Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence (Q36130833)

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English	Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence	scientific article

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scholarly article

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Europe PubMed Central

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12 August 2017

Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence (English)

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Europe PubMed Central

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12 August 2017

DNA methylation

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Peter M. Visscher

13

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12 August 2017

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Jihoon E Joo

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Joseph E. Powell

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Joseph E Powell

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Jeffrey M Craig

14

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Miina Ollikainen

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Miina Ollikainen

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Richard Saffery

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object named as

Richard Saffery

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Lavinia Gordon

1

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Boris Novakovic

5

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12 August 2017

Xin Li

6

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12 August 2017

Roberta Andronikos

7

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12 August 2017

Mark N Cruickshank

8

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12 August 2017

Karen N Conneely

9

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12 August 2017

Alicia K Smith

10

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Reid S Alisch

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Ruth Morley

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publication date

16 July 2012

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Genome Research

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22

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8

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1395-1406

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12 August 2017

describes a project that uses

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22 June 2022

https://europepmc.org/article/PMC/3409253

based on heuristic

inferred from PubMed Central ID database lookup

A conceptual framework for the developmental origins of health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3409253

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Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3409253

2 October 2017

Genome-wide DNA methylation profiling using Infinium® assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3409253

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Identification of type 1 diabetes-associated DNA methylation variable positions that precede disease diagnosis.

1 reference

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Extensive variation and low heritability of DNA methylation identified in a twin study

1 reference

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Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation.

1 reference

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Commentary: Why are children in the same family so different? Non-shared environment three decades later

1 reference

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Epigenetic predictor of age

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Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome

1 reference

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Expression discordance of monozygotic twins at birth: effect of intrauterine environment and a possible mechanism for fetal programming

1 reference

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Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis

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Acute physical activity effects on cardiac gene expression

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Epigenomic disruption: the effects of early developmental exposures

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A longitudinal study of epigenetic variation in twins

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Cellular heterogeneity: do differences make a difference?

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Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome

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Allelic skewing of DNA methylation is widespread across the genome

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Evolution in health and medicine Sackler colloquium: Stochastic epigenetic variation as a driving force of development, evolutionary adaptation, and disease

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DNA methylation-mediated down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta

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Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosus

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Non-imprinted allele-specific DNA methylation on human autosomes.

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Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts

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The relationship of DNA methylation with age, gender and genotype in twins and healthy controls

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DNA methylation profiles in monozygotic and dizygotic twins.

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The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores

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Prospects for epigenetic epidemiology

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2 October 2017

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2 October 2017

Epigenetic mechanisms in the context of complex diseases

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2 October 2017

Environmental effects on gene expression phenotype have regional biases in the human genome

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2 October 2017

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2 October 2017

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2 October 2017

Epigenetic differences arise during the lifetime of monozygotic twins

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Studies of twins: what can they tell us about the fetal origins of adult disease?

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2 October 2017

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2 October 2017

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2 July 2018

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23 September 2018

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

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Aberrant DNA methylation associated with bipolar disorder identified from discordant monozygotic twins

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Power of the Classical Twin Design Revisited

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Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation

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Is the similarity of monozygotic twins due to genetic factors alone?

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based on heuristic

inferred from PubMed ID database lookup

Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/22800725

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1101/GR.136598.111

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

ResearchGate publication ID

0 references

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