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 Beetz, Christian

Class:Id	Person:5603009
_displayName	Beetz, Christian
_timestamp	2014-06-25 13:12:46
created	[InstanceEdit:5602968] Jassal, Bijay, 2014-06-25
firstname	Christian
initial	C
surname	Beetz
(author)	[LiteratureReference:5602916] CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5 [LiteratureReference:5602945] Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia [LiteratureReference:5688173] Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure [LiteratureReference:9909225] Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction
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No pathways have been reviewed or authored by Beetz, Christian (5603009)