(Q34499457)

English

Population-based resequencing of APOA1 in 10,330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Population-based resequencing of APOA1 in 10,330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

based on heuristic

inferred from title

genetic variation

1 reference

based on heuristic

inferred from title

Børge G. Nordestgaard

3

object named as

Børge G Nordestgaard

0 references

Anne Tybjærg-Hansen

4

object named as

Anne Tybjærg-Hansen

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Ruth Frikke-Schmidt

2

object named as

Ruth Frikke-Schmidt

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Christiane L Haase

1

object named as

Christiane L Haase

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

29 November 2012

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

e1003063

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

copyright license

Creative Commons Attribution 4.0 International

29 November 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Deep resequencing reveals excess rare recent variants consistent with explosive population growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

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=3510059

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Amyloid heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Finding the missing heritability of complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review

1 reference

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7 July 2018

Genetically elevated C-reactive protein and ischemic vascular disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Discrete roles of apoA-I and apoE in the biogenesis of HDL species: lessons learned from gene transfer studies in different mouse models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Universal definition of myocardial infarction: Kristian Thygesen, Joseph S. Alpert and Harvey D. White on behalf of the Joint ESC/ACCF/AHA/WHF Task Force for the Redefinition of Myocardial Infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Role of apoA-I, ABCA1, LCAT, and SR-BI in the biogenesis of HDL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Ostertag revisited: the inherited systemic amyloidoses without neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

The effects of altered apolipoprotein A-I structure on plasma HDL concentration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Apolipoprotein AI and transthyretin as components of amyloid fibrils in a kindred with apoAI Leu178His amyloidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3510059

7 July 2018

Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Genetically elevated apolipoprotein A-I, high-density lipoprotein cholesterol levels, and risk of ischemic heart disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Coronary heart disease risk factors ranked by importance for the individual and community. A 21 year follow-up of 12 000 men and women from The Copenhagen City Heart Study

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Association of loss-of-function mutations in the ABCA1 gene with high-density lipoprotein cholesterol levels and risk of ischemic heart disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Enhanced fractional catabolic rate of apo A-I and apo A-II in heterozygous subjects for apo A-I(Zaragoza) (L144R).

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Myocardial infarction redefined—A consensus document of The Joint European Society of Cardiology/American College of Cardiology Committee for the Redefinition of Myocardial Infarction

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003063

21 January 2018

Structural analysis of human apolipoprotein A-I variants. Amino acid substitutions are nonrandomly distributed throughout the apolipoprotein A-I primary structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compound heterozygosity for a structural apolipoprotein A-I variant, apo A-I(L141R)Pisa, and an apolipoprotein A-I null allele in patients with absence of HDL cholesterol, corneal opacifications, and coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of two new human apolipoprotein A-I variants: apolipoprotein A-I Tsushima (Trp-108-->Arg) and A-I Hita (Ala-95-->Asp)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic etiology of isolated low HDL syndrome: incidence and heterogeneity of efflux defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo metabolism of apo A-I and apo A-II in subjects with apo A-I(Lys107-->0) associated with reduced HDL cholesterol and Lp(AI w AII) deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ApoA-IHelsinki (Lys107-->0) associated with reduced HDL cholesterol and LpA-I:A-II deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive intimal apolipoprotein A1-derived amyloid deposits in a patient with an apolipoprotein A1 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human apolipoprotein A-I polymorphism. Identification of amino acid substitutions in three electrophoretic variants of the Münster-3 type

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal lecithin:cholesterol acyltransferase activation by a human apolipoprotein A-I variant in which a single lysine residue is deleted

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in APOA1 predicts increased risk of ischaemic heart disease and total mortality without low HDL cholesterol levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variants of group A apolipoproteins. Rapid methods for screening and characterization without ultracentrifugation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23209431

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1003063

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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