Evidence map›Paper›PMID 26177343›Full record

ArticleBiometrics2015

Retrospective likelihood-based methods for analyzing case-cohort genetic association studies.

Yuanyuan Shen, Tianxi Cai, Yu Chen, Ying Yang, Jinbo Chen

Open access · bronzeAbstract read
In one paragraph

Article in Biometrics, 2015. 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
0.5field-weighted citation impact, top 27% 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, 3 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

5 authors at 1 institution in 1 country.

Yuanyuan ShenDepartment of Biostatistics, Harvard University, Boston, MA 02115.
Tianxi CaiDepartment of Biostatistics, Harvard University, Boston, MA 02115.
Yu ChenDepartment of Population Health, New York University School of Medicine, New York, NY 10016.
Ying YangDepartment of Mathematical Sciences, Tsinghua University, Beijing 100084, P. R. China.
Jinbo ChenDepartment of Biostatistics and Epidemiology, University of Pennsylvania, School of Medicine, Philadelphia, PA 19104.
Tsinghua University · CN

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Research ProjectP50MH106933 · NIMH · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S. · 2014 to 2018
$17.0M
Statistical Methods for Optimizing Personalized Treatment SelectionR01HL089778 · NHLBI · STANFORD UNIVERSITY · PI LU TIAN · 2008 to 2026
$4.8M
Statistical Methods in Genetic Epidemiology ResearchR01ES016626 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI CHEN, JINBO · 2008 to 2012
$1.6M
Statistical Methods for Cancer Absolute Risk PredictionR01CA164305 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHEN, JINBO · 2013 to 2016
$1.4M
Robust Approaches to the Development and Evaluation of Prognostic ClassifiersR01GM079330 · NIGMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI CAI, TIANXI · 2007 to 2014
$1.0M
Efficient Design and Analytic Strategies for Enhancing the Power of Detecting G XR21ES020811 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MUKHERJEE, BHRAMAR · 2012 to 2014
$447k
NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA164305NHLBI NIH HHS R01 HL089778NIEHS NIH HHS R01 ES016626NIEHS NIH HHS R01-ES016626NIEHS NIH HHS R21 ES020811NIEHS NIH HHS R21-ES020811NIGMS NIH HHS R01 GM079330NIGMS NIH HHS R01GM079330NIMH NIH HHS P50 MH106933NIMH NIH HHS P50 MH106999
6 · The paper itself

Abstract

The case cohort (CCH) design is a cost-effective design for assessing genetic susceptibility with time-to-event data especially when the event rate is low. In this work, we propose a powerful pseudo-score test for assessing the association between a single nucleotide polymorphism (SNP) and the event time under the CCH design. The pseudo-score is derived from a pseudo-likelihood which is an estimated retrospective likelihood that treats the SNP genotype as the dependent variable and time-to-event outcome and other covariates as independent variables. It exploits the fact that the genetic variable is often distributed independent of covariates or only related to a low-dimensional subset. Estimates of hazard ratio parameters for association can be obtained by maximizing the pseudo-likelihood. A unique advantage of our method is that it allows the censoring distribution to depend on covariates that are only measured for the CCH sample while not requiring the knowledge of follow-up or covariate information on subjects not selected into the CCH sample. In addition to these flexibilities, the proposed method has high relative efficiency compared with commonly used alternative approaches. We study large sample properties of this method and assess its finite sample performance using both simulated and real data examples.

Indexed as

BiometryCardiovascular DiseasesCase-Control StudiesCohort StudiesComputer SimulationGenetic Association StudiesGenetic Predisposition to DiseaseHumansLikelihood FunctionsPolymorphism, Single NucleotideProportional Hazards ModelsRetrospective StudiesCase-cohort designCox proportional hazards modelGenetic associationInverse probability weightingPolytomous regressionPseudo-likelihood

Identifiers

PMID26177343
PMCPMC4751872
OpenAlexW1805320231

What OpenQuestion holds

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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.