Evidence map›Paper›PMID 36769638›Full record

ArticleJournal of clinical medicine2023

The Role of

Iulia Potorac, Marie Laterre, Olivier Malaise, Vlad Nechifor, Corinne Fasquelle, Orphal Colleye, Nancy Detrembleur, Hannah Verdin, Sofie Symoens, Elfride De Baere and 4 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Advances in the genetic etiology of female infertility.Journal of assisted reproduction and genetics · 2024
    Review
  6. A Human HomozygousGenes · 2024
    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

14 authors.

Iulia PotoracDepartment of Endocrinology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Marie LaterreDepartment of Human Genetics, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Olivier MalaiseDepartment of Rheumatology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.ORCID 0000-0002-2799-2949
Vlad NechiforDepartment of Urology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Corinne FasquelleDepartment of Human Genetics, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Orphal ColleyeDepartment of Pathology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Nancy DetrembleurDepartment of Pathology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Hannah VerdinCenter for Medical Genetics Ghent, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0002-0258-1000
Sofie SymoensCenter for Medical Genetics Ghent, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.
Elfride De BaereCenter for Medical Genetics Ghent, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0002-5609-6895
Adrian F DalyDepartment of Endocrinology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.ORCID 0000-0001-6130-2975
Vincent BoursDepartment of Human Genetics, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Patrick PétrossiansDepartment of Endocrinology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.
Axelle PintiauxDepartment of Gynecology, Centre Hospitalier Universitaire (CHU) de Liège, Domaine Universitaire Sart-Tilman, 4000 Liège, Belgium.

Funding

of the Centre Hospitalier Universitaire de Liège FIRS 2020-2021
6 · The paper itself

Abstract

Infertility in couples is a common problem, with both female and male factors contributing to similar extents. Severe, congenital disorders affecting fertility are, however, rare. While folliculogenesis and spermatogenesis are generally orchestrated via different mechanisms, some genetic anomalies can impair both female and male gametogenesis. Minichromosome maintenance complex component 9 (MCM9) is involved in DNA repair and mutations of the

Indexed as

azoospermiageneticsMCM9non-obstructivepremature ovarian failurepubertySertoli cell only syndrome

Identifiers

PMID36769638
PMCPMC9917496

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.