Maryke Schoonen
6PUBLICATIONS
32CO-AUTHORS
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Publications (6)
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|Jan 31, 2026
Bridging gaps in mitochondrial disease diagnosis: the role of advanced biomarker discovery.Tendai Makwikwi, Maryke Schoonen, Izelle Smuts
|Sep 12, 2025
OXPHOS complex deficiency in congenital myopathy: A systematic review.Megan J du Preez, Maryke Schoonen, Monray E Williams
|Feb 18, 2025
Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort.Maryke Schoonen, Mahmoud Fassad, Krutik Patel
|Jan 14, 2024
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.Michelle Bisschoff, Izelle Smuts, Marli Dercksen
|Dec 25, 2019
A call for global action for rare diseases in Africa.Gareth S Baynam, Stephen Groft, Francois H van der Westhuizen
|Oct 04, 2019
Development of an SNP-based parentage verification panel for lovebirds.H van der Zwan, C Visser, M Schoonen
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Frequent Collaborators
5 joint publications
Francois H van der Westhuizen
3 joint publications
Barend C Vorster
3 joint publications
Izelle Smuts
3 joint publications
Michelle Bisschoff
2 joint publications
Mahmoud R Fassad
1 joint publications
Tendai Makwikwi
1 joint publications
C Visser
1 joint publications
R van der Sluis
1 joint publications
Gareth S Baynam
1 joint publications
Désirée Gavhed
