Stéphanie Maupetit‐Mehouas

Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape

Lenka Veselovská, Sébastien A. Smallwood, Heba Saadeh et al. · Genome biology · 2015 · 241 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

A Maternal Epimutation of GNAS Leads to Albright Osteodystrophy and Parathyroid Hormone Resistance

Virginie Mariot, Stéphanie Maupetit‐Mehouas, Christiane Sinding et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 110 citations

Medicine, Genetics, Molecular Genetics +16

Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with<i>GNAS</i>Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b

Stéphanie Maupetit‐Mehouas, Salah Azzi, Virginie Steunou et al. · Human Mutation · 2013 · 56 citations

Life Sciences, Genetics, Molecular Genetics +16

Quantification of the methylation at the <i>GNAS</i> locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib

Stéphanie Maupetit‐Mehouas, Virginie Mariot, Christelle Reynès et al. · Journal of Medical Genetics · 2010 · 55 citations

Medicine, Genetics, Molecular Genetics +17

Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive

Stéphanie Maupetit‐Mehouas, Bertille Montibus, David Nury et al. · Nucleic Acids Research · 2015 · 48 citations · Full text

Life Sciences, Genetics, Molecular Biology +17