Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks - Wikidata - awgldk - TriplyDB

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

http://www.wikidata.org/entity/Q30411387

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ANGPTL8/betatrophin does not control pancreatic beta cell expansion The ANGPTL3-4-8 model, a molecular mechanism for triglyceride trafficking Insights into blood lipids from rare variant discovery Perspectives on pharmacogenomics of antiretroviral medications and HIV-associated comorbidities Genetic and epigenetic factors influencing chronic kidney disease Insights from exome sequencing for endocrine disorders A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation Progress in methods for rare variant association Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Epidemiology of cardiovascular disease: recent novel outlooks on risk factors and clinical approaches.Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.Association of exome sequences with plasma C-reactive protein levels in >9000 participants.Variant association tools for quality control and analysis of large-scale sequence and genotyping array data RVFam: an R package for rare variant association analysis with family data.The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced Samples Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans.No large-effect low-frequency coding variation found for myocardial infarction Specific collagen XVIII isoforms promote adipose tissue accrual via mechanisms determining adipocyte number and affect fat deposition.A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.A dual role of lipasin (betatrophin) in lipid metabolism and glucose homeostasis: consensus and controversy Is there a link between proprotein convertase PC7 activity and human lipid homeostasis?A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy A lipasin/Angptl8 monoclonal antibody lowers mouse serum triglycerides involving increased postprandial activity of the cardiac lipoprotein lipase.American Heart Association Cardiovascular Genome-Phenome Study: foundational basis and program Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.Rare variant association studies: considerations, challenges and opportunities.Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.Glucokinase regulatory protein: complexity at the crossroads of triglyceride and glucose metabolism.Assessing the Power of Exome Chips.Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study.A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans Family-based approaches: design, imputation, analysis, and beyond.Incorporating Non-Coding Annotations into Rare Variant Analysis.Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations

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P2860

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

http://www.wikidata.org/entity/Q30411387

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2014 nî lūn-bûn

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2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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J.AJHG.2014.01.009

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American Journal of Human Genetics

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Adolfo Correa

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Albert Hofman

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Alexander P Reiner

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Andre G Uitterlinden

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Aniruddh P Patel

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Arend Voorman

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Aron Y Joon

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Brian Davis

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Bruce M Psaty

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Charles Kooperberg

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P2860

Atypical angiopoietin-like protein that regulates ANGPTL3

RETRACTED: Betatrophin: a hormone that controls pancreatic β cell proliferation

Biological, clinical and population relevance of 95 loci for blood lipids

Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

Platelet-activating factor acetylhydrolases

The proprotein convertases and their implication in sterol and/or lipid metabolism

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S)

Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins

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Vilmundur Gudnason

Caroline Hayward

Albert V. Smith

James S. Pankow

José M. Ordovas

Michael Y. Tsai

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