11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic CorrelationsIrène Netchine, Yves Le Bouc, Muriel Houang et al.|The Journal of Clinical Endocrinology & Metabolism|2007Cited by 312
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted lociSalah Azzi, Irène Netchine, Sylvie Rossignol et al.|Human Molecular Genetics|2009Cited by 254
Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restrictionWalid Abi Habib, Irène Netchine, Frédéric Brioude et al.|Genetics in Medicine|2017Cited by 137