Evidence map›Paper›PMID 31724772›Full record

ArticleGenetic epidemiology2020

Identification of gene-environment interactions with marginal penalization.

Sanguo Zhang, Yuan Xue, Qingzhao Zhang, Chenjin Ma, Mengyun Wu, Shuangge Ma

Abstract read
In one paragraph

Article in Genetic epidemiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. High-Dimensional Gene-Environment Interaction Analysis.Annual review of statistics and its application · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Gene-Environment Interaction: A Variable Selection Perspective.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  7. 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

6 authors.

Sanguo ZhangSchool of Mathematics Sciences, University of Chinese Academy of Sciences, Beijing, China.
Yuan XueSchool of Mathematics Sciences, University of Chinese Academy of Sciences, Beijing, China.
Qingzhao ZhangDepartment of Statistics, School of Economics, Xiamen University, Xiamen, China.
Chenjin MaDepartment of Biostatistics, Yale University, New Haven, Connecticut.
Mengyun WuSchool of Statistics and Management, Shanghai University of Finance and Economics, Shanghai, China.
Shuangge MaDepartment of Biostatistics, Yale University, New Haven, Connecticut.ORCID 0000-0001-9001-4999

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI RUTH HALABAN · 2006 to 2026
$43.9M
Novel methods for identifying genetic interactions in cancer prognosisR01CA204120 · NCI · YALE UNIVERSITY · PI Shuangge Ma · 2016 to 2026
$3.5M
NCATS NIH HHS UL1 TR001863NCI NIH HHS P50 CA121974NCI NIH HHS R01 CA204120
6 · The paper itself

Abstract

Gene-environment (G-E) interaction analysis has been extensively conducted for complex diseases. In marginal analysis, the common practice is to conduct likelihood-based (and other "standard") estimation with each marginal model, and then select significant G-E interactions and main effects based on p values and multiple comparisons adjustment. One limitation of this approach is that the identification results often do not respect the "main effects, interactions" hierarchy, which has been stressed in recent G-E interaction analyses. There is some recent effort tackling this problem, however, with very complex formulations. Another limitation of the common practice is that it may not perform well when regularization is needed, for example, because of "non-normal" distributions. In this article, we propose a marginal penalization approach which adopts a novel penalty to directly tackle the aforementioned problems. The proposed approach has a framework more coherent with that of the recently developed joint analysis methods and an intuitive formulation, and can be effectively realized. In simulation, it outperforms the popular significance-based analysis and simple penalization-based alternatives. Promising findings are made in the analysis of a single-nucleotide polymorphism and a gene expression data.

Indexed as

Gene-Environment InteractionModels, GeneticComputer SimulationDiabetes MellitusGenome, HumanHumansMelanomaPolymorphism, Single NucleotideSkin Neoplasmsgene-environment interactionmarginal analysispenalization

Identifiers

PMID31724772
PMCPMC7028443

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Registered trials

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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.