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.

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Details on Person Majewski, Jacek

Class:IdPerson:2458336
_displayNameMajewski, Jacek
_timestamp2012-08-29 12:02:19
created[InstanceEdit:2458286] Jassal, B, 2012-08-29
firstnameJacek
initialJ
surnameMajewski
(author)[LiteratureReference:3318443] Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome
[LiteratureReference:3322890] Mutations in NOTCH2 in families with Hajdu-Cheney syndrome
[LiteratureReference:3928676] Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism
[LiteratureReference:9647275] Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
[LiteratureReference:9681554] ARHGDIA: a novel gene implicated in nephrotic syndrome
[LiteratureReference:9754266] Bmp signaling maintains a mesoderm progenitor cell state in the mouse tailbud
[LiteratureReference:9916626] Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome
[LiteratureReference:9981462] SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase CÉ›) impairing TORC2-dependent AKT activation
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No pathways have been reviewed or authored by Majewski, Jacek (2458336)