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.

Details on Person Broer, Stefan, 2015-08-04

Class:Id	InstanceEdit:6789776
_displayName	Broer, Stefan, 2015-08-04
_timestamp	2015-09-10 08:21:51
author	[Person:352037] Broer, Stefan
created	[InstanceEdit:6789777] Jassal, Bijay, 2015-08-04
dateTime	2015-08-04 16:34:29
modified	[InstanceEdit:6797395] Jassal, Bijay, 2015-09-10 [InstanceEdit:6797396] Jassal, Bijay, 2015-09-10
(reviewed)	[FailedReaction:3560789] Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol [Homo sapiens] [Pathway:3560792] Defective SLC26A2 causes chondrodysplasias [Homo sapiens] [Pathway:5619035] Defective SLC17A5 causes Salla disease (SD) and ISSD [Homo sapiens] [Pathway:5619036] Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6) [Homo sapiens] [Pathway:5619037] Defective transport by SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) [Homo sapiens] [Pathway:5619039] Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) [Homo sapiens] [Pathway:5619040] Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1) [Homo sapiens] [Pathway:5619041] Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG) [Homo sapiens] [Pathway:5619042] Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) [Homo sapiens] [Pathway:5619043] Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) [Homo sapiens] List all 139 refering instances
[Change default viewing format]

No pathways have been reviewed or authored by Broer, Stefan, 2015-08-04 (6789776)