Edith Heard

Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes.

Antisense RNA in imprinting: spreading silence through Air.

Relationship of XIST expression and responses of ovarian cancer to chemotherapy.

Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.

Rb-mediated heterochromatin formation and silencing of E2F target genes during cellular senescence.

Epigenetic dynamics of imprinted X inactivation during early mouse development.

X-chromosome inactivation in mouse embryonic stem cells: analysis of histone modifications and transcriptional activity using immunofluorescence and FISH.

Recent advances in X-chromosome inactivation.

Differential histone H3 Lys-9 and Lys-27 methylation profiles on the X chromosome.

Imprinted X-inactivation in extra-embryonic endoderm cell lines from mouse blastocysts.

Initiation of epigenetic reprogramming of the X chromosome in somatic nuclei transplanted to a mouse oocyte.

Delving into the diversity of facultative heterochromatin: the epigenetics of the inactive X chromosome.

Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inactivation in mice.

Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation.

Mouse polycomb proteins bind differentially to methylated histone H3 and RNA and are enriched in facultative heterochromatin.

Dosage compensation in mammals: fine-tuning the expression of the X chromosome.

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced.

[Cross talk between the Xics].

Non-rigid registration of 3D multi-channel microscopy images of cell nuclei.

The ins and outs of gene regulation and chromosome territory organisation.

X inactive-specific transcript RNA coating and genetic instability of the X chromosome in BRCA1 breast tumors.

A phosphorylated subpopulation of the histone variant macroH2A1 is excluded from the inactive X chromosome and enriched during mitosis.

Chromosome structural proteins and RNA-mediated epigenetic silencing.

[Inactivation of X chromosome: cells know how to count two X chromosomes].

Combined immunofluorescence, RNA fluorescent in situ hybridization, and DNA fluorescent in situ hybridization to study chromatin changes, transcriptional activity, nuclear organization, and X-chromosome inactivation.

Monomethylation of histone H4-lysine 20 is involved in chromosome structure and stability and is essential for mouse development.

Dynamic changes in paternal X-chromosome activity during imprinted X-chromosome inactivation in mice.

X inactivation and the complexities of silencing a sex chromosome.

High-resolution analysis of epigenetic changes associated with X inactivation.

Highly dynamic and sex-specific expression of microRNAs during early ES cell differentiation.

Foreword: Coping with sex chromosome imbalance.

Lessons from comparative analysis of X-chromosome inactivation in mammals.

X chromosome inactivation: when dosage counts.

Epigenetic mechanisms in development and disease.

LINE-1 activity in facultative heterochromatin formation during X chromosome inactivation.

Dynamic plasticity of large-scale chromatin structure revealed by self-assembly of engineered chromosome regions.

Ten years of genetics and genomics: what have we achieved and where are we heading?

Girafe--an R/Bioconductor package for functional exploration of aligned next-generation sequencing reads.

Nuclear organization and dosage compensation.

[Establishing transcriptional silencing of the X chromosome during early embryogenesis].

Rnf12--a jack of all trades in X inactivation?

Eutherian mammals use diverse strategies to initiate X-chromosome inactivation during development.

Live-cell chromosome dynamics and outcome of X chromosome pairing events during ES cell differentiation.

Regulation of X-chromosome inactivation by the X-inactivation centre.

Evolutionary diversity and developmental regulation of X-chromosome inactivation.

The inactive X chromosome adopts a unique three-dimensional conformation that is dependent on Xist RNA.

Function of the sex chromosomes in mammalian fertility.

Deterministic and stochastic allele specific gene expression in single mouse blastomeres.

Fifty years of X-inactivation research.

Naive and primed murine pluripotent stem cells have distinct miRNA expression profiles.

MicroRNA regulation of Cbx7 mediates a switch of Polycomb orthologs during ESC differentiation.

Deep-sequencing protocols influence the results obtained in small-RNA sequencing.

Spatial partitioning of the regulatory landscape of the X-inactivation centre.

Smchd1-dependent and -independent pathways determine developmental dynamics of CpG island methylation on the inactive X chromosome.

