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 Bailey, CG

Class:Id	Person:375466
_displayName	Bailey, CG
_timestamp	2008-08-29 20:23:00
created	[InstanceEdit:375485] D'Eustachio, P, 2008-08-29 20:22:39
firstname	Charles G
initial	CG
modified	[InstanceEdit:375492] D'Eustachio, P, 2008-08-29 20:22:58
surname	Bailey
(author)	[LiteratureReference:375453] Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 [LiteratureReference:5625009] Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria [LiteratureReference:5653856] Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
[Change default viewing format]

No pathways have been reviewed or authored by Bailey, CG (375466)