On the public citation graph
Variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility
0 signed · 77 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00949.xopenalex-snapshot
Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities.
inferredcites →https://doi.org/10.1007/978-3-642-29627-7_30openalex-snapshot
Differential Oestrogen Receptor Binding is Associated with Clinical Outcome in Breast Cancer
inferredcites →https://doi.org/10.1016/j.cell.2013.02.029openalex-snapshot
CTCF and Cohesin: Linking Gene Regulatory Elements with Their Targets
inferredcites →https://doi.org/10.1016/j.cell.2015.07.048openalex-snapshot
Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions
inferredcites →https://doi.org/10.1016/j.cell.2015.08.001openalex-snapshot
Population Variation and Genetic Control of Modular Chromatin Architecture in Humans
inferredcites →https://doi.org/10.1016/j.cell.2015.12.031openalex-snapshot
LRRC8 Proteins Form Volume-Regulated Anion Channels that Sense Ionic Strength
inferredcites →https://doi.org/10.1016/j.cell.2016.03.041openalex-snapshot
Pooled ChIP-Seq Links Variation in Transcription Factor Binding to Complex Disease Risk
inferredcites →https://doi.org/10.1016/j.cell.2016.09.037openalex-snapshot
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters
inferredcites →https://doi.org/10.1016/j.cell.2016.10.026openalex-snapshot
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
inferredcites →https://doi.org/10.1016/j.cell.2016.10.042openalex-snapshot
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
inferredcites →https://doi.org/10.1016/j.cell.2018.04.018openalex-snapshot
Analysis of Genetically Diverse Macrophages Reveals Local and Domain-wide Mechanisms that Control Transcription Factor Binding and Function
inferredcites →https://doi.org/10.1016/j.chom.2014.04.011openalex-snapshot
The Balancing Act of Neutrophils
inferredcites →https://doi.org/10.1016/j.clineuro.2018.04.008openalex-snapshot
CPEB4 regulates glioblastoma cell proliferation and predicts poor outcome of patients
inferredcites →https://doi.org/10.1016/j.devcel.2014.07.008openalex-snapshot
Cpeb4-Mediated Translational Regulatory Circuitry Controls Terminal Erythroid Differentiation
inferredcites →https://doi.org/10.1016/j.molcel.2010.05.004openalex-snapshot
Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
inferredcites →https://doi.org/10.1016/j.tibs.2007.04.004openalex-snapshot
CPEB: a life in translation
inferredcites →https://doi.org/10.1016/j.tig.2015.10.004openalex-snapshot
The Hierarchy of Transcriptional Activation: From Enhancer to Promoter
inferredcites →https://doi.org/10.1038/nature10730openalex-snapshot
Differential oestrogen receptor binding is associated with clinical outcome in breast cancer
inferredcites →https://doi.org/10.1038/nature12615openalex-snapshot
Effect of natural genetic variation on enhancer selection and function
inferredcites →https://doi.org/10.1038/nature13835openalex-snapshot
Genetic and epigenetic fine mapping of causal autoimmune disease variants
inferredcites →https://doi.org/10.1038/ng.2383openalex-snapshot
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng.2770openalex-snapshot
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
inferredcites →https://doi.org/10.1038/ng.3245openalex-snapshot
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
inferredcites →https://doi.org/10.1038/ng.3286openalex-snapshot
Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C
inferredcites →https://doi.org/10.1038/ng.3359openalex-snapshot
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
inferredcites →https://doi.org/10.1038/ng.3432openalex-snapshot
Large-scale identification of sequence variants influencing human transcription factor occupancy in vivo
inferredcites →https://doi.org/10.1038/ng.3467openalex-snapshot
Fine-mapping cellular QTLs with RASQUAL and ATAC-seq
inferredcites →https://doi.org/10.1038/ng.3570openalex-snapshot
Detection and interpretation of shared genetic influences on 42 human traits
inferredcites →https://doi.org/10.1038/ng.3963openalex-snapshot
Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements
inferredcites →https://doi.org/10.1038/ng.543openalex-snapshot
Multiple common variants for celiac disease influencing immune gene expression
inferredcites →https://doi.org/10.1038/nmeth.3582openalex-snapshot
WASP: allele-specific software for robust molecular quantitative trait locus discovery
inferredcites →https://doi.org/10.1038/nprot.2015.127openalex-snapshot
Single-cell Hi-C for genome-wide detection of chromatin interactions that occur simultaneously in a single cell
inferredcites →https://doi.org/10.1038/nrg3891openalex-snapshot
The role of regulatory variation in complex traits and disease
inferredcites →https://doi.org/10.1038/s41467-017-01037-xopenalex-snapshot
Interplay of cis and trans mechanisms driving transcription factor binding and gene expression evolution
inferredcites →https://doi.org/10.1038/s41467-019-08940-5openalex-snapshot
Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression
inferredcites →https://doi.org/10.1038/s41586-018-0321-xopenalex-snapshot
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
inferredcites →https://doi.org/10.1038/s41588-017-0034-3openalex-snapshot
Genetic determinants and epigenetic effects of pioneer-factor occupancy
inferredcites →https://doi.org/10.1038/s41588-018-0156-2openalex-snapshot
Genetic determinants of co-accessible chromatin regions in activated T cells across humans
inferredcites →https://doi.org/10.1038/s41588-018-0278-6openalex-snapshot
