About: Circulation: Cardiovascular Genetics

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journal

Attributes	Values
rdf:type	Item
description	journal (en) revista científica (es) ساینَسی رِسالہٕ (ks) revue scientifique (fr) rivista scientifica (it) науковий журнал (uk) wissenschaftliche Fachzeitschrift (de) wetenschappelijk tijdschrift van Lippincott Williams & Wilkins (nl)
language of work or name	wds:Q15816430-4CB04B6F-15AB-4879-B08F-972B1D201E60
language of work or name	English
OpenCitations bibliographic resource ID	wds:Q15816430-9D068AC4-8E4C-47B3-A0C2-8530B8AB196D
UniProt journal ID	wds:Q15816430-9DF792EC-800A-4DCC-B93A-B8EE51204A08
Scilit journal ID	wds:Q15816430-26DEEA36-B201-4DEC-B5A3-7F85591A2295
Crossref journal ID	wds:Q15816430-0BC34185-C0C3-455B-8227-A83A8C75F059
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1798
UniProt journal ID	uniprot:journals/3813
OpenCitations bibliographic resource ID	1798
UniProt journal ID	3813
Scilit journal ID	1170328
Crossref journal ID	78518
rdfs:label	Circulation: Cardiovascular Genetics (en) Circulation: Cardiovascular Genetics (es) Circulation: Cardiovascular Genetics (it) Circulation: Cardiovascular Genetics (nl) Circulation: Cardiovascular Genetics (ast)
skos:prefLabel	Circulation: Cardiovascular Genetics (en) Circulation: Cardiovascular Genetics (es) Circulation: Cardiovascular Genetics (it) Circulation: Cardiovascular Genetics (nl) Circulation: Cardiovascular Genetics (ast)
name	Circulation: Cardiovascular Genetics (en) Circulation: Cardiovascular Genetics (es) Circulation: Cardiovascular Genetics (it) Circulation: Cardiovascular Genetics (nl) Circulation: Cardiovascular Genetics (ast)
title	wds:Q15816430-573E2885-01AC-4F27-98A9-FAC934C26754 wds:Q15816430-938BBB4D-E0E5-45E4-807D-DB3C1150FF3E
title	Circulation. Cardiovascular genetics (en) Circulation: Cardiovascular Genetics (und)
ERA Journal ID	wds:Q15816430-698171DD-325B-48E6-9E23-E0ED32C483FC
Danish Bibliometri...h Indicator level	wds:Q15816430-35B0F765-6F52-40F3-B673-307EA5F7AB21
Danish Bibliometri...tor (BFI) SNO/CNO	wds:Q15816430-4DAC6DD2-7F7F-4581-AA18-19BB2DAE6FC4
ERA Journal ID	123722
Danish Bibliometri...h Indicator level	1
Danish Bibliometri...tor (BFI) SNO/CNO	6064411
NLM Unique ID	wds:Q15816430-C2EC959F-B223-45E6-8853-F5D82A17FBDA
ACNP journal ID	wds:Q15816430-17F2416A-DB25-4578-9AF3-84F06EA8655F
HAL journal ID	wds:Q15816430-3C9F778A-9716-46EC-B9F9-3E5685964707
NLM Unique ID	101489144
ACNP journal ID	2701478
HAL journal ID	87646
instance of	wds:Q15816430-9ff992b5-4601-5538-bbe7-12c1bbcd6023 wds:Q15816430-AFAAAD05-6B43-4377-ADA2-0E70A21A334D
instance of	scientific journal hybrid open access journal
publisher	wds:Q15816430-EB0C4403-05E3-4677-AB60-777D162A6789
publisher	Lippincott Williams & Wilkins
skos:altLabel	Circulation. Cardiovascular genetics (en)
OpenAlex ID	wds:Q15816430-398E4D21-43B7-41D8-B618-2FE50C6E1ADC
country of origin	wds:Q15816430-915E11C1-54B4-40D4-A524-150F58D93818
official website	wds:Q15816430-19E656B2-8076-4FA4-992A-02D8C0BA2118 wds:Q15816430-7d3d43a4-4260-0e8d-15db-98cfe729a85a
OpenAlex ID	V103446830
country of origin	United States of America
official website	http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=01337497-000000000-00000 https://www.ahajournals.org/journal/circgenetics
Scopus source ID	wds:Q15816430-B88B3A91-3C57-4509-BC6B-33EDAAFE7940
ISSN	wds:Q15816430-1F6D940E-9D67-4B89-8D2D-DB431AB466AD wds:Q15816430-DED9B87B-73DC-4010-92F9-AAA0F604B4A9
ISSN-L	wds:Q15816430-C8FED50A-7C18-475A-A4DC-C46EFC4668FD
indexed in bibliographic review	wds:Q15816430-A8699256-0022-4D9A-9BC6-7E5154A200BF
ISSN	urn:ISSN:1942-325X urn:ISSN:1942-3268
ISSN-L	http://issn.org/resource/ISSN/1942-3268
Scopus source ID	19600166306
ISSN	1942-325X 1942-3268
ISSN-L	1942-3268
indexed in bibliographic review	Scopus
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q15816430
is published in of	Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits A variant in LDLR is associated with abdominal aortic aneurysm A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality Fine mapping study reveals novel candidate genes for carotid intima-media thickness in Dominican Republican families Relationship between the temporal profile of plasma microRNA and left ventricular remodeling in patients after myocardial infarction Circulating MicroRNA-208b and MicroRNA-499 reflect myocardial damage in cardiovascular disease. Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation MicroRNA-150: a novel marker of left ventricular remodeling after acute myocardial infarction. Genetic association of the CCR5 region with lipid levels in at-risk cardiovascular patients. A locus mapping to mouse chromosome 7 determines infarct volume in a mouse model of ischemic stroke Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study Common variants in epithelial sodium channel genes contribute to salt sensitivity of blood pressure: The GenSalt study Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese Clinical and genetic correlates of circulating angiopoietin-2 and soluble Tie-2 in the community Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people Letter by Olesen et al Regarding Article, “MOG1: A New Susceptibility Gene for Brugada Syndrome”

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