Evidence map›Paper›PMID 34811777›Full record

ArticleStatistics in medicine2022

A conditional autoregressive model for genetic association analysis accounting for genetic heterogeneity.

Xiaoxi Shen, Yalu Wen, Yuehua Cui, Qing Lu

Abstract read
In one paragraph

Article in Statistics in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Xiaoxi ShenDepartment of Mathematics, Texas State University, San Marcos, Texas, USA.
Yalu WenDepartment of Statistics, University of Auckland, Auckland, New Zealand.ORCID 0000-0002-0071-5917
Yuehua CuiDepartment of Statistics and Probability, Michigan State University, East Lansing, Michigan, USA.ORCID 0000-0001-8099-1753
Qing LuDepartment of Biostatistics, University of Florida, Gainesville, Florida, USA.ORCID 0000-0002-7943-966X

Funding

Computational Efficient Statistical Tools for Analyzing Substance Dependence Sequencing DataR01DA043501 · NIDA · UNIVERSITY OF FLORIDA · PI LU, QING · 2017 to 2021
$2.1M
Methods and Software for High-dimensional Risk Prediction ResearchR01LM012848 · NLM · UNIVERSITY OF FLORIDA · PI LU, QING · 2018 to 2021
$1.2M
Gene-Gene/Gene-Environment Interactions Associated with Nicotine DependenceK01DA033346 · NIDA · MICHIGAN STATE UNIVERSITY · PI LU, QING · 2013 to 2017
$833k
NIDA NIH HHS K01 DA033346NIDA NIH HHS R01 DA043501NLM NIH HHS R01 LM012848
6 · The paper itself

Abstract

Converging evidence from genetic studies and population genetics theory suggest that complex diseases are characterized by remarkable genetic heterogeneity, and individual rare mutations with different effects could collectively play an important role in human diseases. Many existing statistical models for association analysis assume homogeneous effects of genetic variants across all individuals, and could be subject to power loss in the presence of genetic heterogeneity. To consider possible heterogeneous genetic effects among individuals, we propose a conditional autoregressive model. In the proposed method, the genetic effect is considered as a random effect and a score test is developed to test the variance component of genetic random effect. Through simulations, we compare the type I error and power performance of the proposed method with those of the generalized genetic random field and the sequence kernel association test methods under different disease scenarios. We find that our method outperforms the other two methods when (i) the rare variants have the major contribution to the disease, or (ii) the genetic effects vary in different individuals or subgroups of individuals. Finally, we illustrate the new method by applying it to the whole genome sequencing data from the Alzheimer's Disease Neuroimaging Initiative.

Indexed as

Genetic HeterogeneityModels, GeneticGenetic TestingGenetic VariationHumansModels, Statisticalgenetic heterogeneityscore test

Identifiers

PMID34811777
PMCPMC8792507

What OpenQuestion holds

Textmetadata
LicenceTDM
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.