Evidence map›Paper›PMID 35127102›Full record

ArticleVeterinary record open2022

Genotypic and allelic frequency of a mutation in the

Stefano P Marelli, Rita Rizzi, Alessandra Paganelli, Mara Bagardi, Giulietta Minozzi, Paola G Brambilla, Michele Polli

Open access · goldAbstract read
In one paragraph

Article in Veterinary record open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Stefano P MarelliDepartment of Veterinary Medicine University of Milan Lodi Italy.ORCID https://orcid.org/0000-0001-8027-2193
Rita RizziDepartment of Veterinary Medicine University of Milan Lodi Italy.
Alessandra PaganelliVetogene - ENCI Servizi Milano Italy.
Mara BagardiDepartment of Veterinary Medicine University of Milan Lodi Italy.ORCID https://orcid.org/0000-0002-5247-3796
Giulietta MinozziDepartment of Veterinary Medicine University of Milan Lodi Italy.ORCID https://orcid.org/0000-0002-0020-8798
Paola G BrambillaDepartment of Veterinary Medicine University of Milan Lodi Italy.ORCID https://orcid.org/0000-0003-4255-555X
Michele PolliDepartment of Veterinary Medicine University of Milan Lodi Italy.ORCID https://orcid.org/0000-0003-0129-0161
University of Milan · ITPolitecnico di Milano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA 7.8-kb deletion in intron 4 of the

methodsGenotype data, for the 7.8 kb deletion in intron 4 of the

resultsHealthy carriers were 50%, 45%, 29.6%, 17.3% and 12.5% in SS, NS, BC, AS and RC, respectively. The affected recessive homozygotes were 81.3%, 10.8% and 1.5% in RC, SS and BC, respectively. The CEA allelic frequencies were 0.36, 0.16 and 0.087 in SS, BC and AS, respectively.

conclusionThe results support the usefulness of this type of genetic analysis to optimize the care of dogs where the CEA mutation is present, including assessing the health risk to susceptible dogs within a breed and to provide an objective basis for breeding programmes.

Identifiers

PMID35127102
PMCPMC8800487
OpenAlexW4210561998

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.