A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders

Epigenome-wide DNA methylation changes with development of arsenic-induced skin lesions in Bangladesh: A case-control follow-up study

(2014) Wei Jie Seow et al.   ENVIRONMENTAL AND MOLECULAR MUTAGENESIS

Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation

(2014) Jeannine Gerhardt et al.   JOURNAL OF CELL BIOLOGY

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

(2014) Louise E Docherty et al.   JOURNAL OF MEDICAL GENETICS

Epigenome-Wide Association Study for Parkinson’s Disease

(2014) Kerry Moore et al.   NEUROMOLECULAR MEDICINE

DNA hypermethylation of serotonin transporter gene promoter in drug naïve patients with schizophrenia

(2014) Hamid Mostafavi Abdolmaleky et al.   SCHIZOPHRENIA RESEARCH

Child Abuse and Epigenetic Mechanisms of Disease Risk

(2013) Bao-Zhu Yang et al.   AMERICAN JOURNAL OF PREVENTIVE MEDICINE

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

(2012) D. Wang et al.   BIOINFORMATICS

Epigenome-wide association study in the European Prospective Investigation into Cancer and Nutrition (EPIC-Turin) identifies novel genetic loci associated with smoking

(2012) Natalie S. Shenker et al.   HUMAN MOLECULAR GENETICS

Single-case research in neuropsychology: A comparison of five forms of t-test for comparing a case to controls

(2011) John R. Crawford et al.   CORTEX

Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder

(2011) Emma L. Dempster et al.   HUMAN MOLECULAR GENETICS

Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation

(2011) K. Gronskov et al.   JOURNAL OF MEDICAL GENETICS

Evaluation of the Infinium Methylation 450K technology

(2011) Sarah Dedeurwaerder et al.   Epigenomics

Russell-Silver syndrome

(2010) Thomas Eggermann   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Point and interval estimates of effect sizes for the case-controls design in neuropsychology: Rationale, methods, implementations, and proposed reporting standards

(2010) John R. Crawford et al.   COGNITIVE NEUROPSYCHOLOGY

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

(2009) Salah Azzi et al.   HUMAN MOLECULAR GENETICS

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

(2008) Jet Bliek et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

(2008) Deborah J G Mackay et al.   NATURE GENETICS

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

(2008) Marjolijn J L Ligtenberg et al.   NATURE GENETICS