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 Gravel, RA

Class:Id	Person:71002
_displayName	Gravel, RA
_timestamp	0000-00-00 00:00:00
firstname	Roy A
initial	RA
surname	Gravel
(author)	[LiteratureReference:200732] Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders [LiteratureReference:3095895] Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type [LiteratureReference:3159261] Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation [LiteratureReference:3159262] Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation [LiteratureReference:3159291] Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements [LiteratureReference:3159300] Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism [LiteratureReference:3322111] Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L [LiteratureReference:3325559] Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria [LiteratureReference:3325635] Genetic disorders of vitamin B12 metabolism: eight complementation groups--eight genes [LiteratureReference:3325638] Molecular genetics of biotin metabolism: old vitamin, new science
(chapterAuthors)	[Book:71000] The Metabolic and Molecular Bases of Inherited Disease, 8th ed Scriver, CR Disorders of propionate and methylmalonate metabolism 0079130356
[Change default viewing format]

No pathways have been reviewed or authored by Gravel, RA (71002)