Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765)

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Language	Label	Description	Also known as
English	Common variants at 30 loci contribute to polygenic dyslipidemia	scientific article

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scholarly article

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Common variants at 30 loci contribute to polygenic dyslipidemia (English)

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Francis Collins

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David Altshuler

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Rory Edwards Collins

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Michael Boehnke

58

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Leena Peltonen-Palotie

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David Schlessinger

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Sekar Kathiresan

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Jaakko Tuomilehto

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Johanna Kuusisto

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Candace Guiducci

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Marju Orho-Melander

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Cristen J. Willer

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Kathryn L. Lunetta

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Serkalem Demissie

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José María Ordovás

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Karen L Mohlke

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Anne U Jackson

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Heather M Stringham

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Heather M Stringham

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Lori L Bonnycastle

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Lori L Bonnycastle

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Sarah Parish

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Edward G. Lakatta

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Edward G Lakatta

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Benjamin F. Voight

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Benjamin F Voight

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Jaspal S Kooner

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Richard N. Bergman

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Richard N Bergman

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Eric E Schadt

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L. Adrienne Cupples

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L Adrienne Cupples

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Toshiko Tanaka

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Christopher J O'Donnell

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Christopher J O'Donnell

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Gina M Peloso

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Lee Kaplan

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Mario A. Morken

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Mario A Morken

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Gonçalo Abecasis

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Gonçalo R Abecasis

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43

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Pierre Meneton

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Derrick A Bennett

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Derrick Bennett

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Kiran Musunuru

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Aarti Surti

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Kari A Kubalanza

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Kari A Kubalanza

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Laura J Scott

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Paul I W de Bakker

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Paul I W de Bakker

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9

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Yun Li

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26

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Amy J Swift

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author name string

Gabriel Crawford

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Noel P Burtt

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Robert Clarke

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Jouko Sundvall

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Qiong Yang

35

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John C Chambers

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language of work or name

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publication date

January 2009

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number of pages

10

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Nature Genetics

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41

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1

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56-65

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

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24 March 2017

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

24 March 2017

Control of pancreas and liver gene expression by HNF transcription factors

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24 March 2017

Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters

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24 March 2017

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

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24 March 2017

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24 March 2017

Mapping the genetic architecture of gene expression in human liver

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24 March 2017

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

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24 March 2017

Low-density lipoprotein receptor-related protein interacts with MafB, a regulator of hindbrain development

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24 March 2017

ATP binding cassette transporter G5 and G8 genotypes and plasma lipoprotein levels before and after treatment with atorvastatin

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24 March 2017

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

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24 March 2017

Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolism

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24 March 2017

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

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24 March 2017

Angiopoietin-like protein 4 is a potent hyperlipidemia-inducing factor in mice and inhibitor of lipoprotein lipase

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24 March 2017

Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

24 March 2017

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

1 reference

https://api.crossref.org/works/10.1038/NG.291

22 April 2017

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

7 April 2017

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

7 April 2017

A HapMap harvest of insights into the genetics of common disease

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7 April 2017

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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7 April 2017

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

7 April 2017

LDL-cholesterol concentrations: a genome-wide association study

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

27 September 2017

Identification of Tim4 as a phosphatidylserine receptor

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27 September 2017

Common single-nucleotide polymorphisms act in concert to affect plasma levels of high-density lipoprotein cholesterol.

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27 September 2017

A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

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27 September 2017

Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol

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27 September 2017

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

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27 September 2017

Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

27 September 2017

A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

27 September 2017

Overexpression of PCSK9 accelerates the degradation of the LDLR in a post-endoplasmic reticulum compartment

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881676

27 September 2017

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

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27 September 2017

Post-transcriptional regulation of low density lipoprotein receptor protein by proprotein convertase subtilisin/kexin type 9a in mouse liver.

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27 September 2017

NARC-1/PCSK9 and its natural mutants: zymogen cleavage and effects on the low density lipoprotein (LDL) receptor and LDL cholesterol

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27 September 2017

Factors of risk in the development of coronary heart disease--six year follow-up experience. The Framingham Study

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27 September 2017

Targeted mutation of plasma phospholipid transfer protein gene markedly reduces high-density lipoprotein levels

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27 September 2017

Increased prebeta-high density lipoprotein, apolipoprotein AI, and phospholipid in mice expressing the human phospholipid transfer protein and human apolipoprotein AI transgenes

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27 September 2017

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27 September 2017

Polymorphisms associated with cholesterol and risk of cardiovascular events

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28 November 2018

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease

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28 November 2018

A Polymorphism in the Protease-Like Domain of Apolipoprotein(a) Is Associated With Severe Coronary Artery Disease

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28 November 2018

The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: Design, Recruitment, and Initial Examination

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28 November 2018

The functional Thr130Ile and Val255Met polymorphisms of the hepatocyte nuclear factor-4alpha (HNF4A): gene associations with type 2 diabetes or altered beta-cell function among Danes.

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28 November 2018

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28 November 2018

ISIS-3: a randomised comparison of streptokinase vs tissue plasminogen activator vs anistreplase and of aspirin plus heparin vs aspirin alone among 41,299 cases of suspected acute myocardial infarction. ISIS-3 (Third International Study of Infarct S

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12 December 2020

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The private hepatocyte nuclear factor-1alpha G319S variant is associated with plasma lipoprotein variation in Canadian Oji-Cree

1 reference

https://pubmed.ncbi.nlm.nih.gov/19060906

12 December 2020

based on heuristic

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Cardiovascular risk factor changes in Finland, 1972-1997

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https://pubmed.ncbi.nlm.nih.gov/19060906

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based on heuristic

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An investigation of coronary heart disease in families. The Framingham offspring study

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https://pubmed.ncbi.nlm.nih.gov/19060906

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https://pubmed.ncbi.nlm.nih.gov/19060906

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Reduction of plasma lipids, lipoproteins, and apoproteins by dietary fish oils in patients with hypertriglyceridemia

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https://pubmed.ncbi.nlm.nih.gov/19060906

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The Malmo Diet and Cancer Study. Design and feasibility

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https://pubmed.ncbi.nlm.nih.gov/19060906

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

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