Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Details on Person Wanders, Ronald J A

Class:Id	Person:9859048
_displayName	Wanders, Ronald J A
_timestamp	2024-01-15 09:16:00
created	[InstanceEdit:9859030] Stephan, Ralf, 2024-01-15
firstname	Ronald J A
initial	RJ
surname	Wanders
(author)	[LiteratureReference:9859042] Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria [LiteratureReference:9914020] Peroxisomal fatty acid uptake mechanism in Saccharomyces cerevisiae [LiteratureReference:9914025] Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation [LiteratureReference:9914306] NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism [LiteratureReference:9915309] Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): identification of a Km mutant and an analysis of the mutational sites in the structure [LiteratureReference:9916574] Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation [LiteratureReference:9916629] Clinical and biochemical characterization of four patients with mutations in ECHS1 [LiteratureReference:9916882] HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase [LiteratureReference:9916885] Mutations in the gene encoding 3-hydroxyisobutyryl-CoA hydrolase results in progressive infantile neurodegeneration [LiteratureReference:9916899] Metabolite studies in HIBCH and ECHS1 defects: Implications for screening List all 13 refering instances
[Change default viewing format]

No pathways have been reviewed or authored by Wanders, Ronald J A (9859048)