ArticleFrontiers in genetics2026
Case Report: Identification of two novel
Article in Frontiers in genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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0 citing papers in PubMed.
No citing paper in PubMed yet.
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Authors and funding
4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Background: Alström syndrome (AS) is a rare autosomal recessive ciliopathy caused by biallelic pathogenic variants in the Case Presentation: We report a 27-year-old Chinese female with a body mass index (BMI) of 28.4 kg/m Conclusion: This report describes two novel
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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.