GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing data.
PMID:35234913
Mouse genomic and cellular annotations.
PMID:35124726
Modeling uniquely human gene regulatory function via targeted humanization of the mouse genome.
PMID:35027568
Epigenome rewiring in human pluripotent stem cells.
PMID:34955367
Chromatin accessibility and microRNA expression in nephron progenitor cells during kidney development.
PMID:34942352
Transgenic Model Systems Have Revolutionized the Study of Disease.
PMID:34941457
Evolving features of human cortical development and the emerging roles of non-coding RNAs in neural progenitor cell diversity and function.
PMID:34921638
Characterization of Mammalian In Vivo Enhancers Using Mouse Transgenesis and CRISPR Genome Editing.
PMID:34913122
A single-nucleotide mutation within the TBX3 enhancer increased body size in Chinese horses.
PMID:34906355
Cell-specific alterations in Pitx1 regulatory landscape activation caused by the loss of a single enhancer.
PMID:34903763
RefSeq Functional Elements as experimentally assayed nongenic reference standards and functional interactions in human and mouse.
PMID:34876495
Rare Does Not Mean Worthless: How Rare Diseases Have Shaped Neurodevelopment Research in the NGS Era.
PMID:34827709
SMAD4 target genes are part of a transcriptional network that integrates the response to BMP and SHH signaling during early limb bud patterning.
PMID:34822715
Quantitative spatial and temporal assessment of regulatory element activity in zebrafish.
PMID:34796872
Hearing loss genes reveal patterns of adaptive evolution at the coding and non-coding levels in mammals.
PMID:34784928
A single-cell atlas of chromatin accessibility in the human genome.
PMID:34774128
Perfect and imperfect views of ultraconserved sequences.
PMID:34764456
scEnhancer: a single-cell enhancer resource with annotation across hundreds of tissue/cell types in three species.
PMID:34761274
PANTHER: Making genome-scale phylogenetics accessible to all.
PMID:34717010
Comprehensive multi-omics integration identifies differentially active enhancers during human brain development with clinical relevance.
PMID:34663447
From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries.
PMID:34659337
Many chronological aging clocks can be found throughout the epigenome: Implications for quantifying biological aging.
PMID:34655509
An atlas of gene regulatory elements in adult mouse cerebrum.
PMID:34616068
Single-cell epigenomics reveals mechanisms of human cortical development.
PMID:34616060
Conserved and species-specific chromatin remodeling and regulatory dynamics during mouse and chicken limb bud development.
PMID:34584102
Altered DNA Methylation Profiles in SF3B1 Mutated CLL Patients.
PMID:34502260
ReFeaFi: Genome-wide prediction of regulatory elements driving transcription initiation.
PMID:34491989
lncExplore: a database of pan-cancer analysis and systematic functional annotation for lncRNAs from RNA-sequencing data.
PMID:34464437
The bowfin genome illuminates the developmental evolution of ray-finned fishes.
PMID:34462605
Developmental and evolutionary dynamics of cis-regulatory elements in mouse cerebellar cells.
PMID:34446581
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant.
PMID:34410491
A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome.
PMID:34356064
Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR-FlowFISH.
PMID:34326544
Impact of Genetic Variation in Gene Regulatory Sequences: A Population Genomics Perspective.
PMID:34276769
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
PMID:34256850
Tissue-specific 5-hydroxymethylcytosine landscape of the human genome.
PMID:34253716
DECODE: a Deep-learning framework for Condensing enhancers and refining boundaries with large-scale functional assays.
PMID:34252960
Untangling the genetic link between type 1 and type 2 diabetes using functional genomics.
PMID:34230558
Leveraging three-dimensional chromatin architecture for effective reconstruction of enhancer-target gene regulatory interactions.
PMID:34197622
Accurate prediction of cis-regulatory modules reveals a prevalent regulatory genome of humans.
PMID:34159315
Common DNA methylation dynamics in endometriod adenocarcinoma and glioblastoma suggest universal epigenomic alterations in tumorigenesis.
PMID:34021236
Cardiac cell type-specific gene regulatory programs and disease risk association.
PMID:33990324
Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.
PMID:33960642
Fish-Ing for Enhancers in the Heart.
PMID:33920121
Epigenetic regulation during human cortical development: Seq-ing answers from the brain to the organoid.
PMID:33915225
Human brain region-specific variably methylated regions are enriched for heritability of distinct neuropsychiatric traits.
PMID:33888138
The cis-regulatory effects of modern human-specific variants.
PMID:33885362
A compendium and comparative epigenomics analysis of cis-regulatory elements in the pig genome.
PMID:33850120
A Transcription Start Site Map in Human Pancreatic Islets Reveals Functional Regulatory Signatures.
PMID:33849996
hReg-CNCC reconstructs a regulatory network in human cranial neural crest cells and annotates variants in a developmental context.
PMID:33824393
Heart Enhancers: Development and Disease Control at a Distance.
PMID:33777110
Neuronal enhancers are hotspots for DNA single-strand break repair.
PMID:33767446
HAND transcription factors cooperatively specify the aorta and pulmonary trunk.
PMID:33757801
Remus: A Web Application for Prioritization of Regulatory Regions and Variants in Monogenic Diseases.
PMID:33747049
Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning.
PMID:33686085
An intriguing characteristic of enhancer-promoter interactions.
PMID:33685407
Identification of Novel Genetic Regulatory Region for Proprotein Convertase FURIN and Interferon Gamma in T Cells.
PMID:33679774
Molecular signatures of selection on the human GLI3 associated central nervous system specific enhancers.
PMID:33655411
Comprehensive analysis of single cell ATAC-seq data with SnapATAC.
PMID:33637727
Identification and Characterisation of Putative Enhancer Elements in Mouse Embryonic Stem Cells.
PMID:33623376
Annotation of chromatin states in 66 complete mouse epigenomes during development.
PMID:33619351
CellWalker integrates single-cell and bulk data to resolve regulatory elements across cell types in complex tissues.
