Evidence map›Paper›PMID 19306044›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2009

Replication of long-bone length QTL in the F9-F10 LG,SM advanced intercross.

Elizabeth A Norgard, Joseph P Jarvis, Charles C Roseman, Taylor J Maxwell, Jane P Kenney-Hunt, Kaitlin E Samocha, L Susan Pletscher, Bing Wang, Gloria L Fawcett, Christopher J Leatherwood and 2 more

Open access · greenAbstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2009. 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
3.3field-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

23 citing papers in PubMed, 34 citations in OpenAlex.

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  7. Fine-mapping QTLs in advanced intercross lines and other outbred populations.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Review
  8. Article
  9. Article
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  12. Forward genetic approaches to understanding complex behaviors.Current topics in behavioral neurosciences · 2012
    Review
  13. Identification of quantitative trait loci influencing skeletal architecture in mice: emergence of Cdh11 as a primary candidate gene regulating femoral morphology.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  14. Article
  15. Genetic factors and diet affect long-bone length in the F34 LG,SM advanced intercross.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    Article
  16. Developmental and genetic origins of murine long bone length variation.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2011
    Article
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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

12 authors at 4 institutions in 2 countries.

Elizabeth A NorgardDepartment of Anatomy and Neurobiology, Washington University School of Medicine, Box 8108, 660 South Euclid Avenue, St. Louis, MO 63110, USA. enorgard@artsci.wustl.edu
Joseph P Jarvis
Charles C Roseman
Taylor J Maxwell
Jane P Kenney-Hunt
Kaitlin E Samocha
L Susan Pletscher
Bing Wang
Gloria L Fawcett
Christopher J Leatherwood
Jason B Wolf
James M Cheverud
Washington University in St. Louis · USThe University of Texas at Austin · USUniversity of Manchester · GBUniversity of South Carolina · US

Funding

GENETIC VARIATION IN MURINE LONG BONE GROWTH AND DEVELOPMENTR01AR053224 · NIAMS · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2006 to 2010
$1.6M
Biotechnology and Biological Sciences Research Council BB/C516936/1Intramural NIH HHSNIAMS NIH HHS AR053224NIAMS NIH HHS R01 AR053224
6 · The paper itself

Abstract

Quantitative trait locus (QTL) mapping techniques are frequently used to identify genomic regions associated with variation in phenotypes of interest. However, the F(2) intercross and congenic strain populations usually employed have limited genetic resolution resulting in relatively large confidence intervals that greatly inhibit functional confirmation of statistical results. Here we use the increased resolution of the combined F(9) and F(10) generations (n = 1455) of the LG,SM advanced intercross to fine-map previously identified QTL associated with the lengths of the humerus, ulna, femur, and tibia. We detected 81 QTL affecting long-bone lengths. Of these, 49 were previously identified in the combined F(2)-F(3) population of this intercross, while 32 represent novel contributors to trait variance. Pleiotropy analysis suggests that most QTL affect three to four long bones or serially homologous limb segments. We also identified 72 epistatic interactions involving 38 QTL and 88 novel regions. This analysis shows that using later generations of an advanced intercross greatly facilitates fine-mapping of confidence intervals, resolving three F(2)-F(3) QTL into multiple linked loci and narrowing confidence intervals of other loci, as well as allowing identification of additional QTL. Further characterization of the biological bases of these QTL will help provide a better understanding of the genetics of small variations in long-bone length.

Indexed as

Crosses, GeneticDNA ReplicationQuantitative Trait LociAnimalsBone and BonesFemaleHybridization, GeneticMaleMiceOrgan Size

Identifiers

PMID19306044
PMCPMC2736561
OpenAlexW1965598885

What OpenQuestion holds

Textmetadata
LicenceTDM
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.