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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.

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Details on Person Bykhovskaya, Yelena

Class:IdPerson:6787434
_displayNameBykhovskaya, Yelena
_timestamp2015-07-13 14:32:51
created[InstanceEdit:6787465] May, Bruce, 2015-07-13
firstnameYelena
initialY
surnameBykhovskaya
(author)[LiteratureReference:6787483] Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
[LiteratureReference:6787575] Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylation
[LiteratureReference:6787578] Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)
[LiteratureReference:6793079] Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation
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No pathways have been reviewed or authored by Bykhovskaya, Yelena (6787434)