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 Revy, Patrick

Class:IdPerson:5687230
_displayNameRevy, Patrick
_timestamp2015-04-07 03:11:20
created[InstanceEdit:5687245] Orlic-Milacic, Marija, 2015-04-07
firstnamePatrick
initialP
surnameRevy
(author)[LiteratureReference:5687239] Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly
[LiteratureReference:9686596] Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability
[LiteratureReference:9938482] Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
[LiteratureReference:9947217] Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
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No pathways have been reviewed or authored by Revy, Patrick (5687230)