Author

Shailly Jain

University of Alberta

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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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1

Frequent Co-Authors

Abiola Harrison· 1 shared Alicia Chan· 1 shared Anabelle Tuttle· 1 shared Andrew MuranyiiD· 1 shared Ashley NicolasiD· 1 shared Boris KereniD· 1 shared Cathleen HuculakiD· 1 shared Chaya Nautiyal MuraliiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abiola Harrison

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2 papers

Recent·Most cited

Comparing Cardiac Genetic Testing Pathways: Impacts on Access, Informed Choice, and Decisional Satisfaction

Susan Christian, Talia C. Belcher, Marc Benoit, Alicia Chan, Tara Dzwiniel, Erkan İlhan, Shailly Jain, Karen Katchmer, Omid Kiamanesh, Margaret Lilley, Julien L. Marcadier, Skylar Moreau, Andrew Muranyi, Ashley Nicolas, Priyana Sharma, , Cathleen Huculak

This study compares two genetic testing pathways for cardiac conditions, finding higher uptake and faster access in the mainstreaming model but lower informed decision rates compared to a genetics referral model.

Circulation Genomic and Precision Medicine · Sep 24, 2026Peer-reviewedGenetic & Genomic Medicine

Variants in BSN, encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

Stacy G. Guzman, Sarah McKeown Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan, Zornitza Stark, Natasha J. Brown, Sajel Lala Kana, Anabelle Tuttle, Jair Antonio Tenorio, Pablo Daniel Lapunzina, Julián B. Nevado, Marie McDonald, Courtney Jensen, , Ingo Helbig

The paper identifies BSN variants as a cause of a new neurodevelopmental disorder with a broad phenotypic range, using clinical data and computational phenotyping.

medRxiv · Feb 10, 2025 · PreprintGenetic & Genomic Medicine