(Q38896272)

7 September 2017

title

Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms (English)

1 reference

7 September 2017

1 reference

6

1 reference

7 September 2017

Chiea Chuen Khor

5

0 references

Shyam Prabhakar

7

object named as

Shyam Prabhakar

1 reference

7 September 2017

author name string

Ricardo Cruz-Herrera del Rosario

1

1 reference

7 September 2017

Jeremie Poschmann

2

1 reference

7 September 2017

Sigrid Laure Rouam

3

1 reference

7 September 2017

Eileen Png

4

1 reference

7 September 2017

publication date

23 March 2015

1 reference

7 September 2017

1 reference

7 September 2017

volume

12

1 reference

7 September 2017

issue

5

1 reference

7 September 2017

page(s)

458-464

1 reference

https://scigraph.springernature.com/pub.10.1038/nmeth.3326

7 September 2017

exact match

0 references

cites work

Annotation of functional variation in personal genomes using RegulomeDB

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Genomewide association studies and assessment of the risk of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Systematic localization of common disease-associated variation in regulatory DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Obesity-associated variants within FTO form long-range functional connections with IRX3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Genetic mapping in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

The Genotype-Tissue Expression (GTEx) project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Transcriptome and genome sequencing uncovers functional variation in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Transcriptome genetics using second generation sequencing in a Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Understanding mechanisms underlying human gene expression variation with RNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

High-resolution mapping of expression-QTLs yields insight into human gene regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

DNase I sensitivity QTLs are a major determinant of human expression variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

A map of open chromatin in human pancreatic islets

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Variation in transcription factor binding among humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Heritable individual-specific and allele-specific chromatin signatures in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Simultaneous SNP identification and assessment of allele-specific bias from ChIP-seq data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Extensive variation in chromatin states across humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Identification of genetic variants that affect histone modifications in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

An integrated map of genetic variation from 1,092 human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Combinatorial patterns of histone acetylations and methylations in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Histone modifications at human enhancers reflect global cell-type-specific gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Uniform, optimal signal processing of mapped deep-sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Architecture of the human regulatory network derived from ENCODE data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

An expansive human regulatory lexicon encoded in transcription factor footprints

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Exome sequencing as a tool for Mendelian disease gene discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Systematic cross-validation of 454 sequencing and pyrosequencing for the exact quantification of DNA methylation patterns with single CpG resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Association testing for next-generation sequencing data using score statistics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

A Simplex Method for Function Minimization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

The control of the false discovery rate in multiple testing under dependency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Systematic discovery and characterization of regulatory motifs in ENCODE TF binding experiments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3326

The human genome browser at UCSC

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25799442

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The use of MassARRAY technology for high throughput genotyping

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25799442

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NMETH.3326

1 reference

Dimensions Publication ID

7 September 2017

1003115598

0 references

1 reference