Author

David Ewart Henshall

Roslin InstituteORCID 0000-0001-7377-3969Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Albert TenesaiD· 1 shared Amy FergusoniD· 1 shared Bryan Ronald ConwayiD· 1 shared Cathie L. M. SudlowiD· 1 shared Ed WhittakeriD· 1 shared Konrad RawlikiD· 1 shared Kristiina RannikmäeiD· 1 shared Malcolm Robert MacleodiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Albert TenesaORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineNeurology GeneticsPeer-reviewedAug 24, 2022

Frequency and phenotype associations of rare variants in five monogenic cerebral small vessel disease genes in 200,000 UK Biobank participants with whole exome sequencing data

Amy Ferguson, Sophie Thrippleton, David Ewart Henshall…·Kristiina Rannikmäe

The paper examines rare variants in monogenic cerebral small vessel disease genes in UK Biobank participants, finding limited phenotype associations and suggesting issues with previous gene-phenotype links.

14 citations

humanwhole-exome sequencing

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