Reactome: A Curated Pathway Database

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.

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Details on Person Alkuraya, Fowzan S

Class:IdPerson:4839835
_displayNameAlkuraya, Fowzan S
_timestamp2017-08-22 20:44:46
created[InstanceEdit:4839807] Jassal, B, 2013-11-04
firstnameFowzan S
initialFS
surnameAlkuraya
(author)[LiteratureReference:4839792] Mental retardation, growth retardation, unusual nose, and open mouth: an autosomal recessive entity
[LiteratureReference:4839814] Congenital disorder of glycosylation IIa: the trouble with diagnosing a dysmorphic inborn error of metabolism
[LiteratureReference:5659981] Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
[LiteratureReference:8867078] Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
[LiteratureReference:8870269] A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition
[InstanceEdit:8877098] Alkuraya, Fowzan S, 2016-06-20
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No pathways have been reviewed or authored by Alkuraya, Fowzan S (4839835)