Publications by authors named "Ronald Wanders"

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Molecular and cellular mechanisms underlying gyrate atrophy: Why is the retina primarily affected?
Mark J N Buijs, Berith M Balfoort, Marion M Brands, Anneloor L M A Ten Asbroek, Camiel J F Boon, Ronald J A Wanders

Acta Ophthalmol· November 2025

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Docosahexaenoic acid prevents peroxisomal and mitochondrial protein loss in a murine hepatic organoid model of severe malnutrition.
José M Horcas-Nieto, W Alfredo Rios-Ocampo, Miriam Langelaar-Makkinje, Rinse de Boer, Albert Gerding, Ronald J A Wanders

Biochim Biophys Acta Mol Basis Dis· August 2025

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Syndromic retinitis pigmentosa.
Jessica S Karuntu, Hind Almushattat, Xuan-Thanh-An Nguyen, Astrid S Plomp, Ronald J A Wanders

Prog Retin Eye Res· July 2025

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A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of Metabolism.
Aaron Bender, Pablo Ranea-Robles, Evan G Williams, Mina Mirzaian, J Alexander Heimel, Ronald J Wanders

J Inherit Metab Dis· July 2025

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A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolism.
Aaron Bender, Pablo Ranea-Robles, Evan G Williams, Mina Mirzaian, J Alexander Heimel, Ronald J Wanders

bioRxiv· February 2025

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Disorders of fatty acid homeostasis.
Frédéric M Vaz, Sacha Ferdinandusse, Gajja S Salomons, Ronald J A Wanders

J Inherit Metab Dis· January 2025

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A Dutch translational knowledge agenda for inherited metabolic diseases.
Hans R Waterham, Ronald J A Wanders, Ron A Wevers, Clara D van Karnebeek

J Inherit Metab Dis· January 2025

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Human glyoxylate metabolism revisited: New insights pointing to multi-organ involvement with implications for siRNA-based therapies in primary hyperoxaluria.
Ronald J A Wanders, Jaap W Groothoff, Lisa J Deesker, Eduardo Salido, Sander F Garrelfs

J Inherit Metab Dis· January 2025

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A mini-review on the international gyrate atrophy symposium 2023: More than meets the eye. Focus on outstanding research questions.
Marion Brands, Berith Balfoort, Karabi Acharya, Arthur Bergen, Nicola Brunetti-Pierri, Ronald Wanders

Mol Genet Metab· December 2024

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Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay.
Berith M Balfoort, Gioena Pampalone, Jos P N Ruiter, Simone W Denis, Marion M Brands, Ronald J A Wanders

Mol Genet Metab· October 2024

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Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.
Frédéric M Vaz, Pippa Staps, Jan Bert van Klinken, Henk van Lenthe, Martin Vervaart, Ronald J A Wanders

Biochim Biophys Acta Mol Cell Biol Lipids· March 2024

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Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylate.
Sander F Garrelfs, Serhii Chornyi, Heleen Te Brinke, Jos Ruiter, Jaap Groothoff, Ronald J A Wanders

J Inherit Metab Dis· March 2024

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Tracer-based lipidomics enables the discovery of disease-specific candidate biomarkers in mitochondrial β-oxidation disorders.
Marit Schwantje, Signe Mosegaard, Suzan J G Knottnerus, Jan Bert van Klinken, Ronald J Wanders

FASEB J· February 2024

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Vision on gyrate atrophy: why treat the eye?
Arthur A Bergen, Mark Jn Buijs, Anneloor Lma Ten Asbroek, Berith M Balfoort, Camiel Jf Boon, Ronald Ja Wanders

EMBO Mol Med· January 2024

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Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.
Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend C Vorster, Ronald J A Wanders

Orphanet J Rare Dis· January 2024

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Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene.
Hans R Waterham, Janet Koster, Merel S Ebberink, Pavel Ješina, Jiri Zeman, Ronald J A Wanders

Genet Med· November 2023

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Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy.
Vincenza Gragnaniello, Daniela Gueraldi, Andrea Puma, Anna Commone, Chiara Cazzorla, Ronald J A Wanders

Orphanet J Rare Dis· November 2023

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Functional and structural impact of 10 ACADM missense mutations on human medium chain acyl-Coa dehydrogenase.
Catarina A Madeira, Carolina Anselmo, João M Costa, Cátia A Bonito, Ricardo J Ferreira, Ronald J Wanders

Biochim Biophys Acta Mol Basis Dis· October 2023

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Human peroxisomal NAD/NADH homeostasis is regulated by two independent NAD(H) shuttle systems.
Serhii Chornyi, Cláudio F Costa, Lodewijk IJlst, Marc Fransen, Ronald J A Wanders

Free Radic Biol Med· September 2023

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Maintenance of cellular vitamin B levels and mitochondrial oxidative function depend on pyridoxal 5'-phosphate homeostasis protein.
Jolita Ciapaite, Carlo W T van Roermund, Marjolein Bosma, Johan Gerrits, Sander M Houten, Ronald J A Wanders

J Biol Chem· September 2023

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The malate-aspartate shuttle is important for de novo serine biosynthesis.
Melissa H Broeks, Nils W F Meijer, Denise Westland, Marjolein Bosma, Johan Gerrits, Ronald J A Wanders

Cell Rep· September 2023

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Genetic defects in peroxisome morphogenesis (Pex11β, dynamin-like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid-phospholipid metabolism.
Yuichi Abe, Ronald J A Wanders, Hans R Waterham, Hanna Mandel, Tzipora C Falik-Zaccai

J Inherit Metab Dis· March 2023

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The physiological functions of human peroxisomes.
Ronald J A Wanders, Myriam Baes, Daniela Ribeiro, Sacha Ferdinandusse, Hans R Waterham

Physiol Rev· January 2023

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Multi-omics in classical galactosemia: Evidence for the involvement of multiple metabolic pathways.
Merel E Hermans, Michel van Weeghel, Frédéric M Vaz, Sacha Ferdinandusse, Carla E M Hollak, Ronald J A Wanders

J Inherit Metab Dis· November 2022

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Systematic multi-level analysis of an organelle proteome reveals new peroxisomal functions.
Eden Yifrach, Duncan Holbrook-Smith, Jérôme Bürgi, Alaa Othman, Miriam Eisenstein, Ronald J A Wanders

Mol Syst Biol· September 2022

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