(Q34277727)

1 August 2017

1 reference

title

Imprinting methylation errors in ART. (English)

1 reference

1 August 2017

Hitoshi Hiura

1

1 reference

1 August 2017

Hiroaki Okae

2

1 reference

1 August 2017

Hatsune Chiba

3

1 reference

1 August 2017

Naoko Miyauchi

4

1 reference

1 August 2017

Fumi Sato

5

1 reference

1 August 2017

Akiko Sato

6

1 reference

1 August 2017

Takahiro Arima

7

1 reference

1 August 2017

19 June 2014

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Reproductive Medicine and Biology

1 August 2017

1 reference

1 August 2017

13

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1 August 2017

4

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1 August 2017

193-202

1 reference

https://scigraph.springernature.com/pub.10.1007/s12522-014-0183-3

1 August 2017

0 references

cites work

Childhood outcomes of assisted reproductive technology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Absence of insulin resistance and low-grade inflammation despite early metabolic syndrome manifestations in children born after in vitro fertilization

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

DNA methylation and gene expression differences in children conceived in vitro or in vivo

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Widespread epigenetic abnormalities suggest a broad DNA methylation erasure defect in abnormal human sperm

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

A survey of assisted reproductive technology births and imprinting disorders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

In vitro maturation of human oocytes for assisted reproduction

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Intra- and interindividual epigenetic variation in human germ cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Epigenetic reprogramming in mammals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Incidence of retinoblastoma in children born after in-vitro fertilisation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Intracytoplasmic sperm injection may increase the risk of imprinting defects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

DNA methylation in genomic imprinting, development, and disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Imprinting mechanisms in mammals.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Completion of mouse embryogenesis requires both the maternal and paternal genomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Low and very low birth weight in infants conceived with use of assisted reproductive technology

6 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Imprinting and the initiation of gene silencing in the germ line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

The sins of the fathers and mothers: genomic imprinting in mammalian development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Gene-specific timing and epigenetic memory in oocyte imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Oocyte growth-dependent progression of maternal imprinting in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Aberrant DNA methylation of imprinted loci in superovulated oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Timing of establishment of paternal methylation imprints in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

In vitro fertilization in Sweden: child morbidity including cancer risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Dynamic CpG methylation of the KCNQ1OT1 gene during maturation of human oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Genomic imprinting in disruptive spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Assessing loss of imprint methylation in sperm from subfertile men using novel methylation polymerase chain reaction Luminex analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Methylation defects of imprinted genes in human testicular spermatozoa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Effect of in vitro culture of human embryos on birthweight of newborns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Cardiometabolic differences in children born after in vitro fertilization: follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

In vitro fertilization improves childhood growth and metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Epigenetic reprogramming in mouse primordial germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

A female infant with Silver Russell Syndrome, mesocardia and enlargement of the clitoris.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4182590

Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

28 October 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Allelic imbalance in selected chromosomal regions in ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12522-014-0183-3

Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia

21 January 2018

1 reference

12 December 2020

Congenital malformations in infants born after in vitro fertilization in Sweden

1 reference

12 December 2020

Overgrowth with severe developmental delay following IVF/ICSI: A newly recognized syndrome?

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies

1 reference

12 December 2020

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

1 reference

12 December 2020

Alterations in sperm DNA methylation patterns at imprinted loci in two classes of infertility

1 reference

12 December 2020

Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study

1 reference

12 December 2020

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination

1 reference

12 December 2020

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Aberrant DNA methylation of imprinted H19 gene in human preimplantation embryos

1 reference

12 December 2020

Increased risk of Silver-Russell syndrome after in vitro fertilization?

1 reference

12 December 2020

Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors

1 reference

12 December 2020

Assisted reproductive therapies and imprinting disorders--a preliminary British survey

1 reference

12 December 2020

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

1 reference

12 December 2020

Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs?

1 reference

12 December 2020

Monoallelic expression: 'there can only be one'

1 reference

12 December 2020

10.1007/S12522-014-0183-3

Identifiers

DOI

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference