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 Pierri, Ciro L

Class:Id	Person:9815310
_displayName	Pierri, Ciro L
_timestamp	2022-08-16 22:37:50
created	[InstanceEdit:9815308] D'Eustachio, Peter, 2022-08-16
firstname	Ciro L
initial	CL
modified	[InstanceEdit:9815337] D'Eustachio, Peter, 2022-08-16
surname	Pierri
(author)	[LiteratureReference:9815327] SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency [LiteratureReference:9856976] AGC1 deficiency associated with global cerebral hypomyelination [LiteratureReference:9857411] Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular Transmission [LiteratureReference:9959723] Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study
[Change default viewing format]

No pathways have been reviewed or authored by Pierri, Ciro L (9815310)