Cristina Das Neves

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome

Walid Abi Habib, Salah Azzi, Frédéric Brioude et al. · Human Molecular Genetics · 2014 · 72 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Complex Tissue-Specific Epigenotypes in Russell-Silver Syndrome Associated with 11p15 ICR1 Hypomethylation

Salah Azzi, Annick Blaise, Virginie Steunou et al. · Human Mutation · 2014 · 39 citations

Life Sciences, Genetics, Molecular Genetics +17

11p15 ICR1 Partial Deletions Associated with<i>IGF2/H19</i>DMR Hypomethylation and Silver-Russell Syndrome

Walid Abi Habib, Frédéric Brioude, Salah Azzi et al. · Human Mutation · 2016 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Exhaustive methylation analysis revealed uneven profiles of methylation at <i>IGF2/</i>ICR1<i>/H19</i> 11p15 loci in Russell Silver syndrome

Salah Azzi, Virginie Steunou, Jörg Tost et al. · Journal of Medical Genetics · 2014 · 20 citations

Life Sciences, Genetics, Molecular Genetics +17

Hypercortisolism due to a Pituitary Adenoma Associated with Beckwith-Wiedemann Syndrome

Frédéric Brioude, Carole Nicolas, Isabelle Marey et al. · Hormone Research in Paediatrics · 2016 · 12 citations

Medicine, Endocrinology, Genetics +15