In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene (Q24532045)

4

object named as

Jean-Pierre Siffroi

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author name string

Christine Gicquel

1

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Véronique Gaston

2

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Jacqueline Mandelbaum

3

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Yves Le Bouc

American Journal of Human Genetics

6

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language of work or name

English

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publication date

May 2003

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published in

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volume

72

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page(s)

1338-41

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issue

5

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cites work

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

1 reference

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

24 March 2017

1 reference

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Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

24 March 2017

1 reference

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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180288

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

24 March 2017

1 reference

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

24 March 2017

1 reference

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Chromatin modification and epigenetic reprogramming in mammalian development

24 March 2017

1 reference

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Genomic imprinting: parental influence on the genome

7 April 2017

1 reference

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Intracytoplasmic sperm injection may increase the risk of imprinting defects

7 April 2017

1 reference

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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

27 September 2017

1 reference

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Nuclear cloning and epigenetic reprogramming of the genome

27 September 2017

1 reference

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Perinatal outcome of pregnancy after GnRH antagonist (ganirelix) treatment during ovarian stimulation for conventional IVF or ICSI: a preliminary report

27 September 2017

1 reference

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Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

27 September 2017

1 reference

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Beckwith-Wiedemann syndrome: imprinting in clusters revisited

27 September 2017

1 reference

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

27 September 2017

1 reference

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

27 September 2017

1 reference

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Epigenetic instability in ES cells and cloned mice.

29 November 2018

1 reference

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Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180288

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180288

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

29 November 2018

1 reference

12 December 2020

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

1 reference

12 December 2020

Large offspring syndrome in cattle and sheep

1 reference

12 December 2020

Study of DNA-methylation patterns at chromosome 15q11-q13 in children born after ICSI reveals no imprinting defects

1 reference

12 December 2020