Author

Bailey Gallinger

Hospital for Sick ChildrenORCID 0000-0003-0039-3652Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant effect prediction· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Amit TiroshiD· 1 shared Amy Y. PaniD· 1 shared Anna SzutoiD· 1 shared Chansonette Badduke· 1 shared Chloe E. Mighton· 1 shared Chung Ting Tsoi· 1 shared Clare Sheen· 1 shared Deborah RitteriD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amit TiroshORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedMay 1, 2026

Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease

Deborah Ritter, Chansonette Badduke, Kurston Doonanco…·Raymond H. Kim

The paper describes the development of variant classification specifications for the VHL gene using ACMG/AMP guidelines, resulting in updated evidence codes and improved classification consistency.

2 citationstop 5%

humanwhole-exome sequencing

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Genetic & Genomic MedicinePaediatrics & Child HealthPeer-reviewedSep 1, 2025

Implementing a consultation service for translating genomic research findings into the clinic: lessons from the SickKids Genome Board

Amy Y. Pan, Kenzie Pulsifer, Michelle M. Axford…·Gregory Costain

The paper describes a consultation service for evaluating genomic research findings in a paediatric hospital, highlighting its role in assessing variant pathogenicity and managing clinical implications.

DOI 10.1093/pch/pxaf020

humanwhole-genome sequencing

𝕏 PostBluesky