Reactome: A Curated Pathway Database
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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.

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Details on Person Auray-Blais, Christiane

Class:IdPerson:5625031
_displayNameAuray-Blais, Christiane
_timestamp2014-10-01 12:43:54
created[InstanceEdit:5625030] Jassal, Bijay, 2014-10-01
firstnameChristiane
initialC
surnameAuray-Blais
(author)[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
[LiteratureReference:6797948] Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
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No pathways have been reviewed or authored by Auray-Blais, Christiane (5625031)