PMID:33583425
3D promoter architecture re-organization during iPSC-derived neuronal cell differentiation implicates target genes for neurodevelopmental disorders.
PMID:33545232
Human MiniPromoters for ocular-rAAV expression in ON bipolar, cone, corneal, endothelial, Müller glial, and PAX6 cells.
PMID:33531684
Dbx2 regulation in limbs suggests interTAD sharing of enhancers.
PMID:33497014
Genetic Variation in Enhancers Modifies Cardiomyopathy Gene Expression and Progression.
PMID:33478249
Giant lungfish genome elucidates the conquest of land by vertebrates.
PMID:33461212
Enhancer redundancy in development and disease.
PMID:33442000
intePareto: an R package for integrative analyses of RNA-Seq and ChIP-Seq data.
PMID:33372591
PEREGRINE: A genome-wide prediction of enhancer to gene relationships supported by experimental evidence.
PMID:33320871
Cell-Type-Specific Gene Regulatory Networks Underlying Murine Neonatal Heart Regeneration at Single-Cell Resolution.
PMID:33296652
Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias.
PMID:33263113
A map of cis-regulatory elements and 3D genome structures in zebrafish.
PMID:33239788
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
PMID:33227023
Prioritizing long range interactions in noncoding regions using GWAS and deletions perturbed TADs.
PMID:33209206
dbCNS: A New Database for Conserved Noncoding Sequences.
PMID:33196844
Identification of Prognostic Markers in Cholangiocarcinoma Using Altered DNA Methylation and Gene Expression Profiles.
PMID:33193605
A human cell atlas of fetal chromatin accessibility.
PMID:33184180
Ensembl 2021.
PMID:33137190
VARAdb: a comprehensive variation annotation database for human.
PMID:33095866
Analyzing a putative enhancer of optic disc morphology.
PMID:33092545
Cell-type-specific 3D epigenomes in the developing human cortex.
PMID:33057195
SilencerDB: a comprehensive database of silencers.
PMID:33045745
A survey on deep learning in DNA/RNA motif mining.
PMID:33005921
Altered Enhancer and Promoter Usage Leads to Differential Gene Expression in the Normal and Failed Human Heart.
PMID:32993371
Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder.
PMID:32991838
Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty.
PMID:32986727
Tamoxifen-inducible cardiac-specific Cre transgenic mouse using VIPR2 intron.
PMID:32983955
Interpreting the impact of noncoding structural variation in neurodevelopmental disorders.
PMID:32973355
In Vivo Reporter Assays Uncover Changes in Enhancer Activity Caused by Type 2 Diabetes-Associated Single Nucleotide Polymorphisms.
PMID:32912862
NeuroLab Research Experiences: Extending the CURE Design Framework into an Informal Science Setting Dedicated to Pre-College STEM Instruction.
PMID:32832882
Enhancer evolutionary co-option through shared chromatin accessibility input.
PMID:32778581
Preclinical evidence for the therapeutic value of TBX5 normalization in arrhythmia control.
PMID:32777030
Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis.
PMID:32772801
Ancestral regulatory mechanisms specify conserved midbrain circuitry in arthropods and vertebrates.
PMID:32747566
Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants.
PMID:32732423
The changing mouse embryo transcriptome at whole tissue and single-cell resolution.
PMID:32728245
Spatiotemporal DNA methylome dynamics of the developing mouse fetus.
PMID:32728242
An atlas of dynamic chromatin landscapes in mouse fetal development.
PMID:32728240
Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.
PMID:32717170
Total Functional Score of Enhancer Elements Identifies Lineage-Specific Enhancers That Drive Differentiation of Pancreatic Cells.
PMID:32655276
Single-cell ATAC sequencing analysis: From data preprocessing to hypothesis generation.
PMID:32637041
DNA methylation and hydroxymethylation have distinct genome-wide profiles related to axonal regeneration.
PMID:32633672
A Chromatin Accessibility Atlas of the Developing Human Telencephalon.
PMID:32610082
Mapping and characterization of structural variation in 17,795 human genomes.
PMID:32460305
EpiRegio: analysis and retrieval of regulatory elements linked to genes.
PMID:32459338
Progress, Challenges, and Surprises in Annotating the Human Genome.
PMID:32421357
A statistical framework for predicting critical regions of p53-dependent enhancers.
PMID:32392580
Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate.
PMID:32318854
Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.
PMID:32303558
Gene Regulatory and Expression Differences between Mouse and Pig Limb Buds Provide Insights into the Evolutionary Emergence of Artiodactyl Traits.
PMID:32268095
Loss-of-function tolerance of enhancers in the human genome.
PMID:32243438
Accelerated evolution of an Lhx2 enhancer shapes mammalian social hierarchies.
PMID:32238901
Exploring 3D chromatin contacts in gene regulation: The evolution of approaches for the identification of functional enhancer-promoter interaction.
PMID:32226593
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants.
PMID:32169219
Chromatin interaction analyses elucidate the roles of PRC2-bound silencers in mouse development.
PMID:32094912
Enhancer Domains Predict Gene Pathogenicity and Inform Gene Discovery in Complex Disease.
PMID:32032514
GLI transcriptional repression regulates tissue-specific enhancer activity in response to Hedgehog signaling.
PMID:31989924
Towards a comprehensive catalogue of validated and target-linked human enhancers.
PMID:31988385
Whole-genome fingerprint of the DNA methylome during chemically induced differentiation of the human AML cell line HL-60/S4.
PMID:31988093
ORSO (Online Resource for Social Omics): A data-driven social network connecting scientists to genomics datasets.
PMID:31978042
Chromatin accessibility dynamics in a model of human forebrain development.
PMID:31974223
A Pretraining-Retraining Strategy of Deep Learning Improves Cell-Specific Enhancer Predictions.
PMID:31969903
A Novel Approach to Identify Enhancer lincRNAs by Integrating Genome, Epigenome, and Regulatome.
PMID:31956652
Enhancer-gene maps in the human and zebrafish genomes using evolutionary linkage conservation.
PMID:31943068
The formation of the thumb requires direct modulation of Gli3 transcription by Hoxa13.
