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.

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Details on Person Nelson, Stanley F

Class:IdPerson:3247973
_displayNameNelson, Stanley F
_timestamp2013-04-05 21:36:31
created[InstanceEdit:3247941] Shamovsky, V, 2013-04-05
firstnameStanley F
initialSF
surnameNelson
(author)[LiteratureReference:3247932] C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
[LiteratureReference:3656346] Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1
[LiteratureReference:5610239] Oxysterols are novel activators of the hedgehog signaling pathway in pluripotent mesenchymal cells
[LiteratureReference:6799057] Melanoma whole-exome sequencing identifies (V600E)B-RAF amplification-mediated acquired B-RAF inhibitor resistance
[LiteratureReference:6799059] Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
[LiteratureReference:8879116] SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function
[LiteratureReference:9940680] ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome
[LiteratureReference:9940755] The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition
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No pathways have been reviewed or authored by Nelson, Stanley F (3247973)