Evidence map›Paper›PMID 33671757›Full record

ArticleInternational journal of molecular sciences2021

Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.

Caroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, Selima Fourati Ben Mustapha, Marjorie Whitfield, Charles Coutton, Nicolas Thierry-Mieg, Pierre Di Pizio, Nathalie Rives, Christophe Arnoult and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Guideline
  2. Observational
  3. SUN5 forms a regular protein lattice reinforcing the sperm head-tail junction.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Article
  6. Genetic etiological spectrum of sperm morphological abnormalities.Journal of assisted reproduction and genetics · 2024
    Review
  7. The Development, Differentiation, and Toxicity in Reproduction.International journal of molecular sciences · 2022
    Article
  8. The relevance of sperm morphology in male infertility.Frontiers in reproductive health · 2022
    Article
  9. Review
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

15 authors at 4 institutions in 1 country.

Caroline CazinInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Yasmine BoumerdassiDepartment of Reproductive Biology, Hôpital Jean Verdier, Assistance Publique, Hôpitaux de Paris, F-75004 Paris, France.ORCID 0000-0003-2381-443X
Guillaume MartinezInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Selima Fourati Ben MustaphaCentre d'Aide Médicale à la Procréation, Polyclinique les Jasmin, Centre Urbain Nord, Tunis 1003, Tunisia.
Marjorie WhitfieldInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Charles CouttonInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Nicolas Thierry-MiegTIMC-IMAG, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Pierre Di PizioEA 4308 'Gametogenesis and Gamete Quality, Normandie University, UNIROUEN, F-76000 Rouen, France.
Nathalie RivesEA 4308 'Gametogenesis and Gamete Quality, Normandie University, UNIROUEN, F-76000 Rouen, France.
Christophe ArnoultInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Aminata TouréInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.ORCID 0000-0001-5629-849X
Pierre F RayInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.ORCID 0000-0003-1544-7449
Raoudha ZouariCentre d'Aide Médicale à la Procréation, Polyclinique les Jasmin, Centre Urbain Nord, Tunis 1003, Tunisia.
Christophe SiferDepartment of Reproductive Biology, Hôpital Jean Verdier, Assistance Publique, Hôpitaux de Paris, F-75004 Paris, France.
Zine-Eddine KherrafInstitute for Advanced Biosciences, INSERM, CNRS, Université Grenoble Alpes, F-38000 Grenoble, France.
Centre National de la Recherche Scientifique · FRInstitut polytechnique de Grenoble · FRAssistance Publique – Hôpitaux de Paris · FRNormandie Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acephalic spermatozoa syndrome (ASS) is a rare but extremely severe type of teratozoospermia, defined by the presence of a majority of headless flagella and a minority of tail-less sperm heads in the ejaculate. Like the other severe monomorphic teratozoospermias, ASS has a strong genetic basis and is most often caused by bi-allelic variants in

Indexed as

AdultAfrica, NorthernAneuploidyCase-Control StudiesExome SequencingGenetic VariationHaplotypesHomozygoteHumansIn Situ Hybridization, FluorescenceMaleMembrane ProteinsMiddle AgedSpermatozoaTeratozoospermiaMembrane ProteinsSUN5 protein, humanacephalic spermatozoa syndromegenetics of male infertilitySUN5teratozoospermiawhole exome sequencing

Identifiers

PMID33671757
PMCPMC7927044
OpenAlexW3132069990

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.