Evidence map›Paper›PMID 16245029›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2005

Quantitative trait loci for hip dysplasia in a cross-breed canine pedigree.

Rory J Todhunter, Raluca Mateescu, George Lust, Nancy I Burton-Wurster, Nathan L Dykes, Stuart P Bliss, Alma J Williams, Margaret Vernier-Singer, Elizabeth Corey, Carlos Harjes and 7 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Emerging insights into the genetic basis of canine hip dysplasia.Veterinary medicine (Auckland, N.Z.) · 2015
    Review
  9. Article
  10. Review
  11. Article
  12. Multiple loci associated with canine hip dysplasia (CHD) in German shepherd dogs.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Canine hip dysplasia is predictable by genotyping.Osteoarthritis and cartilage · 2011
    Article
  19. 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

17 authors at 4 institutions in 1 country.

Rory J TodhunterDepartment of Clinical Sciences, Box 32 College of Veterinary Medicine, Cornell University, Ithaca, New York 14853, USA. rjt2@cornell.edu
Raluca Mateescu
George Lust
Nancy I Burton-Wurster
Nathan L Dykes
Stuart P Bliss
Alma J Williams
Margaret Vernier-Singer
Elizabeth Corey
Carlos Harjes
Richard L Quaas
Zhiwu Zhang
Robert O Gilbert
Dietrich Volkman
George Casella
Rongling Wu
Gregory M Acland
Cornell University · USNew York State College of Veterinary Medicine · USUniversity of Florida · USNew York State College of Agriculture & Life Sciences · US

Funding

Impact Damage, Apoptosis, and Early OsteoarthritisR01AR047558 · NIAMS · CORNELL UNIVERSITY ITHACA · PI BURTON-WURSTER, NANCY I · 2001 to 2003
$835k
NIAMS NIH HHS R01 AR47558
6 · The paper itself

Abstract

Canine hip dysplasia is a common developmental inherited trait characterized by hip laxity, subluxation or incongruity of the femoral head and acetabulum in affected hips. The inheritance pattern is complex and the mutations contributing to trait expression are unknown. In the study reported here, 240 microsatellite markers distributed in 38 autosomes and the X chromosome were genotyped on 152 dogs from three generations of a crossbred pedigree based on trait-free Greyhound and dysplastic Labrador Retriever founders. Interval mapping was undertaken to map the QTL underlying the quantitative dysplastic traits of maximum passive hip laxity (the distraction index), the dorsolateral subluxation score, and the Norberg angle. Permutation testing was used to derive the chromosome-wide level of significance at p<0.05 for each QTL. Chromosomes 4, 9, 10, 11 (p<0.01), 16, 20, 22, 25, 29 (p<0.01), 30, 35, and 37 harbor putative QTL for one or more traits. Successful detection of QTL was due to the cross-breed pedigree, multiple-trait measurements, control of environmental background, and marked advancement in canine mapping tools.

Indexed as

PhenotypeQuantitative Trait LociAnimalsChromosome MappingCrosses, GeneticDogsGenetics, PopulationGenotypeHip Dysplasia, CanineMicrosatellite RepeatsPedigreeRadiographyRegression AnalysisSpecies Specificity

Identifiers

PMID16245029
OpenAlexW2054574487

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.