DNA drug

Aliases

DNA, DNA (>1000 bps), DNA molecules, DNA samples, DNA sequence, Genomic DNA, deoxyribonucleic acid, double-stranded DNA, dsDNA, genomic DNA, high molecular weight DNA, immunoprecipitated DNA, input DNA, saliva DNA sample

External links

DrugBank · PubChem

Related entities (43)

Mentioned in (307)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Genome modelling and design across all domains of life with Evo 2. (2026)
• A guide to transcriptomic deconvolution in cancer. (2026)
• Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
• Whole-genome landscapes of 1,364 breast cancers. (2026)
• LINE-1 retrotransposons mediate cis-acting transcriptional control in human pluripotent stem cells and regulate early brain development. (2025)
• Annotating the genome at single-nucleotide resolution with DNA foundation models. (2025)
• Enhancer activation from transposable elements in extrachromosomal DNA. (2025)
• Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
• Connectome-seq: High-throughput Mapping of Neuronal Connectivity at Single-Synapse Resolution via Barcode Sequencing. (2025)
• ChromoGen: Diffusion model predicts single-cell chromatin conformations. (2025)
• Rapid brain tumor classification from sparse epigenomic data. (2025)
• Microfluidic purification of genomic DNA. (2025)
• Chromosomal instability as a driver of cancer progression. (2025)
• Efficient and accurate search in petabase-scale sequence repositories. (2025)
• Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Three-dimensional genome landscape of primary human cancers. (2025)
• Single cell and spatial alternative splicing analysis with Nanopore long read sequencing. (2025)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
• Alcohol Exposure May Increase Prenatal Choline Needs Through Redirection of Choline into Lipid Synthesis Rather than Methyl Donation. (2025)
• Foundation models in bioinformatics. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• DNA breathing integration with deep learning foundational model advances genome-wide binding prediction of human transcription factors. (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Sequence modeling and design from molecular to genome scale with Evo. (2024)
• Transient loss of Polycomb components induces an epigenetic cancer fate. (2024)
• Oral supplementation of choline attenuates the development of alcohol-related liver disease (ALD). (2024)
• Alternative splicing of transcript mediates the response of circadian clocks to temperature changes. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. (2024)
• The Application of Long-Read Sequencing to Cancer. (2024)
• ENPP1 Immunobiology as a Therapeutic Target. (2023)
• Cell-Free DNA Fragmentomics: The Novel Promising Biomarker. (2023)
• A DNA methylation atlas of normal human cell types. (2023)
• Validation of the new EPIC DNA methylation microarray (900K EPIC v2) for high-throughput profiling of the human DNA methylome. (2023)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• GenSLMs: Genome-scale language models reveal SARS-CoV-2 evolutionary dynamics. (2022)
• At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
• Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smoking. (2022)
• Epigenetic analysis of cell-free DNA by fragmentomic profiling. (2022)
• Nanopore sequencing of RNA and cDNA molecules in . (2022)
• Epigenetic profiling of social communication trajectories and co-occurring mental health problems: a prospective, methylome-wide association study. (2022)
• Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data. (2022)
• Massively parallel reporter perturbation assays uncover temporal regulatory architecture during neural differentiation. (2022)
• Estimation of tumor cell total mRNA expression in 15 cancer types predicts disease progression. (2022)
• Sequence aligners can guarantee accuracy in almost <i>O</i> ( <i>m</i> log <i>n</i> ) time: a rigorous average-case analysis of the seed-chain-extend heuristic (2022)
• Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• DNA methylation in relation to gestational age and brain dysmaturation in preterm infants. (2022)
• Nanopore sequencing technology, bioinformatics and applications. (2021)
• Maternal choline supplementation mitigates alcohol exposure effects on neonatal brain volumes. (2021)
• Autosomal sex-associated co-methylated regions predict biological sex from DNA methylation. (2021)
• Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
• Application of third-generation sequencing in cancer research. (2021)
• A practical guide to cancer subclonal reconstruction from DNA sequencing. (2021)
• Placental genomic risk scores and early neurodevelopmental outcomes. (2021)
• A Comprehensive Circulating Tumor DNA Assay for Detection of Translocation and Copy-Number Changes in Pediatric Sarcomas. (2021)
• Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
• Early-life nicotine or cotinine exposure produces long-lasting sleep alterations and downregulation of hippocampal corticosteroid receptors in adult mice. (2021)
• Accurate detection of circulating tumor DNA using nanopore consensus sequencing. (2021)
• Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
• NUP98-NSD1 Driven MDS/MPN in Childhood Masquerading as JMML. (2021)
• Simultaneous epigenetic perturbation and genome imaging reveal distinct roles of H3K9me3 in chromatin architecture and transcription. (2020)
• Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
• Structural variation in the sequencing era. (2020)
• UMI-linked consensus sequencing enables phylogenetic analysis of directed evolution. (2020)
• Patterns of Reliability: Assessing the Reproducibility and Integrity of DNA Methylation Measurement. (2020)
• Klotho gene polymorphism, brain structure and cognition in early-life development. (2020)
• Inferring structural variant cancer cell fraction. (2020)
• Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. (2020)
• Folding Keratin Gene Clusters during Skin Regional Specification. (2020)