PMID:31896583
A novel enhancer RNA, Hmrhl, positively regulates its host gene, phkb, in chronic myelogenous leukemia.
PMID:31891018
Lessons from eRNAs: understanding transcriptional regulation through the lens of nascent RNAs.
PMID:31856658
Genetic and Epigenetic Control of Heart Development.
PMID:31818853
Recapitulation-like developmental transitions of chromatin accessibility in vertebrates.
PMID:31807314
Interrogating the Grainyhead-like 2 (Grhl2) genomic locus identifies an enhancer element that regulates palatogenesis in mouse.
PMID:31782997
Genetic Predisposition to Glioma Mediated by a MAPKAP1 Enhancer Variant.
PMID:31773361
Ranking of non-coding pathogenic variants and putative essential regions of the human genome.
PMID:31748530
EnhancerAtlas 2.0: an updated resource with enhancer annotation in 586 tissue/cell types across nine species.
PMID:31740966
The ALK-1/SMAD/ATOH8 axis attenuates hypoxic responses and protects against the development of pulmonary arterial hypertension.
PMID:31719172
UCSC Genome Browser enters 20th year.
PMID:31691824
Identification of gene specific cis-regulatory elements during differentiation of mouse embryonic stem cells: An integrative approach using high-throughput datasets.
PMID:31682597
Decoding regulatory structures and features from epigenomics profiles: A Roadmap-ENCODE Variational Auto-Encoder (RE-VAE) model.
PMID:31672653
ENdb: a manually curated database of experimentally supported enhancers for human and mouse.
PMID:31665430
A reference map of murine cardiac transcription factor chromatin occupancy identifies dynamic and conserved enhancers.
PMID:31659164
Identification and Massively Parallel Characterization of Regulatory Elements Driving Neural Induction.
PMID:31631012
Identification of atrial fibrillation associated genes and functional non-coding variants.
PMID:31628324
Organoid single-cell genomic atlas uncovers human-specific features of brain development.
PMID:31619793
Contribution of retrotransposition to developmental disorders.
PMID:31604926
Distinct enhancer signatures in the mouse gastrula delineate progressive cell fate continuum during embryo development.
PMID:31591447
Widespread cis-regulatory convergence between the extinct Tasmanian tiger and gray wolf.
PMID:31533979
Bioinformatics Discovery of Putative Enhancers within Mouse Odorant Receptor Gene Clusters.
PMID:31529021
Genomic architecture of Shh-dependent cochlear morphogenesis.
PMID:31488567
MPRAnalyze: statistical framework for massively parallel reporter assays.
PMID:31477158
Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development.
PMID:31417368
Whole genome and transcriptome sequencing of post-mortem cardiac tissues from sudden cardiac death victims identifies a gene regulatory variant in NEXN.
PMID:31392414
Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes.
PMID:31367015
Computational Biology Solutions to Identify Enhancers-target Gene Pairs.
PMID:31316726
Stable enhancers are active in development, and fragile enhancers are associated with evolutionary adaptation.
PMID:31307522
Open chromatin dynamics in prosensory cells of the embryonic mouse cochlea.
PMID:31227770
Genome-wide enhancer annotations differ significantly in genomic distribution, evolution, and function.
PMID:31221079
On the traces of tcf12: Investigation of the gene expression pattern during development and cranial suture patterning in zebrafish (Danio rerio).
PMID:31188878
Pax3 cooperates with Ldb1 to direct local chromosome architecture during myogenic lineage specification.
PMID:31127120
RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants.
PMID:31106382
Cardiac Reprogramming Factors Synergistically Activate Genome-wide Cardiogenic Stage-Specific Enhancers.
PMID:31080136
Identification and Conservation Analysis of Cis-Regulatory Elements in Pig Liver.
PMID:31067820
Chromatin Conformation Links Putative Enhancers in Intracranial Aneurysm-Associated Regions to Potential Candidate Genes.
PMID:30994044
Improved Prediction of Regulatory Element Using Hybrid Abelian Complexity Features with DNA Sequences.
PMID:30959806
Taiji: System-level identification of key transcription factors reveals transcriptional waves in mouse embryonic development.
PMID:30944857
Trim33 is required for appropriate development of pre-cardiogenic mesoderm.
PMID:30940539
Predicting enhancers in mammalian genomes using supervised hidden Markov models.
PMID:30917778
Hoxa13 regulates expression of common Hox target genes involved in cartilage development to coordinate the expansion of the autopodal anlage.
PMID:30895612
Enhancer and super-enhancer: Positive regulators in gene transcription.
PMID:30891562
ClinTAD: a tool for copy number variant interpretation in the context of topologically associated domains.
PMID:30765865
Twenty-Seven Tamoxifen-Inducible iCre-Driver Mouse Strains for Eye and Brain, Including Seventeen Carrying a New Inducible-First Constitutive-Ready Allele.
PMID:30765420
Variational infinite heterogeneous mixture model for semi-supervised clustering of heart enhancers.
PMID:30753279
Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562.
PMID:30737237
CERENKOV2: improved detection of functional noncoding SNPs using data-space geometric features.
PMID:30727967
Sequence Characteristics Distinguish Transcribed Enhancers from Promoters and Predict Their Breadth of Activity.
PMID:30696717
EnhancerDB: a resource of transcriptional regulation in the context of enhancers.
PMID:30689845
RAEdb: a database of enhancers identified by high-throughput reporter assays.
PMID:30624654
A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens.
PMID:30612741
Functional characterization of the ZEB2 regulatory landscape.
PMID:30590588
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology.
PMID:30583798
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
PMID:30582786
High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human.
PMID:30568279
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
PMID:30565424
The Role of De Novo Noncoding Regulatory Mutations in Neurodevelopmental Disorders.
PMID:30563709
Dichotomy in redundant enhancers points to presence of initiators of gene regulation.
PMID:30563465
TET2-Dependent Hydroxymethylome Plasticity Reduces Melanoma Initiation and Progression.
