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 Turner, Emily H

Class:Id	Person:5652089
_displayName	Turner, Emily H
_timestamp	2014-11-27 15:51:40
created	[InstanceEdit:5652118] Jassal, Bijay, 2014-11-27
firstname	Emily H
initial	EH
surname	Turner
(author)	[LiteratureReference:5652121] Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation [LiteratureReference:9944939] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome [LiteratureReference:9969682] Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia [LiteratureReference:9969740] Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms
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No pathways have been reviewed or authored by Turner, Emily H (5652089)