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.
Pathways reviewed by Belaya, Katsiaryna (5633214)
| DB_ID | Name |
|---|---|
| 4793950 | Defective MAN1B1 causes MRT15 |
| 4687000 | Defective MPDU1 causes CDG-1f |
| 5633231 | Defective ALG14 causes ALG14-CMS |
| 4549380 | Defective ALG1 causes CDG-1k |
| 4549349 | Defective ALG2 causes CDG-1i |
| 4551295 | Defective ALG11 causes CDG-1p |
| 4570571 | Defective RFT1 causes CDG-1n |
| 4720475 | Defective ALG3 causes CDG-1d |
| 4720454 | Defective ALG9 causes CDG-1l |
| 4720489 | Defective ALG12 causes CDG-1g |
| 4724289 | Defective ALG6 causes CDG-1c |
| 4724325 | Defective ALG8 causes CDG-1h |
| 4549356 | Defective DPAGT1 causes CDG-1j, CMSTA2 |
| 4793952 | Defective MGAT2 causes CDG-2a |
| 4793954 | Defective MOGS causes CDG-2b |
| 4793953 | Defective B4GALT1 causes CDG-2d |
| 3781860 | Diseases associated with N-glycosylation of proteins |
Details on Person Belaya, Katsiaryna
| Class:Id | Person:5633214 |
|---|---|
| _displayName | Belaya, Katsiaryna |
| _timestamp | 2014-11-10 10:36:15 |
| created | [InstanceEdit:5633234] Jassal, Bijay, 2014-10-31 |
| firstname | Katsiaryna |
| initial | K |
| modified | [InstanceEdit:5634130] Jassal, Bijay, 2014-11-03 [InstanceEdit:5637452] Jassal, Bijay, 2014-11-10 |
| surname | Belaya |
| (author) | [LiteratureReference:4549335] Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates [LiteratureReference:5633222] Congenital myasthenic syndromes due to mutations in ALG2 and ALG14 [LiteratureReference:5633243] Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1 [InstanceEdit:5633220] Belaya, Katsiaryna, 2014-10-31 |
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