Marco Tartaglia
Université de Bordeaux(FR)Bordeaux Population Health(FR)Bambino Gesù Children's Hospital(IT)Istituti di Ricovero e Cura a Carattere Scientifico(IT)
Publications by Year
Research Areas
Protein Tyrosine Phosphatases, Galectins and Cancer Biology, RNA modifications and cancer, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome(2001)1,728 cited
- → Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia(2003)1,034 cited
- → PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity(2002)787 cited
- → Noonan syndrome(2013)755 cited
- → Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy(2007)696 cited
- → Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome(2010)695 cited