(Q81490137)

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9 January 2020

title

Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation (English)

1 reference

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9 January 2020

author name string

Kristi Kerkel

1

1 reference

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9 January 2020

Alexandra Spadola

2

1 reference

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9 January 2020

Eric Yuan

3

1 reference

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9 January 2020

Jolanta Kosek

4

1 reference

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9 January 2020

Le Jiang

5

1 reference

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9 January 2020

Eldad Hod

6

1 reference

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9 January 2020

Kerry Li

7

1 reference

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9 January 2020

Vundavalli V Murty

8

1 reference

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9 January 2020

Nicole Schupf

9

1 reference

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9 January 2020

Eric Vilain

10

1 reference

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9 January 2020

Mitzi Morris

11

1 reference

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9 January 2020

Fatemeh Haghighi

12

1 reference

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9 January 2020

Benjamin Tycko

13

1 reference

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9 January 2020

publication date

22 June 2008

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9 January 2020

1 reference

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9 January 2020

volume

40

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9 January 2020

issue

7

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9 January 2020

page(s)

904-908

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Allele-specific methylation of the human c-Ha-ras-1 gene

9 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Inheritance of allelic blueprints for methylation patterns.

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

A single nucleotide polymorphism chip-based method for combined genetic and epigenetic profiling: validation in decitabine therapy and tumor/normal comparisons.

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Genetics of alcohol and tobacco use in humans.

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Widespread monoallelic expression on human autosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Monoallelic expression: 'there can only be one'

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Monoallelic expression of multiple genes in the CNS.

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Inherited epimutation or a haplotypic basis for the propensity to silence?

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

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%2FNG.174

7 January 2021

Polymorphic NF-Y dependent regulation of human nicotine C-oxidase (CYP2A6).

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Identification of a single nucleotide polymorphism in the TATA box of the CYP2A6 gene: impairment of its promoter activity

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

A nicotine C-oxidase gene (CYP2A6) polymorphism important for promoter activity

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning

1 reference

https://api.crossref.org/works/10.1038%2FNG.174

7 January 2021

Identifiers

DOI

10.1038/NG.174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18568024%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference