Published in Epigenetics Chromatin on March 03, 2013
Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays. Bioinformatics (2014) 5.93
DNA Methylation and Somatic Mutations Converge on the Cell Cycle and Define Similar Evolutionary Histories in Brain Tumors. Cancer Cell (2015) 1.87
The human placenta methylome. Proc Natl Acad Sci U S A (2013) 1.86
Abnormalities in human pluripotent cells due to reprogramming mechanisms. Nature (2014) 1.81
A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies. Genome Biol (2015) 1.71
Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci. Nat Neurosci (2015) 1.60
A comprehensive overview of Infinium HumanMethylation450 data processing. Brief Bioinform (2013) 1.49
DUSP4 deficiency caused by promoter hypermethylation drives JNK signaling and tumor cell survival in diffuse large B cell lymphoma. J Exp Med (2015) 1.48
Methylomic trajectories across human fetal brain development. Genome Res (2015) 1.35
The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes. Genome Res (2014) 1.29
Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia. Mol Hum Reprod (2013) 1.25
The transcriptional landscape of age in human peripheral blood. Nat Commun (2015) 1.20
Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biol (2014) 1.20
Prenatal exposure to maternal cigarette smoking and DNA methylation: epigenome-wide association in a discovery sample of adolescents and replication in an independent cohort at birth through 17 years of age. Environ Health Perspect (2014) 1.17
Reducing the risk of false discovery enabling identification of biologically significant genome-wide methylation status using the HumanMethylation450 array. BMC Genomics (2014) 1.16
Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation. Hum Mol Genet (2014) 1.15
Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Res (2014) 1.13
Statistical methods for detecting differentially methylated loci and regions. Front Genet (2014) 1.06
Analysis pipelines and packages for Infinium HumanMethylation450 BeadChip (450k) data. Methods (2014) 1.03
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation. Genome Biol (2016) 1.02
Concordant and discordant DNA methylation signatures of aging in human blood and brain. Epigenetics Chromatin (2015) 1.01
Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in Down syndrome. BMC Med Genomics (2013) 1.01
Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes. Epigenetics (2015) 1.00
Lifetime stress accelerates epigenetic aging in an urban, African American cohort: relevance of glucocorticoid signaling. Genome Biol (2015) 0.96
5-hydroxymethylcytosine marks promoters in colon that resist DNA hypermethylation in cancer. Genome Biol (2015) 0.93
Leishmania donovani infection causes distinct epigenetic DNA methylation changes in host macrophages. PLoS Pathog (2014) 0.92
Nucleated red blood cells impact DNA methylation and expression analyses of cord blood hematopoietic cells. Clin Epigenetics (2015) 0.90
Short-term diesel exhaust inhalation in a controlled human crossover study is associated with changes in DNA methylation of circulating mononuclear cells in asthmatics. Part Fibre Toxicol (2014) 0.90
Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta. PLoS One (2013) 0.90
Characterization of whole-genome autosomal differences of DNA methylation between men and women. Epigenetics Chromatin (2015) 0.90
Meta-analysis of human methylomes reveals stably methylated sequences surrounding CpG islands associated with high gene expression. Epigenetics Chromatin (2014) 0.89
Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis. PLoS One (2015) 0.89
Adiposity is associated with DNA methylation profile in adipose tissue. Int J Epidemiol (2014) 0.88
A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data. Aging (Albany NY) (2015) 0.88
Epigenetic signatures of alcohol abuse and hepatitis infection during human hepatocarcinogenesis. Oncotarget (2014) 0.87
Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains. Hum Mol Genet (2013) 0.87
Pervasive polymorphic imprinted methylation in the human placenta. Genome Res (2016) 0.86
Base resolution methylome profiling: considerations in platform selection, data preprocessing and analysis. Epigenomics (2015) 0.86
