ArticleAmerican journal of human genetics2016
Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome.
Article in American journal of human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
20 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Recommendations for Human Sperm Morphology Assessment in 2025: An Expert Review From the French BLEFCO Group.Andrology · 2026Guideline
- Comparative sperm proteomics in IVF patients with differential fertilization rates identifies FAM205A as a novel biomarker for male infertility.Asian journal of andrology · 2026Article
- Molecular models of the sperm head-tail coupling apparatus.Journal of cell science · 2025Review
- Article
- Genome-Wide Association Screening Determines Peripheral Players in Male Fertility Maintenance.International journal of molecular sciences · 2022Article
- Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report.World journal of clinical cases · 2022Article
- Novel mutations of PMFBP1 in a man with acephalic spermatozoa defects.Molecular genetics & genomic medicine · 2022Article
- Semen parameters are seriously affected in acephalic spermatozoa syndrome.Basic and clinical andrology · 2022Article
- CEP128 is involved in spermatogenesis in humans and mice.Nature communications · 2022Article
- Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.International journal of molecular sciences · 2021Article
- Pathogenic Variants inFrontiers in cell and developmental biology · 2021Article
- A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.Human genetics · 2021Review
- Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.Molecular genetics & genomic medicine · 2020Article
- Sperm Head-Tail Linkage Requires Restriction of Pericentriolar Material to the Proximal Centriole End.Developmental cell · 2020Article
- Microtubular Dysfunction and Male Infertility.The world journal of men's health · 2020Review
- Recent advances and future opportunities to diagnose male infertility.Current sexual health reports · 2019Article
- Associations between DNAH1 gene polymorphisms and male infertility: A retrospective study.Medicine · 2018Article
- SPATC1L maintains the integrity of the sperm head-tail junction.EMBO reports · 2018Article
- The involvement of the nuclear lamina in human and rodent spermiogenesis: a systematic review.Basic and clinical andrology · 2018Article
- Biallelic mutations inAsian journal of andrologyArticle
Corrections and comments
- Erratum for
Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Identifiers
What OpenQuestion holds
Registered trials
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.