Frequency and characterization of DNA methylation defects in children born SGA

Association of genomic instability and the methylation status of imprinted genes and mismatch-repair genes, with neural tube defects

(2012) Zhuo Liu et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples

(2012) Christel Eckmann-Scholz et al.   PLoS One

Systematic cross-validation of 454 sequencing and pyrosequencing for the exact quantification of DNA methylation patterns with single CpG resolution

(2011) Anna Potapova et al.   BMC BIOTECHNOLOGY

Structural and Regulatory Characterization of the Placental Epigenome at Its Maternal Interface

(2011) Tianjiao Chu et al.   PLoS One

Impact of the Genome on the Epigenome Is Manifested in DNA Methylation Patterns of Imprinted Regions in Monozygotic and Dizygotic Twins

(2011) Marcel W. Coolen et al.   PLoS One

Investigation of 90 patients referred for molecular cytogenetic analysis using aCGH uncovers previously unsuspected anomalies of imprinting

(2010) Rebecca L. Poole et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prader-Willi syndrome and Angelman syndrome

(2010) Karin Buiting   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Beckwith-Wiedemann syndrome

(2010) Sanaa Choufani et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

(2010) M Begemann et al.   CLINICAL GENETICS

Epigenetic modulation of theIGF2/H19imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction

(2010) Silvia Tabano et al.   Epigenetics

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci

(2010) Claire Louise Susan Turner et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia

(2010) D.K. Bourque et al.   PLACENTA

Inter- and Intra-Individual Variation in Allele-Specific DNA Methylation and Gene Expression in Children Conceived using Assisted Reproductive Technology

(2010) Nahid Turan et al.   PLoS Genetics

Hunting for the 5th base: Techniques for analyzing DNA methylation

(2009) Ole Ammerpohl et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Segmental maternal UPD(7q) in Silver-Russell syndrome

(2009) T Eggermann et al.   CLINICAL GENETICS

Continuous growth reference from 24thweek of gestation to 24 months by gender

(2008) Aimon Niklasson et al.   BMC Pediatrics

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae

(2008) Lin Guo et al.   DEVELOPMENTAL BIOLOGY

Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster

(2008) Karin Buiting et al.   HUMAN MUTATION

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

(2008) Masayo Kagami et al.   NATURE GENETICS