About: Huw R Morris

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

researcher (ORCID 0000-0002-5473-3774)

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (ORCID 0000-0002-5473-3774) (en)
rdfs:label	Huw R Morris (en) Huw R Morris (es) Huw R Morris (nl) Huw R Morris (sl) Huw R Morris (ast)
skos:prefLabel	Huw R Morris (en) Huw R Morris (es) Huw R Morris (nl) Huw R Morris (sl) Huw R Morris (ast)
name	Huw R Morris (en) Huw R Morris (es) Huw R Morris (nl) Huw R Morris (sl) Huw R Morris (ast)
given name	wds:Q42586947-3A82962D-E895-4632-B084-2825E216AF75
given name	Huw
instance of	wds:Q42586947-74F3F122-CEF8-48B9-87A4-617C2D94D356
instance of	Homo sapiens
Loop ID	wds:Q42586947-FD7A0472-DF08-4D53-9E8E-C4DD26CE3253
Loop ID	352625
skos:altLabel	Huw Morris (en)
occupation	wds:Q42586947-916FB189-7E19-4EB8-AD15-193AC89301B8
employer	wds:Q42586947-D7C69937-7901-4D86-ABDF-3CCCD5C17895
sex or gender	wds:Q42586947-03E05EC1-2888-4CF2-9D57-058CAE93994B
date of birth	wds:Q42586947-2C8FC369-49C7-4997-80D4-24B69A491383
family name	wds:Q42586947-329DC858-0DA1-47DB-A650-C14DD63C0963
official website	wds:Q42586947-D4978466-EFD3-48C0-8BD8-35D6F320F030
occupation	researcher
employer	University College London
sex or gender	male
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Morris
official website	http://iris.ucl.ac.uk/iris/browse/profile?upi=HRMOR79
ORCID iD	wds:Q42586947-26079407-C99A-4595-90D7-5AB45F600899 wds:Q42586947-2CA1F49E-A335-49D5-8309-9F6618FDF5CA
ORCID iD	https://orcid.org/0000-0001-9188-3934 https://orcid.org/0000-0002-5473-3774
ORCID iD	0000-0001-9188-3934 0000-0002-5473-3774
ResearcherID	wds:Q42586947-45EBE65D-D6F1-4632-ABF3-BB88EBEABCB4
Publons author ID	wds:Q42586947-9c197181-5603-48ba-bd10-7681fc8567a4
ResearcherID	B-8527-2008
Publons author ID	2884880
is owl:sameAs of	Huw R Morris
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42586947
is author of	Aripiprazole associated with severe exacerbation of Parkinson's disease A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure SGCE mutations cause psychiatric disorders: clinical and genetic characterization A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data Genetics of Parkinson's disease Creation of an open-access, mutation-defined fibroblast resource for neurological disease research Equating scores of the University of Pennsylvania Smell Identification Test and Sniffin' Sticks test in patients with Parkinson's disease Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Prevalence and age of onset of Parkinson's disease in Cardiff: a community based cross sectional study and meta-analysis The genetic and pathological classification of familial frontotemporal dementia. Mutation in the tau exon 10 splice site region in familial frontotemporal dementia. Early myoclonic status and outcome after cardiorespiratory arrest Clinical genetics of familial progressive supranuclear palsy. Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion Late onset startle induced tics Variation in tau isoform expression in different brain regions and disease states Parkinson's disease in GTP cyclohydrolase 1 mutation carriers Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease Recent advances in Parkinson’s disease genetics. The frequency of spinocerebellar ataxia type 23 in a UK population. Client and therapist views on exercise programmes for early-mid stage Parkinson's disease and Huntington's disease The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. Hyposmia in progressive supranuclear palsy. Parkinson's disease--the debate on the clinical phenomenology, aetiology, pathology and pathogenesis The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK. Chromosome 9 ALS and FTD locus is probably derived from a single founder Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease Sequence analysis of tau in familial and sporadic progressive supranuclear palsy. Case control analysis of repeat expansion size in ataxia. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review.

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