Evidence map›Paper›PMID 31615056›Full record

ArticleGenes2019

A

Petra Hug, Patricia Kern, Vidhya Jagannathan, Tosso Leeb

Open access · goldAbstract readCase Reports
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

4 authors at 1 institution in 1 country.

Petra HugInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. petra.hug@vetsuisse.unibe.ch.
Patricia KernTierarztpraxis Spiegelberg AG, 4566 Halten, Switzerland. info@tierarztpraxis-spiegelberg.ch.
Vidhya JagannathanInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. vidhya.jagannathan@vetsuisse.unibe.ch.ORCID 0000-0002-8155-0041
Tosso LeebInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. tosso.leeb@vetsuisse.unibe.ch.ORCID 0000-0003-0553-4880
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A single male domestic shorthair cat that did not complete puberty was reported. At four years of age, it still had primary dentition, testicular hypoplasia, and was relatively small for its age. We hypothesized that the phenotype might have been due to an inherited form of hypogonadotropic hypogonadism (HH). We sequenced the genome of the affected cat and compared the data to 38 genomes from control cats. A search for private variants in 40 candidate genes associated with human HH revealed a single protein-changing variant in the affected cat. It was located in the

Indexed as

Mutation, MissenseAnimalsCat DiseasesCatsHypogonadismMaleNeurokinin BReceptors, Neurokinin-3Sexual MaturationTachykininsTestisTooth AbnormalitiesTooth, DeciduousNeurokinin BReceptors, Neurokinin-3Tachykininsanimal modeldevelopmentdisorder of sexual developmentFelis catus L.neurokinin Bprecision medicinepubertywhole genome sequence

Identifiers

PMID31615056
PMCPMC6826659
OpenAlexW2979572550

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.