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 Klopstock, Thomas

Class:Id	Person:5657586
_displayName	Klopstock, Thomas
_timestamp	2014-12-15 12:08:04
created	[InstanceEdit:5657574] Jupe, Steve, 2014-12-15
firstname	Thomas
initial	T
surname	Klopstock
(author)	[LiteratureReference:5657576] High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease [LiteratureReference:6787419] MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention [LiteratureReference:8868768] Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearing [LiteratureReference:8956303] The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations [LiteratureReference:9832377] Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant Mice [LiteratureReference:9856701] Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia [LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
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No pathways have been reviewed or authored by Klopstock, Thomas (5657586)