High-resolution genetic mapping of putative causal interactions between regions of open chromatin
inferredcites →https://doi.org/10.1038/s41588-018-0322-6openalex-snapshot
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals
inferredcites →https://doi.org/10.1038/srep22223openalex-snapshot
Significant impact of miRNA–target gene networks on genetics of human complex traits
inferredcites →https://doi.org/10.1073/pnas.1530509100openalex-snapshot
Statistical significance for genomewide studies
inferredcites →https://doi.org/10.1074/jbc.m513471200openalex-snapshot
Phospholipase Cϵ Suppresses Integrin Activation
inferredcites →https://doi.org/10.1084/jem.20041535openalex-snapshot
Dynamic regulation of PU.1 expression in multipotent hematopoietic progenitors
inferredcites →https://doi.org/10.1084/jem.20122220openalex-snapshot
Diverse novel functions of neutrophils in immunity, inflammation, and beyond
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btv562openalex-snapshot
regioneR: an R/Bioconductor package for the association analysis of genomic regions based on permutation tests
inferredcites →https://doi.org/10.1093/nar/gkw257openalex-snapshot
deepTools2: a next generation web server for deep-sequencing data analysis
inferredcites →https://doi.org/10.1093/nar/gkx618openalex-snapshot
Automatic identification of informative regions with epigenomic changes associated to hematopoiesis
inferredcites →https://doi.org/10.1101/003905openalex-snapshot
LIMIX: genetic analysis of multiple traits
inferredcites →https://doi.org/10.1101/gad.13.11.1398openalex-snapshot
Direct interaction of hematopoietic transcription factors PU.1 and GATA-1: functional antagonism in erythroid cells
inferredcites →https://doi.org/10.1101/gad.176826.111openalex-snapshot
Pioneer transcription factors: establishing competence for gene expression
inferredcites →https://doi.org/10.1101/gad.293910.116openalex-snapshot
Comprehensive characterization of neutrophil genome topology
inferredcites →https://doi.org/10.1101/gr.131201.111openalex-snapshot
Effects of sequence variation on differential allelic transcription factor occupancy and gene expression
inferredcites →https://doi.org/10.1101/gr.136184.111openalex-snapshot
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
inferredcites →https://doi.org/10.1101/gr.155192.113openalex-snapshot
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
inferredcites →https://doi.org/10.1101/gr.185272.114openalex-snapshot
The pluripotent regulatory circuitry connecting promoters to their long-range interacting elements
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04399.xopenalex-snapshot
Phospholipase C‐related inactive protein is implicated in the constitutive internalization of GABAAreceptors mediated by clathrin and AP2 adaptor complex
inferredcites →https://doi.org/10.1111/j.1582-4934.2009.00757.xopenalex-snapshot
PU.1 and partners: regulation of haematopoietic stem cell fate in normal and malignant haematopoiesis
inferredcites →https://doi.org/10.1126/science.1183621openalex-snapshot
Variation in Transcription Factor Binding Among Humans
inferredcites →https://doi.org/10.1126/science.1222794openalex-snapshot
Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
inferredcites →https://doi.org/10.1126/science.1242429openalex-snapshot
Identification of Genetic Variants That Affect Histone Modifications in Human Cells
inferredcites →https://doi.org/10.1126/science.1242463openalex-snapshot
Coordinated Effects of Sequence Variation on DNA Binding, Chromatin Structure, and Transcription
inferredcites →https://doi.org/10.1126/science.1242510openalex-snapshot
Extensive Variation in Chromatin States Across Humans
inferredcites →https://doi.org/10.1182/blood-2002-03-0835openalex-snapshot
The in vivo profile of transcription factors during neutrophil differentiation in human bone marrow
inferredcites →https://doi.org/10.1182/blood-2016-07-730135openalex-snapshot
Reduced PU.1 expression underlies aberrant neutrophil maturation and function in β-thalassemia mice and patients
inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot
Model-based Analysis of ChIP-Seq (MACS)
inferredcites →https://doi.org/10.1186/gb-2013-14-11-r124openalex-snapshot
AHT-ChIP-seq: a completely automated robotic protocol for high-throughput chromatin immunoprecipitation
inferredcites →https://doi.org/10.1186/s13059-016-0992-2openalex-snapshot
CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data
inferredcites →https://doi.org/10.1186/s13059-017-1156-8openalex-snapshot
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types
inferredcites →https://doi.org/10.12688/f1000research.7334.1openalex-snapshot
HiCUP: pipeline for mapping and processing Hi-C data
inferredcites →https://doi.org/10.1371/journal.pgen.1002599openalex-snapshot
Widespread Site-Dependent Buffering of Human Regulatory Polymorphism
inferredcites →https://doi.org/10.1371/journal.pgen.1004383openalex-snapshot
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
inferredcites →https://doi.org/10.1371/journal.pgen.1004798openalex-snapshot
Quantitative Genetics of CTCF Binding Reveal Local Sequence Effects and Different Modes of X-Chromosome Association
inferredcites →https://doi.org/10.7554/elife.21926openalex-snapshot
Global reorganisation of cis-regulatory units upon lineage commitment of human embryonic stem cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2020.01.15.907436openalex-snapshot
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.