(Q34014319)

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Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology

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scholarly article

1 reference

Europe PubMed Central

30 July 2017

Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology (English)

1 reference

Europe PubMed Central

30 July 2017

DNA methylation

0 references

author name string

Nahid Turan

1

1 reference

Europe PubMed Central

30 July 2017

Sunita Katari

2

1 reference

Europe PubMed Central

30 July 2017

Leigh F Gerson

3

1 reference

Europe PubMed Central

30 July 2017

Raffi Chalian

4

1 reference

Europe PubMed Central

30 July 2017

Michael W Foster

5

1 reference

Europe PubMed Central

30 July 2017

John P Gaughan

6

1 reference

Europe PubMed Central

30 July 2017

Christos Coutifaris

7

1 reference

Europe PubMed Central

30 July 2017

Carmen Sapienza

8

1 reference

Europe PubMed Central

30 July 2017

publication date

22 July 2010

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

6

1 reference

Europe PubMed Central

30 July 2017

7

1 reference

Europe PubMed Central

30 July 2017

e1001033

1 reference

Europe PubMed Central

30 July 2017

copyright license

Creative Commons Attribution 4.0 International

22 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Time course analysis of RNA stability in human placenta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Imprinting disorders and assisted reproductive technology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

A survey of assisted reproductive technology births and imprinting disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Limited evolutionary conservation of imprinting in the human placenta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Homeobox gene HLX1 expression is decreased in idiopathic human fetal growth restriction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Genomic imprinting and reproduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Assisted reproductive technologies and the risk of birth defects--a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Imprinted chromosomal regions of the human genome have unusually high recombination rates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

CTCF maintains differential methylation at the Igf2/H19 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Intracytoplasmic sperm injection may increase the risk of imprinting defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Epigenetic reprogramming in mammalian development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Natural selection and the function of genome imprinting: beyond the silenced minority

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Imprinting mechanisms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Heritability of X chromosome--inactivation phenotype in a large family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Conservation of a maternal-specific methylation signal at the human IGF2R locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Insulin-like growth factors and their binding proteins: biological actions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Numerology of development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Monoallelic expression of the human H19 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

28 July 2018

Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Aberrant DNA methylation of imprinted loci in superovulated oocytes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Selective loss of imprinting in the placenta following preimplantation development in culture

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Gene-specific timing and epigenetic memory in oocyte imprinting.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Superovulation alters the expression of imprinted genes in the midgestation mouse placenta.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Long-term effect of in vitro culture of mouse embryos with serum on mRNA expression of imprinting genes, development, and behavior.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Mouse embryo culture induces changes in postnatal phenotype including raised systolic blood pressure

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Human imprinted chromosomal regions are historical hot-spots of recombination.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Mammalian recombination hot spots: properties, control and evolution.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Interactions of IGF-II with the IGF2R/cation-independent mannose-6-phosphate receptor mechanism and biological outcomes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Genomic imprinting. Imprinting with and without methylation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

GAPDH, 18S rRNA and YWHAZ are suitable endogenous reference genes for relative gene expression studies in placental tissues from human idiopathic fetal growth restriction

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Size at birth and cord blood levels of insulin, insulin-like growth factor I (IGF-I), IGF-II, IGF-binding protein-1 (IGFBP-1), IGFBP-3, and the soluble IGF-II/mannose-6-phosphate receptor in term human infants. The ALSPAC Study Team. Avon Longitudin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908687

29 October 2018

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001033

21 January 2018

Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A longitudinal study of X-inactivation ratio in human females

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Placental IGF2 Expression in Normal and Intrauterine Growth Restricted (IUGR) Pregnancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental genomic imprinting of the human IGF2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

1 reference

https://pubmed.ncbi.nlm.nih.gov/20661447

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1001033

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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