Evidence map›Paper›PMID 38222269›Full record

ArticleThe annals of applied statistics2019

A SIMPLE, CONSISTENT ESTIMATOR OF SNP HERITABILITY FROM GENOME-WIDE ASSOCIATION STUDIES.

Armin Schwartzman, Andrew J Schork, Rong Zablocki, Wesley K Thompson

Abstract read
In one paragraph

Article in The annals of applied statistics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Interpreting SNP heritability in admixed populations.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Trade-offs of Linear Mixed Models in Genome-Wide Association Studies.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  10. Article
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.

Armin SchwartzmanUniversity of California, San Diego, La Jolla, CA and.
Andrew J SchorkInstitute of Biological Psychiatry, Mental Health Center St. Hans, Mental Health Services Copenhagen, Roskilde, Denmark.
Rong ZablockiUniversity of California, San Diego, La Jolla, CA and.
Wesley K ThompsonUniversity of California, San Diego, La Jolla, CA and.

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
Polygenicity, Pleiotrophy and Power: Novel Statistical Methods for Gene DiscoveryR01GM104400 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI THOMPSON, WESLEY KURT · 2014 to 2017
$1.6M
NIGMS NIH HHS R01 GM104400NIMH NIH HHS R01 MH128923
6 · The paper itself

Abstract

Analysis of genome-wide association studies (GWAS) is characterized by a large number of univariate regressions where a quantitative trait is regressed on hundreds of thousands to millions of single-nucleotide polymorphism (SNP) allele counts, one at a time. This article proposes an estimator of the SNP heritability of the trait, defined here as the fraction of the variance of the trait explained by the SNPs in the study. The proposed GWAS heritability (GWASH) estimator is easy to compute, highly interpretable, and is consistent as the number of SNPs and the sample size increase. More importantly, it can be computed from summary statistics typically reported in GWAS, not requiring access to the original data. The estimator takes full account of the linkage disequilibrium (LD) or correlation between the SNPs in the study through moments of the LD matrix, estimable from auxiliary datasets. Unlike other proposed estimators in the literature, we establish the theoretical properties of the GWASH estimator and obtain analytical estimates of the precision, allowing for power and sample size calculations for SNP heritability estimates, and forming a firm foundation for future methodological development.

Indexed as

62F1062J0592D10high dimensional datamassively univariate regressionPrimary 62H20secondary 62P10single nucleotide polymorphismsummary statistics

Identifiers

PMID38222269
PMCPMC10786410

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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.