PMID:30538121
Borders of Cis-Regulatory DNA Sequences Preferentially Harbor the Divergent Transcription Factor Binding Motifs in the Human Genome.
PMID:30524473
Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.
PMID:30503521
Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development.
PMID:30478328
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics.
PMID:30445463
CisPi: a transcriptomic score for disclosing cis-acting disease-associated lincRNAs.
PMID:30423099
CNEFinder: finding conserved non-coding elements in genomes.
PMID:30423090
Phenotype loss is associated with widespread divergence of the gene regulatory landscape in evolution.
PMID:30413698
Nervous System Regionalization Entails Axial Allocation before Neural Differentiation.
PMID:30343898
Characterization of cis-regulatory elements for Fgf10 expression in the chick embryo.
PMID:30325084
An intronic genetic variation of MGMT affects enhancer activity and is associated with glioma susceptibility.
PMID:30310321
NG2 expression in NG2 glia is regulated by binding of SoxE and bHLH transcription factors to a Cspg4 intronic enhancer.
PMID:30306660
Prediction of gene regulatory enhancers across species reveals evolutionarily conserved sequence properties.
PMID:30286077
HACER: an atlas of human active enhancers to interpret regulatory variants.
PMID:30247654
Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease.
PMID:30224808
Genomic analysis of transcriptional networks directing progression of cell states during MGE development.
PMID:30217225
Enhancer reprogramming in mammalian genomes.
PMID:30200877
Genome-wide DNA methylation profiling of primary colorectal laterally spreading tumors identifies disease-specific epimutations on common pathways.
PMID:30183087
Nascent RNA sequencing analysis provides insights into enhancer-mediated gene regulation.
PMID:30139328
Differential analysis of chromatin accessibility and histone modifications for predicting mouse developmental enhancers.
PMID:30137428
Independent erosion of conserved transcription factor binding sites points to shared hindlimb, vision and external testes loss in different mammals.
PMID:30137416
Genome-wide Identification and Characterization of Enhancers Across 10 Human Tissues.
PMID:30123079
Analysis of diet-induced differential methylation, expression, and interactions of lncRNA and protein-coding genes in mouse liver.
PMID:30069000
Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon.
PMID:30014848
A promoter interaction map for cardiovascular disease genetics.
PMID:29988018
Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks.
PMID:29955040
VRTN is Required for the Development of Thoracic Vertebrae in Mammals.
PMID:29904281
GWAS reveals loci associated with velopharyngeal dysfunction.
PMID:29855589
Genome-wide prediction of cis-regulatory regions using supervised deep learning methods.
PMID:29855387
Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes.
PMID:29805044
Towards a map of cis-regulatory sequences in the human genome.
PMID:29733395
High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development.
PMID:29719267
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
PMID:29700473
Mapping genetic variants for cranial vault shape in humans.
PMID:29698431
PREDICTD PaRallel Epigenomics Data Imputation with Cloud-based Tensor Decomposition.
PMID:29643364
iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.
PMID:29621297
Mammalian genomic regulatory regions predicted by utilizing human genomics, transcriptomics, and epigenetics data.
PMID:29618048
Homo sapiens-Specific Binding Site Variants within Brain Exclusive Enhancers Are Subject to Accelerated Divergence across Human Population.
PMID:29608725
Genetic susceptibility to neuroblastoma: current knowledge and future directions.
PMID:29589100
De novo mutations in regulatory elements in neurodevelopmental disorders.
PMID:29562236
Mapping of Human FOXP2 Enhancers Reveals Complex Regulation.
PMID:29515369
An information-theoretic approach to the modeling and analysis of whole-genome bisulfite sequencing data.
PMID:29514626
Assessing sufficiency and necessity of enhancer activities for gene expression and the mechanisms of transcription activation.
PMID:29491135
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors.
PMID:29440260
Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation.
PMID:29438503
Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation.
PMID:29434377
Enhancer redundancy provides phenotypic robustness in mammalian development.
PMID:29420474
Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin.
PMID:29321672
The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis.
PMID:29307494
Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.
PMID:29301908
Regulatory variants of FOXG1 in the context of its topological domain organisation.
PMID:29289958
Transcription-factor-dependent enhancer transcription defines a gene regulatory network for cardiac rhythm.
PMID:29280435
PITX1 promotes chondrogenesis and myogenesis in mouse hindlimbs through conserved regulatory targets.
PMID:29273440
Promoter-enhancer interactions identified from Hi-C data using probabilistic models and hierarchical topological domains.
PMID:29269730
Multiple enhancer regions govern the transcription of CCN2 during embryonic development.
PMID:29256171
Noncoding copy-number variations are associated with congenital limb malformation.
PMID:29236091
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
PMID:29198719
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience.
PMID:29183403
Software for rapid time dependent ChIP-sequencing analysis (TDCA).
PMID:29178831
Conserved non-coding elements: developmental gene regulation meets genome organization.
PMID:29121339
High-throughput annotation of full-length long noncoding RNAs with capture long-read sequencing.
PMID:29106417
The BRAIN Initiative Cell Census Consortium: Lessons Learned toward Generating a Comprehensive Brain Cell Atlas.
PMID:29096072
Appendages and gene regulatory networks: Lessons from the limbless.
PMID:29076617
DiseaseEnhancer: a resource of human disease-associated enhancer catalog.
PMID:29059320
Genomic Patterns of De Novo Mutation in Simplex Autism.
PMID:28965761
A tissue-specific, Gata6-driven transcriptional program instructs remodeling of the mature arterial tree.
PMID:28952437
Composition and dosage of a multipartite enhancer cluster control developmental expression of Ihh (Indian hedgehog).
PMID:28846100
Limb-Enhancer Genie: An accessible resource of accurate enhancer predictions in the developing limb.
PMID:28827824
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.
PMID:28735859
Short DNA sequence patterns accurately identify broadly active human enhancers.
PMID:28716036
Putative enhancer sites in the bovine genome are enriched with variants affecting complex traits.
PMID:28683716
Silencing Effect of Hominoid Highly Conserved Noncoding Sequences on Embryonic Brain Development.
