Evidence map›Paper›PMID 41542651›Full record

ArticlebioRxiv : the preprint server for biology2026

Partitioning Fraction of Variance Explained into Strong Localized Effects and Weak Diffuse Effects.

Fang Nan, David Azriel, Armin Schwartzman

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Fang NanDivision of Biostatistics, University of California San Diego, La Jolla, CA, USA.ORCID 0009-0004-4351-0323
David AzrielFaculty of Data and Decision Sciences, The Technion, Haifa, Israel.ORCID 0000-0002-9569-576X
Armin SchwartzmanDivision of Biostatistics, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-5335-1611

Funding

Estimating The Fraction of Variance Explained by Genetics and Neuroanatomy in Neuropsychiatric ConditionsR01MH128923 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Armin Schwartzman, Wesley Kurt Thompson · 2022 to 2026
$2.9M
NIMH NIH HHS R01 MH128923
6 · The paper itself

Abstract

High-dimensional genetic data present substantial challenges for estimating the fraction of variance explained (FVE) by genome-wide single-nucleotide polymorphisms (SNPs). In the context of genetics the VFE is called SNP heritability. Standard approaches for FVE estimation, such as GWAS heritability (GWASH) and linkage disequilibrium score (LDSC) regression, typically assume Gaussian distributions for SNP effect sizes. However, empirical evidence indicates that SNP effects are often heavy-tailed, with a small subset of variants exerting disproportionately large influence. Such settings violate the recently established bounded-kurtosis effect (BKE) condition, under which these FVE estimators are consistent. Consequently, widely used methods may yield severely biased estimates when strong effects are present. We introduce a decomposed FVE estimation framework that accommodates heavy-tailed and heterogeneous SNP effect distributions. The proposed approach partitions total heritability into contributions from strong and weak genetic effects, estimating the former using low-dimensional adjusted

Identifiers

PMID41542651
PMCPMC12803106

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.