Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

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.

Name Email address

Details on Person Vockley, J

Class:IdPerson:70737
_displayNameVockley, J
_timestamp0000-00-00 00:00:00
firstnameJerry
initialJ
surnameVockley
(author)[LiteratureReference:70731] Structure of human isovaleryl-CoA dehydrogenase at 2.6 A resolution: structural basis for substrate specificity
[LiteratureReference:70813] 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism
[LiteratureReference:70864] Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans
[LiteratureReference:508471] Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases
[LiteratureReference:5695992] Identification and characterization of new long chain acyl-CoA dehydrogenases
[LiteratureReference:9914730] Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity
[LiteratureReference:9914747] Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysis
[LiteratureReference:9945087] Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay
[Change default viewing format]
No pathways have been reviewed or authored by Vockley, J (70737)