Epigenome-wide association study identifies Behçet’s disease-associated methylation loci in Han Chinese

Gender differences of B cell signature related to estrogen-induced IFI44L/BAFF in systemic lupus erythematosus

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Epigenome-wide analysis links SMAD3 methylation at birth to asthma in children of asthmatic mothers

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Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet's disease in Han Chinese

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Ocular Behcet’s disease is associated with aberrant methylation of interferon regulatory factor 8 (IRF8) in monocyte-derived dendritic cells

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Reduced DNA methylation and psychopathology following endogenous hypercortisolism – a genome-wide study

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Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in TP53-Associated Cancer Susceptibility

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Epigenome-wide association study of triglyceride postprandial responses to a high-fat dietary challenge

(2016) Chao-Qiang Lai et al.   JOURNAL OF LIPID RESEARCH

Quantitative comparison of DNA methylation assays for biomarker development and clinical applications

(2016) Christoph Bock et al.   NATURE BIOTECHNOLOGY

Increased DNA methylation variability in type 1 diabetes across three immune effector cell types

(2016) Dirk S. Paul et al.   Nature Communications

Genome-wide epigenomic profiling for biomarker discovery

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Epigenome-wide association data implicates DNA methylation-mediated genetic risk in psoriasis

(2016) Fusheng Zhou et al.   Clinical Epigenetics

FASGene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese

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FKBP5 Genotype-Dependent DNA Methylation and mRNA Regulation After Psychosocial Stress in Remitted Depression and Healthy Controls

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Genome-wide DNA methylation analysis in dermal fibroblasts from patients with diffuse and limited systemic sclerosis reveals common and subset-specific DNA methylation aberrancies

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Accounting for Population Stratification in DNA Methylation Studies

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Predisposition to Behçet’s disease and VKH syndrome by genetic variants of miR-182

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Child Abuse, Depression, and Methylation in Genes Involved With Stress, Neural Plasticity, and Brain Circuitry

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Epigenome-Wide Scan Identifies a Treatment-Responsive Pattern of Altered DNA Methylation Among Cytoskeletal Remodeling Genes in Monocytes and CD4+ T Cells From Patients With Behçet's Disease

(2014) Travis Hughes et al.   Arthritis & Rheumatology

Genome-Wide DNA Methylation Study Identifies Significant Epigenomic Changes in Osteoarthritic Cartilage

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DNA hypermethylation and DNA hypomethylation is present at different loci in chronic kidney disease

(2013) Laura J Smyth et al.   Epigenetics

Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis

(2013) Yun Liu et al.   NATURE BIOTECHNOLOGY

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

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TH17 Cell Differentiation Is Regulated by the Circadian Clock

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Polymorphisms in ESR1 and FLJ43663 are associated with breast cancer risk in the Han population

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MicroRNA-146aandEts-1gene polymorphisms in ocular Behçet's disease and Vogt–Koyanagi–Harada syndrome

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Identification of a susceptibility locus inSTAT4for Behçet's disease in Han Chinese in a genome-wide association study

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IMA: an R package for high-throughput analysis of Illumina's 450K Infinium methylation data

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Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease

(2012) Luke Jostins et al.   NATURE

SWAN: Subset-quantile Within Array Normalization for Illumina Infinium HumanMethylation450 BeadChips

(2012) Jovana Maksimovic et al.   GENOME BIOLOGY

NFIL3/E4BP4 controls type 2 T helper cell cytokine expression

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E4BP4: an unexpected player in the immune response

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Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

(2010) Nobuhisa Mizuki et al.   NATURE GENETICS

Genome-wide association study identifies variants in the MHC class I, IL10 and IL23R-IL12RB2 regions associated with Behçet's disease

(2010) Elaine F Remmers et al.   NATURE GENETICS

Rapidly denoising pyrosequencing amplicon reads by exploiting rank-abundance distributions

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Association of FKBP5 Polymorphisms and Childhood Abuse With Risk of Posttraumatic Stress Disorder Symptoms in Adults

(2008) Elisabeth B. Binder   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION