About: Bryan Traynor

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

Irish neuroscientist

Attributes	Values
rdf:type	Item
description	neurowetenschapper (nl) Irish neuroscientist (en) neurólogo irlandés (es)
rdfs:label	Bryan Traynor (en) Bryan Traynor (es) Bryan Traynor (nl) Bryan Traynor (ast)
skos:prefLabel	Bryan Traynor (en) Bryan Traynor (es) Bryan Traynor (nl) Bryan Traynor (ast)
name	Bryan Traynor (en) Bryan Traynor (es) Bryan Traynor (nl) Bryan Traynor (ast)
Scopus author ID	wds:Q28777952-c05e5973-4cd4-14d3-8f33-6c3df6e67aac
Scopus author ID	6701852117
given name	wds:Q28777952-47B2777F-432A-48CD-A544-7140D87D36AE
given name	Bryan
instance of	wds:Q28777952-285d7026-4c2a-2201-526e-62c12718b5ee
instance of	Homo sapiens
award received	wds:Q28777952-19f7f3bd-4852-c5f0-4ccb-f8b2ada8efaa
award received	Potamkin Prize
Google Knowledge Graph ID	wds:Q28777952-A9127314-E5AE-43FB-AF8B-7FC68BA07427
Google Knowledge Graph ID	http://g.co/kg/g/11hynbgdpg
Google Knowledge Graph ID	/g/11hynbgdpg
skos:altLabel	Bryan J. Traynor (en) Bryan J. Traynor (es)
occupation	wds:Q28777952-b5a47a7c-4be1-2432-2cd3-44efeac587d3
employer	wds:Q28777952-ecb891f6-4b1d-5646-097d-730510778bcd
place of birth	wds:Q28777952-E3DD50CA-AEAB-48BF-A292-A9A58BF41C5F
sex or gender	wds:Q28777952-61658aad-4b32-146f-57e2-68260dd24aa1
VIAF ID	wds:Q28777952-b42c7f54-4baa-c5d0-2394-b733475178b8
GND ID	wds:Q28777952-e3c3ef15-4e9d-8f81-6278-0cab9a44db36
Library of Congress authority ID	wds:Q28777952-C87CA695-A76C-4F1D-8CD5-D6FCD78E3EB7
date of birth	wds:Q28777952-3CED4C54-6E03-47B7-B2E7-1BB32831A8C3
educated at	wds:Q28777952-1fb88678-4a97-f9f5-6ec1-4c4d7b479595 wds:Q28777952-e4578dfb-755c-4b13-b89a-ed9c42b25655
family name	wds:Q28777952-D8BE1B8A-10CE-473A-9B02-B3BAFA07B59E
WorldCat Identities ID (superseded)	wds:Q28777952-1CFB8025-DCD5-40CC-890B-DE16952A84DC
VIAF ID	http://viaf.org/viaf/311463942
GND ID	https://d-nb.info/gnd/1065777310
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2014189968
occupation	neuroscientist
employer	National Institute on Aging
place of birth	Dublin
sex or gender	male
VIAF ID	311463942
GND ID	1065777310
Library of Congress authority ID	n2014189968
date of birth	1969-08-12 00:00:00Z (xsd:dateTime)
educated at	Harvard Medical School University College Dublin
family name	Traynor
WorldCat Identities ID (superseded)	lccn-n2014189968
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28777952 Bryan J. Traynor https://es.wikipedia.org/wiki/Bryan_Traynor
is author of	State of play in amyotrophic lateral sclerosis genetics The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype? Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis Ethnic variation in the incidence of ALS: a systematic review Towards a complete resolution of the genetic architecture of disease Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Large C9orf72 repeat expansions are not a common cause of Parkinson's disease Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD The epidemiology of ALS and the role of population-based registries Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain Common genetic variants influence human subcortical brain structures SNCA variants are associated with increased risk for multiple system atrophy Genetic comorbidities in Parkinson's disease Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Genome-wide meta-analysis identifies new susceptibility loci for migraine Genotype, haplotype and copy-number variation in worldwide human populations Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis A genome-wide association study of sporadic ALS in a homogenous Irish population. Exome sequencing reveals VCP mutations as a cause of familial ALS An outcome study of riluzole in amyotrophic lateral sclerosis--a population-based study in Ireland, 1996-2000. TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis Genome-wide association study reveals genetic risk underlying Parkinson's disease Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population Extensive genetics of ALS: a population-based study in Italy RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases Novel genetic loci underlying human intracranial volume identified through genome-wide association Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

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