Author

Riaan van Coller

University of PretoriaORCID 0000-0001-6250-363XUnclaimed 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

Elizna MaasdorpiD· 1 shared Ignacio Fernandez MataiD· 1 shared Jonathan Ambrose CarriD· 1 shared Kathryn StepiD· 1 shared Lusanda MadulaiD· 1 shared Marlo MölleriD· 1 shared Nicole KuznetsoviD· 1 shared Soraya BardieniD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Elizna MaasdorpORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineClinical Parkinsonism & Related DisordersPeer-reviewedJan 1, 2026

Comprehensive genetic screening of the South African Parkinson's disease study collection using the NeuroBooster array

Kathryn Step, Lusanda Madula, Nicole Kuznetsov…·Soraya Bardien

This study performs genetic screening of South African Parkinson's disease patients, identifying rare variants and CNVs in known PD genes, highlighting their contribution to disease in an underrepresented population.

DOI 10.1016/j.prdoa.2026.100508

humanwhole-exome sequencing

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