Author

Catherine Doust

University of Edinburgh

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· 1

Signature Assays, Organisms & Methods

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Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Research Focus:polygenic risk· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam AutoniD· 1 shared Alan M. KwongiD· 1 shared Aly Azeem KhaniD· 1 shared Anjali J. Shastri· 1 shared Barry Hicks· 1 shared Catherine H. Weldon· 1 shared Chris GermaniD· 1 shared Chris Q. EijsboutsiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam AutonORCID

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Author profile →

1 paper

Recent·Most cited

Multivariate genome-wide association analysis of quantitative reading skill and dyslexia improves gene discovery

Hayley S. Mountford, Else Eising, Pierre Fontanillas, Adam Auton, Stella W. Aslibekyan, Robert K. Bell, Katelyn Kukar Bond, Zayn Cochinwala, Sayantan Das, Kahsaia de Brito, Emily DelloRusso, Chris Q. Eijsbouts, Sarah L. Elson, Chris German, Julie M. Granka, , Michelle Luciano A

This study uses a multivariate GWAS approach to identify genetic loci associated with reading ability and dyslexia, finding 35 new genome-wide significant loci and estimating SNP heritability at 24%.

Translational Psychiatry · Aug 18, 2025Peer-reviewedGenetic & Genomic Medicine