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 Janecke, Andreas R

Class:Id	Person:508037
_displayName	Janecke, Andreas R
_timestamp	2015-06-17 20:37:51
created	[InstanceEdit:508032] D'Eustachio, P, 2010-02-10
firstname	Andreas R
initial	AR
modified	[InstanceEdit:508096] D'Eustachio, P, 2010-02-10 [InstanceEdit:6783922] D'Eustachio, Peter, 2015-06-17
surname	Janecke
(author)	[LiteratureReference:508064] Mutations in PYCR1 cause cutis laxa with progeroid features [LiteratureReference:2471628] Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy [LiteratureReference:3636877] Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome [LiteratureReference:6814319] Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function [LiteratureReference:9941057] Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint Laxity [LiteratureReference:9941167] Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome
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No pathways have been reviewed or authored by Janecke, Andreas R (508037)