(Q21563383)

2 September 2022

23

David Schlessinger

David

Schlessinger

1 reference

2 September 2022

1

Serena Sanna

Serena

Sanna

1 reference

2 September 2022

22

Manuela Uda

Manuela

Uda

1 reference

2 September 2022

17

Jaakko Tuomilehto

Jaakko

Tuomilehto

1 reference

2 September 2022

15

Markku Laakso

Markku

Laakso

1 reference

2 September 2022

3

Antonella Mulas

Antonella

Mulas

1 reference

2 September 2022

14

Inger Njølstad

Inger

Njølstad

1 reference

2 September 2022

19

Rainer Rauramaa

Rainer

Rauramaa

1 reference

2 September 2022

16

Kristian Hveem

Kristian

Hveem

1 reference

2 September 2022

8

Gianluca Usala

Gianluca

Usala

1 reference

2 September 2022

7

Maria Grazia Piras

Maria Grazia

Piras

1 reference

2 September 2022

4

Carlo Sidore

Carlo

Sidore

1 reference

2 September 2022

Timo A Lakka

18

Timo A

Lakka

1 reference

2 September 2022

Francesco Cucca

21

Francesco

Cucca

1 reference

2 September 2022

6

Anne U Jackson

Anne U

Jackson

1 reference

2 September 2022

5

Hyun M Kang

Hyun M

Kang

1 reference

2 September 2022

Bingshan Li

2

Bingshan

Li

1 reference

2 September 2022

Giuseppe Maninchedda

9

Giuseppe

Maninchedda

1 reference

2 September 2022

Alessandro Sassu

10

Alessandro

Sassu

1 reference

2 September 2022

Fabrizio Serra

11

Fabrizio

Serra

1 reference

2 September 2022

Maria Antonietta Palmas

12

Maria Antonietta

Palmas

1 reference

2 September 2022

William H Wood

13

William H 3rd

Wood

1 reference

2 September 2022

Ramaiah Nagaraja

24

Ramaiah

Nagaraja

1 reference

2 September 2022

Gonçalo R Abecasis

25

Gonçalo R

Abecasis

1 reference

Creative Commons Attribution 4.0 International

2 September 2022

language of work or name

English

0 references

publication date

July 2011

0 references

published in

PLOS Genetics

0 references

volume

7

0 references

issue

7

0 references

page(s)

e1002198

0 references

copyright license

start time

28 July 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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=3145627

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Finding the missing heritability of complex diseases

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Variants in MTNR1B influence fasting glucose levels

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Common variants at 30 loci contribute to polygenic dyslipidemia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

LocusZoom: regional visualization of genome-wide association scan results

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Rare variants create synthetic genome-wide associations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related 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=3145627

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Synthetic associations are unlikely to account for many common disease genome-wide association signals

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease: 3 independent studies and meta-analyses

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Uncovering the roles of rare variants in common disease through whole-genome sequencing

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Family-based association tests for genomewide association scans

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Heritability of cardiovascular and personality traits in 6,148 Sardinians

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Improved inference of relationship for pairs of individuals

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

Low-coverage sequencing: implications for design of complex trait association studies

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145627

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.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371/JOURNAL.PGEN.1002198

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371/JOURNAL.PGEN.1002198

Human E apoprotein heterogeneity. Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/21829380

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21829380

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002198

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1653651

Fatcat ID

release_uxmcjk7embalbjiu6ry6osg6za

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/uxmcjk7embalbjiu6ry6osg6za

mapped directly with Wikidata item

24 November 2022

based on heuristic

OpenCitations bibliographic resource ID

1653651

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1653651

PMC publication ID

3145627

0 references