Query author contributions in Reactome

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Details on Person Stratton, MR

Class:Id	Person:1614179
_displayName	Stratton, MR
_timestamp	2011-09-27 13:31:47
created	[InstanceEdit:1614178] Rothfels, K, 2011-09-27
firstname	Michael R
initial	MR
surname	Stratton
(author)	[LiteratureReference:1614272] Somatic mutations of the protein kinase gene family in human lung cancer [LiteratureReference:1637891] Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes [LiteratureReference:2018771] Patterns of somatic mutation in human cancer genomes [LiteratureReference:3318337] COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer [LiteratureReference:4836527] Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation [LiteratureReference:5661011] Natural history of Christianson syndrome [LiteratureReference:5661048] SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome [LiteratureReference:5672236] Mutations of the BRAF gene in human cancer [LiteratureReference:6799043] COSMIC: exploring the world's knowledge of somatic mutations in human cancer [LiteratureReference:9606466] Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma List all 12 refering instances
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No pathways have been reviewed or authored by Stratton, MR (1614179)