ReviewClinics in perinatology2026
Genetics and Stillbirth.
Review in Clinics in perinatology, 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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Stillbirth affects over 3 million pregnancies globally and remains unexplained in roughly half of US cases. Genetic testing has uncovered chromosomal causes in approximately 6% to 13% of stillbirths, while exome sequencing has identified Mendelian variants in an additional approximately 5% to 10%. Family-based genome sequencing may allow identification of inherited and de novo pathogenic variants with increased diagnostic yield. We reviewed current knowledge ranging from rare monogenic disorders and polygenic risk to epigenetic dysregulation contributing to stillbirth. We provide a clinical framework aimed at refining stillbirth diagnosis toward improved clinical management of stillbirth in future pregnancies.
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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.