Dietary flavanols modulate the transcription of genes associated with cardiovascular pathology without changes in their DNA methylation state. PLoS One (2014) 0.85
Whole genome DNA methylation signature of HER2-positive breast cancer. Epigenetics (2014) 0.83
Epigenetic profiling of ADHD symptoms trajectories: a prospective, methylome-wide study. Mol Psychiatry (2016) 0.83
Current and Future Prospects for Epigenetic Biomarkers of Substance Use Disorders. Genes (Basel) (2015) 0.83
A CpG-methylation-based assay to predict survival in clear cell renal cell carcinoma. Nat Commun (2015) 0.83
Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects. Clin Epigenetics (2016) 0.83
Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents. Eur J Hum Genet (2014) 0.82
Epigenome-wide and transcriptome-wide analyses reveal gestational diabetes is associated with alterations in the human leukocyte antigen complex. Clin Epigenetics (2015) 0.82
Body mass index associated with genome-wide methylation in breast tissue. Breast Cancer Res Treat (2015) 0.81
An evaluation of statistical methods for DNA methylation microarray data analysis. BMC Bioinformatics (2015) 0.81
DNA methylation signature of human fetal alcohol spectrum disorder. Epigenetics Chromatin (2016) 0.80
Comparison of Methyl-capture Sequencing vs. Infinium 450K methylation array for methylome analysis in clinical samples. Epigenetics (2016) 0.80
Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies. BMC Genomics (2015) 0.80
DNA Methylation Profiling in Inflammatory Bowel Disease Provides New Insights into Disease Pathogenesis. J Crohns Colitis (2015) 0.80
The epigenomic landscape of African rainforest hunter-gatherers and farmers. Nat Commun (2015) 0.80
Statistical challenges in analyzing methylation and long-range chromosomal interaction data. Stat Biosci (2016) 0.79
DaVIE: Database for the Visualization and Integration of Epigenetic data. Front Genet (2014) 0.79
Current advances in systems and integrative biology. Comput Struct Biotechnol J (2014) 0.79
Improved reporting of DNA methylation data derived from studies of the human placenta. Epigenetics (2014) 0.79
Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions. Hum Mol Genet (2016) 0.78
Racial differences in genome-wide methylation profiling and gene expression in breast tissues from healthy women. Epigenetics (2015) 0.78
Epigenetic silencing of neurofilament genes promotes an aggressive phenotype in breast cancer. Epigenetics (2015) 0.78
Methylomic markers of persistent childhood asthma: a longitudinal study of asthma-discordant monozygotic twins. Clin Epigenetics (2015) 0.78
The interplay between the lysine demethylase KDM1A and DNA methyltransferases in cancer cells is cell cycle dependent. Oncotarget (2016) 0.77
DNA methylation levels are highly correlated between pooled samples and averaged values when analysed using the Infinium HumanMethylation450 BeadChip array. Clin Epigenetics (2015) 0.77
CpGFilter: model-based CpG probe filtering with replicates for epigenome-wide association studies. Bioinformatics (2015) 0.77
Genome-wide DNA methylation detection by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison. Sci Rep (2015) 0.77
Profiling placental and fetal DNA methylation in human neural tube defects. Epigenetics Chromatin (2016) 0.77
Shared genetic control of expression and methylation in peripheral blood. BMC Genomics (2016) 0.77
Methylomic analysis of monozygotic twins discordant for childhood psychotic symptoms. Epigenetics (2015) 0.77
DMRforPairs: identifying differentially methylated regions between unique samples using array based methylation profiles. BMC Bioinformatics (2014) 0.77
Global hypermethylation in fetal cortex of Down syndrome due to DNMT3L overexpression. Hum Mol Genet (2016) 0.77
Widespread DNA hypomethylation and differential gene expression in Turner syndrome. Sci Rep (2016) 0.76
Comparative methylome analysis identifies new tumour subtypes and biomarkers for transformation of nephrogenic rests into Wilms tumour. Genome Med (2015) 0.76
Mapping epigenetic changes to the host cell genome induced by Burkholderia pseudomallei reveals pathogen-specific and pathogen-generic signatures of infection. Sci Rep (2016) 0.76
