About: Nicholas W. Wood

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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) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Nicholas W. Wood (en) Nicholas W. Wood (es) Nicholas W. Wood (nl) Nicholas W. Wood (sl) Nicholas W. Wood (ast) নিকোলাস ডাব্লিউ উড (bn)
skos:prefLabel	Nicholas W. Wood (en) Nicholas W. Wood (es) Nicholas W. Wood (nl) Nicholas W. Wood (sl) Nicholas W. Wood (ast) নিকোলাস ডাব্লিউ উড (bn)
name	Nicholas W. Wood (en) Nicholas W. Wood (es) Nicholas W. Wood (nl) Nicholas W. Wood (sl) Nicholas W. Wood (ast) নিকোলাস ডাব্লিউ উড (bn)
Scopus author ID	wds:Q42592839-C42F8037-22CF-4F62-93A2-0E7F533A797D wds:Q42592839-E92E76F9-26C7-4746-89D4-57F7F126ECAD
Scopus author ID	57207702408 7202960784
given name	wds:Q42592839-F2D8EFAC-CA65-432D-98E5-92F309E512AC
given name	Nicholas
instance of	wds:Q42592839-F5426751-5AD9-4A78-8A60-FF21A54E45FD
instance of	Homo sapiens
Semantic Scholar author ID	wds:Q42592839-9AEE24ED-2611-4CD0-B10B-EF052E4B807D
Semantic Scholar author ID	144859175
skos:altLabel	Nicholas Wood (en) N W Wood (en) NW Wood (en) Nicholas W Wood (en)
occupation	wds:Q42592839-382E64E9-CCDB-4F2B-8597-A15CAFD547CA
employer	wds:Q42592839-5D58C861-8DBB-4C3D-A9B1-B1C30DB6DAC9
NUKAT ID	wds:Q42592839-2E8B2B2E-E932-4ABE-8465-7234C0A92D42
sex or gender	wds:Q42592839-A3D81A57-098A-4C0A-8F0B-FE0C11FF1B1A
VIAF ID	wds:Q42592839-B8637132-D051-41B0-BA82-BCF32321C301
IdRef ID	wds:Q42592839-CF89EEBF-B348-43B5-8A7B-DF28DBC0690C
educated at	wds:Q42592839-24D0BE57-F358-42FF-88E0-FE927FD5A940 wds:Q42592839-2ACFD27C-7458-43CD-A3E5-297AFB23A7B0 wds:Q42592839-6D1B489C-A1E9-4216-BE26-FDC2E97D0281 wds:Q42592839-A860E763-5D83-4B4D-AC3C-A9CDF09AF9F5
family name	wds:Q42592839-A6DAADAA-BFA1-45FD-8B38-58105056BD40
VIAF ID	http://viaf.org/viaf/56117654
IdRef ID	http://www.idref.fr/226264041/id
occupation	researcher
employer	University College London
NUKAT ID	n01090675
sex or gender	male
VIAF ID	56117654
IdRef ID	226264041
educated at	University of Birmingham John Ffowcs Williams Royal College of Physicians, London
family name	Wood
ORCID iD	wds:Q42592839-F6926DE9-F809-45EB-A376-68A6CF99745A
ORCID iD	https://orcid.org/0000-0002-9500-3348
ORCID iD	0000-0002-9500-3348
ResearcherID	wds:Q42592839-D7D94B1A-26C7-4FAA-8A61-221C57E33A4C
Publons author ID	wds:Q42592839-cc44a9b9-6684-41cf-913f-8b467c6aa1e1
ResearcherID	C-2505-2009
Publons author ID	2862370
is owl:sameAs of	Nicholas W. Wood
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42592839
is author of	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption Single-Molecule Imaging of Individual Amyloid Protein Aggregates in Human Biofluids Rare individual amyloid-β oligomers act on astrocytes to initiate neuronal damage ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia. The phenotypic spectrum of DYT24 due to ANO3 mutations Multiple sclerosis and the HLA-D region: linkage and association studies Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin's effect on neuronal survival Parkin mutations are frequent in patients with isolated early-onset parkinsonism. Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial-cervical or upper limb onset Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter GeneABCB1 Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

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