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 Michaud, Jacques L

Class:IdPerson:3247906
_displayNameMichaud, Jacques L
_timestamp2013-04-05 21:35:38
created[InstanceEdit:3247941] Shamovsky, V, 2013-04-05
firstnameJacques L
initialJL
surnameMichaud
(author)[LiteratureReference:3247931] Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus
[LiteratureReference:6797787] Mutations in the calcium-related gene IL1RAPL1 are associated with autism
[LiteratureReference:9916626] Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome
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No pathways have been reviewed or authored by Michaud, Jacques L (3247906)