Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses

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18. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
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23. Genetic variations of DNA bindings of FOXA1 and co-factors in breast cancer susceptibility
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24. Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors
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26. Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions
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27. Robust Causal Structure Learning with Some Hidden Variables
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28. Transcriptome-Wide Association Study for Inflammatory Bowel Disease Reveals Novel Candidate Susceptibility Genes in Specific Colon Subsites and Tissue Categories
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30. Genetic Variants That Impact Alternative Polyadenylation in Cancer Represent Candidate Causal Risk Loci
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31. Single nucleus RNA-sequencing integrated into risk variant colocalization discovers 17 cell-type-specific abdominal obesity genes for metabolic dysfunction-associated steatotic liver disease
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32. Integrating muti-omics data to identify tissue-specific DNA methylation biomarkers for cancer risk
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33. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
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34. QRank: a novel quantile regression tool for eQTL discovery
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35. Evidence for a potential role of miR-1908-5p and miR-3614-5p in autoimmune disease risk using integrative bioinformatics
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36. Expression of the readthrough transcript CiDRE in alveolar macrophages boosts SARS-CoV-2 susceptibility and promotes COVID-19 severity
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37. Genetic regulation of human brain proteome reveals proteins implicated in psychiatric disorders
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38. Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability
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39. Effects of Type 1 Diabetes Risk Alleles on Immune Cell Gene Expression
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43. Transcriptome diversity is a systematic source of variation in RNA-sequencing data
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44. Functional Characterization of Genetic Variant Effects on Expression
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45. HEFT: eQTL analysis of many thousands of expressed genes while simultaneously controlling for hidden factors
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47. A common polymorphism in the Intelectin-1 gene influences mucus plugging in severe asthma
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50. Diverse approaches to predicting drug-induced liver injury using gene-expression profiles
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51. Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease
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85. Host Genetic Risk Factors for Chlamydia trachomatis-Related Infertility in Women
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89. Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations
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91. Functional and dynamic profiling of transcript isoforms reveals essential roles of alternative splicing in interferon response
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92. Using genomic annotations increases statistical power to detect eGenes
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93. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease
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94. Considerations for reproducible omics in aging research
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95. Secreted Protein Profiling of Human Aortic Smooth Muscle Cells Identifies Vascular Disease Associations
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96. Rate of brain aging and APOE ε4 are synergistic risk factors for Alzheimer’s disease
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