About: Alexander S Doney

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

About: Alexander S Doney 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) researcher (en) 연구원 (ko) 研究者 (ja) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) հետազոտող (hy) onderzoeker (nl)
rdfs:label	Alexander S Doney (en) Alexander S Doney (es) Alexander S Doney (nl) Alexander S Doney (ast)
skos:prefLabel	Alexander S Doney (en) Alexander S Doney (es) Alexander S Doney (nl) Alexander S Doney (ast)
name	Alexander S Doney (en) Alexander S Doney (es) Alexander S Doney (nl) Alexander S Doney (ast)
given name	wds:Q57327614-B93E83FE-89D8-4668-84C0-9FCB95F79849
given name	Aleksandr
instance of	wds:Q57327614-85A40961-3BC0-468B-95AB-871E77037187
instance of	Homo sapiens
skos:altLabel	A S F Doney (en) Alex S Doney (en) Alex S F Doney (en) Alex Sf Doney (en) Alexander Doney (en) Alexander Doney (en)
occupation	wds:Q57327614-42E4131D-06C2-4600-AC21-5F3D1D1E4B10
employer	wds:Q57327614-e5095c03-48a8-9cc4-ef6c-b3dd09186bac
sex or gender	wds:Q57327614-077F2B44-1BF5-4796-8FD4-AEBCC799B628
DBLP author ID	wds:Q57327614-9F166EAD-724C-49AA-BD77-697AF20D44AA
DBLP author ID	https://dblp.org/pid/21/9253.rdf
occupation	researcher
employer	University of Dundee
sex or gender	male
DBLP author ID	21/9253
ORCID iD	wds:Q57327614-B61A6504-48A5-4890-8FFF-96C47030A19C
ORCID iD	https://orcid.org/0000-0002-6210-5620
ORCID iD	0000-0002-6210-5620
ResearcherID	wds:Q57327614-2BE92949-C79C-438F-9465-86CA6866A4D8
ResearcherID	P-7437-2017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57327614
is author of	Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility Common variants near MC4R are associated with fat mass, weight and risk of obesity Genetic studies of body mass index yield new insights for obesity biology Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes Peroxisome proliferator-activated receptor-delta genotype influences metabolic phenotype and may influence lipid response to statin therapy in humans: a genetics of diabetes audit and research Tayside study. Effect of Metformin on mortality in patients with heart failure and type 2 diabetes mellitus Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis Haplotype analysis of the PPARgamma Pro12Ala and C1431T variants reveals opposing associations with body weight. Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis The effect of obesity on glycaemic response to metformin or sulphonylureas in Type 2 diabetes. Variants in MTNR1B influence fasting glucose levels Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data Common nonsynonymous substitutions in SLCO1B1 predispose to statin intolerance in routinely treated individuals with type 2 diabetes: a go-DARTS study A paucimorphic variant in the HMG-CoA reductase gene is associated with lipid-lowering response to statin treatment in diabetes: a GoDARTS study. Apolipoprotein E genotypes are associated with lipid-lowering responses to statin treatment in diabetes: a Go-DARTS study. Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. Intracellular ATP influences synaptic plasticity in area CA1 of rat hippocampus via metabolism to adenosine and activity-dependent activation of adenosine A1 receptors Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus A genome-wide association search for type 2 diabetes genes in African Americans New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Common variants associated with plasma triglycerides and risk for coronary artery disease Discovery and refinement of loci associated with lipid levels Large-scale association analysis identifies new risk loci for coronary artery disease Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study Genetic association analysis of LARS2 with type 2 diabetes New genetic loci link adipose and insulin biology to body fat distribution Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function Loss-of-function CYP2C9 variants improve therapeutic response to sulfonylureas in type 2 diabetes: a Go-DARTS study. A role for coding functional variants in HNF4A in type 2 diabetes susceptibility Public attitudes to the storage of blood left over from routine general practice tests and its use in research. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Defining the role of common variation in the genomic and biological architecture of adult human height The cost of cerebral ischaemia. The genetic architecture of type 2 diabetes The FTO gene is associated with an atherogenic lipid profile and myocardial infarction in patients with type 2 diabetes: a Genetics of Diabetes Audit and Research Study in Tayside Scotland (Go-DARTS) study Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease Robust association of the LPA locus with low-density lipoprotein cholesterol lowering response to statin treatment in a meta-analysis of 30 467 individuals from both randomized control trials and observational studies and association with [...] Genome-wide association and functional follow-up reveals new loci for kidney function Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

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, 188 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software