(Q39812286)

14 September 2017

Allele-specific transcription factor binding in liver and cervix cells unveils many likely drivers of GWAS signals (English)

1 reference

genome-wide association study

14 September 2017

0 references

author name string

Gang Pan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Helena Nord

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Emelie Wallén Arzt

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Ola Wallerman

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

language of work or name

1 reference

25 April 2016

1 reference

14 September 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

volume

107

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

page(s)

248-254

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27126307%20AND%20SRC:MED&resulttype=core&format=json

The support of human genetic evidence for approved drug indications

4 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

A prostate cancer susceptibility allele at 6q22 increases RFX6 expression by modulating HOXB13 chromatin binding.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

An integrated encyclopedia of DNA elements in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

The Genotype-Tissue Expression (GTEx) project

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Integrative analysis of 111 reference human epigenomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

CTCF-Mediated Human 3D Genome Architecture Reveals Chromatin Topology for Transcription.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Genome-wide mapping of promoter-anchored interactions with close to single-enhancer resolution

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Differential binding and co-binding pattern of FOXA1 and FOXA3 and their relation to H3K4me3 in HepG2 cells revealed by ChIP-seq

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

AlleleSeq: analysis of allele-specific expression and binding in a network framework

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Mapping the genetic architecture of gene expression in human liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Nucleosome regulatory dynamics in response to TGFβ

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

SLiCE: a novel bacterial cell extract-based DNA cloning method

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

The haplotype-resolved genome and epigenome of the aneuploid HeLa cancer cell line

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Annotation of functional variation in personal genomes using RegulomeDB

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

Quantifying the effect of sequence variation on regulatory interactions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

MAPPER: a search engine for the computational identification of putative transcription factor binding sites in multiple genomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

iASeq: integrative analysis of allele-specificity of protein-DNA interactions in multiple ChIP-seq datasets

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

ALEA: a toolbox for allele-specific epigenomics analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006

FTO Obesity Variant Circuitry and Adipocyte Browning in Humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2016.04.006