About: Anthony W Ryan

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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) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Anthony W Ryan (en) Anthony W Ryan (es) Anthony W Ryan (nl) Anthony W Ryan (ast)
skos:prefLabel	Anthony W Ryan (en) Anthony W Ryan (es) Anthony W Ryan (nl) Anthony W Ryan (ast)
name	Anthony W Ryan (en) Anthony W Ryan (es) Anthony W Ryan (nl) Anthony W Ryan (ast)
LinkedIn personal profile ID	wds:Q42425569-A3F8F8D9-1D40-4433-B045-3E5A94AD61FC
LinkedIn personal profile ID	anthonywryan
given name	wds:Q42425569-8C4BD148-9894-4991-8427-CED02AA91F6E
given name	Anthony
instance of	wds:Q42425569-159D1B03-D13A-45A0-980B-D7E3391E3218
instance of	Homo sapiens
skos:altLabel	Anthony Ryan (en) Tony Ryan (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q42425569-55c48a5c-aef4-47b4-8933-6b772d8bc815
occupation	wds:Q42425569-7A57318F-CE30-4CC4-9D2D-538D5D472EF7
employer	wds:Q42425569-05616876-26F5-4522-8764-06EB0083B975 wds:Q42425569-61D2C13F-0D8E-479E-83B7-56D0465DA796 wds:Q42425569-9AD0F51A-E583-40CE-BA1E-F04C1B1638D2 wds:Q42425569-E98C46E8-933B-4556-9B15-752C4CAD1E62
sex or gender	wds:Q42425569-71A0DF4E-17B3-4220-9A7F-F1406F663DE8
VIAF ID	wds:Q42425569-C2DCFB11-5D91-4B2B-A4C8-5CD2B7519F8D
Library of Congress authority ID	wds:Q42425569-CC38FF91-71F6-4F82-A117-E06C36290E92
IdRef ID	wds:Q42425569-1fbb8b31-7c1e-4195-b0c1-6cd068b743b8
educated at	wds:Q42425569-B972AF95-B9CB-4FDF-BC9D-272D2C4F2769 wds:Q42425569-EE16991B-6EAA-4283-9B83-EF163141232F
family name	wds:Q42425569-A331B650-6E97-4226-B464-634CCCEC54A1
WorldCat Identities ID (superseded)	wds:Q42425569-D52D2C9B-F12B-464C-A1C2-864905E7EAA9
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p405024738
VIAF ID	http://viaf.org/viaf/10146522437832392644
Library of Congress authority ID	http://id.loc.gov/authorities/names/nb2015023145
IdRef ID	http://www.idref.fr/190540001/id
Nationale Thesaurus voor Auteursnamen ID	405024738
occupation	researcher
employer	Max Planck Institute for Evolutionary Anthropology Trondhjem Biological Station University College Dublin Genomics Medicine (Ireland)
sex or gender	male
VIAF ID	10146522437832392644
Library of Congress authority ID	nb2015023145
IdRef ID	190540001
educated at	University of Galway University College Dublin
family name	Ryan
WorldCat Identities ID (superseded)	lccn-nb2015023145
ORCID iD	wds:Q42425569-8EE7984E-501F-43C6-86F2-D33EDEBF5E05
Dimensions author ID	wds:Q42425569-1B1AC971-4768-4F0D-8CBC-EE8335C56ECF
ORCID iD	https://orcid.org/0000-0001-5005-3344
ORCID iD	0000-0001-5005-3344
Dimensions author ID	011246333177.72
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42425569
is author of	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci Newly identified genetic risk variants for celiac disease related to the immune response Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Variants in linkage disequilibrium with the late cornified envelope gene cluster deletion are associated with susceptibility to psoriatic arthritis Evidence to support IL-13 as a risk locus for psoriatic arthritis but not psoriasis vulgaris Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling The pregnane X receptor locus is associated with susceptibility to inflammatory bowel disease. Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study Haplotypes in the CTLA4 region are associated with coeliac disease in the Irish population. A genome-wide approach to identify genetic loci with a signature of natural selection in the Irish population Sequence and phylogenetic analysis of the gene for surface layer protein, slpA, from 14 PCR ribotypes of Clostridium difficile. Epigenetic modulation in the treatment of atherosclerotic disease Variants inRUNX3Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground With Ankylosing Spondylitis Levels of interpopulation differentiation among different functional classes of immunologically important genes Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus Genes of the interleukin-18 pathway are associated with susceptibility to Barrett's esophagus and esophageal adenocarcinoma. Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. Apolipoprotein E genotype in senile dementia and Down's syndrome Eastern and Western Poor Cod (Trisopterus minutus capelanus) Populations in the Mediterranean Sea: Evidence from Allozyme and Minisatellite Loci Gene polymorphism and requirement for vasopressor infusion after cardiac surgery

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