Evidence map›Paper›PMID 26482791›Full record

ArticleGenetics2015

Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method.

Qi Yan, Daniel E Weeks, Juan C Celedón, Hemant K Tiwari, Bingshan Li, Xiaojing Wang, Wan-Yu Lin, Xiang-Yang Lou, Guimin Gao, Wei Chen and 1 more

Abstract read
In one paragraph

Article in Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  3. Review
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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

11 authors.

Qi YanDivision of Pulmonary Medicine, Allergy and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, University of Pittsburgh, Pennsylvania 15224.
Daniel E WeeksDepartments of Human Genetics and Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261.
Juan C CeledónDivision of Pulmonary Medicine, Allergy and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, University of Pittsburgh, Pennsylvania 15224 Departments of Human Genetics and Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261.
Hemant K TiwariDepartment of Biostatistics, University of Alabama at Birmingham, Alabama 35294.
Bingshan LiDepartments of Molecular Physiology and Biophysics and Neurology, Vanderbilt University Medical Center, Nashville, Tennessee 37232.
Xiaojing WangAnalytics of Metrics Central, Global QARAC Headquarters, ConvaTec, Inc., Greensboro, North Carolina 27409.
Wan-Yu LinInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Xiang-Yang LouDepartment of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana 70112.
Guimin GaoDepartment of Public Health Sciences, University of Chicago, Illinois 60637.
Wei ChenDivision of Pulmonary Medicine, Allergy and Immunology, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh Medical Center, University of Pittsburgh, Pennsylvania 15224 Departments of Human Genetics and Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pennsylvania 15261 nliu@uab.edu wei.chen@chp.edu.
Nianjun LiuDepartment of Biostatistics, University of Alabama at Birmingham, Alabama 35294 nliu@uab.edu wei.chen@chp.edu.

Funding

Predictors of hemorrhage among patients on direct acting oral anticoagulantsR01HL092173 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIMDI, NITA A · 2008 to 2023
$10.4M
Epigenetic Variation and Childhood Asthma in Puerto RicansR01HL117191 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS · 2013 to 2020
$5.8M
UAB Multidisciplinary Clinical Research CenterP60AR064172 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRIDGES, S LOUIS · 2013 to 2018
$4.5M
The Genetic Epidemiology of COPD in Costa RicaR01HL073373 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS · 2005 to 2009
$3.5M
Statistical methods for population and family-based whole-genome sequence dataR01HG007358 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2018
$1.7M
Design and analysis of sequencing studies for gene mapping in familiesR01HG006857 · NHGRI · VANDERBILT UNIVERSITY · PI LI, BINGSHAN · 2013 to 2016
$1.5M
Genome Wide Haplotype Association AnalysisR01GM081488 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2008 to 2012
$1.3M
Haplotyping and QTL Mapping in Pedigrees with Missing DataR01GM073766 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI GAO, GUIMIN · 2007 to 2011
$1.3M
AMD genetics: methods and analysis for progression, prediction, and associationR01EY024226 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2016
$899k
Secondary analysis and risk prediction of dental caries and oral cleftsR03DE024198 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2015 to 2016
$456k
NEI NIH HHS R01 EY024226NEI NIH HHS R01-EY024226NHGRI NIH HHS R01 HG006857NHGRI NIH HHS R01-HG006857NHGRI NIH HHS R01 HG007358NHGRI NIH HHS R01-HG007358NHLBI NIH HHS HL-073373NHLBI NIH HHS HL-117191NHLBI NIH HHS R01 HL073373NHLBI NIH HHS R01 HL092173NHLBI NIH HHS R01-HL092173NHLBI NIH HHS R01 HL117191NIAMS NIH HHS P60 AR064172NIAMS NIH HHS P60-AR064172NIDCR NIH HHS R03 DE024198NIDCR NIH HHS R03-DE024198NIGMS NIH HHS GM-081488NIGMS NIH HHS R01 GM073766NIGMS NIH HHS R01-GM073766NIGMS NIH HHS R01 GM081488
6 · The paper itself

Abstract

The recent development of sequencing technology allows identification of association between the whole spectrum of genetic variants and complex diseases. Over the past few years, a number of association tests for rare variants have been developed. Jointly testing for association between genetic variants and multiple correlated phenotypes may increase the power to detect causal genes in family-based studies, but familial correlation needs to be appropriately handled to avoid an inflated type I error rate. Here we propose a novel approach for multivariate family data using kernel machine regression (denoted as MF-KM) that is based on a linear mixed-model framework and can be applied to a large range of studies with different types of traits. In our simulation studies, the usual kernel machine test has inflated type I error rates when applied directly to familial data, while our proposed MF-KM method preserves the expected type I error rates. Moreover, the MF-KM method has increased power compared to methods that either analyze each phenotype separately while considering family structure or use only unrelated founders from the families. Finally, we illustrate our proposed methodology by analyzing whole-genome genotyping data from a lung function study.

Indexed as

Computer SimulationGenetic VariationModels, GeneticModels, StatisticalQuantitative Trait LociAdultAlgorithmsChildFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenome, HumanHumansLungMaleMultivariate Analysisfamily sampleskernel functionlinear mixed modelmultivariate traitsrare variants

Identifiers

PMID26482791
PMCPMC4676518

What OpenQuestion holds

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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.