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 Odent, Sylvie

Class:IdPerson:2453900
_displayNameOdent, Sylvie
_timestamp2012-08-17 13:27:32
created[InstanceEdit:2453822] Jassal, Bijay, 2012-08-17
firstnameSylvie
initialS
surnameOdent
(author)[LiteratureReference:2453872] Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia
[LiteratureReference:5358217] Functional characterization of sonic hedgehog mutations associated with holoprosencephaly
[LiteratureReference:5358247] The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis
[LiteratureReference:5617061] POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardation
[LiteratureReference:9940699] Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly
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No pathways have been reviewed or authored by Odent, Sylvie (2453900)