(Q37961876)

26 August 2017

Epigenetic discordance at imprinting control regions in twins (English)

1 reference

26 August 2017

Miina Ollikainen

1

1 reference

PubMed ID

22122339

26 August 2017

Jeffrey M Craig

series ordinal

2

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26 August 2017

1 June 2011

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26 August 2017

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26 August 2017

3

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26 August 2017

3

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26 August 2017

295-306

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Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

26 August 2017

1 reference

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

21 January 2018

1 reference

Failure to confirm CNVs as of aetiological significance in twin pairs discordant for schizophrenia.

21 January 2018

1 reference

Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance?

21 January 2018

1 reference

Intra-individual change over time in DNA methylation with familial clustering

21 January 2018

1 reference

Metabolic plasticity during mammalian development is directionally dependent on early nutritional status.

21 January 2018

1 reference

Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome

21 January 2018

1 reference

Diet-induced hypermethylation at agouti viable yellow is not inherited transgenerationally through the female.

21 January 2018

1 reference

Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension

21 January 2018

1 reference

Neonatal leptin treatment reverses developmental programming

21 January 2018

1 reference

Phenotypic plasticity and the epigenetics of human disease

21 January 2018

1 reference

Persistent epigenetic differences associated with prenatal exposure to famine in humans

21 January 2018

1 reference

Loss of imprinting of IGF2: a common epigenetic modifier of intestinal tumor risk

21 January 2018

1 reference

The epigenetic progenitor origin of human cancer

21 January 2018

1 reference

Epigenomics reveals a functional genome anatomy and a new approach to common disease

21 January 2018

1 reference

Epigenetics and human disease

21 January 2018

1 reference

Imprinting evolution and the price of silence.

21 January 2018

1 reference

A census of mammalian imprinting.

21 January 2018

1 reference

Transient neonatal diabetes, a disorder of imprinting.

21 January 2018

1 reference

Allele-specific expression of imprinted genes in mouse migratory primordial germ cells.

21 January 2018

1 reference

Timing of establishment of paternal methylation imprints in the mouse.

21 January 2018

1 reference

The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development.

21 January 2018

1 reference

Epigenetic modifications necessary for normal development are established during oocyte growth in mice.

21 January 2018

1 reference

Maternal primary imprinting is established at a specific time for each gene throughout oocyte growth

21 January 2018

1 reference

Dnmt3L and the establishment of maternal genomic imprints.

21 January 2018

1 reference

Role for DNA methylation in genomic imprinting

21 January 2018

1 reference

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

21 January 2018

1 reference

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

21 January 2018

1 reference

New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

21 January 2018

1 reference

Monozygotic twins discordant for the Russell-Silver syndrome

21 January 2018

1 reference

Monozygotic twins discordant for the Russell-Silver syndrome

21 January 2018

1 reference

Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR.

21 January 2018

1 reference

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

21 January 2018

1 reference

Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region.

21 January 2018

1 reference

Embryologic development and monozygotic twinning.

21 January 2018

1 reference

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

21 January 2018

1 reference

Variation, patterns, and temporal stability of DNA methylation: considerations for epigenetic epidemiology

21 January 2018

1 reference

DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome.

21 January 2018

1 reference

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

Transient neonatal diabetes mellitus type 1.

21 January 2018

1 reference

Imprinting errors and developmental asymmetry

21 January 2018

1 reference

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

21 January 2018

1 reference

A review of known imprinting syndromes and their association with assisted reproduction technologies.

21 January 2018

1 reference

Identical twins and in vitro fertilization

21 January 2018

1 reference

Assisted reproductive technologies and monozygous twins: implications for future study and clinical practice

21 January 2018

1 reference

Monozygotic twinning following assisted conception: an analysis of 81 consecutive cases

21 January 2018

1 reference

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

21 January 2018

1 reference

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

21 January 2018

1 reference

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

21 January 2018

1 reference

Beckwith-Wiedemann syndrome and IVF: a case-control study

21 January 2018

1 reference

Finding the fifth base: genome-wide sequencing of cytosine methylation.

21 January 2018

1 reference

Genome-wide DNA methylation profiling using Infinium® assay

21 January 2018

1 reference

Genome-wide identification of new imprinted genes.

21 January 2018

1 reference

Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes

21 January 2018

1 reference

Characterization of differentially methylated regions in 3 bovine imprinted genes: a model for studying human germ-cell and embryo development.

21 January 2018

1 reference

A longitudinal study of epigenetic variation in twins

21 January 2018

1 reference

Mechanisms regulating imprinted genes in clusters.

21 January 2018

1 reference

DNA methylation and human disease

21 January 2018

1 reference

Genomic imprinting, monozygous twinning, and X inactivation

21 January 2018

1 reference

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

21 January 2018

1 reference

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

21 January 2018

1 reference

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies

21 January 2018

1 reference

Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.2217/EPI.11.18

1 reference

26 August 2017

1 reference

PubMed ID

22122339