DUX4 Binding to Retroelements Creates Promoters That Are Active in FSHD Muscle and Testis

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Transposable Elements Re-Wire and Fine-Tune the Transcriptome

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Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD

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Transposable Elements Are Major Contributors to the Origin, Diversification, and Regulation of Vertebrate Long Noncoding RNAs

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

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Long non-coding antisense RNA controls Uchl1 translation through an embedded SINEB2 repeat

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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

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Landscape of Somatic Retrotransposition in Human Cancers

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Transposable elements reveal a stem cell-specific class of long noncoding RNAs

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No-Nonsense Functions for Long Noncoding RNAs

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DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy

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Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

(2011) Mark Richards et al.   HUMAN GENETICS

BRCA1 tumour suppression occurs via heterochromatin-mediated silencing

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Transposon-mediated rewiring of gene regulatory networks contributed to the evolution of pregnancy in mammals

(2011) Vincent J Lynch et al.   NATURE GENETICS

PIWI-interacting small RNAs: the vanguard of genome defence

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The UCSC Genome Browser database: extensions and updates 2011

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The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression

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Aberrant Overexpression of Satellite Repeats in Pancreatic and Other Epithelial Cancers

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Facioscapulohumeral muscular dystrophy and DUX4: breaking the silence

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DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

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A family history of DUX4: phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene

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Epigenetic Regulation of Pericentromeric Heterochromatin during Mammalian Meiosis

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CD8+ T Cells in Facioscapulohumeral Muscular Dystrophy Patients with Inflammatory Features at Muscle MRI

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KAP1 controls endogenous retroviruses in embryonic stem cells

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Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET

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Transposable elements have rewired the core regulatory network of human embryonic stem cells

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Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphoma

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A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

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Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene

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Estimating enrichment of repetitive elements from high-throughput sequence data

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Endogenous retroviral LTRs as promoters for human genes: A critical assessment

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Detection of nonneutral substitution rates on mammalian phylogenies

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RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

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The Notch Effector Hey1 Associates with Myogenic Target Genes to Repress Myogenesis

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Embryonic stem cells use ZFP809 to silence retroviral DNAs

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The regulated retrotransposon transcriptome of mammalian cells

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(2009) Richard Cordaux et al.   NATURE REVIEWS GENETICS

Complex Evolution of a Y-Chromosomal Double Homeobox 4 (DUX4)-Related Gene Family in Hominoids

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Analysis of Homeodomain Specificities Allows the Family-wide Prediction of Preferred Recognition Sites

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An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

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Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event

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Evolution of the mammalian transcription factor binding repertoire via transposable elements

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Transposable elements and the evolution of regulatory networks

(2008) Cédric Feschotte   NATURE REVIEWS GENETICS