Genome-wide methylation profiling of ovarian cancer patient-derived xenografts treated with the demethylating agent decitabine identifies novel epigenetically regulated genes and pathways. Genome Med (2016) 0.76
DNA methylation and substance-use risk: a prospective, genome-wide study spanning gestation to adolescence. Transl Psychiatry (2016) 0.76
Genome-scale methylation assessment did not identify prognostic biomarkers in oral tongue carcinomas. Clin Epigenetics (2016) 0.76
The defining DNA methylation signature of Floating-Harbor Syndrome. Sci Rep (2016) 0.76
A targeted analysis reveals relevant shifts in the methylation and transcription of genes responsible for bile acid homeostasis and drug metabolism in non-alcoholic fatty liver disease. BMC Genomics (2016) 0.76
DNA methylation levels and long-term trihalomethane exposure in drinking water: an epigenome-wide association study. Epigenetics (2015) 0.76
One-night sleep deprivation induces changes in the DNA methylation and serum activity indices of stearoyl-CoA desaturase in young healthy men. Lipids Health Dis (2016) 0.76
Potential roles of DNA methylation in the initiation and establishment of replicative senescence revealed by array-based methylome and transcriptome analyses. PLoS One (2017) 0.75
Methylome analysis of extreme chemoresponsive patients identifies novel markers of platinum sensitivity in high-grade serous ovarian cancer. BMC Med (2017) 0.75
RAB25 expression is epigenetically downregulated in oral and oropharyngeal squamous cell carcinoma with lymph node metastasis. Epigenetics (2016) 0.75
Familial resemblances in blood leukocyte DNA methylation levels. Epigenetics (2016) 0.75
"Gap hunting" to characterize clustered probe signals in Illumina methylation array data. Epigenetics Chromatin (2016) 0.75
Epigenetic signatures of internal migration in Italy. Int J Epidemiol (2014) 0.75
Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease. Clin Epigenetics (2017) 0.75
Infinium monkeys: Infinium 450K array for the Cynomolgus macaque (Macaca fascicularis). G3 (Bethesda) (2014) 0.75
Comprehensive characterization, annotation and innovative use of Infinium DNA methylation BeadChip probes. Nucleic Acids Res (2016) 0.75
Methylomic changes during conversion to psychosis. Mol Psychiatry (2016) 0.75
Epigenomics of Total Acute Sleep Deprivation in Relation to Genome-Wide DNA Methylation Profiles and RNA Expression. OMICS (2016) 0.75
Risk of re-identification of epigenetic methylation data: a more nuanced response is needed. Clin Epigenetics (2015) 0.75
Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study. Br J Cancer (2016) 0.75
Mutant IDH1 expression is associated with down-regulation of monocarboxylate transporters. Oncotarget (2016) 0.75
Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome. BMC Med (2017) 0.75
Periconceptional folate consumption is associated with neonatal DNA methylation modifications in neural crest regulatory and cancer development genes. Epigenetics (2015) 0.75
Genetic-epigenetic interactions in cis: a major focus in the post-GWAS era. Genome Biol (2017) 0.75
DNA methylation analysis of paediatric low-grade astrocytomas identifies a tumour-specific hypomethylation signature in pilocytic astrocytomas. Acta Neuropathol Commun (2016) 0.75
Lists of HumanMethylation450 BeadChip probes with nucleotide-variant information obtained from the Phase 3 data of the 1000 Genomes Project. Genom Data (2015) 0.75
Longitudinal genome-wide methylation study of Roux-en-Y gastric bypass patients reveals novel CpG sites associated with essential hypertension. BMC Med Genomics (2016) 0.75
BLAT--the BLAST-like alignment tool. Genome Res (2002) 126.78
The UCSC Table Browser data retrieval tool. Nucleic Acids Res (2004) 25.12
CpG islands in vertebrate genomes. J Mol Biol (1987) 23.16
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet (2007) 20.22
The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores. Nat Genet (2009) 18.90
DNA methylation profiling of human chromosomes 6, 20 and 22. Nat Genet (2006) 18.08
lumi: a pipeline for processing Illumina microarray. Bioinformatics (2008) 17.19
Principles and challenges of genomewide DNA methylation analysis. Nat Rev Genet (2010) 10.71