• AmpliconReconstructor integrates NGS and optical mapping to resolve the complex structures of focal amplifications. (2020)
• Biological embedding of experience: A primer on epigenetics. (2020)
• FQSqueezer: k-mer-based compression of sequencing data. (2020)
• Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
• Establishing guidelines to harmonize tumor mutational burden (TMB): in silico assessment of variation in TMB quantification across diagnostic platforms: phase I of the Friends of Cancer Research TMB Harmonization Project. (2020)
• Data structures based on <i>k</i> -mers for querying large collections of sequencing datasets (2019)
• Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• Ploidy- and Purity-Adjusted Allele-Specific DNA Analysis Using CLONETv2. (2019)
• Passenger hotspot mutations in cancer driven by APOBEC3A and mesoscale genomic features. (2019)
• CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. (2019)
• Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study. (2019)
• CUT&RUNTools: a flexible pipeline for CUT&RUN processing and footprint analysis. (2019)
• Genome-Informed Targeted Therapy for Osteosarcoma. (2019)
• Genome-wide cell-free DNA fragmentation in patients with cancer. (2019)
• RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
• Persistent Changes in Stress-Regulatory Genes in Pregnant Women or Children Exposed Prenatally to Alcohol. (2019)
• Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
• Comparison of Illumina 450K and EPIC arrays in placental DNA methylation. (2019)
• Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
• Heritability of obsessive-compulsive trait dimensions in youth from the general population. (2018)
• Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. (2018)
• Collider scope: when selection bias can substantially influence observed associations. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
• Comparison of DNA methylation measured by Illumina 450K and EPIC BeadChips in blood of newborns and 14-year-old children. (2018)
• Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
• Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3β Are Modulators of Anxiety and Glutamatergic Neurotransmission. (2018)
• The Human Transcription Factors. (2018)
• Oxytocin Receptor Gene Variant Interacts with Intervention Delivery Format in Predicting Intervention Outcomes for Youth with Conduct Problems. (2018)
• The Immune Landscape of Cancer. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• Prenatal Alcohol Exposure: Profiling Developmental DNA Methylation Patterns in Central and Peripheral Tissues. (2018)
• Nanopore sequencing and assembly of a human genome with ultra-long reads. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Molecular profiling and sequential somatic mutation shift in hypermutator tumours harbouring POLE mutations. (2018)
• PDGFRA gene, maternal binge drinking and obstructive heart defects. (2018)
• Accurate Recycling of Parental Histones Reproduces the Histone Modification Landscape during DNA Replication. (2018)
• Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. (2018)
• Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
• Nanopore Sequencing Reveals High-Resolution Structural Variation in the Cancer Genome (2017)
• GAVIN: Gene-Aware Variant INterpretation for medical sequencing. (2017)
• HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
• Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
• Genetic effects on gene expression across human tissues. (2017)
• A pooled mutational analysis identifies ionizing radiation-associated mutational signatures conserved between mouse and human malignancies. (2017)
• Maternal choline supplementation during murine pregnancy modulates placental markers of inflammation, apoptosis and vascularization in a fetal sex-dependent manner. (2017)
• Patient-derived xenografts undergo mouse-specific tumor evolution. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• CHN2 Promoter Methylation Change May Be Associated With Methamphetamine Dependence. (2017)
• GRIDSS: sensitive and specific genomic rearrangement detection using positional de Bruijn graph assembly. (2017)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• Sex differences in DNA methylation of the cord blood are related to sex-bias psychiatric diseases. (2017)
• Mapping and phasing of structural variation in patient genomes using nanopore sequencing. (2017)
• DNA replication timing during development anticipates transcriptional programs and parallels enhancer activation. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• Epigenetics studies of fetal alcohol spectrum disorder: where are we now? (2017)
• ReMixT: clone-specific genomic structure estimation in cancer. (2017)
• Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential. (2017)
• Impact of cytosine methylation on DNA binding specificities of human transcription factors. (2017)
• Copy-number signatures and mutational processes in ovarian carcinoma (2017)
• Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity. (2017)
• An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
• DNA Methylation Analysis: Choosing the Right Method. (2016)
• Statistical modeling for sensitive detection of low-frequency single nucleotide variants. (2016)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Integrated digital error suppression for improved detection of circulating tumor DNA. (2016)
• GeneiASE: Detection of condition-dependent and static allele-specific expression from RNA-seq data without haplotype information. (2016)
• Somatic cancer variant curation and harmonization through consensus minimum variant level data. (2016)
• The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Global analysis of somatic structural genomic alterations and their impact on gene expression in diverse human cancers. (2016)
• Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
• Alteration of Gene Expression, DNA Methylation, and Histone Methylation in Free Radical Scavenging Networks in Adult Mouse Hippocampus following Fetal Alcohol Exposure. (2016)
• Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
