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 Hubert, Laurence

Class:IdPerson:6792632
_displayNameHubert, Laurence
_timestamp2015-08-25 14:11:53
created[InstanceEdit:6792635] Jassal, Bijay, 2015-08-25
firstnameLaurence
initialL
surnameHubert
(author)[LiteratureReference:6792624] Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase
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No pathways have been reviewed or authored by Hubert, Laurence (6792632)