| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Ross Hardison | Q27063030 |
| P2860 | cites work | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project | Q21061203 |
| A user's guide to the encyclopedia of DNA elements (ENCODE) | Q21092716 | ||
| Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS | Q21563317 | ||
| Transcriptional Regulatory Elements in the Human Genome | Q22065387 | ||
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| Mapping and quantifying mammalian transcriptomes by RNA-Seq | Q22122035 | ||
| An integrated encyclopedia of DNA elements in the human genome | Q22122150 | ||
| Complement factor H polymorphism in age-related macular degeneration | Q24553334 | ||
| Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose | Q24611198 | ||
| High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells | Q24614543 | ||
| Cluster analysis and display of genome-wide expression patterns | Q24644463 | ||
| DOT1L/KMT4 recruitment and H3K79 methylation are ubiquitously coupled with gene transcription in mammalian cells | Q24655388 | ||
| A haplotype map of the human genome | Q24679827 | ||
| High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
| Chromatin modifications and their function | Q27861067 | ||
| Genome-wide location and function of DNA binding proteins | Q28131765 | ||
| Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome | Q28131828 | ||
| A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly | Q28184095 | ||
| Large-scale transcriptional activity in chromosomes 21 and 22 | Q28216457 | ||
| ChIP-seq accurately predicts tissue-specific activity of enhancers | Q28235102 | ||
| Histone modifications at human enhancers reflect global cell-type-specific gene expression | Q28238467 | ||
| Discovering hematopoietic mechanisms through genome-wide analysis of GATA factor chromatin occupancy | Q28265885 | ||
| GATA-binding transcription factors in hematopoietic cells | Q36354435 | ||
| DNase I sensitivity QTLs are a major determinant of human expression variation | Q36408973 | ||
| Myc versus USF: discrimination at the cad gene is determined by core promoter elements | Q36568034 | ||
| Sequence census methods for functional genomics | Q37047820 | ||
| Genome-wide approaches to studying chromatin modifications | Q37077306 | ||
| Global mapping of protein-DNA interactions in vivo by digital genomic footprinting | Q37157318 | ||
| Functional enhancers at the gene-poor 8q24 cancer-linked locus. | Q37279616 | ||
| The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer | Q37390854 | ||
| 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response | Q39048288 | ||
| Regulation of inducible and tissue-specific gene expression | Q39656942 | ||
| The Human Gene Mutation Database: 2008 update | Q41809836 | ||
| Multiple loci on 8q24 associated with prostate cancer susceptibility | Q50582715 | ||
| The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. | Q51565310 | ||
| A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus. | Q54314374 | ||
| A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8 | Q57666866 | ||
| Structural gene sets active in embryos and adult tissues of the sea urchin | Q67852805 | ||
| A major positive regulatory region located far upstream of the human alpha-globin gene locus | Q68624475 | ||
| High-resolution mapping and characterization of open chromatin across the genome | Q28266995 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 | Q28469186 | ||
| The ENCODE (ENCyclopedia Of DNA Elements) Project | Q29547219 | ||
| Mapping and analysis of chromatin state dynamics in nine human cell types | Q29547552 | ||
| Discovery and characterization of chromatin states for systematic annotation of the human genome | Q29614411 | ||
| McKusick's Online Mendelian Inheritance in Man (OMIM) | Q29614446 | ||
| Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins | Q29614507 | ||
| Human genetic variation and its contribution to complex traits | Q29614580 | ||
| Genome-wide association studies for common diseases and complex traits | Q29615822 | ||
| Common and rare variants in multifactorial susceptibility to common diseases | Q29616282 | ||
| Epigenetics: a landscape takes shape | Q29616623 | ||
| Identification of functional elements and regulatory circuits by Drosophila modENCODE | Q29617551 | ||
| Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing | Q29618021 | ||
| Gene regulatory networks and the evolution of animal body plans | Q29618587 | ||
| Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease | Q29619085 | ||
| The NIH Roadmap Epigenomics Mapping Consortium | Q29619856 | ||
| Position-independent, high-level expression of the human beta-globin gene in transgenic mice | Q29620032 | ||
| PhenCode: connecting ENCODE data with mutations and phenotype | Q31103056 | ||
| Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes | Q33576732 | ||
| Genome-wide views of chromatin structure | Q33611702 | ||
| A map of open chromatin in human pancreatic islets | Q33687905 | ||
| Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data | Q33995474 | ||
| Nuclease hypersensitive sites in chromatin | Q34164152 | ||
| Controlling the double helix | Q34172152 | ||
| Quantitative trait loci in Drosophila | Q34186032 | ||
| Comprehensive genome-wide protein-DNA interactions detected at single-nucleotide resolution | Q34239260 | ||
| Linking disease associations with regulatory information in the human genome | Q34298038 | ||
| Locating mammalian transcription factor binding sites: a survey of computational and experimental techniques | Q34575437 | ||
| Mendelian Inheritance in Man and its online version, OMIM | Q34577589 | ||
| Translational and rotational settings of H2A.Z nucleosomes across the Saccharomyces cerevisiae genome. | Q34613479 | ||
| A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression | Q35001653 | ||
| Finding genes that underlie complex traits | Q35031309 | ||
| Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes | Q35056061 | ||
| Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration | Q35451782 | ||
| ATA box transcription mutation in beta-thalassemia | Q35679382 | ||
| Applied bioinformatics for the identification of regulatory elements | Q35766840 | ||
| Unsupervised pattern discovery in human chromatin structure through genomic segmentation | Q35923331 | ||
| Evidence for a locus activation region: the formation of developmentally stable hypersensitive sites in globin-expressing hybrids | Q36102094 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial | Q6936496 |
| P433 | issue | 37 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | regulation of gene expression | Q411391 |
| genome-wide association study | Q1098876 | ||
| genetic epigenesis | Q64443099 | ||
| genetic predisposition to disease | Q64843122 | ||
| multifactorial inheritance | Q67200773 | ||
| P1104 | number of pages | 9 | |
| P304 | page(s) | 30932-30940 | |
| P577 | publication date | 2012-09-05 | |
| 2012-09-07 | |||
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Genome-wide epigenetic data facilitate understanding of disease susceptibility association studies | |
| P478 | volume | 287 |
| Q55332265 | A catalog of potential putative functional variants in psoriasis genome-wide association regions. |
| Q41825238 | Accurate and reproducible functional maps in 127 human cell types via 2D genome segmentation |
| Q26999711 | Advances in inflammatory bowel disease pathogenesis: linking host genetics and the microbiome |
| Q34744860 | Comprehensive functional annotation of seventy-one breast cancer risk Loci |
| Q38726840 | Epigenetic Combinatorial Patterns Predict Disease Variants |
| Q36737217 | Epigenetic Modulation of Mood Disorders |
| Q27023811 | Epigenetic landscape of Parkinson's disease: emerging role in disease mechanisms and therapeutic modalities |
| Q39285701 | Epigenetics in Schizophrenia: A Pilot Study of Global DNA Methylation in Different Brain Regions Associated with Higher Cognitive Functions |
| Q26853555 | Epigenetics: the fine-tuner in inflammatory bowel disease? |
| Q36301611 | Epigenomic data facilitate genetic studies for osteoporosis in post-GWAS era. |
| Q34357186 | Functional annotation of colon cancer risk SNPs |
| Q36954041 | GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications |
| Q39817009 | Identification of a Potential Regulatory Variant for Colorectal Cancer Risk Mapping to 3p21.31 in Chinese Population |
| Q35779205 | Identification of a Potential Regulatory Variant for Colorectal Cancer Risk Mapping to Chromosome 5q31.1: A Post-GWAS Study |
| Q37376508 | Identification of a functional variant for colorectal cancer risk mapping to chromosome 5q31.1. |
| Q35702332 | Inferring regulatory element landscapes and transcription factor networks from cancer methylomes |
| Q34503932 | Integrative annotation of chromatin elements from ENCODE data |
| Q38776927 | Jointly characterizing epigenetic dynamics across multiple human cell types |
| Q51041886 | Non-coding RNAs in cardiovascular diseases: diagnostic and therapeutic perspectives. |
| Q38886326 | Polycomb repressive complex 2 epigenomic signature defines age-associated hypermethylation and gene expression changes. |
| Q38898009 | Spectacle: fast chromatin state annotation using spectral learning |
| Q35051466 | Systematic classification of non-coding RNAs by epigenomic similarity |
| Q30275429 | Using GWAS to identify novel therapeutic targets for osteoporosis |
| Q26865379 | Using the ENCODE Resource for Functional Annotation of Genetic Variants |
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