Evidence map›Paper›PMID 31579362›Full record

ArticleStatistica Sinica2019

SEMIPARAMETRIC TRANSFORMATION MODELS WITH MULTILEVEL RANDOM EFFECTS FOR CORRELATED DISEASE ONSET IN FAMILIES.

Baosheng Liang, Yuanjia Wang, Donglin Zeng

Open access · greenAbstract read
In one paragraph

Article in Statistica Sinica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 92% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

3 authors at 3 institutions in 2 countries.

Baosheng LiangDepartment of Statistics and Actuarial Science, The University of Hong Kong, Hong Kong.
Yuanjia WangDepartment of Biostatistics, Columbia University, New York, USA.
Donglin ZengDepartment of Biostatistics, University of North Carolina at Chapel Hill, North Carolina, USA.
Columbia University · USUniversity of Hong Kong · HKUniversity of North Carolina at Chapel Hill · US

Funding

Epidemiology of Biomarkers of Risk and Progression in LOADR01AG037212 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAYEUX, RICHARD P, SCHUPF, NICOLE · 2010 to 2015
$10.1M
Statistical Methods for Integrating Mixed-type Biomarkers and Phenotypes in Neurodegenerative Disease ModelingR01NS073671 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WANG, YUANJIA · 2011 to 2025
$3.9M
Statistical and Machine Learning Methods to Improve Dynamic Treatment Regimens Estimation Using Real World Data.R01GM124104 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yuanjia Wang, Donglin Zeng · 2018 to 2026
$3.1M
Semiparametric Regression Analysis of Censored DataR01GM047845 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, DANYU · 1997 to 2018
$2.9M
Identifying Huntington's disease markers by modern statistical learning methods.U01NS082062 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WANG, YUANJIA · 2014 to 2016
$1.1M
NIA NIH HHS R01 AG037212NIGMS NIH HHS R01 GM047845NIGMS NIH HHS R01 GM124104NINDS NIH HHS R01 NS073671NINDS NIH HHS U01 NS082062
6 · The paper itself

Abstract

Large cohort studies are commonly launched to study risk of genetic variants or other risk factors on age at onset (AAO) of a chronic disorder. In these studies, family history data including AAO of disease in family members are collected to provide additional information and can be used to improve efficiency. Statistical analysis of these data is challenging due to missing genotypes in family members and the heterogeneous dependence attributed to both shared genetic back-ground and shared environmental factors (e.g., life style). In this paper, we propose a class of semiparametric transformation models with multilevel random effects to tackle these challenges. The proposed models include both proportional hazards model and proportional odds model as special cases. The multilevel random effects contain individual-specific random effects including kinship correlation structure dependent on the family pedigree, and a shared random effect to account for unobserved environment exposure. We use nonparametric maximum likelihood approach for inference and propose an expectation-maximization algorithm for computation in the presence of missing genotypes among family members. The obtained estimators are shown to be consistent, asymptotically normal, and semiparametrically efficient. Simulation studies demonstrate that the proposed method performs well with finite sample sizes. Finally, the proposed method is applied to study genetic risks in an Alzheimer's disease study.

Indexed as

Alzheimer’s diseaseFamily dataMultilevel random effectsNonparametric maximum likelihood estimationSemiparametric efficiency

Identifiers

PMID31579362
PMCPMC6774630
OpenAlexW2810870972

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.