Evidence map›Paper›PMID 35709088›Full record

ArticlePLoS genetics2022

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats.

Heidi Anderson, Stephen Davison, Katherine M Lytle, Leena Honkanen, Jamie Freyer, Julia Mathlin, Kaisa Kyöstilä, Laura Inman, Annette Louviere, Rebecca Chodroff Foran and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Genetic Testing: practical dos and don'ts for cats.Journal of feline medicine and surgery · 2024
    Review
  12. Online Mendelian Inheritance in Animals (OMIA): a genetic resource for vertebrate animals.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    Review
  13. Article
  14. Article
  15. Genetic Basis of Hypertrophic Cardiomyopathy in Cats.Current issues in molecular biology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Dystrophin (International journal of molecular sciences · 2023
    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

13 authors at 1 institution in 1 country.

Heidi AndersonWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-5561-0901
Stephen DavisonWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-7999-7119
Katherine M LytleWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-7826-0107
Leena HonkanenWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0001-8864-6532
Jamie FreyerWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-0223-8747
Julia MathlinWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.
Kaisa KyöstiläDepartment of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
Laura InmanWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-5004-2888
Annette LouviereWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0001-9726-8131
Rebecca Chodroff ForanWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0001-7210-9329
Oliver P FormanWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0003-2817-2165
Hannes LohiDepartment of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.ORCID 0000-0003-1087-5532
Jonas DonnerWisdom Panel Research Team, Wisdom Panel, Kinship, Portland, Oregon, United States of America.ORCID 0000-0002-9874-8484
University of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the largest DNA-based study of domestic cats to date, 11,036 individuals (10,419 pedigreed cats and 617 non-pedigreed cats) were genotyped via commercial panel testing elucidating the distribution and frequency of known disease, blood type, and physical trait associated genetic variants across cat breeds. This study provides allele frequencies for many disease-associated variants for the first time and provides updates on previously reported information with evidence suggesting that DNA testing has been effectively used to reduce disease associated variants within certain pedigreed cat populations over time. We identified 13 disease-associated variants in 47 breeds or breed types in which the variant had not previously been documented, highlighting the relevance of comprehensive genetic screening across breeds. Three disease-associated variants were discovered in non-pedigreed cats only. To investigate the causality of nine disease-associated variants in cats of different breed backgrounds our veterinarians conducted owner interviews, reviewed clinical records, and invited cats to have follow-up clinical examinations. Additionally, genetic variants determining blood types A, B and AB, which are relevant clinically and in cat breeding, were genotyped. Appearance-associated genetic variation in all cats is also discussed. Lastly, genome-wide SNP heterozygosity levels were calculated to obtain a comparable measure of the genetic diversity in different cat breeds. This study represents the first comprehensive exploration of informative Mendelian variants in felines by screening over 10,000 pedigreed cats. The results qualitatively contribute to the understanding of feline variant heritage and genetic diversity and demonstrate the clinical utility and importance of such information in supporting breeding programs and the research community. The work also highlights the crucial commitment of pedigreed cat breeders and registries in supporting the establishment of large genomic databases, that when combined with phenotype information can advance scientific understanding and provide insights that can be applied to improve the health and welfare of cats.

Indexed as

Genetic VariationGenomeAnimalsCatsGene FrequencyMolecular EpidemiologyPhenotype

Identifiers

PMID35709088
PMCPMC9202916
OpenAlexW4283011740

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.