About: Christopher G. Mathew

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) araştırmacı (tr) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
rdfs:label	Christopher G Mathew (nl) Christopher G Mathew (sl) Christopher G. Mathew (en) Christopher G. Mathew (es) Christopher G. Mathew (it) Christopher Mathew (fr)
skos:prefLabel	Christopher G Mathew (nl) Christopher G Mathew (sl) Christopher G. Mathew (en) Christopher G. Mathew (es) Christopher G. Mathew (it) Christopher Mathew (fr)
name	Christopher G Mathew (nl) Christopher G Mathew (sl) Christopher G. Mathew (en) Christopher G. Mathew (es) Christopher G. Mathew (it) Christopher Mathew (fr)
Scopus author ID	wds:Q30348903-15EF5DA5-25E1-4D4D-AE49-38BB92F09A50
Scopus author ID	7004609303
given name	wds:Q30348903-FB611FC5-1673-4DBE-8852-C001068E70C6
given name	Christopher
instance of	wds:Q30348903-FFEFF553-71BB-46D4-9A08-7D06ED6A91A8
instance of	Homo sapiens
skos:altLabel	Christopher Mathew (en)
occupation	wds:Q30348903-A81FC217-243C-4C8F-A107-4598FEE93504
employer	wds:Q30348903-0F7839E7-FAC0-4269-9E56-31678144B1E6 wds:Q30348903-3D15D566-AB7D-468D-B914-38308006810F wds:Q30348903-82731458-4c29-4b47-8cb8-b41c482a0712 wds:Q30348903-BA0B3171-8723-48A2-96F9-E1B71C448C26
sex or gender	wds:Q30348903-14C172A7-707D-4521-984B-73DABDA39F9E
ISNI	wds:Q30348903-2883C796-9F46-4CA5-880C-30C8D63EB48A
VIAF ID	wds:Q30348903-2BA11F51-215E-49CA-997A-C00552980F5F
IdRef ID	wds:Q30348903-DF3ED17D-80DB-4D1E-9B41-EEF8D2050F3A
educated at	wds:Q30348903-C6E7C19C-7565-417E-8004-02BD96B2738D
National Library of Israel J9U ID	wds:Q30348903-FEA4DB53-BECF-425D-81C0-7D80BAFA82D1
official website	wds:Q30348903-72FA23E4-88A4-4678-927A-A71909F6F5F9
VIAF ID	http://viaf.org/viaf/24677061
IdRef ID	http://www.idref.fr/085969648/id
occupation	researcher
employer	University of the Witwatersrand Faculty of Health Sciences King's College London
sex or gender	male
ISNI	0000000028506629
VIAF ID	24677061
IdRef ID	085969648
educated at	University of London
National Library of Israel J9U ID	987007431638705171
official website	https://kclpure.kcl.ac.uk/portal/en/persons/christopher-mathew(4dd29378-7879-4a22-800b-b74ceb49362d).html
Springer Nature person ID	wds:Q30348903-A73A9152-7C13-4FBD-BF7B-F0B9A27F6CF0
ORCID iD	wds:Q30348903-66C19394-40A0-4645-B384-6B8F0565DE35
Dimensions author ID	wds:Q30348903-5FCAFA02-2803-4AD7-AA7E-52AD25543FBA
ORCID iD	https://orcid.org/0000-0003-4178-1838
Springer Nature person ID	01313422073.62
ORCID iD	0000-0003-4178-1838
Dimensions author ID	01313422073.62
Gateway to Research person ID	wds:Q30348903-5EF01C59-3C6D-4002-A9F5-A61707C4F82B
Gateway to Research person ID	8E8A81F1-A264-4E23-8C60-0E41B53E2096
ResearcherID	wds:Q30348903-D4929638-0A8F-4A91-9BF7-A238C80AF962
Publons author ID	wds:Q30348903-29f0c321-b61d-456f-b22b-23267e27325b
ResearcherID	G-3434-2015
Publons author ID	2401143
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30348903
is author of	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis High frequency of large intragenic deletions in the Fanconi anemia group A gene Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.

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