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 Cheadle, Jeremy P

Class:IdPerson:9606217
_displayNameCheadle, Jeremy P
_timestamp2018-04-20 15:05:12
created[InstanceEdit:9606215] Orlic-Milacic, Marija, 2018-04-20
firstnameJeremy P
initialJP
surnameCheadle
(author)[LiteratureReference:9606219] Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors
[LiteratureReference:9606238] Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations
[LiteratureReference:9606249] Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH
[LiteratureReference:9606269] Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis
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No pathways have been reviewed or authored by Cheadle, Jeremy P (9606217)