Query author contributions in Reactome

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Details on Person Riess, Olaf

Class:Id	Person:5658553
_displayName	Riess, Olaf
_timestamp	2014-12-19 16:11:24
created	[InstanceEdit:5658493] Jupe, Steve, 2014-12-19
firstname	Olaf
initial	O
surname	Riess
(author)	[LiteratureReference:5658512] Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease [LiteratureReference:5660758] Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease [LiteratureReference:5689067] Asian origin for the worldwide-spread mutational event in Machado-Joseph disease [LiteratureReference:9856701] Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia
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No pathways have been reviewed or authored by Riess, Olaf (5658553)