Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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Multiple loci identified in a genome-wide association study of prostate cancer

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Network Properties of Complex Human Disease Genes Identified through Genome-Wide Association Studies

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Gene set analysis of SNP data: benefits, challenges, and future directions

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A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

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Exome sequencing and complex disease: practical aspects of rare variant association studies

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The impact of human copy number variation on gene expression: Figure 1

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A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection

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Multiple sclerosis genetics—is the glass half full, or half empty?

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Molecular genetics in glaucoma

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Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain

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Efficient Replication of over 180 Genetic Associations with Self-Reported Medical Data

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Minireview: Epigenetics of Obesity and Diabetes in Humans

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High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction

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SomamiR 2.0: a database of cancer somatic mutations altering microRNA–ceRNA interactions

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Coexpression network based on natural variation in human gene expression reveals gene interactions and functionsPreprint

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3DSNP: a database for linking human noncoding SNPs to their three-dimensional interacting genes

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Epigenetics and Cardiovascular Disease

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Mind the gap: Why many geneticists and psychological scientists have discrepant views about gene–environment interaction (G×E) research.

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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

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PolymiRTS Database 2.0: linking polymorphisms in microRNA target sites with human diseases and complex traits

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Characteristics of Skin Lesions Associated With Anti–Tumor Necrosis Factor Therapy in Patients With Inflammatory Bowel Disease

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Alzheimer’s disease variants with the genome-wide significance are significantly enriched in immune pathways and active in immune cells

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Genetics of cardiovascular disease: Importance of sex and ethnicity

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Cis and Trans Effects of Human Genomic Variants on Gene Expression

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Genome-Wide Variation of Cytosine Modifications Between European and African Populations and the Implications for Complex Traits

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Structural variants caused by Alu insertions are associated with risks for many human diseases

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Single-cell nascent RNA sequencing unveils coordinated global transcription

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Objective assessment of cancer genes for drug discovery

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Mapping Rare and Common Causal Alleles for Complex Human Diseases

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Universal annotation of the human genome through integration of over a thousand epigenomic datasets

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A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension

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Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update

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kmer-SVM: a web server for identifying predictive regulatory sequence features in genomic data sets

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A new way to protect privacy in large-scale genome-wide association studies

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Type 2 Diabetes Risk Alleles Demonstrate Extreme Directional Differentiation among Human Populations, Compared to Other Diseases

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IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma

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Capture Hi-C identifies putative target genes at 33 breast cancer risk loci

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Whole genome sequencing in psychiatric disorders: the WGSPD consortium

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An update of miRNASNP database for better SNP selection by GWAS data, miRNA expression and online tools

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Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

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Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model

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Marine N-3 Polyunsaturated Fatty Acids Are Inversely Associated with Risk of Type 2 Diabetes in Asians: A Systematic Review and Meta-Analysis

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Snx3 Regulates Recycling of the Transferrin Receptor and Iron Assimilation

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Selection and Adaptation in the Human Genome

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Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk

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The Power of Meta-Analysis in Genome-Wide Association Studies

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Gene co-expression network connectivity is an important determinant of selective constraint

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Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes

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Association of Genetic Risk Variants With Expression of Proximal Genes Identifies Novel Susceptibility Genes for Cardiovascular Disease

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Multiple Loci Are Associated with White Blood Cell Phenotypes

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Modeling RNA-Binding Protein Specificity In Vivo by Precisely Registering Protein-RNA Crosslink Sites

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Exposure Science and the Exposome: An Opportunity for Coherence in the Environmental Health Sciences

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Long noncoding RNA lincRNA-p21 is the major mediator of UVB-induced and p53-dependent apoptosis in keratinocytes

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Gene regulatory mechanisms underpinning prostate cancer susceptibility

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Accounting for eXentricities: Analysis of the X Chromosome in GWAS Reveals X-Linked Genes Implicated in Autoimmune Diseases

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Candidate gene association studies and risk of childhood acute lymphoblastic leukemia: a systematic review and meta-analysis

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Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

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Epigenetic Regulation of Monocyte and Macrophage Function

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Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locusPreprint

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Genetic basis of autoimmunity

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Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

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A genetic perspective on coeliac disease

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Leveraging Multilayered “Omics” Data for Atopic Dermatitis: A Road Map to Precision Medicine

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Epigenetics Analysis and Integrated Analysis of Multiomics Data, Including Epigenetic Data, Using Artificial Intelligence in the Era of Precision Medicine

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Genic and nongenic contributions to natural variation of quantitative traits in maizePreprint

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Genome-wide association study implicates a novel RNA gene, the lincRNA AC068718.1, as a risk factor for post-traumatic stress disorder in women

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Convergence of genetic findings for nicotine dependence and smoking related diseases with chromosome 15q24-25

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Functional annotation of colon cancer risk SNPs

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Genetic Basis of Autoantibody Positive and Negative Rheumatoid Arthritis Risk in a Multi-ethnic Cohort Derived from Electronic Health Records

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Investigating Natural Variation in Drosophila Courtship Song by the Evolve and Resequence Approach

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Pooled ChIP-Seq Links Variation in Transcription Factor Binding to Complex Disease Risk

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Genome-wide Analysis of STAT3-Mediated Transcription during Early Human Th17 Cell Differentiation

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HACER: an atlas of human active enhancers to interpret regulatory variants

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Single-Cell Epigenomics and Functional Fine-Mapping of Atherosclerosis GWAS Loci

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Characterizing genetic interactions in human disease association studies using statistical epistasis networks

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Human Gene-Centered Transcription Factor Networks for Enhancers and Disease Variants

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A Chronic Obstructive Pulmonary Disease Susceptibility Gene, FAM13A , Regulates Protein Stability of β-Catenin

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Traumatic Brain Injury Induces Genome-Wide Transcriptomic, Methylomic, and Network Perturbations in Brain and Blood Predicting Neurological Disorders

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A Brief Review on the Human Encyclopedia of DNA Elements (ENCODE) Project

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