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.

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Details on Person Shaag, A

Class:Id	Person:380175
_displayName	Shaag, A
_timestamp	2008-11-08 17:24:47
created	[InstanceEdit:380210] D'Eustachio, P, 2008-11-08 17:23:03
firstname	Avraham
initial	A
modified	[InstanceEdit:380247] D'Eustachio, P, 2008-11-08 17:24:20
surname	Shaag
(author)	[LiteratureReference:380182] Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia [LiteratureReference:3702145] West syndrome caused by ST3Gal-III deficiency [LiteratureReference:5653606] Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis [LiteratureReference:6787460] Acute infantile liver failure due to mutations in the TRMU gene
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No pathways have been reviewed or authored by Shaag, A (380175)