(Q34325361)

1 August 2017

title

Low frequency of imprinting defects in ICSI children born small for gestational age. (English)

1 reference

1 August 2017

2

Karin Buiting

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author name string

Deniz Kanber

1

1 reference

1 August 2017

Michael Zeschnigk

3

1 reference

1 August 2017

Michael Ludwig

4

1 reference

1 August 2017

Bernhard Horsthemke

5

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1 August 2017

publication date

22 October 2008

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European Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

17

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1 August 2017

issue

1

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1 August 2017

page(s)

22-29

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Outcome of assisted reproduction.

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

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=2985955

The centromeric 11p15 imprinting centre is also involved in Silver-Russell 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=2985955

Epimutations in human 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=2985955

Assisted reproduction: the epigenetic perspective

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

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=2985955

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=2985955

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 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=2985955

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=2985955

A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

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=2985955

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=2985955

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

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=2985955

The role of imprinted genes in fetal growth

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2985955

6 July 2018

Resourceful imprinting.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Aberrant DNA methylation of imprinted loci in superovulated oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

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/10.1038%2FEJHG.2008.177

Genomic imprinting in disruptive spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.177

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

21 January 2018

1 reference

12 December 2020

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation

1 reference

12 December 2020

Pregnancy course and outcome after intracytoplasmic sperm injection: a controlled, prospective cohort study

1 reference

12 December 2020

Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA

1 reference

12 December 2020

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

1 reference

12 December 2020

IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2008.177

1 reference

1 August 2017

1 reference

1 August 2017

1 reference