Evidence map›Paper›PMID 25270232›Full record

ArticleBMC genomics2014

Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers.

Enrique Sánchez-Molano, John A Woolliams, Ricardo Pong-Wong, Dylan N Clements, Sarah C Blott, Pamela Wiener

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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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

6 authors at 3 institutions in 1 country.

Enrique Sánchez-Molano
John A Woolliams
Ricardo Pong-Wong
Dylan N Clements
Sarah C Blott
Pamela WienerThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian EH25 9RG, Scotland, UK. pam.wiener@roslin.ed.ac.uk.
Roslin Institute · GBUniversity of Edinburgh · GBAnimal Health Trust · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H017798/1Biotechnology and Biological Sciences Research Council BB/H019073/1Biotechnology and Biological Sciences Research Council BB/J004243/1Biotechnology and Biological Sciences Research Council BBS/E/D/05191132Medical Research Council MR/K001744/1
6 · The paper itself

Abstract

backgroundCanine hip dysplasia (CHD) is characterised by a malformation of the hip joint, leading to osteoarthritis and lameness. Current breeding schemes against CHD have resulted in measurable but moderate responses. The application of marker-assisted selection, incorporating specific markers associated with the disease, or genomic selection, incorporating genome-wide markers, has the potential to dramatically improve results of breeding schemes. Our aims were to identify regions associated with hip dysplasia or its related traits using genome and chromosome-wide analysis, study the linkage disequilibrium (LD) in these regions and provide plausible gene candidates. This study is focused on the UK Labrador Retriever population, which has a high prevalence of the disease and participates in a recording program led by the British Veterinary Association (BVA) and The Kennel Club (KC).

resultsTwo genome-wide and several chromosome-wide QTLs affecting CHD and its related traits were identified, indicating regions related to hip dysplasia.

conclusionConsistent with previous studies, the genetic architecture of CHD appears to be based on many genes with small or moderate effect, suggesting that genomic selection rather than marker-assisted selection may be an appropriate strategy for reducing this disease.

Indexed as

Chromosome MappingPhenotypeAnimalsChromosomes, MammalianDogsGenomicsHip Dysplasia, CaninePolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID25270232
PMCPMC4190382
OpenAlexW2104891172

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.