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.

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Details on Person Freisinger, Peter

Class:Id	Person:5638234
_displayName	Freisinger, Peter
_timestamp	2014-11-13 15:45:58
created	[InstanceEdit:5638236] Jassal, Bijay, 2014-11-13
firstname	Peter
initial	P
surname	Freisinger
(author)	[LiteratureReference:5638214] Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin [LiteratureReference:6786797] ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy [LiteratureReference:9839690] Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA [LiteratureReference:9859455] Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects [LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
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No pathways have been reviewed or authored by Freisinger, Peter (5638234)