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 Steel, Gary

Class:Id	Person:70626
_displayName	Steel, Gary
_timestamp	2015-06-17 20:38:11
firstname	Gary
initial	G
modified	[InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Steel
(author)	[LiteratureReference:70619] Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter [LiteratureReference:70640] Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. [LiteratureReference:517459] Functional consequences of PRODH missense mutations [LiteratureReference:9036548] Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis
[Change default viewing format]

No pathways have been reviewed or authored by Steel, Gary (70626)