PMID:28633494
GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.
PMID:28605766
Taking promoters out of enhancers in sequence based predictions of tissue-specific mammalian enhancers.
PMID:28589862
HAND2 Target Gene Regulatory Networks Control Atrioventricular Canal and Cardiac Valve Development.
PMID:28538179
Perspectives on Gene Regulatory Network Evolution.
PMID:28528721
An imprinted non-coding genomic cluster at 14q32 defines clinically relevant molecular subtypes in osteosarcoma across multiple independent datasets.
PMID:28506242
Comparative transcriptomics in human and mouse.
PMID:28479595
Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval.
PMID:28470180
Cytosine modifications modulate the chromatin architecture of transcriptional enhancers.
PMID:28396520
Potential energy landscapes identify the information-theoretic nature of the epigenome.
PMID:28346445
Global reorganisation of cis-regulatory units upon lineage commitment of human embryonic stem cells.
PMID:28332981
Improved regulatory element prediction based on tissue-specific local epigenomic signatures.
PMID:28193886
eMouseAtlas: An atlas-based resource for understanding mammalian embryogenesis.
PMID:28161522
New insights from GWAS for the cleft palate among han Chinese population.
PMID:28160584
Mapping cell type-specific transcriptional enhancers using high affinity, lineage-specific Ep300 bioChIP-seq.
PMID:28121289
Chromatin dynamics regulate mesenchymal stem cell lineage specification and differentiation to osteogenesis.
PMID:28077316
Editing the Neuronal Genome: a CRISPR View of Chromatin Regulation in Neuronal Development, Function, and Plasticity.
PMID:28018138
A regulatory sequence from the retinoid X receptor γ gene directs expression to horizontal cells and photoreceptors in the embryonic chicken retina.
PMID:28003731
CRISPRi-based genome-scale identification of functional long noncoding RNA loci in human cells.
PMID:27980086
Distal Limb Patterning Requires Modulation of cis-Regulatory Activities by HOX13.
PMID:27974206
EP-DNN: A Deep Neural Network-Based Global Enhancer Prediction Algorithm.
PMID:27929098
Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding.
PMID:27923844
Determinants of orofacial clefting II: Effects of 5-Aza-2'-deoxycytidine on gene methylation during development of the first branchial arch.
PMID:27923600
Cancer somatic mutations cluster in a subset of regulatory sites predicted from the ENCODE data.
PMID:27887606
Genomic approaches to the assessment of human spina bifida risk.
PMID:27883265
The Shh Topological Domain Facilitates the Action of Remote Enhancers by Reducing the Effects of Genomic Distances.
PMID:27867070
Progressive Loss of Function in a Limb Enhancer during Snake Evolution.
PMID:27768887
Formation of new chromatin domains determines pathogenicity of genomic duplications.
PMID:27706140
Genome-wide compendium and functional assessment of in vivo heart enhancers.
PMID:27703156
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.
PMID:27699255
An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility.
PMID:27692237
LMethyR-SVM: Predict Human Enhancers Using Low Methylated Regions based on Weighted Support Vector Machines.
PMID:27662487
Epigenomic and metabolic responses of hypothalamic POMC neurons to gestational nicotine exposure in adult offspring.
PMID:27609221
ANGIOGENES: knowledge database for protein-coding and noncoding RNA genes in endothelial cells.
PMID:27582018
EnhancerAtlas: a resource for enhancer annotation and analysis in 105 human cell/tissue types.
PMID:27515742
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels.
PMID:27357396
Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluid.
PMID:27357110
A unique stylopod patterning mechanism by Shox2-controlled osteogenesis.
PMID:27287812
IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation.
PMID:27282637
Distinct transcription factor complexes act on a permissive chromatin landscape to establish regionalized gene expression in CNS stem cells.
PMID:27197220
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
PMID:27195815
Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis.
PMID:27172222
rAAV-compatible MiniPromoters for restricted expression in the brain and eye.
PMID:27164903
Origin and evolution of developmental enhancers in the mammalian neocortex.
PMID:27114548
Jointly characterizing epigenetic dynamics across multiple human cell types.
PMID:27095202
A uniform survey of allele-specific binding and expression over 1000-Genomes-Project individuals.
PMID:27089393
Systematic identification of gene family regulators in mouse and human embryonic stem cells.
PMID:27084933
Cis-regulatory architecture of a brain signaling center predates the origin of chordates.
PMID:27064252
Distinct epigenetic signatures elucidate enhancer-gene relationships that delineate CIMP and non-CIMP colorectal cancers.
PMID:27049830
A Mammalian enhancer trap resource for discovering and manipulating neuronal cell types.
PMID:26999799
Comprehensive benchmarking reveals H2BK20 acetylation as a distinctive signature of cell-state-specific enhancers and promoters.
PMID:26957309
The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons.
PMID:26950095
Active DNA demethylation at enhancers during the vertebrate phylotypic period.
PMID:26928226
Early developmental gene enhancers affect subcortical volumes in the adult human brain.
PMID:26890892
Ensembl regulation resources.
PMID:26888907
Mapping of Variable DNA Methylation Across Multiple Cell Types Defines a Dynamic Regulatory Landscape of the Human Genome.
PMID:26888867
Enrichment analysis of Alu elements with different spatial chromatin proximity in the human genome.
PMID:26861146
The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data.
PMID:26808208
Role of non-coding sequence variants in cancer.
PMID:26781813
Accelerated Evolution of Enhancer Hotspots in the Mammal Ancestor.
PMID:26715627
Genetic Regulation of Sinoatrial Node Development and Pacemaker Program in the Venous Pole.
PMID:26682210
Progress and challenges in bioinformatics approaches for enhancer identification.
PMID:26634919
Lynx: a knowledge base and an analytical workbench for integrative medicine.
PMID:26590263
Hemichordate genomes and deuterostome origins.
PMID:26580012
ORegAnno 3.0: a community-driven resource for curated regulatory annotation.
PMID:26578589
EMERGE: a flexible modelling framework to predict genomic regulatory elements from genomic signatures.
