About: Hreinn Stefansson

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Hreinn Stefansson Goto Sponge NotDistinct Permalink

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) investigador (es) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) ഗവേഷകന്‍ (ml) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
rdfs:label	Hreinn Stefansson (de) Hreinn Stefansson (en) Hreinn Stefansson (es) Hreinn Stefansson (fr) Hreinn Stefansson (nl) Hreinn Stefansson (sl) Hreinn Stefansson (ast)
skos:prefLabel	Hreinn Stefansson (de) Hreinn Stefansson (en) Hreinn Stefansson (es) Hreinn Stefansson (fr) Hreinn Stefansson (nl) Hreinn Stefansson (sl) Hreinn Stefansson (ast)
name	Hreinn Stefansson (de) Hreinn Stefansson (en) Hreinn Stefansson (es) Hreinn Stefansson (fr) Hreinn Stefansson (nl) Hreinn Stefansson (sl) Hreinn Stefansson (ast)
instance of	wds:Q28050141-3C7874E7-A1B5-4527-90E5-F03C638C2142
instance of	Homo sapiens
occupation	wds:Q28050141-A07100E8-6A3F-41B3-B63D-1EF8BFD359A0
employer	wds:Q28050141-77C7F4CB-E838-4E38-9542-44F781D77663
sex or gender	wds:Q28050141-3d37c78f-4ade-6c31-718e-99c74290f226
VIAF ID	wds:Q28050141-85356FE6-201E-4086-8388-98E7BAB47C06
GND ID	wds:Q28050141-1ccd125b-3795-47a0-8dfe-3926a9853f72
Library of Congress authority ID	wds:Q28050141-91E25E1F-E045-469A-B7C0-FBAA78B2371B
date of birth	wds:Q28050141-6EC1C459-B767-4990-9FD3-2C6D3E860B80
educated at	wds:Q28050141-032A7E67-2A7C-40EE-AD12-AE565DF8B968
WorldCat Identities ID (superseded)	wds:Q28050141-191D4065-6A30-4D6C-8585-60C09526178F
VIAF ID	http://viaf.org/viaf/314899048
GND ID	https://d-nb.info/gnd/1118530241
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2015181473
occupation	researcher
employer	deCODE genetics
sex or gender	male
VIAF ID	314899048
GND ID	1118530241
Library of Congress authority ID	n2015181473
date of birth	1964-01-01 00:00:00Z (xsd:dateTime)
educated at	Lund University
WorldCat Identities ID (superseded)	lccn-n2015181473
Springer Nature person ID	wds:Q28050141-39084BB6-0C43-465C-BDA9-D78914285E60
ORCID iD	wds:Q28050141-5F5FBB69-5685-44B1-85AB-737FB5E548A6
Dimensions author ID	wds:Q28050141-13C649DD-D5EC-4BA7-B0D3-C3BAA7AABE3C
ORCID iD	https://orcid.org/0000-0002-9331-6666
Springer Nature person ID	0611467633.09
ORCID iD	0000-0002-9331-6666
Dimensions author ID	0611467633.09
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28050141
is author of	A rare variant in MYH6 is associated with high risk of sick sinus syndrome Many sequence variants affecting diversity of adult human height Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma Seven new loci associated with age-related macular degeneration Variant of TREM2 Associated with the Risk of Alzheimer's Disease A genetic risk factor for periodic limb movements in sleep A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease CNVs conferring risk of autism or schizophrenia affect cognition in controls A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations. Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility Multiple novel transcription initiation sites for NRG1 Neuregulin1 (NRG1) signaling through Fyn modulates NMDA receptor phosphorylation: differential synaptic function in NRG1+/- knock-outs compared with wild-type mice. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration Disruption of the neurexin 1 gene is associated with schizophrenia Expanding the range of ZNF804A variants conferring risk of psychosis Association between microdeletion and microduplication at 16p11.2 and autism Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype. Common variants conferring risk of schizophrenia Association of neuregulin 1 with schizophrenia confirmed in a Scottish population Neuregulin 1 and susceptibility to schizophrenia

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software