Proper Use of Allele-Specific Expression Improves Statistical Power forcis-eQTL Mapping with RNA-Seq Data

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An integrated map of genetic variation from 1,092 human genomes

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Breast cancer risk–associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

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A Statistical Framework for eQTL Mapping Using RNA-seq Data

(2011) Wei Sun   BIOMETRICS

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A general framework for studying genetic effects and gene-environment interactions with missing data

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Understanding mechanisms underlying human gene expression variation with RNA sequencing

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Identification of a Functional Genetic Variant at 16q12.1 for Breast Cancer Risk: Results from the Asia Breast Cancer Consortium

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Mapping complex disease traits with global gene expression

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Simple and Efficient Analysis of Disease Association with Missing Genotype Data

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