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 Salomons, Gajja S

Class:Id	Person:70948
_displayName	Salomons, Gajja S
_timestamp	2015-01-02 21:54:49
firstname	Gajja S
initial	GS
modified	[InstanceEdit:5659966] D'Eustachio, Peter, 2015-01-02
surname	Salomons
(author)	[LiteratureReference:70944] Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT) [LiteratureReference:71326] Transaldolase deficiency: liver cirrhosis associated with a new inborn error in the pentose phosphate pathway. [LiteratureReference:177786] Ribose-5-phosphate isomerase deficiency: new inborn error in the pentose phosphate pathway associated with a slowly progressive leukoencephalopathy [LiteratureReference:200390] X-linked creatine transporter defect: an overview [LiteratureReference:880003] Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria [LiteratureReference:5659986] A newborn with severe liver failure, cardiomyopathy and transaldolase deficiency [LiteratureReference:5659993] Novel association of early onset hepatocellular carcinoma with transaldolase deficiency [LiteratureReference:5659994] Transaldolase deficiency in a two-year-old boy with cirrhosis [LiteratureReference:9853642] IDH2 mutations in patients with D-2-hydroxyglutaric aciduria
[Change default viewing format]

No pathways have been reviewed or authored by Salomons, Gajja S (70948)