Testing genetic association with rare and common variants in family data

scientific article

Testing genetic association with rare and common variants in family data is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/GEPI.21823
P932PMC publication ID4324976
P698PubMed publication ID25112186
P5875ResearchGate publication ID264712671

P50authorHan ChenQ37632693
P2093author name stringCong Li
Dörthe Malzahn
Julia N Bailey
Brunilda Balliu
P2860cites workTransmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)Q24671756
Pooled association tests for rare variants in exon-resequencing studiesQ28743126
Missing heritability and strategies for finding the underlying causes of complex diseaseQ29614586
Multipoint quantitative-trait linkage analysis in general pedigreesQ29614967
SNP set association analysis for familial dataQ30564362
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigreesQ30879437
Kernel score statistic for dependent dataQ30879460
Combining information from linkage and association mapping for next-generation sequencing longitudinal family dataQ30879707
Extended T(2) tests for longitudinal family data in whole genome sequencing studiesQ30879724
Random-effects Cox proportional hazards model: general variance components methods for time-to-event dataQ30975696
Optimal tests for rare variant effects in sequencing association studiesQ31065241
Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed modelsQ31140023
Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed modelsQ33346484
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence dataQ33359015
A groupwise association test for rare mutations using a weighted sum statisticQ33408787
A data-adaptive sum test for disease association with multiple common or rare variantsQ33562753
Comprehensive Approach to Analyzing Rare Genetic VariantsQ33745005
Testing for an unusual distribution of rare variantsQ33847792
Rare-variant association testing for sequencing data with the sequence kernel association testQ33954046
Evaluation of the power and type I error of recently proposed family-based tests of association for rare variantsQ34085617
Adjusting for population stratification and relatedness with sequencing dataQ34085660
Adjustment of familial relatedness in association test for rare variants.Q34086243
Detecting rare variant associations by identity-by-descent mapping in case-control studiesQ34248911
Powerful SNP-set analysis for case-control genome-wide association studiesQ34544433
Variance component model to account for sample structure in genome-wide association studiesQ34971144
A general framework for detecting disease associations with rare variants in sequencing studiesQ35204927
Rare genetic variant analysis on blood pressure in related samplesQ35527986
Family-based Bayesian collapsing method for rare-variant association studyQ35528003
A comparison of whole genome sequencing with exome sequencing for family-based association studiesQ35528453
Principles for the post-GWAS functional characterization of cancer risk lociQ35887461
Robust variance-components approach for assessing genetic linkage in pedigreesQ35889010
Family-based association studies for next-generation sequencing.Q36017127
Family-based association tests for genomewide association scansQ36492206
Sequence kernel association test for quantitative traits in family samplesQ36812083
A geometric framework for evaluating rare variant tests of associationQ37031565
A powerful and flexible multilocus association test for quantitative traitsQ37149380
New approaches to population stratification in genome-wide association studiesQ37765137
An evaluation of statistical approaches to rare variant analysis in genetic association studiesQ39941009
Generalized T2 test for genome association studiesQ41048589
Asymptotic tests of association with multiple SNPs in linkage disequilibriumQ41854759
Genome-wide efficient mixed-model analysis for association studiesQ41961596
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).Q51928874
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.Q52079461
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.Q52432442
Population Structure and Cryptic Relatedness in Genetic Association StudiesQ57393113
Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculationsQ68834082
Statistical properties of the haplotype relative riskQ69627803
P304page(s)S37-43
P577publication date2014-09-01
P1433published inGenetic EpidemiologyQ5532864
P1476titleTesting genetic association with rare and common variants in family data
P478volume38 Suppl 1

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cites work (P2860)
Q39146309Drinking from the Holy Grail: analysis of whole-genome sequencing from the Genetic Analysis Workshop 18.
Q35920852Filtering genetic variants and placing informative priors based on putative biological function.
Q60910682Modeling gene-environment interactions in longitudinal family studies: a comparison of methods and their application to the association between the IGF pathway and childhood obesity
Q31094385Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples

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