Sylvie Rossignol

The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

Sylvie Rossignol, Virginie Steunou, Céline Chalas et al. · Journal of Medical Genetics · 2006 · 220 citations · Full text

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

Igf2 Expression, Epigenetic Change, Genetics +20

Mutation update for the<i>GPC3</i>gene involved in Simpson-Golabi-Behmel syndrome and review of the literature

Marie‐Laure Vuillaume, Marie‐Pierre Moizard, Sylvie Rossignol et al. · Human Mutation · 2018 · 33 citations

Genetics, Pathology, Molecular Biology +17

Increasing knowledge in <i>IGF1R</i> defects: lessons from 35 new patients

Éloïse Giabicani, Marjolaine Willems, Virginie Steunou et al. · Journal of Medical Genetics · 2019 · 27 citations · Full text

Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population

Yasmine El Allali, Coralie Hermetet, Justine Bacchetta et al. · European Journal of Endocrinology · 2020 · 20 citations