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 Vuillaumier-Barrot, Sandrine

Class:Id	Person:4724305
_displayName	Vuillaumier-Barrot, Sandrine
_timestamp	2013-10-23 15:24:28
created	[InstanceEdit:4724314] Jassal, B, 2013-10-23
firstname	Sandrine
initial	S
surname	Vuillaumier-Barrot
(author)	[LiteratureReference:4724324] A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation [LiteratureReference:5617061] POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardation [LiteratureReference:9937278] A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis [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 Vuillaumier-Barrot, Sandrine (4724305)