Evidence map›Paper›PMID 33198087›Full record

ArticleInternational journal of molecular sciences2020

Identification of a New QTL Region on Mouse Chromosome 1 Responsible for Male Hypofertility: Phenotype Characterization and Candidate Genes.

Magalie Vatin, Marie-Sophie Girault, Virginie Firlej, Carmen Marchiol, Côme Ialy-Radio, Xavier Montagutelli, Daniel Vaiman, Sandrine Barbaux, Ahmed Ziyyat

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Deletion of theInternational journal of molecular sciences · 2021
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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

9 authors at 2 institutions in 1 country.

Magalie VatinInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.
Marie-Sophie GiraultInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.
Virginie FirlejInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.ORCID 0000-0003-4132-0695
Carmen MarchiolInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.ORCID 0000-0002-9666-7939
Côme Ialy-RadioInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.
Xavier MontagutelliMouse Genetics Laboratory, Institut Pasteur, F-75015 Paris, France.ORCID 0000-0002-9372-5398
Daniel VaimanInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.ORCID 0000-0002-1915-0717
Sandrine BarbauxInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.
Ahmed ZiyyatInstitut Cochin, Université de Paris, INSERM, CNRS, F-75014 Paris, France.ORCID 0000-0001-9724-3831
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male fertility disorders often have their origin in disturbed spermatogenesis, which can be induced by genetic factors. In this study, we used interspecific recombinant congenic mouse strains (IRCS) to identify genes responsible for male infertility. Using ultrasonography, in vivo and in vitro fertilization (IVF) and electron microscopy, the phenotyping of several IRCS carrying mouse chromosome 1 segments of

Indexed as

AcrosomeAnimalsCell NucleusChromosomes, Human, Pair 1EpididymisFemaleHumansInfertility, MaleMaleMicePhenotypeQuantitative Trait LociSpermatidsSpermatogenesisSpermatozoaTeratozoospermiaglobozoospermiainfertilityIRCSspermatogenesisteratozoospermia

Identifiers

PMID33198087
PMCPMC7697627
OpenAlexW3098034908

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.