scholarly article | Q13442814 |
P50 | author | Han Chen | Q37632693 |
P2093 | author name string | Cong Li | |
Dörthe Malzahn | |||
Julia N Bailey | |||
Brunilda Balliu | |||
P2860 | cites work | Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM) | Q24671756 |
Pooled association tests for rare variants in exon-resequencing studies | Q28743126 | ||
Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 | ||
Multipoint quantitative-trait linkage analysis in general pedigrees | Q29614967 | ||
SNP set association analysis for familial data | Q30564362 | ||
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees | Q30879437 | ||
Kernel score statistic for dependent data | Q30879460 | ||
Combining information from linkage and association mapping for next-generation sequencing longitudinal family data | Q30879707 | ||
Extended T(2) tests for longitudinal family data in whole genome sequencing studies | Q30879724 | ||
Random-effects Cox proportional hazards model: general variance components methods for time-to-event data | Q30975696 | ||
Optimal tests for rare variant effects in sequencing association studies | Q31065241 | ||
Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models | Q31140023 | ||
Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models | Q33346484 | ||
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
A data-adaptive sum test for disease association with multiple common or rare variants | Q33562753 | ||
Comprehensive Approach to Analyzing Rare Genetic Variants | Q33745005 | ||
Testing for an unusual distribution of rare variants | Q33847792 | ||
Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
Evaluation of the power and type I error of recently proposed family-based tests of association for rare variants | Q34085617 | ||
Adjusting for population stratification and relatedness with sequencing data | Q34085660 | ||
Adjustment of familial relatedness in association test for rare variants. | Q34086243 | ||
Detecting rare variant associations by identity-by-descent mapping in case-control studies | Q34248911 | ||
Powerful SNP-set analysis for case-control genome-wide association studies | Q34544433 | ||
Variance component model to account for sample structure in genome-wide association studies | Q34971144 | ||
A general framework for detecting disease associations with rare variants in sequencing studies | Q35204927 | ||
Rare genetic variant analysis on blood pressure in related samples | Q35527986 | ||
Family-based Bayesian collapsing method for rare-variant association study | Q35528003 | ||
A comparison of whole genome sequencing with exome sequencing for family-based association studies | Q35528453 | ||
Principles for the post-GWAS functional characterization of cancer risk loci | Q35887461 | ||
Robust variance-components approach for assessing genetic linkage in pedigrees | Q35889010 | ||
Family-based association studies for next-generation sequencing. | Q36017127 | ||
Family-based association tests for genomewide association scans | Q36492206 | ||
Sequence kernel association test for quantitative traits in family samples | Q36812083 | ||
A geometric framework for evaluating rare variant tests of association | Q37031565 | ||
A powerful and flexible multilocus association test for quantitative traits | Q37149380 | ||
New approaches to population stratification in genome-wide association studies | Q37765137 | ||
An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 | ||
Generalized T2 test for genome association studies | Q41048589 | ||
Asymptotic tests of association with multiple SNPs in linkage disequilibrium | Q41854759 | ||
Genome-wide efficient mixed-model analysis for association studies | Q41961596 | ||
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 Studies | Q57393113 | ||
Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations | Q68834082 | ||
Statistical properties of the haplotype relative risk | Q69627803 | ||
P304 | page(s) | S37-43 | |
P577 | publication date | 2014-09-01 | |
P1433 | published in | Genetic Epidemiology | Q5532864 |
P1476 | title | Testing genetic association with rare and common variants in family data | |
P478 | volume | 38 Suppl 1 |
Q39146309 | Drinking from the Holy Grail: analysis of whole-genome sequencing from the Genetic Analysis Workshop 18. |
Q35920852 | Filtering genetic variants and placing informative priors based on putative biological function. |
Q60910682 | Modeling gene-environment interactions in longitudinal family studies: a comparison of methods and their application to the association between the IGF pathway and childhood obesity |
Q31094385 | Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples |
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