ArticleAmerican journal of human genetics2026
A flexible and unified framework for single- and multi-outcome Mendelian randomization using summary statistics.
Article in American journal of human genetics, 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.
- Recalibrating Mendelian randomization under winner's curse, sample structure and polygenicity.medRxiv : the preprint server for health sciences · 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
11 authors.
Funding
Abstract
Mendelian randomization (MR) is widely used to evaluate causal effects of complex trait exposures on disease outcomes. Recently, MR has been increasingly applied to molecular traits, such as gene expression, to map risk genes. However, transcriptome-wide MR (TWMR) faces unique challenges. The number of available cis-QTLs as instrumental variables (IVs) is often limited, and horizontal pleiotropy is pervasive, violating core MR assumptions and compromising inference validity. We introduce FusioMR, a robust MR framework tailored for molecular trait exposures while also applicable to complex trait exposures. Our single-outcome model, FusioMR
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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.