppressor mutations in Mecp2-null mice that alleviate Rett syndrome symptoms by modulating DNA damage response pathways.

Genome Research · Apr 1, 2020Peer-reviewedGenetics