Author

Eriskay Liston

University of TorontoORCID 0000-0003-1380-9274Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Research Focus:variant effect prediction· 2 Research Focus:database / resource· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Amy Y. PaniD· 2 shared Gregory CostainiD· 2 shared Laura A ZahavichiD· 2 shared Michelle M. AxfordiD· 2 shared Miriam S. ReuteriD· 2 shared Andrew McFadyeniD· 1 shared Anna SzutoiD· 1 shared Anne S. BassettiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Amy Y. PanORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 23, 2026

A Generalizable, Governance-Embedded Pathway for Assessing Patient-Level Opportunities for Genetic Medicines

David Cheerie, Amy Y. Pan, Meryl Acker…·Gregory Costain

The paper describes a structured initiative to assess patient eligibility for genetic medicines, showing high uptake and feasibility of a multidisciplinary approach.

DOI 10.64898/2026.09.22.26363712

humanexperimental assay

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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

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GenomicsFrontiers in GeneticsPeer-reviewedSep 15, 2020

Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences

Roozbeh Manshaei, Daniele Merico, Miriam S. Reuter…·Anne S. Bassett

This paper identifies ultra-rare variants in NOTCH1 and FLT4 associated with tetralogy of Fallot using burden analysis of genome sequences from 231 individuals.

36 citations

humanwhole-exome sequencing

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