ArticleMedComm2026
Cerebrospinal Fluid Genetics Enhance Risk Stratification in Bipolar Disorder.
Article in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Cross-ancestry pleiotropic analysis of imaging-derived phenotypes enhances risk stratification of depression.Molecular psychiatry · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bipolar disorder (BD) research confronts challenges: blood-based biomarkers offer limited insights into neurobiology, while cerebrospinal fluid (CSF) collection is clinically unusual. Linking genetic susceptibility to pathophysiology remains crucial for biologically informed risk stratification. We integrated cohort data and genome-wide association study (GWAS) summary statistics: the largest BD meta-analysis, CSF multi-omics profiles including 3107 proteomic and 2602 metabolomic participants, and a validation cohort of 247,834 UK Biobank participants. Unsupervised clustering revealed four single-nucleotide variant (SNV) clusters: metabolic-imbalance, metabolic-active, human leukocyte antigen (HLA)+immune, and HLA-immune. These clusters exhibited distinct clinical features, with the metabolic-imbalance cluster showing multi-directional associations with 21 psychiatric traits, while the HLA-immune cluster was associated with emotional instability in BD patients (odds ratio [OR] = 1.14,
Indexed as
Identifiers
What Socratic 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 Socratic graph.