About: Robert A. Hegele

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

researcher ORCID ID = 0000-0003-2861-5325

Attributes	Values
rdf:type	Item
description	kanadischer Arzt (de) Canadees arts (nl) médicu canadianu (ast) researcher ORCID ID = 0000-0003-2861-5325 (en)
rdfs:label	Robert A. Hegele (ca) Robert A. Hegele (de) Robert A. Hegele (en) Robert A. Hegele (es) Robert A. Hegele (fr) Robert A. Hegele (ga) Robert A. Hegele (nl) Robert A. Hegele (sl) Robert A. Hegele (sq) Robert A. Hegele (ast)
skos:prefLabel	Robert A. Hegele (ca) Robert A. Hegele (de) Robert A. Hegele (en) Robert A. Hegele (es) Robert A. Hegele (fr) Robert A. Hegele (ga) Robert A. Hegele (nl) Robert A. Hegele (sl) Robert A. Hegele (sq) Robert A. Hegele (ast)
name	Robert A. Hegele (ca) Robert A. Hegele (de) Robert A. Hegele (en) Robert A. Hegele (es) Robert A. Hegele (fr) Robert A. Hegele (ga) Robert A. Hegele (nl) Robert A. Hegele (sl) Robert A. Hegele (sq) Robert A. Hegele (ast)
given name	wds:Q58046422-fbad1129-4d41-81c6-9349-e6cabae7fe5a
given name	Robert
instance of	wds:Q58046422-BEC178E5-2A55-4464-A643-8CBE88AF341F
instance of	Homo sapiens
skos:altLabel	R A Hegele (en) Rob Hegele (en) Rob Hegele (fr) Robert A Hegele (en) Robert A Hegele (fr) Robert Hegele (en) Robert Hegele (fr)
occupation	wds:Q58046422-86e72074-4e75-d723-4298-1976d2bd765d
employer	wds:Q58046422-b4fff232-4e14-a109-2f71-782ec91fc775 wds:Q58046422-b6625ead-4361-fbbd-593d-f64b5ed71083
sex or gender	wds:Q58046422-33ba1b7b-4930-3d8a-4b44-ebf06d3f9efc
country of citizenship	wds:Q58046422-465e3ffd-47ed-2a0b-dadd-3ab24a050c25
family name	wds:Q58046422-5BD47C70-9FD7-4197-8907-9E45961EDBCA
occupation	physician
employer	Western University Robarts Research Institute
sex or gender	male
country of citizenship	Malawi
family name	Hegele
ORCID iD	wds:Q58046422-A76A58D9-E119-4B38-86C2-62DA4FE4C771
ORCID iD	https://orcid.org/0000-0003-2861-5325
ORCID iD	0000-0003-2861-5325
Mendeley person ID	wds:Q58046422-22F19634-582C-4BC1-AA04-EE6E21CCBA55
Mendeley person ID	robert-hegele
is owl:sameAs of	Robert A. Hegele
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58046422
is author of	Genetic determinants of the metabolic syndrome Plasma lipoproteins: genetic influences and clinical implications Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals 2012 update of the Canadian Cardiovascular Society guidelines for the diagnosis and treatment of dyslipidemia for the prevention of cardiovascular disease in the adult Uncloaking the genetic determinants of metabolic syndrome Intellectual disability associated with a homozygous missense mutation in THOC6 Exome sequencing: new insights into lipoprotein disorders Mining the genome for lipid genes Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample Blood pressure among the Inuit (Eskimo) populations in the Arctic Substance P (NK1)- and neurokinin A (NK2)-receptor gene expression in inflammatory airway diseases Phenomics, lipodystrophy, and the metabolic syndrome Utility of non-high-density lipoprotein cholesterol in assessing incident type 2 diabetes risk. Allelic and phenotypic spectrum of plasma triglycerides Cerebral cholesterol granuloma in homozygous familial hypercholesterolemia Complete Apo AI deficiency in an Iraqi Mandaean family: case studies and review of the literature Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci Comprehensive analysis of genomic variation in the LPA locus and its relationship to plasma lipoprotein(a) in South Asians, Chinese, and European Caucasians Environmental modulation of atherosclerosis end points in familial hypercholesterolemia Methylenetetrahydrofolate reductase polymorphism 677C>T is associated with peripheral arterial disease in type 2 diabetes Complications of Type 2 Diabetes Among Aboriginal Canadians: prevalence and associated risk factors Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH). Association of parity with risk of type 2 diabetes and related metabolic disorders An apolipoprotein CII mutation, CIILys19----Thr' identified in patients with hyperlipidemia DNA polymorphisms in ITPA including basis of inosine triphosphatase deficiency A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society Canadian Cardiovascular Society position statement on familial hypercholesterolemia Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability The 2010 Canadian Hypertension Education Program recommendations for the management of hypertension: part 2 - therapy Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy Biological, clinical and population relevance of 95 loci for blood lipids Genetics of metabolic syndrome Narrative review: statin-related myopathy

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