Evidence map›Paper›PMID 38317324›Full record

ArticleGenetic epidemiology2024

Gene-based association tests in family samples using GWAS summary statistics.

Peng Wang, Xiao Xu, Ming Li, Xiang-Yang Lou, Siqi Xu, Baolin Wu, Guimin Gao, Ping Yin, Nianjun Liu

Abstract read
In one paragraph

Article in Genetic epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Peng WangDepartment of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Hubei, People's Republic of China.
Xiao XuDepartment of Epidemiology and Biostatistics, Indiana University School of Public Health-Bloomington, Bloomington, Indiana, USA.ORCID 0000-0003-1083-3834
Ming LiDepartment of Epidemiology and Biostatistics, Indiana University School of Public Health-Bloomington, Bloomington, Indiana, USA.ORCID 0000-0003-0273-6217
Xiang-Yang LouDepartment of Biostatistics, College of Public Health and Health Professions and College of Medicine, University of Florida, Gainesville, Florida, USA.
Siqi XuDepartment of Statistics and Actuarial Science, The University of Hong Kong, Hong Kong, Hong Kong.
Baolin WuDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota, USA.
Guimin GaoDepartment of Public Health Sciences, University of Chicago, Chicago, Illinois, USA.
Ping YinDepartment of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Hubei, People's Republic of China.
Nianjun LiuDepartment of Epidemiology and Biostatistics, Indiana University School of Public Health-Bloomington, Bloomington, Indiana, USA.

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
Random Field Modelling of genetic and epigenetic association underlying congenital heart defects in the presence of disease heterogeneityK01HL140333 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI LI, MING · 2018 to 2021
$724k
Random Field Methods for integrative genomic analysis and high-dimensional risk prediction of congenital heart defectsR56HL164477 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI LI, MING · 2023 to 2023
$488k
High-dimensional statistical genetic methods for dental caries and orofacial cleftsR03DE025646 · NIDCR · TRUSTEES OF INDIANA UNIVERSITY · PI LIU, NIANJUN · 2016 to 2017
$468k
Secondary analysis and risk prediction of dental caries and oral cleftsR03DE024198 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2015 to 2016
$456k
Gene-by-Gene and Gene-by-Environment Interactions Underlying Congenital Heart DefectsR03HD092854 · NICHD · TRUSTEES OF INDIANA UNIVERSITY · PI LI, MING · 2018 to 2019
$171k
NHGRI NIH HHS U54 HG003079NHLBI NIH HHS K01 HL140333NHLBI NIH HHS R56 HL164477NICHD NIH HHS R03 HD092854NIDCR NIH HHS R03 DE024198NIDCR NIH HHS R03 DE025646NIH HHS
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have led to rapid growth in detecting genetic variants associated with various phenotypes. Owing to a great number of publicly accessible GWAS summary statistics, and the difficulty in obtaining individual-level genotype data, many existing gene-based association tests have been adapted to require only GWAS summary statistics rather than individual-level data. However, these association tests are restricted to unrelated individuals and thus do not apply to family samples directly. Moreover, due to its flexibility and effectiveness, the linear mixed model has been increasingly utilized in GWAS to handle correlated data, such as family samples. However, it remains unknown how to perform gene-based association tests in family samples using the GWAS summary statistics estimated from the linear mixed model. In this study, we show that, when family size is negligible compared to the total sample size, the diagonal block structure of the kinship matrix makes it possible to approximate the correlation matrix of marginal Z scores by linkage disequilibrium matrix. Based on this result, current methods utilizing summary statistics for unrelated individuals can be directly applied to family data without any modifications. Our simulation results demonstrate that this proposed strategy controls the type 1 error rate well in various situations. Finally, we exemplify the usefulness of the proposed approach with a dental caries GWAS data set.

Indexed as

Dental CariesGenome-Wide Association StudyHumansModels, GeneticPhenotypePolymorphism, Single Nucleotidefamily samplegene-based association testGWAS summary dataLD matrixlinear mixed model

Identifiers

PMID38317324
PMCPMC12421949

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.