(Q28943439)

13

0 references

Robert A. Hegele

21

object named as

Robert A. Hegele

0 references

Sekar Kathiresan

20

object named as

Sekar Kathiresan

1 reference

14 March 2017

18

Salim Yusuf

1 reference

14 March 2017

12

Benjamin F. Voight

1 reference

14 March 2017

5

Adam D. McIntyre

1 reference

14 March 2017

Christopher J O'Donnell

15

object named as

Christopher J. O'Donnell

1 reference

14 March 2017

Christopher T. Johansen

1

1 reference

14 March 2017

Jian Wang

2

1 reference

14 March 2017

Matthew B. Lanktree

3

1 reference

14 March 2017

Henian Cao

4

1 reference

14 March 2017

Matthew R. Ban

6

1 reference

14 March 2017

Rebecca A. Martins

7

1 reference

14 March 2017

Brooke A. Kennedy

8

1 reference

14 March 2017

Reina G. Hassell

9

1 reference

14 March 2017

Maartje E. Visser

10

1 reference

14 March 2017

Stephen M. Schwartz

11

1 reference

14 March 2017

Geesje M. Dallinga-Thie

16

1 reference

14 March 2017

Sonia S. Anand

17

1 reference

14 March 2017

Murray W. Huff

describes a project that uses

19

1 reference

14 March 2017

language of work or name

English

0 references

publication date

1 August 2010

1 reference

14 March 2017

1 reference

14 March 2017

42

1 reference

14 March 2017

684–687

1 reference

14 March 2017

8

1 reference

14 March 2017

genome-wide association study

1 reference

Finding the missing heritability of complex diseases

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Common variants at 30 loci contribute to polygenic dyslipidemia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

PLINK: a tool set for whole-genome association and population-based linkage analyses

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Hypertriglyceridemia: its etiology, effects and treatment

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Population structure and eigenanalysis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Principal components analysis corrects for stratification in genome-wide association studies

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Common disorders are quantitative traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Plasma lipoproteins: genetic influences and clinical implications

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Polygenic determinants of severe hypertriglyceridemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Common disorders are quantitative traits

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)

26 November 2018

1 reference

12 December 2020

Computing measures of explained variation for logistic regression models

1 reference

12 December 2020

APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia

1 reference

12 December 2020

Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.628

1 reference

299778

299778

1 reference

1 reference

1 reference