Evidence map›Paper›PMID 24466169›Full record

ArticlePloS one2014

A chromosomal region on ECA13 is associated with maxillary prognathism in horses.

Heidi Signer-Hasler, Markus Neuditschko, Christoph Koch, Sylvie Froidevaux, Christine Flury, Dominik Burger, Tosso Leeb, Stefan Rieder

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Orthodontics and Genetics.Dental press journal of orthodontics · 2019
    Article
  4. Article
  5. Article
  6. 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

8 authors at 4 institutions in 1 country.

Heidi Signer-HaslerSchool of Agricultural, Forest and Food Sciences, Bern University of Applied Sciences, Zollikofen, Switzerland.
Markus NeuditschkoSwiss National Stud Farm, Agroscope, Avenches, Switzerland.
Christoph KochSwiss Institute of Equine Medicine ISME, Vetsuisse Faculty University of Bern and Agroscope, Bern, Switzerland.
Sylvie FroidevauxSwiss Institute of Equine Medicine ISME, Vetsuisse Faculty University of Bern and Agroscope, Bern, Switzerland.
Christine FlurySchool of Agricultural, Forest and Food Sciences, Bern University of Applied Sciences, Zollikofen, Switzerland.
Dominik BurgerSwiss Institute of Equine Medicine ISME, Vetsuisse Faculty University of Bern and Agroscope, Bern, Switzerland.
Tosso LeebInstitute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Stefan RiederSwiss National Stud Farm, Agroscope, Avenches, Switzerland.
Agroscope · CHBern University of Applied Sciences · CHUniversity of Bern · CHSwiss Institute of Equine Medicine · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary variations in head morphology and head malformations are known in many species. The most common variation encountered in horses is maxillary prognathism. Prognathism and brachygnathism are syndromes of the upper and lower jaw, respectively. The resulting malocclusion can negatively affect teeth wear, and is considered a non-desirable trait in breeding programs. We performed a case-control analysis for maxillary prognathism in horses using 96 cases and 763 controls. All horses had been previously genotyped with a commercially available 50 k SNP array. We analyzed the data with a mixed-model considering the genomic relationships in order to account for population stratification. Two SNPs within a region on the distal end of chromosome ECA 13 reached the Bonferroni corrected genome-wide significance level. There is no known prognathism candidate gene located within this region. Therefore, our findings in the horse offer the possibility of identifying a novel gene involved in the complex genetics of prognathism that might also be relevant for humans and other livestock species.

Indexed as

AnimalsBreedingCase-Control StudiesChromosomesGenome-Wide Association StudyGenotypeHorse DiseasesHorsesMaxillary DiseasesPhenotypePolymorphism, Single NucleotidePrognathism

Identifiers

PMID24466169
PMCPMC3897735
OpenAlexW2038750541

What OpenQuestion holds

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LicenceCC BY
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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.