About: Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

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description	articolo scientifico (it) artículu científicu espublizáu en 2010 (ast) наукова стаття, опублікована в серпні 2010 (uk) 2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած (hyw) 2010 թվականի օգոստոսին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في أغسطس 2010) (ar) wetenschappelijk artikel (gepubliceerd op 2010/08/01) (nl) scientific journal article (en) im August 2010 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28943439-41E6D2A9-326C-47CE-9683-C3F02BC6A6D4
publication date	2010-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28943439-1BB4C455-9DAE-4378-92C2-A658D38CA136
language of work or name	English
cites work	wds:Q28943439-17BDB4BB-0BCF-47C9-A2D2-07CD5CA82B6B wds:Q28943439-1C0C2966-8EE2-457A-A3C5-8B39F2BB7D7E wds:Q28943439-1F3FED90-E585-4B1F-A0C4-A8E06E2A34FB wds:Q28943439-273BDE0D-AE52-486C-B3BC-985EF58D91A6 wds:Q28943439-40830716-EE64-4322-926C-23628112E670 wds:Q28943439-4891C1C8-ABE3-4089-B66F-DF7FCE663088 wds:Q28943439-4CFFEE93-4C0F-48C4-A7BB-FD6632251211 wds:Q28943439-5B0ED0CE-052B-4B0E-B99A-E9F7EB835206 wds:Q28943439-5EA40049-1122-4786-A101-DF22842C1913 wds:Q28943439-71B1655B-145D-4B1E-9D59-AF2B9A8A1823 wds:Q28943439-8CEB00BB-596B-4969-AA26-6846E08E0091 wds:Q28943439-975A9A62-2239-4727-A594-A91EEB1941EA wds:Q28943439-97EFD9A3-8A40-48C5-A8BD-DBC94AE89524 wds:Q28943439-997B519F-0F25-41E6-9D5B-FB62C52064C0 wds:Q28943439-9B5E4B00-0C43-46AD-90B1-EB0797CD9067 wds:Q28943439-9CA13568-3819-49E1-8B50-2DCE062D1888 wds:Q28943439-A3F2BF11-F555-426E-A479-089B3C856A1F wds:Q28943439-AB8AF1A4-06B3-476D-A879-D57D2232FD69 wds:Q28943439-B1E7D0BE-19B2-4CC0-81BE-02081A89B8BC wds:Q28943439-B9B3CC19-43B9-4955-8566-1235995BD4C4 wds:Q28943439-BC1242BF-D1B7-43A2-A145-4E3DE96D3283 wds:Q28943439-BE41F842-4410-4425-AE83-2A8EE54706D4 wds:Q28943439-C3BF2D6E-606E-4303-A5E3-4BBF4BC76BA9 wds:Q28943439-E2D48AD5-4090-4410-96CE-7C01CBF9F72B wds:Q28943439-E48ACAB8-1FA8-4214-986C-D2F33F4C6086 wds:Q28943439-F16DE497-51C2-439A-B36D-8E16A40474DC wds:Q28943439-F25CD359-0A10-4DA2-A6CE-658255AAC95A
cites work	Plasma lipoproteins: genetic influences and clinical implications Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL. Finding the missing heritability of complex diseases Common variants at 30 loci contribute to polygenic dyslipidemia Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Genome-wide association analysis of metabolic traits in a birth cohort from a founder population PLINK: a tool set for whole-genome association and population-based linkage analyses Principal components analysis corrects for stratification in genome-wide association studies Newly identified loci that influence lipid concentrations and risk of coronary artery disease Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Population structure and eigenanalysis Most rare missense alleles are deleterious in humans: implications for complex disease and association studies Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia Common disorders are quantitative traits Common disorders are quantitative traits Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE) Polygenic determinants of severe hypertriglyceridemia Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650) Hypertriglyceridemia: its etiology, effects and treatment APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia Computing measures of explained variation for logistic regression models
author name string	wds:Q28943439-00E86BA5-A2EA-4148-AE61-9DA823839637 wds:Q28943439-0498C1C5-48E8-429C-8EF8-973BA2BE5320 wds:Q28943439-0D864008-58A5-40F2-BE88-089C3BC21C4F wds:Q28943439-2FFFF126-9391-47C6-AE0E-D923BD71675B wds:Q28943439-4EE7864D-4CD3-4FF9-85EA-792B49485C04 wds:Q28943439-5A9D14DB-D966-472B-8F28-6FDD25A8B548 wds:Q28943439-760BB9A5-1FFF-47C2-AD00-3CFDF8D85B52 wds:Q28943439-7FA0C387-7ECE-4AE3-841B-610045B27422 wds:Q28943439-84CCB5CB-0555-4C77-A67C-EED3EC983302 wds:Q28943439-8C912551-646C-464D-B0CC-4D98531FA6CA wds:Q28943439-B1BCAC09-315E-4000-A2B2-082CF124C427 wds:Q28943439-BE010132-FBA3-49B2-800B-E40A37F5C916 wds:Q28943439-CFB221E6-C065-4D0B-814B-99DF2B65BA74
OpenCitations bibliographic resource ID	wds:Q28943439-C85D98BD-1EC8-4143-8512-37E4FDBBB23E
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/299778
author name string	Jian Wang Stephen M. Schwartz Henian Cao Murray W. Huff Sonia S. Anand Matthew B. Lanktree Geesje M. Dallinga-Thie Brooke A. Kennedy Christopher T. Johansen Maartje E. Visser Matthew R. Ban Rebecca A. Martins Reina G. Hassell
OpenCitations bibliographic resource ID	299778
rdfs:label	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia (en) Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia (ast)
skos:prefLabel	Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia (en)

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