• A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. (2016)
• CEL-Seq2: sensitive highly-multiplexed single-cell RNA-Seq. (2016)
• Three decades of nanopore sequencing. (2016)
• Parasail: SIMD C library for global, semi-global, and local pairwise sequence alignments. (2016)
• Oxidative stress signaling to chromatin in health and disease. (2016)
• Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
• STRUCTURAL AND FUNCTIONAL CONNECTIVITY IN POSTTRAUMATIC STRESS DISORDER: ASSOCIATIONS WITH FKBP5. (2016)
• Direct Transcriptional Effects of Apolipoprotein E. (2016)
• Establishment of human iPSC-based models for the study and targeting of glioma initiating cells. (2016)
• Integrating basic research with prevention/intervention to reduce risky substance use among college students. (2015)
• Tools and best practices for data processing in allelic expression analysis. (2015)
• The National Birth Defects Prevention Study: A review of the methods. (2015)
• EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions. (2015)
• What is the DNA repair defect underlying Fanconi anemia? (2015)
• limma powers differential expression analyses for RNA-sequencing and microarray studies. (2015)
• Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data. (2015)
• Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
• ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
• Spatial reconstruction of single-cell gene expression data. (2015)
• Lead exposure induces changes in 5-hydroxymethylcytosine clusters in CpG islands in human embryonic stem cells and umbilical cord blood. (2015)
• ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide. (2015)
• Interparental Relationship Sensitivity Leads to Adolescent Internalizing Problems: Different Genotypes, Different Pathways. (2015)
• Epigenomics and the structure of the living genome. (2015)
• Droplet barcoding for single-cell transcriptomics applied to embryonic stem cells. (2015)
• Post-translational modifications of histones that influence nucleosome dynamics. (2015)
• Clinically relevant genetic biomarkers from the brain in alcoholism with representation on high resolution chromosome ideograms. (2015)
• A comprehensive view of the epigenetic landscape part I: DNA methylation, passive and active DNA demethylation pathways and histone variants. (2015)
• Orchestrating high-throughput genomic analysis with Bioconductor. (2015)
• Systematic pan-cancer analysis of tumour purity. (2015)
• RNA imaging. Spatially resolved, highly multiplexed RNA profiling in single cells. (2015)
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. (2015)
• Comprehensive genomic profiles of small cell lung cancer. (2015)
• MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
• Condensins are Required for Maintenance of Nuclear Architecture. (2014)
• Polymorphisms in ABC transporter genes and concentrations of mercury in newborns--evidence from two Mediterranean birth cohorts. (2014)
• Detecting ultralow-frequency mutations by Duplex Sequencing. (2014)
• RADIA: RNA and DNA integrated analysis for somatic mutation detection. (2014)
• MAGeCK enables robust identification of essential genes from genome-scale CRISPR/Cas9 knockout screens. (2014)
• The role of BAF (mSWI/SNF) complexes in mammalian neural development. (2014)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Fetal alcohol programming of hypothalamic proopiomelanocortin system by epigenetic mechanisms and later life vulnerability to stress. (2014)
• Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
• Clonal evolution in hematological malignancies and therapeutic implications. (2014)
• Fetal alcohol spectrum disorders and their transmission through genetic and epigenetic mechanisms. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
• Choline partially prevents the impact of ethanol on the lipid raft dependent functions of l1 cell adhesion molecule. (2014)
• PyClone: statistical inference of clonal population structure in cancer. (2014)
• Gestational choline supplementation normalized fetal alcohol-induced alterations in histone modifications, DNA methylation, and proopiomelanocortin (POMC) gene expression in β-endorphin-producing POMC neurons of the hypothalamus. (2013)
• RNA in unexpected places: long non-coding RNA functions in diverse cellular contexts. (2013)
• Alcohol modulates expression of DNA methyltranferases and methyl CpG-/CpG domain-binding proteins in murine embryonic fibroblasts. (2013)
• Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer. (2013)
• Cancer genome landscapes. (2013)
• THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data. (2013)
• Ewing sarcoma protein: a key player in human cancer. (2013)
• Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
• A simple consensus approach improves somatic mutation prediction accuracy. (2013)
• In utero alcohol exposure, epigenetic changes, and their consequences. (2013)
• Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome. (2013)
• Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
• Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition. (2013)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects. (2013)
• ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. (2013)
• Gene expression in the human brain: the current state of the study of specificity and spatiotemporal dynamics. (2013)
• Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
• Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
• Charting a dynamic DNA methylation landscape of the human genome. (2013)
• Coordinated cell type-specific epigenetic remodeling in prefrontal cortex begins before birth and continues into early adulthood. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• The Genomic Revolution and Beliefs about Essential Racial Differences: A Backdoor to Eugenics? (2013)
• Characterizing and measuring bias in sequence data. (2013)
• Alcohol exposure during development: Impact on the epigenome. (2013)
• ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. (2012)
• Absolute quantification of somatic DNA alterations in human cancer. (2012)