HiTC: exploration of high-throughput 'C' experiments.

ncPRO-seq: a tool for annotation and profiling of ncRNAs in sRNA-seq data.

Recent advances in X-chromosome inactivation research.

Unusual chromatin status and organization of the inactive X chromosome in murine trophoblast giant cells.

Role and control of X chromosome dosage in mammalian development.

The dynamics of epigenetic changes in a range of organisms.

Small RNAs derived from structural non-coding RNAs.

Cell nucleus.

Epigenetic functions of smchd1 repress gene clusters on the inactive X chromosome and on autosomes.

Segmental folding of chromosomes: a basis for structural and regulatory chromosomal neighborhoods?

The pluripotent genome in three dimensions is shaped around pluripotency factors.

Live-cell imaging combined with immunofluorescence, RNA, or DNA FISH to study the nuclear dynamics and expression of the X-inactivation center.

Cohesin-based chromatin interactions enable regulated gene expression within preexisting architectural compartments.

RNAi-dependent and independent control of LINE1 accumulation and mobility in mouse embryonic stem cells.

Changes in the organization of the genome during the mammalian cell cycle.

Jarid2 Is Implicated in the Initial Xist-Induced Targeting of PRC2 to the Inactive X Chromosome.

The two active X chromosomes in female ESCs block exit from the pluripotent state by modulating the ESC signaling network.

Developmental dynamics and disease potential of random monoallelic gene expression.

Transgenerational epigenetic inheritance: myths and mechanisms.

Predictive polymer modeling reveals coupled fluctuations in chromosome conformation and transcription.

MOF-associated complexes ensure stem cell identity and Xist repression.

X-chromosome inactivation in development and cancer.

Noncoding RNAs and epigenetic mechanisms during X-chromosome inactivation.

[Initiation of X chromosome inactivation during early embryogenesis in mice and in humans].

High-resolution 3D DNA FISH using plasmid probes and computational correction of optical aberrations to study chromatin structure at the sub-megabase scale.

Jarid2 Methylation via the PRC2 Complex Regulates H3K27me3 Deposition during Cell Differentiation.

The inactive X chromosome is epigenetically unstable and transcriptionally labile in breast cancer.

Systematic discovery of Xist RNA binding proteins.

Correction: RNAi-Dependent and Independent Control of LINE1 Accumulation and Mobility in Mouse Embryonic Stem Cells.

X-chromosome inactivation: new insights into cis and trans regulation.

[The legacy of Mary F. Lyon (1925-2014)].

Structural and functional diversity of Topologically Associating Domains.

HiC-Pro: an optimized and flexible pipeline for Hi-C data processing.

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation.

Structural Fluctuations of the Chromatin Fiber within Topologically Associating Domains.

Random monoallelic expression of genes on autosomes: Parallels with X-chromosome inactivation.

Structural organization of the inactive X chromosome in the mouse.

LINE-1 Activity in Facultative Heterochromatin Formation during X Chromosome Inactivation.

Ordered chromatin changes and human X chromosome reactivation by cell fusion-mediated pluripotent reprogramming.

Genomes of Ellobius species provide insight into the evolutionary dynamics of mammalian sex chromosomes.

A symmetric toggle switch explains the onset of random X inactivation in different mammals.

Advances in epigenetics link genetics to the environment and disease.

Xist RNA in action: Past, present, and future.

A Conserved Noncoding Locus Regulates Random Monoallelic Xist Expression across a Topological Boundary.

SPEN integrates transcriptional and epigenetic control of X-inactivation.

Parental-to-embryo switch of chromosome organization in early embryogenesis.

Locus specific epigenetic modalities of random allelic expression imbalance.

Noncoding RNAs: biology and applications-a Keystone Symposia report.

Gene regulation in time and space during X-chromosome inactivation.

The X chromosome from telomere to telomere: key achievements and future opportunities.

Molecular biology for green recovery-A call for action.

XIST loss impairs mammary stem cell differentiation and increases tumorigenicity through Mediator hyperactivation.