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 Varusai, Thawfeek, 2017-07-26
| Class:Id | InstanceEdit:9014026 |
|---|
| _displayName | Varusai, Thawfeek, 2017-07-26 |
|---|
| _timestamp | 2017-07-26 13:24:07 |
|---|
| author | [Person:8952429] Varusai, Thawfeek |
|---|
| dateTime | 2017-07-26 17:21:37 |
|---|
| (created) | [Person:9014023] Callewaert, Bert
[Person:9014024] Vanakker, Olivier
[Person:9014025] Takahara, Kazuhiko
[LiteratureReference:9014027] Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
[Person:9014028] Hoffman, Guy G
[Person:9014029] De Backer, Julie
[Person:9014030] Coucke, Paul
[LiteratureReference:9014031] Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type I
[Person:9014032] Smith, Lynne T
[Person:9014033] Byers, Peter H |
|---|
| (modified) | [Summation:9013586] Mutations in procollagen peptide type V (COL5A1) can cause d...
[Reaction:9013588] Defective procollagen type V [Homo sapiens]
[DefinedSet:9013596] COL5A1 mutants [endoplasmic reticulum lumen] [Homo sapiens] |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Varusai, Thawfeek, 2017-07-26 (9014026)
