Author

Solomon K. Guyler

Queensland University of TechnologyORCID 0009-0007-3779-6160Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Heidi G. E. SutherlandiD· 1 shared Lyn Robyn GriffithsiD· 1 shared Mohammed M. AlfayyadhiD· 1 shared Neven MaksemousiD· 1 shared Robert A. Smith· 1 shared Rod A. LeaiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Heidi G. E. SutherlandORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 16, 2026

Whole Exome Sequencing of Suspected Monogenic Cerebral Small Vessel Disease Patients reveals Novel Gene Associations

Solomon K. Guyler, Mohammed M. Alfayyadh, Neven Maksemous…·Lyn Robyn Griffiths

The paper performs whole exome sequencing on CSVD patients to identify novel gene associations and finds significant variants in ABCC6, MYH11, NOTCH1, and seven other genes.

DOI 10.64898/2026.02.08.26345868

humanwhole-exome sequencing

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