(Q34595528)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

review article

1 reference

title

A review of known imprinting syndromes and their association with assisted reproduction technologies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

author name string

Jane Halliday

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

language of work or name

English

0 references

publication date

14 August 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

page(s)

2826-2834

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18703582%20AND%20SRC:MED&resulttype=core&format=json

A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus.

12 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Cell microarrays and RNA interference chip away at gene function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

A survey of assisted reproductive technology births and imprinting disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Intracytoplasmic sperm injection may increase the risk of imprinting defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

An imprinted locus associated with transient neonatal diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Genetic imprinting during impaired spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Assisted reproduction: the epigenetic perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Imprinted expression of SNRPN in human preimplantation embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Culture of preimplantation embryos and its long-term effects on gene expression and phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Follow-up of cognitive and motor development of 10-year-old singleton children born after ICSI compared with spontaneously conceived children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Imprinting diseases and IVF: Danish National IVF cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Computational and experimental identification of novel human imprinted genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

In vitro fertilization improves childhood growth and metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

The use of amplified cDNA to investigate the expression of seven imprinted genes in human oocytes and preimplantation embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Aberrant DNA methylation of imprinted loci in superovulated oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310

Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN310