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 Omran, H

Class:Id	Person:508567
_displayName	Omran, H
_timestamp	2010-02-12 22:53:44
created	[InstanceEdit:508568] D'Eustachio, P, 2010-02-12
firstname	Heymut
initial	H
modified	[InstanceEdit:508575] D'Eustachio, P, 2010-02-12
surname	Omran
(author)	[LiteratureReference:508571] Mutations in antiquitin in individuals with pyridoxine-dependent seizures [LiteratureReference:5579051] Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism [LiteratureReference:5638367] When cilia go bad: cilia defects and ciliopathies [LiteratureReference:6790338] Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytoma [LiteratureReference:6800633] Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma [LiteratureReference:9945663] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia [LiteratureReference:9960341] Multicilin drives centriole biogenesis via E2f proteins [LiteratureReference:9960886] De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry [LiteratureReference:9961915] Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells [LiteratureReference:9961934] Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia List all 28 refering instances
[Change default viewing format]

No pathways have been reviewed or authored by Omran, H (508567)