Evidence map›Paper›PMID 16951076›Full record

ArticleGenetics2006

Complex genetic architecture revealed by analysis of high-density lipoprotein cholesterol in chromosome substitution strains and F2 crosses.

Ioannis M Stylianou, Shirng-Wern Tsaih, Keith DiPetrillo, Naoki Ishimori, Renhua Li, Beverly Paigen, Gary Churchill

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  9. Review
  10. Review
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  13. Article
  14. Genetic resistance to diet-induced obesity in chromosome substitution strains of mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  15. Article
  16. Article
  17. Genetic factors for resistance to diet-induced obesity and associated metabolic traits on mouse chromosome 17.Mammalian genome : official journal of the International Mammalian Genome Society · 2009
    Article
  18. Article
  19. Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  20. Article
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

7 authors at 2 institutions in 2 countries.

Ioannis M StylianouThe Jackson Laboratory, Maine 04609, USA.
Shirng-Wern Tsaih
Keith DiPetrillo
Naoki Ishimori
Renhua Li
Beverly Paigen
Gary Churchill
Jackson Laboratory · USNovartis (United States) · US

Funding

Systems Genetic Analysis of Multi-parent CrossesR01GM070683 · NIGMS · JACKSON LABORATORY · PI BROMAN, KARL W, CHURCHILL, GARY A · 2004 to 2022
$6.8M
From QTL to Gene for HDL CholesterolR37HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2009 to 2018
$4.3M
From QTL to Gene for HDL CholesterolR01HL077796 · NHLBI · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2004 to 2008
$2.1M
NHLBI NIH HHS HL77796NHLBI NIH HHS R01 HL077796NHLBI NIH HHS R37 HL077796NIGMS NIH HHS GM070638NIGMS NIH HHS R01 GM070683
6 · The paper itself

Abstract

Intercrosses between inbred lines provide a traditional approach to analysis of polygenic inheritance in model organisms. Chromosome substitution strains (CSSs) have been developed as an alternative to accelerate the pace of gene identification in quantitative trait mapping. We compared a classical intercross and three CSS intercrosses to examine the genetic architecture underlying plasma high-density lipoprotein cholesterol (HDL) levels in the C57BL/6J (B) and A/J (A) mouse strains. The B x A intercross revealed significant quantitative trait loci (QTL) for HDL on chromosomes 1, 4, 8, 15, 17, 18, and 19. A CSS survey revealed that many have significantly different HDL levels compared to the background strain B, including chromosomes with no significant QTL in the intercross and, in some cases (CSS-1, CSS-17), effects that are opposite to those observed in the B x A intercross population. Intercrosses between B and three CSSs (CSS-3, CSS-11, and CSS-8) revealed significant QTL but with some unexpected differences from the B x A intercross. Our inability to predict the results of CSS intercrosses suggests that additional complexity will be revealed by further crosses and that the CSS mapping strategy should be viewed as a complement to, rather than a replacement for, classical intercross mapping.

Indexed as

Crosses, GeneticAnimalsCholesterol, HDLChromosomes, MammalianFemaleMaleMiceMice, Inbred AMice, Inbred C57BLSpecies SpecificityCholesterol, HDL

Identifiers

PMID16951076
PMCPMC1602087
OpenAlexW2107189114

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.