Mapping cis- and trans-regulatory effects across multiple tissues in twins

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5. Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
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7. Exploring the molecular basis of age-related disease comorbidities using a multi-omics graphical model
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14. Functional Genomic Annotation of Genetic Risk Loci Highlights Inflammation and Epithelial Biology Networks in CKD
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15. Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions
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19. An Integrated Systems Genetics and Omics Toolkit to Probe Gene Function
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20. Global Properties and Functional Complexity of Human Gene Regulatory Variation
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21. CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits
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23. Genetic variants in Hippo pathway genesYAP1,TEAD1andTEAD4are associated with melanoma-specific survival
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24. Genome-wide association study of recalcitrant atopic dermatitis in Korean children
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25. The canine era: the rise of a biomedical model
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26. Genome-wide identification of microRNA-related variants associated with risk of Alzheimer’s disease
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27. Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution
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28. Emerging Methods and Resources for Biological Interrogation of Neuropsychiatric Polygenic Signal
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29. A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius
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30. CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation
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31. From Loci to Biology
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32. Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk
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33. B cell OX40L supports T follicular helper cell development and contributes to SLE pathogenesis
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34. Trans-Ancestral Studies Fine Map the SLE-Susceptibility Locus TNFSF4
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35. Expression of Phosphofructokinase in Skeletal Muscle Is Influenced by Genetic Variation and Associated With Insulin Sensitivity
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36. Genetic Variants in MicroRNAs and Their Binding Sites Are Associated with the Risk of Parkinson Disease
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37. The Nature and Extent of Mutational Pleiotropy in Gene Expression of Male Drosophila serrata
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38. An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma
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39. Functional genomics bridges the gap between quantitative genetics and molecular biology
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40. Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC
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41. Evidence of reduced recombination rate in human regulatory domains
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42. Expression quantitative trait loci in sheep liver and muscle contribute to variations in meat traits
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43. Genetic variability of VEGF pathway genes in six randomized phase III trials assessing the addition of bevacizumab to standard therapy
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44. The Relationship of Common Risk Variants and Polygenic Risk for Schizophrenia to Sensorimotor Gating
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45. Heritability and genetic basis of protein level variation in an outbred population
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46. Extent, Causes, and Consequences of Small RNA Expression Variation in Human Adipose Tissue
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47. Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx
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48. Phenotype and Tissue Expression as a Function of Genetic Risk in Polycystic Ovary Syndrome
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49. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
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50. Simultaneous quantification of mRNA and protein in single cells reveals post-transcriptional effects of genetic variation
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51. Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort
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52. Wnt signaling pathway pharmacogenetics in non-small cell lung cancer
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53. A Genetic Variant in the Seed Region of miR-4513 Shows Pleiotropic Effects on Lipid and Glucose Homeostasis, Blood Pressure, and Coronary Artery Disease
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54. Generalised Anxiety Disorder – A Twin Study of Genetic Architecture, Genome-Wide Association and Differential Gene Expression
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55. Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity
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56. A Genome-Wide Association Study Identifies a Novel Locus for Bortezomib-Induced Peripheral Neuropathy in European Patients with Multiple Myeloma
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60. Genetic Architecture of Adaptive Immune System Identifies Key Immune Regulators
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61. Accuracy of Gene Expression Prediction From Genotype Data With PrediXcan Varies Across and Within Continental Populations
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62. Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis
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63. ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition—implications for COVID-19
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64. Predicting gene expression using DNA methylation in three human populations
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65. Analysis of Allele-Specific Expression in Mouse Liver by RNA-Seq: A Comparison With Cis-eQTL Identified Using Genetic Linkage
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66. Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits
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67. Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart
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70. GBAT: a gene-based association test for robust detection of trans-gene regulation
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71. Expression Quantitative Trait Loci Acting Across Multiple Tissues Are Enriched in Inherited Risk for Coronary Artery Disease
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74. Genome-wide DNA methylation analysis reveals loci that distinguish different types of adipose tissue in obese individuals
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76. Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
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77. Characterization of candidate genes in inflammatory bowel disease–associated risk loci
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80. Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
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81. Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients
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82. DNA variants affecting the expression of numerous genes in trans have diverse mechanisms of action and evolutionary histories
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83. Genetic variant rs763361 regulates multiple sclerosis CD226 gene expression
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84. TNF/TNFR Superfamily Members in Costimulation of T Cell Responses—Revisited
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86. Preferential Binding to Elk-1 by SLE-Associated IL10 Risk Allele Upregulates IL10 Expression
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87. A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood
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88. Metabolomics profiling reveals novel markers for leukocyte telomere length
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89. A Polymorphic Antioxidant Response Element Links NRF2/sMAF Binding to Enhanced MAPT Expression and Reduced Risk of Parkinsonian Disorders
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90. Epigenetics and individuality: from concepts to causality across timescales
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91. Variation and Genetic Control of Gene Expression in Primary Immunocytes across Inbred Mouse Strains
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92. Independent phenotypic plasticity axes define distinct obesity sub-types
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93. Integrative DNA methylome analysis of pan-cancer biomarkers in cancer discordant monozygotic twin-pairs
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94. Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes
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95. Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length
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96. An omnidirectional visualization model of personalized gene regulatory networks
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97. TreeQTL: hierarchical error control for eQTL findings
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98. Single cell transcriptomics of noncoding RNAs and their cell‐specificity
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99. Melanoma risk loci as determinants of melanoma recurrence and survival
    Justin Rendleman, Shulian Shang, Christine Dominianni, Jerry Shields, Patrick Scanlon, Christina Adaniel, Alexis Desrichard, Michelle Ma, Richard L. Shapiro, Russell S. Berman et al. · 2013 · Journal of Translational Medicine
100. Circulating Metabolites and Survival Among Patients With Pancreatic Cancer
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