A genome-wide analysis of CpG dinucleotides in the human genome distinguishes two distinct classes of promoters. Proc Natl Acad Sci U S A (2006) 10.63
Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts. Nat Genet (2009) 10.54
Increased methylation variation in epigenetic domains across cancer types. Nat Genet (2011) 8.92
Epigenome-wide association studies for common human diseases. Nat Rev Genet (2011) 7.96
Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis. BMC Bioinformatics (2010) 7.78
Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome. Epigenetics (2011) 7.38
Genome-wide methylation profiles reveal quantitative views of human aging rates. Mol Cell (2012) 6.50
DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol (2011) 6.48
A unique regulatory phase of DNA methylation in the early mammalian embryo. Nature (2012) 6.34
Comprehensive methylome map of lineage commitment from haematopoietic progenitors. Nature (2010) 6.06
Rapid DNA methylation changes after exposure to traffic particles. Am J Respir Crit Care Med (2009) 5.20
SWAN: Subset-quantile within array normalization for illumina infinium HumanMethylation450 BeadChips. Genome Biol (2012) 4.99
Evaluation of the Infinium Methylation 450K technology. Epigenomics (2011) 4.90
Genetic control of individual differences in gene-specific methylation in human brain. Am J Hum Genet (2010) 3.91
A re-annotation pipeline for Illumina BeadArrays: improving the interpretation of gene expression data. Nucleic Acids Res (2009) 3.50
Factors underlying variable DNA methylation in a human community cohort. Proc Natl Acad Sci U S A (2012) 3.20
Large-scale human promoter mapping using CpG islands. Nat Genet (2000) 3.02
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder. Hum Mol Genet (2011) 2.99
Dependence of transcriptional repression on CpG methylation density. Mol Cell Biol (1994) 2.97
DNA methylation of the first exon is tightly linked to transcriptional silencing. PLoS One (2011) 2.80
Global DNA hypomethylation is associated with high serum-persistent organic pollutants in Greenlandic Inuit. Environ Health Perspect (2008) 2.29
Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray. Genomics (2011) 2.19
An evaluation of new criteria for CpG islands in the human genome as gene markers. Bioinformatics (2004) 2.19
On the presence and role of human gene-body DNA methylation. Oncotarget (2012) 2.10
Population-specificity of human DNA methylation. Genome Biol (2012) 2.04
Prospects for epigenetic epidemiology. Am J Epidemiol (2009) 2.00
Commentary: The seven plagues of epigenetic epidemiology. Int J Epidemiol (2012) 1.88
Effect of polymorphisms within probe-target sequences on olignonucleotide microarray experiments. Nucleic Acids Res (2008) 1.80
Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation. Hum Genet (2011) 1.60
DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia. Eur J Hum Genet (2010) 1.55
Guthrie card methylomics identifies temporally stable epialleles that are present at birth in humans. Genome Res (2012) 1.45
On the analysis of the illumina 450k array data: probes ambiguously mapped to the human genome. Front Genet (2012) 1.33
Report on the Infinium 450k methylation array analysis workshop: April 20, 2012 UCL, London, UK. Epigenetics (2012) 1.10
Illuminating potential technical artifacts of DNA-methylation array probes. Am J Hum Genet (2012) 1.00
Genome-wide sperm deoxyribonucleic acid methylation is altered in some men with abnormal chromatin packaging or poor in vitro fertilization embryogenesis. Fertil Steril (2011) 0.92
A comprehensive analysis of common copy-number variations in the human genome. Am J Hum Genet (2006) 8.61
The functional role of long non-coding RNA in human carcinomas. Mol Cancer (2011) 6.37
RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approach. Mol Cell Biol (2002) 5.04
Low early-life social class leaves a biological residue manifested by decreased glucocorticoid and increased proinflammatory signaling. Proc Natl Acad Sci U S A (2009) 4.11
Transcriptional control in the segmentation gene network of Drosophila. PLoS Biol (2004) 3.47
Factors underlying variable DNA methylation in a human community cohort. Proc Natl Acad Sci U S A (2012) 3.20
