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 Al-Gazali, Lihadh

Class:Id	Person:508046
_displayName	Al-Gazali, Lihadh
_timestamp	2015-06-17 20:37:43
created	[InstanceEdit:508032] D'Eustachio, P, 2010-02-10
firstname	Lihadh
initial	L
modified	[InstanceEdit:508096] D'Eustachio, P, 2010-02-10 [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Al-Gazali
(author)	[LiteratureReference:508064] Mutations in PYCR1 cause cutis laxa with progeroid features [LiteratureReference:1675802] Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies [LiteratureReference:3621752] Faulty initiation of proteoglycan synthesis causes cardiac and joint defects [LiteratureReference:4420007] SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder [LiteratureReference:5624829] Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome [LiteratureReference:5656257] Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine [LiteratureReference:5656262] Functional analysis of NBC1 mutants associated with proximal renal tubular acidosis and ocular abnormalities [LiteratureReference:9725148] An SCN9A channelopathy causes congenital inability to experience pain [LiteratureReference:9944961] A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome
[Change default viewing format]

No pathways have been reviewed or authored by Al-Gazali, Lihadh (508046)