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 Gabriel, S

Class:IdPerson:1228021
_displayNameGabriel, S
_timestamp2011-03-16 17:46:54
created[InstanceEdit:1228023] Orlic-Milacic, Marija, 2011-03-16
firstnameStacey
initialS
surnameGabriel
(author)[LiteratureReference:1228027] EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy
[LiteratureReference:1637882] Drug-sensitive FGFR2 mutations in endometrial carcinoma
[LiteratureReference:2008165] Epidermal growth factor receptor activation in glioblastoma through novel missense mutations in the extracellular domain
[LiteratureReference:5693126] Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy
[LiteratureReference:8865651] Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome
[LiteratureReference:9647303] Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
[LiteratureReference:9673534] Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1
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No pathways have been reviewed or authored by Gabriel, S (1228021)