ArticlePharmacogenomics and personalized medicine2026
Association Between
Article in Pharmacogenomics and personalized medicine, 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
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Purpose: Propofol, a commonly used intravenous sedative in general anesthesia, exhibits significant inter-individual variability in clinical effects; however, the underlying mechanisms remain uncertain. We aimed to assess the association between the UGT1A9 rs13418420 polymorphism and individual propofol response, as assessed by the time required for the bispectral index (BIS) to decrease to 60. Patients and Methods: A total of 75 Chinese female patients undergoing painless abortion, cervical conization, or hysteroscopy under intravenous anesthesia without endotracheal intubation were recruited. Based on bioinformatic analysis and our preliminary sequencing experiments in the Chinese population, Results: Our results revealed that patients with the TT genotype of Conclusion: Patients carrying the TT genotype of
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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.