Stanislas Lyonnet
Hôpital Necker-Enfants Malades(FR)Inserm(FR)Inserm(FR)Université Paris Cité(FR)Commissariat à l'Énergie Atomique et aux Énergies Alternatives(FR)Université Paris-Saclay(FR)Institut Necker Enfants Malades(FR)Assistance Publique – Hôpitaux de Paris(FR)Assistance Publique – Hôpitaux de Paris(FR)Direction de la Recherche Fondamentale(FR)CEA Paris-Saclay(FR)Human Genetic of Infectious Diseases(FR)Institut des Maladies Génétiques Imagine(FR)
Publications by Year
Research Areas
Congenital gastrointestinal and neural anomalies, Genomics and Rare Diseases, Congenital heart defects research, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Lamin A Truncation in Hutchinson-Gilford Progeria(2003)1,454 cited
- → Hirschsprung disease, associated syndromes and genetics: a review(2007)1,197 cited
- → Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family(1997)925 cited
- → Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma(2008)890 cited
- → Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome(2003)854 cited
- → SOX10 mutations in patients with Waardenburg-Hirschsprung disease(1998)818 cited