PMID:26531828
CEGA--a catalog of conserved elements from genomic alignments.
PMID:26527719
Handling Permutation in Sequence Comparison: Genome-Wide Enhancer Prediction in Vertebrates by a Novel Non-Linear Alignment Scoring Principle.
PMID:26505748
MEPD: medaka expression pattern database, genes and more.
PMID:26450962
Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus.
PMID:26443638
Shared Enhancer Activity in the Limbs and Phallus and Functional Divergence of a Limb-Genital cis-Regulatory Element in Snakes.
PMID:26439399
Chromatin Architecture of the Pitx2 Locus Requires CTCF- and Pitx2-Dependent Asymmetry that Mirrors Embryonic Gut Laterality.
PMID:26411685
Sequential Binding of MEIS1 and NKX2-5 on the Popdc2 Gene: A Mechanism for Spatiotemporal Regulation of Enhancers during Cardiogenesis.
PMID:26411676
Disruptions in a cluster of computationally identified enhancers near FOXC1 and GMDS may influence brain development.
PMID:26382291
Enhancer divergence and cis-regulatory evolution in the human and chimp neural crest.
PMID:26365491
DENdb: database of integrated human enhancers.
PMID:26342387
Activation of Six1 Expression in Vertebrate Sensory Neurons.
PMID:26313368
A shift in anterior-posterior positional information underlies the fin-to-limb evolution.
PMID:26283004
Nuclear Fractionation Reveals Thousands of Chromatin-Tethered Noncoding RNAs Adjacent to Active Genes.
PMID:26257179
The Evolution of Bony Vertebrate Enhancers at Odds with Their Coding Sequence Landscape.
PMID:26253316
The frequent evolutionary birth and death of functional promoters in mouse and human.
PMID:26228054
A semi-supervised approach uncovers thousands of intragenic enhancers differentially activated in human cells.
PMID:26169177
A Simple Predictive Enhancer Syntax for Hindbrain Patterning Is Conserved in Vertebrate Genomes.
PMID:26131856
Comprehensive identification and analysis of human accelerated regulatory DNA.
PMID:26104583
CASC15-S Is a Tumor Suppressor lncRNA at the 6p22 Neuroblastoma Susceptibility Locus.
PMID:26100672
Occupancy by key transcription factors is a more accurate predictor of enhancer activity than histone modifications or chromatin accessibility.
PMID:25984238
DNase I hypersensitivity analysis of the mouse brain and retina identifies region-specific regulatory elements.
PMID:25972927
Principles of long noncoding RNA evolution derived from direct comparison of transcriptomes in 17 species.
PMID:25959816
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions.
PMID:25959774
ChIP-Array 2: integrating multiple omics data to construct gene regulatory networks.
PMID:25916854
Human gene-centered transcription factor networks for enhancers and disease variants.
PMID:25910213
Widespread macromolecular interaction perturbations in human genetic disorders.
PMID:25910212
Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP.
PMID:25888893
The ensembl regulatory build.
PMID:25887522
A distinct regulatory region of the Bmp5 locus activates gene expression following adult bone fracture or soft tissue injury.
PMID:25886903
The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancers.
PMID:25857663
Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum.
PMID:25849986
Integrating motif, DNA accessibility and gene expression data to build regulatory maps in an organism.
PMID:25791631
Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.
PMID:25786657
Spectacle: fast chromatin state annotation using spectral learning.
PMID:25786205
A diverse epigenetic landscape at human exons with implication for expression.
PMID:25765649
Extrapolating histone marks across developmental stages, tissues, and species: an enhancer prediction case study.
PMID:25765133
Evolutionary genomics. Evolutionary changes in promoter and enhancer activity during human corticogenesis.
PMID:25745175
Identifying transcriptional cis-regulatory modules in animal genomes.
PMID:25704908
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD).
PMID:25701871
Developmental enhancers revealed by extensive DNA methylome maps of zebrafish early embryos.
PMID:25697895
Integrative analysis of haplotype-resolved epigenomes across human tissues.
PMID:25693566
Intermediate DNA methylation is a conserved signature of genome regulation.
PMID:25691127
Genomic perspectives of transcriptional regulation in forebrain development.
PMID:25569346
A discrete transition zone organizes the topological and regulatory autonomy of the adjacent tfap2c and bmp7 genes.
PMID:25569170
Scl binds to primed enhancers in mesoderm to regulate hematopoietic and cardiac fate divergence.
PMID:25564442
Identification and computational analysis of gene regulatory elements.
PMID:25561628
Mammalian transcriptional hotspots are enriched for tissue specific enhancers near cell type specific highly expressed genes and are predicted to act as transcriptional activator hubs.
PMID:25547756
Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain.
PMID:25539921
A Sox2 distal enhancer cluster regulates embryonic stem cell differentiation potential.
PMID:25512558
An integrative computational approach for prioritization of genomic variants.
PMID:25506935
An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator.
PMID:25493341
Histone H3 K27 acetylation marks a potent enhancer element on the adipogenic master regulator gene Pparg2.
PMID:25485585
HAND2 targets define a network of transcriptional regulators that compartmentalize the early limb bud mesenchyme.
PMID:25453830
GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes.
PMID:25428361
Constrained transcription factor spacing is prevalent and important for transcriptional control of mouse blood cells.
PMID:25428352
Monoallelic expression of the human FOXP2 speech gene.
PMID:25422445
The long non-coding RNA Dali is an epigenetic regulator of neural differentiation.
PMID:25415054
Principles of regulatory information conservation between mouse and human.
PMID:25409826
DEEP: a general computational framework for predicting enhancers.
PMID:25378307
A large scale expression study associates uc.283-plus lncRNA with pluripotent stem cells and human glioma.
PMID:25352916
Deletions of chromosomal regulatory boundaries are associated with congenital disease.
PMID:25315429
Genome-wide identification of signaling center enhancers in the developing limb.
PMID:25273087
Dynamic GATA4 enhancers shape the chromatin landscape central to heart development and disease.
PMID:25249388
Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families.
