(Q83093485)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Corinna Zogel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Stefan Böhringer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Stephanie Gross

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Raymonda Varon

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Karin Buiting

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Bernhard Horsthemke

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

1 June 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

752-758

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201602

19 January 2020

exact match

0 references

cites work

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Imprinting-mutation mechanisms in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

The imprinting box of the Prader-Willi/Angelman syndrome domain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

The imprinting mechanism of the Prader-Willi/Angelman regional control center

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T and 1298A-->C mutations are associated with DNA hypomethylation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Epigenetic reprogramming in mammals

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Median-joining networks for inferring intraspecific phylogenies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Transmission/disequilibrium tests for multiallelic loci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Somatic mosaicism in patients with Angelman syndrome and an imprinting defect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Control elements within the PWS/AS imprinting box and their function in the imprinting process

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201602

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201602

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16596119%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference