Ronald J. Wanders

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 22 publications

A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolism.

A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolism.

Journal: bioRxiv : the preprint server for biology

Published: March 03, 2025

A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of Metabolism.

A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of Metabolism.

Journal: Journal of inherited metabolic disease

Published: January 12, 2025

Diagnosis and Metabolic Management of Adult Refsum Disease: Guidance From the Medical and Scientific Committee of Global DARE (Defeat Adult Refsum Everywhere).

Diagnosis and Metabolic Management of Adult Refsum Disease: Guidance From the Medical and Scientific Committee of Global DARE (Defeat Adult Refsum Everywhere).

Journal: Journal of inherited metabolic disease

Published: October 28, 2024

Vision on gyrate atrophy: why treat the eye?

Vision on gyrate atrophy: why treat the eye?

Journal: EMBO molecular medicine

Published: July 17, 2023

Functional and structural impact of 10 ACADM missense mutations on human medium chain acyl-Coa dehydrogenase.

Functional and structural impact of 10 ACADM missense mutations on human medium chain acyl-Coa dehydrogenase.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: February 06, 2023

Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophy.

Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophy.

Journal: The Journal of clinical investigation

Published: July 22, 2020

Mutations in TIMM50 cause severe mitochondrial dysfunction by targeting key aspects of mitochondrial physiology.

Mutations in TIMM50 cause severe mitochondrial dysfunction by targeting key aspects of mitochondrial physiology.

Journal: Human mutation

Published: October 10, 2018

Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution.

Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: May 03, 2018

Increased cardiac fatty acid oxidation in a mouse model with decreased malonyl-CoA sensitivity of CPT1B.

Increased cardiac fatty acid oxidation in a mouse model with decreased malonyl-CoA sensitivity of CPT1B.

Journal: Cardiovascular research

Published: March 15, 2018

Pyruvate dehydrogenase complex plays a central role in brown adipocyte energy expenditure and fuel utilization during short-term beta-adrenergic activation.

Pyruvate dehydrogenase complex plays a central role in brown adipocyte energy expenditure and fuel utilization during short-term beta-adrenergic activation.

Journal: Scientific reports

Published: February 16, 2018

Stability of the ABCD1 Protein with a Missense Mutation: A Novel Approach to Finding Therapeutic Compounds for X-Linked Adrenoleukodystrophy.

Stability of the ABCD1 Protein with a Missense Mutation: A Novel Approach to Finding Therapeutic Compounds for X-Linked Adrenoleukodystrophy.

Journal: JIMD reports

Published: September 01, 2017

Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history.

Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history.

Journal: Nature reviews. Endocrinology

Published: June 18, 2016

Showing 1-12 of 22

Last Updated: 09/26/2026