PMID:25231166
Identification of a face enhancer reveals direct regulation of LIM homeobox 8 (Lhx8) by wingless-int (WNT)/β-catenin signaling.
PMID:25190800
Tissue-specific RNA expression marks distant-acting developmental enhancers.
PMID:25188404
A 'tool box' for deciphering neuronal circuits in the developing chick spinal cord.
PMID:25147209
Tracing the evolution of lineage-specific transcription factor binding sites in a birth-death framework.
PMID:25144359
Concerted bioinformatic analysis of the genome-scale blood transcription factor compendium reveals new control mechanisms.
PMID:25133983
Dnmt3a regulates global gene expression in olfactory sensory neurons and enables odorant-induced transcription.
PMID:25123312
A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock.
PMID:25089931
Integrating diverse datasets improves developmental enhancer prediction.
PMID:24967590
UCbase 2.0: ultraconserved sequences database (2014 update).
PMID:24951797
Lynx web services for annotations and systems analysis of multi-gene disorders.
PMID:24948611
Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence.
PMID:24934569
Functional analysis of limb transcriptional enhancers in the mouse.
PMID:24920384
Genome-scale functional characterization of Drosophila developmental enhancers in vivo.
PMID:24896182
Targeted CNS Delivery Using Human MiniPromoters and Demonstrated Compatibility with Adeno-Associated Viral Vectors.
PMID:24761428
Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis.
PMID:24752179
Comparative epigenomics in distantly related teleost species identifies conserved cis-regulatory nodes active during the vertebrate phylotypic period.
PMID:24709821
The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.
PMID:24709820
FIREWACh: high-throughput functional detection of transcriptional regulatory modules in mammalian cells.
PMID:24658142
Obesity-associated variants within FTO form long-range functional connections with IRX3.
PMID:24646999
Multiple conserved regulatory domains promote Fezf2 expression in the developing cerebral cortex.
PMID:24618363
Transcriptional enhancers: from properties to genome-wide predictions.
PMID:24614317
Conservation and divergence of regulatory strategies at Hox Loci and the origin of tetrapod digits.
PMID:24465181
Association of the hepatocyte growth factor gene with keratoconus in an Australian population.
PMID:24416191
Functional and topological characteristics of mammalian regulatory domains.
PMID:24398455
Ensembl 2014.
PMID:24316576
Lynx: a database and knowledge extraction engine for integrative medicine.
PMID:24270788
EMAGE mouse embryo spatial gene expression database: 2014 update.
PMID:24265223
Single site-specific integration targeting coupled with embryonic stem cell differentiation provides a high-throughput alternative to in vivo enhancer analyses.
PMID:24244860
Many human accelerated regions are developmental enhancers.
PMID:24218637
The mystery of extreme non-coding conservation.
PMID:24218634
Functional characterization of SIM1-associated enhancers.
PMID:24203700
Nencki Genomics Database--Ensembl funcgen enhanced with intersections, user data and genome-wide TFBS motifs.
PMID:24089456
Functional analysis of limb enhancers in the developing fin.
PMID:24068387
The enhancer landscape during early neocortical development reveals patterns of dense regulation and co-option.
PMID:24009522
Epigenetic memory at embryonic enhancers identified in DNA methylation maps from adult mouse tissues.
PMID:23995138
Pax7 is regulated by cMyb during early neural crest development through a novel enhancer.
PMID:23942518
A yeast one-hybrid and microfluidics-based pipeline to map mammalian gene regulatory networks.
PMID:23917988
Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational model.
PMID:23892608
A compact, in vivo screen of all 6-mers reveals drivers of tissue-specific expression and guides synthetic regulatory element design.
PMID:23867016
Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression.
PMID:23835950
The evolution of lineage-specific regulatory activities in the human embryonic limb.
PMID:23827682
Computational methods to detect conserved non-genic elements in phylogenetically isolated genomes: application to zebrafish.
PMID:23814184
Machine learning and genome annotation: a match meant to be?
PMID:23731483
GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.
PMID:23723249
The genomic landscape of cohesin-associated chromatin interactions.
PMID:23704192
Candidate gene association studies: a comprehensive guide to useful in silico tools.
PMID:23656885
From remote enhancers to gene regulation: charting the genome's regulatory landscapes.
PMID:23650632
TRACER: a resource to study the regulatory architecture of the mouse genome.
PMID:23547943
Systematic dissection of regulatory motifs in 2000 predicted human enhancers using a massively parallel reporter assay.
PMID:23512712
Distinct cis regulatory elements govern the expression of TAG1 in embryonic sensory ganglia and spinal cord.
PMID:23469119
Comparative genomics using teleost fish helps to systematically identify target gene bodies of functionally defined human enhancers.
PMID:23432897
A high-resolution enhancer atlas of the developing telencephalon.
PMID:23375746
Genetic and functional modularity of Hox activities in the specification of limb-innervating motor neurons.
PMID:23359544
Computational tools and resources for prediction and analysis of gene regulatory regions in the chick genome.
PMID:23355428
Function and regulation of AUTS2, a gene implicated in autism and human evolution.
PMID:23349641
Dlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneurons.
PMID:23312518
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
PMID:23307621
Enhancer chip: detecting human copy number variations in regulatory elements.
PMID:23284961
Vertebrate paralogous conserved noncoding sequences may be related to gene expressions in brain.
PMID:23267051
Differences in enhancer activity in mouse and zebrafish reporter assays are often associated with changes in gene expression.
PMID:23253453
Genome-wide identification of enhancers in skeletal muscle: the role of MyoD1.
PMID:23249738
Cell specific CD44 expression in breast cancer requires the interaction of AP-1 and NFκB with a novel cis-element.
PMID:23226410
Ensembl 2013.
PMID:23203987
Pitx1 broadly associates with limb enhancers and is enriched on hindlimb cis-regulatory elements.
PMID:23201014
UCNEbase--a database of ultraconserved non-coding elements and genomic regulatory blocks.
PMID:23193254
Facilitators and impediments of the pluripotency reprogramming factors' initial engagement with the genome.
