Reactome: A Curated Pathway Database
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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.

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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:IdPerson:5633214
_displayNameBelaya, Katsiaryna
_timestamp2014-11-10 10:36:15
created[InstanceEdit:5633234] Jassal, Bijay, 2014-10-31
firstnameKatsiaryna
initialK
modified[InstanceEdit:5634130] Jassal, Bijay, 2014-11-03
[InstanceEdit:5637452] Jassal, Bijay, 2014-11-10
surnameBelaya
(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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