(Q34649888)

English

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

3 August 2017

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained (English)

1 reference

Europe PubMed Central

3 August 2017

1 reference

based on heuristic

inferred from title

21

1 reference

Europe PubMed Central

3 August 2017

Eric Boerwinkle

8

object named as

Eric Boerwinkle

0 references

Johanna Kuusisto

53

object named as

Johanna Kuusisto

0 references

67

object named as

Matti Uusitupa

0 references

Jaakko Tuomilehto

66

object named as

Jaakko Tuomilehto

0 references

Loic Le Marchand

24

object named as

Loic Le Marchand

0 references

Alena Stančáková

32

object named as

Alena Stančáková

1 reference

Europe PubMed Central

3 August 2017

Francis Collins

44

object named as

Francis S Collins

0 references

29

object named as

Narisu Narisu

1 reference

Europe PubMed Central

3 August 2017

50

object named as

Kristian Hveem

1 reference

Europe PubMed Central

3 August 2017

Charles Kooperberg

72

object named as

Charles Kooperberg

1 reference

Europe PubMed Central

3 August 2017

Thomas Quertermous

62

object named as

Thomas Quertermous

1 reference

Europe PubMed Central

3 August 2017

Rainer Rauramaa

63

object named as

Rainer Rauramaa

1 reference

Europe PubMed Central

3 August 2017

object named as

Wen-Chang Wang

36

0 references

Jyh-Ming Jimmy Juang

object named as

Jyh-Ming J Juang

51

0 references

object named as

I-Te Lee

56

0 references

object named as

Tzung-Dau Wang

68

0 references

object named as

Steven Buyske

5

0 references

object named as

Timo A Lakka

55

0 references

77

object named as

Karen L Mohlke

1 reference

Europe PubMed Central

3 August 2017

Jerome I Rotter

64

object named as

Jerome I Rotter

1 reference

Europe PubMed Central

3 August 2017

40

object named as

Linda S Adair

1 reference

Europe PubMed Central

3 August 2017

object named as

Dana C Crawford

74

0 references

Inger Njølstad

60

object named as

Inger Njølstad

1 reference

Europe PubMed Central

3 August 2017

54

object named as

Markku Laakso

1 reference

Europe PubMed Central

3 August 2017

Michael Boehnke

69

object named as

Michael Boehnke

1 reference

Europe PubMed Central

3 August 2017

3

object named as

Anne U Jackson

1 reference

Europe PubMed Central

3 August 2017

Lori L Bonnycastle

9

object named as

Lori L Bonnycastle

1 reference

Europe PubMed Central

3 August 2017

6

object named as

Devin Absher

1 reference

Europe PubMed Central

3 August 2017

Christopher A. Haiman

70

object named as

Christopher A Haiman

1 reference

Europe PubMed Central

3 August 2017

Brian E. Henderson

18

object named as

Brian E Henderson

1 reference

Europe PubMed Central

3 August 2017

7

object named as

Donna K Arnett

1 reference

Europe PubMed Central

3 August 2017

49

object named as

Steven C Hunt

1 reference

Europe PubMed Central

3 August 2017

58

object named as

Tara C Matise

1 reference

Europe PubMed Central

3 August 2017

76

object named as

Kari E North

1 reference

Europe PubMed Central

3 August 2017

Nora Franceschini

16

object named as

Nora Franceschini

1 reference

Europe PubMed Central

3 August 2017

Lucia A Hindorff

19

object named as

Lucia A Hindorff

1 reference

Europe PubMed Central

3 August 2017

38

object named as

Tom Wilsgaard

1 reference

Europe PubMed Central

3 August 2017

61

object named as

Ulrike Peters

1 reference

Europe PubMed Central

3 August 2017

Christie M. Ballantyne

41

object named as

Christie M Ballantyne

1 reference

Europe PubMed Central

3 August 2017

71

object named as

Yii-Der I Chen

1 reference

Europe PubMed Central

3 August 2017

17

object named as

Xiuqing Guo

1 reference

Europe PubMed Central

3 August 2017

Aravinda Chakravarti

43

object named as

Aravinda Chakravarti

1 reference

Europe PubMed Central

3 August 2017

Lindsay L Waite

2

object named as

Lindsay L Waite

1 reference

Europe PubMed Central

3 August 2017

Wayne Huey-Herng Sheu

4

object named as

Wayne H-H Sheu

1 reference

Europe PubMed Central

3 August 2017

23

object named as

Wen-Jane Lee

1 reference

Europe PubMed Central

3 August 2017

57

object named as

Mark F Leppert

1 reference

Europe PubMed Central

3 August 2017

Themistocles L Assimes

73

object named as

Themistocles L Assimes

1 reference

Europe PubMed Central

3 August 2017

Antero Kesäniemi

52

object named as

Antero Y Kesäniemi

1 reference

Europe PubMed Central

3 August 2017

Lynne R. Wilkens

37

object named as

Lynne Wilkens

1 reference

Europe PubMed Central

3 August 2017

Damien C Croteau-Chonka

13

object named as

Damien C Croteau-Chonka

1 reference

Europe PubMed Central

3 August 2017

35

object named as

Amy J Swift

1 reference

Europe PubMed Central

3 August 2017

Charles B Eaton

15

object named as

Charles B Eaton

1 reference

Europe PubMed Central

3 August 2017

author name string

Ying Wu

1

1 reference

Europe PubMed Central

3 August 2017

Cara L Carty

10

1 reference

Europe PubMed Central

3 August 2017

Iona Cheng

11

1 reference

Europe PubMed Central

3 August 2017

Barbara Cochran

12

1 reference

Europe PubMed Central

3 August 2017

Logan Dumitrescu

14

1 reference

Europe PubMed Central

3 August 2017

Eric Kim

20

1 reference

Europe PubMed Central

3 August 2017

Pirjo Komulainen

22

1 reference

Europe PubMed Central

3 August 2017

Yi Lin

25

1 reference

Europe PubMed Central

3 August 2017

Jaana Lindström

26

1 reference

Europe PubMed Central

3 August 2017

Oddgeir Lingaas-Holmen

27

1 reference

Europe PubMed Central

3 August 2017

Sabrina L Mitchell

28

1 reference

Europe PubMed Central

3 August 2017

Jennifer G Robinson

30

1 reference

Europe PubMed Central

3 August 2017

Fred Schumacher

31

1 reference

Europe PubMed Central

3 August 2017

Jouko Sundvall

33

1 reference

Europe PubMed Central

3 August 2017

Yun-Ju Sung

34

1 reference

Europe PubMed Central

3 August 2017

Alicia M Young

39

1 reference

Europe PubMed Central

3 August 2017

Petra Bůžková

42

1 reference

Europe PubMed Central

3 August 2017

David Duggan

45

1 reference

Europe PubMed Central

3 August 2017

Alan B Feranil

46

1 reference

Europe PubMed Central

3 August 2017

Low-Tone Ho

47

1 reference

Europe PubMed Central

3 August 2017

Yi-Jen Hung

48

