Evidence map›Paper›PMID 42182162›Full record

ArticlebioRxiv : the preprint server for biology2026

When can whole-genome SNP heritability be reliably estimated from summary statistics?

Benjamin Pham, Samuel Davenport, 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

4 authors.

Benjamin PhamHalicioğlu Data Science Institute, University of California San Diego.ORCID 0009-0005-5994-3593
Samuel DavenportDivision of Biostatistics, University of California San Diego.
David AzrielFaculty of Data and Decision Sciences, The Technion, Haifa, Israel.ORCID 0000-0002-9569-576X
Armin SchwartzmanHalicioğlu Data Science Institute, University of California San Diego.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

LD Score Regression (LDSC) is a prominent method, which estimates whole-genome SNP heritability from summary statistics via the slope of a linear regression of GWAS test statistics corresponding to a trait of interest against LD scores. It was claimed by the LDSC authors that the free intercept in the regression accounts for confounding bias such as population stratification. In this study, we argue that the intercept in LDSC must be fixed to 1 for accurate SNP heritability estimation. We show both theoretically and with simulations that the estimated intercept does not accurately capture population stratification effects, and that it adversely affects the accuracy of the heritability estimate introducing bias and increasing variance. Fixing the intercept to 1 eliminates bias and reduces variance when no population stratification is present. On the other hand, under population stratification, LDSC is biased with both the free and the fixed intercept. Additionally, we show that estimated standard errors in LDSC are underestimated, potentially leading to false-positives in downstream GWAS analyses.

Identifiers

PMID42182162
PMCPMC13192620

What Socratic 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 Socratic graph.