Terkko Navigator / Clinical Epigenetics

Aberrant DNA hydroxymethylation reshapes transcription factor binding in myeloid neoplasms

Low reliability of DNA methylation across Illumina Infinium platforms in cord blood: implications for replication studies and meta-analyses of prenatal exposures

Mitochondrial DNA methylation profiling of the human prefrontal cortex and nucleus accumbens: correlations with aging and drug use

Maternal epigenetic clocks measured during pregnancy do not predict gestational age at delivery or offspring birth outcomes: a replication study in metropolitan Cebu, Philippines

Targeted genetic and epigenetic profiling of esophageal adenocarcinomas and non-dysplastic Barrett’s esophagus

Evaluation of short-term epigenetic age fluctuation

An epigenome-wide study of DNA methylation profiles and lung function among American Indians in the Strong Heart Study

Detection of ovarian cancer using plasma cell-free DNA methylomes

Cardiovascular health and four epigenetic clocks

Lifetime exposure to smoking, epigenetic aging, and morbidity and mortality in older adults

Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances

Cross talk between acetylation and methylation regulators reveals histone modifier expression patterns posing prognostic and therapeutic implications on patients with colon cancer

DNA methylation and expression profiles of placenta and umbilical cord blood reveal the characteristics of gestational diabetes mellitus patients and offspring

Genome-wide promoter methylation profiling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival

Correction to: Silencing or inhibition of H3K79 methyltransferase DOT1L induces cell cycle arrest by epigenetically modulating c-Myc expression in colorectal cancer

The mediating effect of DNA methylation in the association between maternal sleep during pregnancy and offspring adiposity status: a prospective cohort study

Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature

Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia

Folic acid intervention during pregnancy alters DNA methylation, affecting neural target genes through two distinct mechanisms

Characterising sex differences of autosomal DNA methylation in whole blood using the Illumina EPIC array

DNA methylation analysis of tumor suppressor genes in liquid biopsy components of early stage NSCLC: a promising tool for early detection

Androgen receptor reprogramming demarcates prognostic, context-dependent gene sets in primary and metastatic prostate cancer

Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis

Batch-effect detection, correction and characterisation in Illumina HumanMethylation450 and MethylationEPIC BeadChip array data

Epigenome-wide association study of bronchopulmonary dysplasia in preterm infants: results from the discovery-BPD program

Technical considerations in PCR-based assay design for diagnostic DNA methylation cancer biomarkers

Effects of stressful life-events on DNA methylation in panic disorder and major depressive disorder

Predicting male fertility from the sperm methylome: application to 120 bulls with hundreds of artificial insemination records

Epigenome-wide contributions to individual differences in childhood phenotypes: a GREML approach

Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B12

LINC00114 stimulates growth and glycolysis of esophageal cancer cells by recruiting EZH2 to enhance H3K27me3 of DLC1

DNA methylation regulates TIGIT expression within the melanoma microenvironment, is prognostic for overall survival, and predicts progression-free survival in patients treated with anti-PD-1 immunotherapy

Selective hypermethylation is evident in small intestine samples from infants with necrotizing enterocolitis

Epigenetics of early-life adversity in youth: cross-sectional and longitudinal associations

Regulation of oxytocin receptor gene expression in obsessive–compulsive disorder: a possible role for the microbiota-host epigenetic axis

Integrative analysis of DNA methylation and gene expression reveals key molecular signatures in acute myocardial infarction

Ethical implications of epigenetics in the era of personalized medicine

Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny

Multi-omic alterations of the SWI/SNF complex define a clinical subgroup in lung adenocarcinoma

Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences

Increases in ambient air pollutants during pregnancy are linked to increases in methylation of IL4, IL10, and IFNγ

Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes

Chromatin accessibility and transcriptome integrative analysis revealed AP-1-mediated genes potentially modulate histopathology features in psoriasis

SEEMLIS: a flexible semi-automated method for enrichment of methylated DNA from low-input samples

Correction to: ZMYND10, an epigenetically regulated tumor suppressor, exerts tumor-suppressive functions via miR145-5p/NEDD9 axis in breast cancer

Data mining of bulk and single-cell RNA sequencing introduces OBI1-AS1 as an astrocyte marker with possible role in glioma recurrence and progression

Roles for the methyltransferase SETD8 in DNA damage repair

Methyl-qPCR: a new method to investigate Epstein–Barr virus infection in post-transplant lymphoproliferative diseases

Atheroprotective mechanism by which folic acid regulates monocyte subsets and function through DNA methylation

Cell-type heterogeneity: Why we should adjust for it in epigenome and biomarker studies