Linking cell cycle to histone modifications: SBF and H2B monoubiquitination machinery and cell-cycle regulation of H3K79 dimethylation. Mol Cell (2009) 2.91
DNA methylation in ES cells requires the lysine methyltransferase G9a but not its catalytic activity. EMBO J (2008) 2.81
Silencing of the mammalian X chromosome. Annu Rev Genomics Hum Genet (2005) 2.47
Human cancer long non-coding RNA transcriptomes. PLoS One (2011) 2.38
Different measures of "genome-wide" DNA methylation exhibit unique properties in placental and somatic tissues. Epigenetics (2012) 2.17
Epigenetic vestiges of early developmental adversity: childhood stress exposure and DNA methylation in adolescence. Child Dev (2011) 2.07
Validation of a genomic classifier that predicts metastasis following radical prostatectomy in an at risk patient population. J Urol (2013) 2.07
The specificity and topology of chromatin interaction pathways in yeast. Mol Cell (2011) 2.04
Population-specificity of human DNA methylation. Genome Biol (2012) 2.04
The human placenta methylome. Proc Natl Acad Sci U S A (2013) 1.86
Social stress up-regulates inflammatory gene expression in the leukocyte transcriptome via β-adrenergic induction of myelopoiesis. Proc Natl Acad Sci U S A (2013) 1.81
Translating dosage compensation to trisomy 21. Nature (2013) 1.75
R-loop-mediated genome instability in mRNA cleavage and polyadenylation mutants. Genes Dev (2012) 1.69
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. Hum Genet (2005) 1.67
Slx4 regulates DNA damage checkpoint-dependent phosphorylation of the BRCT domain protein Rtt107/Esc4. Mol Biol Cell (2005) 1.66
Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation. Hum Genet (2011) 1.60
Channel interaction in cochlear implant users evaluated using the electrically evoked compound action potential. Audiol Neurootol (2004) 1.58
DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia. Eur J Hum Genet (2010) 1.55
YEATS domain proteins: a diverse family with many links to chromatin modification and transcription. Biochem Cell Biol (2009) 1.44
Epigenomics: mapping the methylome. Cell Cycle (2006) 1.42
Genome-wide mapping of boundary element-associated factor (BEAF) binding sites in Drosophila melanogaster links BEAF to transcription. Mol Cell Biol (2009) 1.40
Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors. BMC Genomics (2011) 1.39
Fertility and aging: do reproductive-aged Canadian women know what they need to know? Fertil Steril (2009) 1.36
Mechanisms of X-chromosome inactivation. Front Biosci (2006) 1.34
Dot1 and histone H3K79 methylation in natural telomeric and HM silencing. Mol Cell (2011) 1.32
Splitting the task: Ubp8 and Ubp10 deubiquitinate different cellular pools of H2BK123. Genes Dev (2011) 1.30
Widespread DNA hypomethylation at gene enhancer regions in placentas associated with early-onset pre-eclampsia. Mol Hum Reprod (2013) 1.25
Inactive X chromosome-specific reduction in placental DNA methylation. Hum Mol Genet (2009) 1.22
Targeting of EZH2 to a defined genomic site is sufficient for recruitment of Dnmt3a but not de novo DNA methylation. Epigenetics (2009) 1.22
Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Birth Defects Res A Clin Mol Teratol (2005) 1.21
Roles for H2A.Z and its acetylation in GAL1 transcription and gene induction, but not GAL1-transcriptional memory. PLoS Biol (2010) 1.20
MECP2 promoter methylation and X chromosome inactivation in autism. Autism Res (2008) 1.19
Internal auditory canal morphology in children with cochlear nerve deficiency. Otol Neurotol (2006) 1.19
The clinical application of potentials evoked from the peripheral auditory system. Hear Res (2008) 1.18
NuA4 and SWR1-C: two chromatin-modifying complexes with overlapping functions and components. Biochem Cell Biol (2009) 1.18
Epigenetics of cancer progression. Pharmacogenomics (2008) 1.18
DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF. Hum Reprod (2012) 1.16
Decreased fibronectin production significantly contributes to dysregulated repair of asthmatic epithelium. Am J Respir Crit Care Med (2010) 1.14
Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes. PLoS One (2009) 1.14
Characterization of expression at the human XIST locus in somatic, embryonal carcinoma, and transgenic cell lines. Genomics (2003) 1.14