• An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. (2012)
• Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
• Early second trimester maternal plasma choline and betaine are related to measures of early cognitive development in term infants. (2012)
• Clustered mutations in yeast and in human cancers can arise from damaged long single-strand DNA regions. (2012)
• The future of DNA sequence archiving. (2012)
• Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (2012)
• A cross-sample statistical model for SNP detection in short-read sequencing data. (2012)
• Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. (2012)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
• Ultrasensitive detection of rare mutations using next-generation targeted resequencing. (2012)
• Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. (2012)
• The Pediatric Cancer Genome Project. (2012)
• Summarizing and correcting the GC content bias in high-throughput sequencing. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• Massive genomic rearrangement acquired in a single catastrophic event during cancer development. (2011)
• Association among SNAP-25 gene DdeI and MnlI polymorphisms and hemodynamic changes during methylphenidate use: a functional near-infrared spectroscopy study. (2011)
• Alcohol alters DNA methylation patterns and inhibits neural stem cell differentiation. (2011)
• BRCA1 and BRCA2: different roles in a common pathway of genome protection. (2011)
• Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications. (2011)
• Regulation of chromatin by histone modifications. (2011)
• Effects of ethanol and NAP on cerebellar expression of the neural cell adhesion molecule L1. (2011)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
• ViennaRNA Package 2.0. (2011)
• Focus on: epigenetics and fetal alcohol spectrum disorders. (2011)
• An integrated ChIP-seq analysis platform with customizable workflows. (2011)
• CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing. (2011)
• Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
• Molecular mechanisms of long noncoding RNAs. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• Allele-specific copy number analysis of tumors. (2010)
• Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
• Genetics of psychiatric disorders methods: molecular approaches. (2010)
• Temporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter. (2010)
• Molecular maps of the reorganization of genome-nuclear lamina interactions during differentiation. (2010)
• DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
• A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
• Histone methylation regulates memory formation. (2010)
• Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification. (2010)
• A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. (2010)
• The basics of brain development. (2010)
• Maternal folate-related gene environment interactions and congenital heart defects. (2010)
• Childhood maltreatment and telomere shortening: preliminary support for an effect of early stress on cellular aging. (2010)
• Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. (2010)
• Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
• The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants. (2010)
• Conserved role of intragenic DNA methylation in regulating alternative promoters. (2010)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. (2009)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
• A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
• High-resolution mapping of copy-number alterations with massively parallel sequencing. (2009)
• Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. (2009)
• Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. (2009)
• An exploration of attitudes among black Americans towards psychiatric genetic research. (2009)
• The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
• Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. (2009)
• Copy-number-variation and copy-number-alteration region detection by cumulative plots. (2009)
• Genome-wide association study of alcohol dependence. (2009)
• A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder. (2009)
• Computation for ChIP-seq and RNA-seq studies. (2009)
• QPCR: Application for real-time PCR data management and analysis. (2009)
• The relationship of 5HTT (SLC6A4) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption Studies. (2008)
• Alterations in ethyl alcohol pharmacokinetics during oral consumption of malt liquor beverages in African Americans. (2008)
• Adrenomedullin signaling is necessary for murine lymphatic vascular development. (2008)
• Chromatin immunoprecipitation (ChIP) coupled to detection by quantitative real-time PCR to study transcription factor binding to DNA in Caenorhabditis elegans. (2008)
• Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)
• Molecular specification and patterning of progenitor cells in the lateral and medial ganglionic eminences. (2008)
• Effect of in utero and early-life conditions on adult health and disease. (2008)
• Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. (2007)
• DNA methylation, insulin resistance, and blood pressure in offspring determined by maternal periconceptional B vitamin and methionine status. (2007)
• Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. (2006)
• Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)
• Population structure and eigenanalysis. (2006)
• Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome. (2006)
• Taverna: a tool for building and running workflows of services. (2006)
• Environmental programming of stress responses through DNA methylation: life at the interface between a dynamic environment and a fixed genome. (2005)
• Pituitary adenylate cyclase-activating polypeptide protects rat cerebellar granule neurons against ethanol-induced apoptotic cell death. (2002)
• Rapid Sex Determination Using PCR Technique Compared to Classic Cytogenetics - PMC

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