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 Rothfels, Karen, 2024-07-26

Class:Id	InstanceEdit:9916927
_displayName	Rothfels, Karen, 2024-07-26
_timestamp	2024-07-26 17:51:51
author	[Person:1226097] Rothfels, Karen
dateTime	2024-07-26 17:51:49
(modified)	[Summation:9914208] The following mutations in MCCC1 have been identified in pat... [Summation:9914212] The following mutations have been identified in patients wit... [Summation:9914341] The following mutations have been identified in patients wit... [Summation:9915283] Mutations in ACAT1 have been identified in cases of beta-ket... [Pathway:9916722] 3-hydroxyisobutyryl-CoA hydrolase deficiency [Homo sapiens] [EntityFunctionalStatus:9916723] loss_of_function of HIBCH mutants [mitochondrial matrix] [DefinedSet:9916724] HIBCH mutants [mitochondrial matrix] [Homo sapiens] [FailedReaction:9916727] HIBCH mutants don't synthesize beta-hydroxyisobutyrate [Homo sapiens] [Summation:9916904] 3-hydroxyisobutyryl-CoA hydrolase deficiency is an autosomal...
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No pathways have been reviewed or authored by Rothfels, Karen, 2024-07-26 (9916927)