The brain-specific microRNA miR-128b regulates the formation of fear-extinction memory. Nat Neurosci (2011) 1.13
Extensive epigenetic reprogramming in human somatic tissues between fetus and adult. Epigenetics Chromatin (2011) 1.13
A cross-species comparison of X-chromosome inactivation in Eutheria. Genomics (2007) 1.11
Relationship of preoperative findings and ossicular discontinuity in chronic otitis media. Otol Neurotol (2003) 1.11
Inducible XIST-dependent X-chromosome inactivation in human somatic cells is reversible. Proc Natl Acad Sci U S A (2007) 1.09
Electrical suppression of tinnitus with high-rate pulse trains. Otol Neurotol (2003) 1.07
Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies. Epigenetics Chromatin (2011) 1.07
Epigenetic mechanisms mediating vulnerability and resilience to psychiatric disorders. Neurosci Biobehav Rev (2011) 1.06
Auditory neuropathy characteristics in children with cochlear nerve deficiency. Ear Hear (2006) 1.05
Asf1-like structure of the conserved Yaf9 YEATS domain and role in H2A.Z deposition and acetylation. Proc Natl Acad Sci U S A (2009) 1.05
Methylated DNA immunoprecipitation. J Vis Exp (2009) 1.04
DNA methylation profiles of airway epithelial cells and PBMCs from healthy, atopic and asthmatic children. PLoS One (2012) 1.04
X-chromosome inactivation: molecular mechanisms from the human perspective. Hum Genet (2011) 1.03
Threshold prediction using the auditory steady-state response and the tone burst auditory brain stem response: a within-subject comparison. Ear Hear (2005) 1.01
A skewed view of X chromosome inactivation. J Clin Invest (2008) 1.01
NMR structure of the amino-terminal domain from the Tfb1 subunit of TFIIH and characterization of its phosphoinositide and VP16 binding sites. Biochemistry (2005) 1.01
Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in Down syndrome. BMC Med Genomics (2013) 1.01
DNA methylation, genotype and gene expression: who is driving and who is along for the ride? Genome Biol (2013) 1.00
Telomere length and reproductive aging. Hum Reprod (2009) 1.00
Chromosome driven spatial patterning of proteins in bacteria. PLoS Comput Biol (2010) 1.00
Comparison of auditory steady-state response and auditory brainstem response thresholds in children. J Am Acad Audiol (2002) 1.00
Histone H3 lysine 36 methylation targets the Isw1b remodeling complex to chromatin. Mol Cell Biol (2012) 1.00
Outcome of cochlear implantation in pediatric auditory neuropathy. Otol Neurotol (2002) 1.00
Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome. Genome Biol (2013) 0.99
Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay. Eur J Hum Genet (2002) 0.98
Cochlear implantation for children with GJB2-related deafness. Laryngoscope (2004) 0.97
Correlation between sequence hydrophobicity and surface-exposure pattern of database proteins. Protein Sci (2004) 0.96
p300/CBP-associated factor selectively regulates the extinction of conditioned fear. J Neurosci (2012) 0.94
Interaction of Fcp1 phosphatase with elongating RNA polymerase II holoenzyme, enzymatic mechanism of action, and genetic interaction with elongator. J Biol Chem (2004) 0.94
Action and outcome activity state patterns in the anterior cingulate cortex. Cereb Cortex (2012) 0.93
Hypomethylation of the LEP gene in placenta and elevated maternal leptin concentration in early onset pre-eclampsia. Mol Cell Endocrinol (2012) 0.93
Reading chromatin: insights from yeast into YEATS domain structure and function. Epigenetics (2010) 0.92
Loss of H3 K79 trimethylation leads to suppression of Rtt107-dependent DNA damage sensitivity through the translesion synthesis pathway. J Biol Chem (2010) 0.92
Speech perception using maps based on neural response telemetry measures. Ear Hear (2002) 0.92
How the epigenome contributes to the development of psychiatric disorders. Dev Psychobiol (2010) 0.92
Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation. Hum Genet (2002) 0.92
Histone H3K4 demethylation is negatively regulated by histone H3 acetylation in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A (2012) 0.92
Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expression. Bioessays (2014) 0.91