Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Polygene risk scores and randomized experiments.

The Behavioral and brain sciences - 11 Sept 2023

Ross Lauren N, Kendler Kenneth S, Woodward James F

Abstract excerpt

We explore Madole & Harden's (2022) suggestion that single-nucleotide polymorphism (SNP)/trait correlations are analogous to randomized experiments and thus can be given a causal interpretation.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Multifactorial Inheritance
Share to Polymorphism, Single Nucleotide
Share to Risk Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37694930
DOI: 10.1017/S0140525X22002151

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polygene risk scores and randomized experiments.PMID 37694930Read ↗

Highly parameterized polygenic scores tend to overfit to population stratification via random effectsSemantic proximity Read ↗

Optimizing genomic control in mixed model associations with binary diseases.Semantic proximity Read ↗

Optimal Genomic Control in Large-scale Genetic Associations for Binary DiseasesSemantic proximity Read ↗

Policy gradient-guided ensemble learning for enhanced polygenic risk prediction in ultra-high-dimensional genomicsSemantic proximity Read ↗

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.Semantic proximity Read ↗

Correction for hidden confounders in the genetic analysis of gene expression.Semantic proximity Read ↗

Estimating causal effects with a non-paranormal method for the design of efficient intervention experiments.Semantic proximity Read ↗

GAW10: simulated family data for a common oligogenic disease with quantitative risk factors.Semantic proximity Read ↗

Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternativesSemantic proximity Read ↗

Causal inference in genetic trio studies.Semantic proximity Read ↗

Integrating genetic data in target trial emulations improves their design and informs the value of polygenic scores for prognostic and predictive enrichmentSemantic proximity Read ↗

Identifying Causal Genotype-Phenotype Relationships for Population-Sampled Parent-Child Trios.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.