Irène Netchine
Inserm(FR)Sorbonne Université(FR)Hôpital Armand-Trousseau(FR)Centre de Recherche Saint-Antoine(FR)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation, Prenatal Screening and Diagnostics, Growth Hormone and Insulin-like Growth Factors, Birth, Development, and Health
Most-Cited Works
- → Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement(2018)584 cited
- → Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome(2005)504 cited
- → Diagnosis and management of Silver–Russell syndrome: first international consensus statement(2016)495 cited
- → Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency(2000)366 cited
- → Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective(2019)337 cited
- → 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 Correlations(2007)312 cited