Alvaro Rada-Iglesias

Some microsatellites may act as novel polymorphic cis-regulatory elements through transcription factor binding.

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays.

The promoter of inducible nitric oxide synthase implicated in glaucoma based on genetic analysis and nuclear factor binding.

In vitro analysis of DNA-protein interactions by proximity ligation.

Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.

Monte Carlo feature selection for supervised classification.

Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders.

Histone acetylation and methylation at sites initiating divergent polycistronic transcription in Trypanosoma cruzi.

Histone H3 lysine 27 trimethylation in adult differentiated colon associated to cancer DNA hypermethylation.

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

Two polypyrimidine tracts in the nitric oxide synthase 2 gene: similar regulatory sequences with different properties.

Nucleosomes are well positioned in exons and carry characteristic histone modifications.

CHD7 cooperates with PBAF to control multipotent neural crest formation.

Integrative epigenomic and genomic analysis of malignant pheochromocytoma.

A unique chromatin signature uncovers early developmental enhancers in humans.

Sequence-specific regulator Prdm14 safeguards mouse ESCs from entering extraembryonic endoderm fates.

Epigenomics of human embryonic stem cells and induced pluripotent stem cells: insights into pluripotency and implications for disease.

The homeodomain-leucine zipper (HD-Zip) class I transcription factors ATHB7 and ATHB12 modulate abscisic acid signalling by regulating protein phosphatase 2C and abscisic acid receptor gene activities.

Epigenomic annotation of enhancers predicts transcriptional regulators of human neural crest.

Pioneering barren land: mitotic bookmarking by transcription factors.

Human genetic variation within neural crest enhancers: molecular and phenotypic implications.

Genetic variation within transcriptional regulatory elements and its implications for human disease.

Foxd3 Promotes Exit from Naive Pluripotency through Enhancer Decommissioning and Inhibits Germline Specification.

Epigenomics-Based Identification of Major Cell Identity Regulators within Heterogeneous Cell Populations.

GARLIC: a bioinformatic toolkit for aetiologically connecting diseases and cell type-specific regulatory maps.

Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.

PRC2 Facilitates the Regulatory Topology Required for Poised Enhancer Function during Pluripotent Stem Cell Differentiation.