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 Ensenauer, R

Class:IdPerson:69963
_displayNameEnsenauer, R
_timestamp0000-00-00 00:00:00
firstnameRegina
initialR
surnameEnsenauer
(author)[LiteratureReference:70832] 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency Is caused by mutations in the HADH2 gene
[LiteratureReference:5695992] Identification and characterization of new long chain acyl-CoA dehydrogenases
[LiteratureReference:9914296] Mutations in the AUH gene cause 3-methylglutaconic aciduria type I
[LiteratureReference:9914730] Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity
[LiteratureReference:9957583] Management and outcome of neonatal-onset ornithine transcarbamylase deficiency following liver transplantation at 60 days of life
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No pathways have been reviewed or authored by Ensenauer, R (69963)