PMID:23159369
Hundreds of conserved non-coding genomic regions are independently lost in mammals.
PMID:23042682
A cis-element in the Notch1 locus is involved in the regulation of gene expression in interneuron progenitors.
PMID:23022658
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus.
PMID:23022097
Annotation of functional variation in personal genomes using RegulomeDB.
PMID:22955989
Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors.
PMID:22950945
Sequencing and analysis of a South Asian-Indian personal genome.
PMID:22938532
Gene isoform specificity through enhancer-associated antisense transcription.
PMID:22937057
POU-III transcription factors (Brn1, Brn2, and Oct6) influence neurogenesis, molecular identity, and migratory destination of upper-layer cells of the cerebral cortex.
PMID:22892427
Human developmental enhancers conserved between deuterostomes and protostomes.
PMID:22876195
A map of the cis-regulatory sequences in the mouse genome.
PMID:22763441
Systematic elucidation and in vivo validation of sequences enriched in hindbrain transcriptional control.
PMID:22759862
Extensive conservation of ancient microsynteny across metazoans due to cis-regulatory constraints.
PMID:22722344
The cis-regulatory dynamics of the Drosophila CNS determinant castor are controlled by multiple sub-pattern enhancers.
PMID:22691242
Evidence for additional FREM1 heterogeneity in Manitoba oculotrichoanal syndrome.
PMID:22690109
Axonal patterns and targets of dA1 interneurons in the chick hindbrain.
PMID:22539838
Chromatin state signatures associated with tissue-specific gene expression and enhancer activity in the embryonic limb.
PMID:22421546
A machine learning approach for identifying novel cell type-specific transcriptional regulators of myogenesis.
PMID:22412381
ReLA, a local alignment search tool for the identification of distal and proximal gene regulatory regions and their conserved transcription factor binding sites.
PMID:22253291
An ancient genomic regulatory block conserved across bilaterians and its dismantling in tetrapods by retrogene replacement.
PMID:22234889
Combinatorial binding in human and mouse embryonic stem cells identifies conserved enhancers active in early embryonic development.
PMID:22215994
Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers.
PMID:22208168
Gli2 and MEF2C activate each other's expression and function synergistically during cardiomyogenesis in vitro.
PMID:22199256
A distal modular enhancer complex acts to control pituitary- and nervous system-specific expression of the LHX3 regulatory gene.
PMID:22194342
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.
PMID:22178994
A mammalian conserved element derived from SINE displays enhancer properties recapitulating Satb2 expression in early-born callosal projection neurons.
PMID:22174821
GWASdb: a database for human genetic variants identified by genome-wide association studies.
PMID:22139925
Large-scale discovery of enhancers from human heart tissue.
PMID:22138689
Enhancer-driven chromatin interactions during development promote escape from silencing by a long non-coding RNA.
PMID:22085535
Thousands of cis-regulatory sequence combinations are shared by Arabidopsis and poplar.
PMID:22058225
Identification of a retina-specific Otx2 enhancer element active in immature developing photoreceptors.
PMID:21963459
VISTA Region Viewer (RViewer)--a computational system for prioritizing genomic intervals for biomedical studies.
PMID:21791533
Towards resolving the transcription factor network controlling myelin gene expression.
PMID:21729871
Decoding the genome with an integrative analysis tool: combinatorial CRM Decoder.
PMID:21724599
Contrasting 5' and 3' evolutionary histories and frequent evolutionary convergence in Meis/hth gene structures.
PMID:21680890
Epigenetic signatures distinguish multiple classes of enhancers with distinct cellular functions.
PMID:21632746
Genome-wide identification of conserved regulatory function in diverged sequences.
PMID:21628450
Ascl1/Mash1 is a novel target of Gli2 during Gli2-induced neurogenesis in P19 EC cells.
PMID:21559470
Genetics of nonsyndromic orofacial clefts.
PMID:21545302
Disease and phenotype data at Ensembl.
PMID:21400687
Identification of a dopaminergic enhancer indicates complexity in vertebrate dopamine neuron phenotype specification.
PMID:21276790
A unique chromatin signature uncovers early developmental enhancers in humans.
PMID:21160473
Integrative analysis of genomic, functional and protein interaction data predicts long-range enhancer-target gene interactions.
PMID:21109530
Motor and dorsal root ganglion axons serve as choice points for the ipsilateral turning of dI3 axons.
PMID:21084609
Statistical analysis strategies for association studies involving rare variants.
PMID:20940738
ChIP-Seq identification of weakly conserved heart enhancers.
PMID:20729851
The ANISEED database: digital representation, formalization, and elucidation of a chordate developmental program.
PMID:20647237
The importance of being cis: evolution of orthologous fish and mammalian enhancer activity.
PMID:20494938
Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development.
PMID:20426846
Sequence composition similarities with the 7SL RNA are highly predictive of functional genomic features.
PMID:20392819
Translog, a web browser for studying the expression divergence of homologous genes.
PMID:20122234
Genome-wide discovery of human heart enhancers.
PMID:20075146
Exonic remnants of whole-genome duplication reveal cis-regulatory function of coding exons.
PMID:19969543
Combinatorial binding predicts spatio-temporal cis-regulatory activity.
PMID:19890324
G-compass: a web-based comparative genome browser between human and other vertebrate genomes.
PMID:19846439
Conserved expression patterns predict microRNA targets.
PMID:19779543
Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes.
PMID:19698106
Transcriptional control of axonal guidance and sorting in dorsal interneurons by the Lim-HD proteins Lhx9 and Lhx1.
PMID:19545367
ChIP-seq accurately predicts tissue-specific activity of enhancers.
PMID:19212405
cneViewer: a database of conserved non-coding elements for studies of tissue-specific gene regulation.
PMID:18718943
Ancora: a web resource for exploring highly conserved noncoding elements and their association with developmental regulatory genes.
PMID:18279518
ORegAnno: an open-access community-driven resource for regulatory annotation.
PMID:18006570
CONDOR: a database resource of developmentally associated conserved non-coding elements.
PMID:17760977