Evidence map›Paper›PMID 17767904›Full record

ReviewCell metabolism2007

Genetic and genomic insights into the molecular basis of atherosclerosis.

Yaoyu Chen, Jarod Rollins, Beverly Paigen, Xiaosong Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell metabolism, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 3 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. Genetics of murine type 2 diabetes and comorbidities.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Review
  7. Review
  8. Review
  9. Effects of Exercise to Improve Cardiovascular Health.Frontiers in cardiovascular medicine · 2019
    Review
  10. Article
  11. Article
  12. Genetic determinants of atherosclerosis, obesity, and energy balance in consomic mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Article
  13. Article
  14. Article
  15. Controlling complexity: the clinical relevance of mouse complex genetics.European journal of human genetics : EJHG · 2013
    Review
  16. Article
  17. Article
  18. High-resolution association mapping of atherosclerosis loci in mice.Arteriosclerosis, thrombosis, and vascular biology · 2012
    Article
  19. Genetics of atherosclerosis.Trends in genetics : TIG · 2012
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Yaoyu ChenThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Jarod Rollins
Beverly Paigen
Xiaosong Wang
Jackson Laboratory · USNovartis (United States) · US

Funding

From QTL to Gene for HDL CholesterolR37HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2009 to 2018
$4.3M
Cloning QTL Genes for Plasma HDL CholesterolR01HL081162 · NHLBI · JACKSON LABORATORY · PI KORSTANJE, RONNY · 2006 to 2013
$3.3M
From QTL to Gene for HDL CholesterolR01HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2008
$2.1M
Identifying Genes Regulating HDL Cholesterol LevelsR01HL074086 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2007
$994k
NHLBI NIH HHS HL74086NHLBI NIH HHS HL77796NHLBI NIH HHS HL81162NHLBI NIH HHS R01 HL074086NHLBI NIH HHS R01 HL077796NHLBI NIH HHS R01 HL081162NHLBI NIH HHS R37 HL077796
6 · The paper itself

Abstract

Atherosclerosis is a complex disease involving genetic and environmental risk factors, acting on their own or in synergy. Within the general population, polymorphisms within genes in lipid metabolism, inflammation, and thrombogenesis are probably responsible for the wide range of susceptibility to myocardial infarction, a fatal consequence of atherosclerosis. Genetic linkage studies have been carried out in both humans and mouse models to identify these polymorphisms. Approximately 40 quantitative trait loci for atherosclerotic disease have been found in humans, and approximately 30 in mice. Recently, genome-wide association studies have been used to identify atherosclerosis-susceptibility polymorphisms. Although discovering new atherosclerosis genes through these approaches remains challenging, the pace at which these polymorphisms are being found is accelerating due to rapidly improving bioinformatics resources and biotechnologies. The outcome of these efforts will not only unveil the molecular basis of atherosclerosis but also facilitate the discovery of drug targets and individualized medication against the disease.

Indexed as

AnimalsAtherosclerosisChromosome MappingEnzyme InhibitorsGenetic LinkageGenetic Predisposition to DiseaseHumansQuantitative Trait LociRisk FactorsEnzyme Inhibitors

Identifiers

PMID17767904
PMCPMC2083632
OpenAlexW2082602361

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.