Evidence map›Paper›PMID 29708978›Full record

ArticlePLoS genetics2018

Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs.

Jonas Donner, Heidi Anderson, Stephen Davison, Angela M Hughes, Julia Bouirmane, Johan Lindqvist, Katherine M Lytle, Balasubramanian Ganesan, Claudia Ottka, Päivi Ruotanen and 5 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
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  11. A 120-y time series of genomes reveals the consequences of closed breeding in German Shepherd Dogs.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Article
  14. PCR-based detection of hereditary mutations inJournal of veterinary science · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Whole exome sequencing as a screening tool in dogs: A pilot study.Computational and structural biotechnology journal · 2025
    Article
  20. A new future for dog breeding.Animal welfare (South Mimms, England) · 2025
    Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 2 countries.

Jonas DonnerGenoscoper Laboratories, Helsinki, Finland.ORCID 0000-0002-9874-8484
Heidi AndersonGenoscoper Laboratories, Helsinki, Finland.
Stephen DavisonWisdom Health, Waltham-on-the-Wolds, Leicestershire, United Kingdom.
Angela M HughesWisdom Health, Vancouver, Washington, United States of America.
Julia BouirmaneGenoscoper Laboratories, Helsinki, Finland.
Johan LindqvistGenoscoper Laboratories, Helsinki, Finland.
Katherine M LytleWisdom Health, Vancouver, Washington, United States of America.
Balasubramanian GanesanWisdom Health, Vancouver, Washington, United States of America.
Claudia OttkaGenoscoper Laboratories, Helsinki, Finland.
Päivi RuotanenGenoscoper Laboratories, Helsinki, Finland.
Maria KaukonenResearch Programs Unit-Molecular Neurology, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-2146-4694
Oliver P FormanWisdom Health, Waltham-on-the-Wolds, Leicestershire, United Kingdom.
Neale FretwellWisdom Health, Vancouver, Washington, United States of America.
Cynthia A ColeWisdom Health, Vancouver, Washington, United States of America.
Hannes LohiGenoscoper Laboratories, Helsinki, Finland.
Wisdom Health (United States) · USUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge on the genetic epidemiology of disorders in the dog population has implications for both veterinary medicine and sustainable breeding. Limited data on frequencies of genetic disease variants across breeds exists, and the disease heritage of mixed breed dogs remains poorly explored to date. Advances in genetic screening technologies now enable comprehensive investigations of the canine disease heritage, and generate health-related big data that can be turned into action. We pursued population screening of genetic variants implicated in Mendelian disorders in the largest canine study sample examined to date by examining over 83,000 mixed breed and 18,000 purebred dogs representing 330 breeds for 152 known variants using a custom-designed beadchip microarray. We further announce the creation of MyBreedData (www.mybreeddata.com), an online updated inherited disorder prevalence resource with its foundation in the generated data. We identified the most prevalent, and rare, disease susceptibility variants across the general dog population while providing the first extensive snapshot of the mixed breed disease heritage. Approximately two in five dogs carried at least one copy of a tested disease variant. Most disease variants are shared by both mixed breeds and purebreds, while breed- or line-specificity of others is strongly suggested. Mixed breed dogs were more likely to carry a common recessive disease, whereas purebreds were more likely to be genetically affected with one, providing DNA-based evidence for hybrid vigor. We discovered genetic presence of 22 disease variants in at least one additional breed in which they were previously undescribed. Some mutations likely manifest similarly independently of breed background; however, we emphasize the need for follow up investigations in each case and provide a suggested validation protocol for broader consideration. In conclusion, our study provides unique insight into genetic epidemiology of canine disease risk variants, and their relevance for veterinary medicine, breeding programs and animal welfare.

Indexed as

AnimalsBreedingDatabases, GeneticDog DiseasesDogsFemaleGene FrequencyGenes, RecessiveGenetic Predisposition to DiseaseGenetic TestingGenetic VariationHybrid VigorMaleMolecular EpidemiologyOligonucleotide Array Sequence AnalysisPrevalence

Identifiers

PMID29708978
PMCPMC5945203
OpenAlexW2801601697

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.