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 Jassal, Bijay, 2014-11-03

Class:Id	InstanceEdit:5634120
_displayName	Jassal, Bijay, 2014-11-03
_timestamp	2014-11-03 11:41:14
author	[Person:73447] Jassal, Bijay
dateTime	2014-11-03 16:40:25
(created)	[Person:5634118] Nakaki, Toshio [InstanceEdit:5634119] Nakaki, Toshio, 2014-11-03
(modified)	[Pathway:5578995] Defective TPMT causes TPMT deficiency [Homo sapiens] [Pathway:5578996] Defective CYP27A1 causes CTX [Homo sapiens] [Pathway:5578997] Defective AHCY causes HMAHCHD [Homo sapiens] [Pathway:5578998] Defective OPLAH causes OPLAHD [Homo sapiens] [Pathway:5578999] Defective GCLC causes HAGGSD [Homo sapiens] [Pathway:5579000] Defective CYP1B1 causes Glaucoma [Homo sapiens] [Pathway:5579002] Defective UGT1A1 causes hyperbilirubinemia [Homo sapiens] [Pathway:5579004] Defective CYP26C1 causes FFDD4 [Homo sapiens] [Pathway:5579005] Defective CYP4F22 causes ARCI5 [Homo sapiens] [Pathway:5579006] Defective GSS causes GSS deficiency [Homo sapiens] List all 69 refering instances
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-11-03 (5634120)