1 reference

Europe PubMed Central

3 August 2017

Leena Moilanen

59

1 reference

Europe PubMed Central

3 August 2017

Jouko Saramies

65

1 reference

Europe PubMed Central

3 August 2017

Chao A Hsiung

75

1 reference

Europe PubMed Central

3 August 2017

publication date

21 March 2013

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

9

1 reference

Europe PubMed Central

3 August 2017

e1003379

1 reference

Europe PubMed Central

3 August 2017

3

1 reference

Europe PubMed Central

3 August 2017

copyright license

Creative Commons CC0 License

21 March 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

0 references

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Haplotype variation and genotype imputation in African populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Quantifying the underestimation of relative risks from genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Variants in ZNF365 isoform D are associated with Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Hundreds of variants clustered in genomic loci and biological pathways affect human height

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

LocusZoom: regional visualization of genome-wide association scan results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

METAL: fast and efficient meta-analysis of genomewide association scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Cohort profile: the Cebu longitudinal health and nutrition survey

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A functional polymorphism in the HMGCR promoter affects transcriptional activity but not the risk for Alzheimer disease in Swedish populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Genome-wide association studies in diverse populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A method and server for predicting damaging missense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Patterns of linkage disequilibrium in different populations: implications and opportunities for lipid-associated loci identified from genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Methodological challenges of genome-wide association analysis in Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

GWAF: an R package for genome-wide association analyses with family data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Degradation of LDLR protein mediated by 'gain of function' PCSK9 mutants in normal and ARH cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

The functional interaction on in vitro gene expression of APOA5 SNPs, defining haplotype APOA52, and their paradoxical association with plasma triglyceride but not plasma apoAV levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A functional mutation in the LDLR promoter (-139C>G) in a patient with familial hypercholesterolemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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=3605054

7 July 2018

The proprotein convertase (PC) PCSK9 is inactivated by furin and/or PC5/6A: functional consequences of natural mutations and post-translational modifications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Molecular characterization of loss-of-function mutations in PCSK9 and identification of a compound heterozygote

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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=3605054

7 July 2018

A haplotype map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Determination of the functionality of common APOA5 polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

The multiethnic cohort study: exploring genes, lifestyle and cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Hepatic lipase: a marker for cardiovascular disease risk and response to therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Type III hyperlipoproteinemia and spontaneous atherosclerosis in mice resulting from gene replacement of mouse Apoe with human Apoe*2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Structural basis for receptor binding heterogeneity of apolipoprotein E from type III hyperlipoproteinemic subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Heterogeneity in multifactorial inheritance of plasma lipids and lipoproteins in ethnically diverse families in Jerusalem

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

7 July 2018

APOE genotype, lipids, and coronary heart disease risk: a prospective population study

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Functional importance of apolipoprotein A5 185G in the activation of lipoprotein lipase.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Enhanced apoB48 metabolism in lipoprotein lipase X447 homozygotes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjects.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Genetic variation of PLTP modulates lipoprotein profiles in hypoalphalipoproteinemia

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Heritabilities of apolipoprotein and lipid levels in three countries

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Identifying candidate causal variants via trans-population fine-mapping.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Design of the Women’s Health Initiative Clinical Trial and Observational Study

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Rapid changes in the prevalence of obesity and known diabetes in an adult Norwegian population. The Nord-Trøndelag Health Surveys: 1984-1986 and 1995-1997.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Incidence of and risk factors for type-2 diabetes in a general population: the Tromsø Study

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Heritabilities of lipids in young European American and African American twins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3605054

26 October 2018

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Implementation of the women's health initiative study design

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003379

21 January 2018

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23555291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Casting a wider net for diabetes susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23555291

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1003379

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34649888&oldid=2063173277"