Andra Ion
St George's, University of London(GB)
Publications by Year
Research Areas
Protein Tyrosine Phosphatases, RNA modifications and cancer, Galectins and Cancer Biology, Connective tissue disorders research, Bone and Dental Protein Studies
Most-Cited Works
- → Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome(2001)1,728 cited
- → PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity(2002)787 cited
- → Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development(2007)228 cited
- → Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome(2002)51 cited
- → Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6(2000)18 cited
- → Correction: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome(2001)5 cited
- Erratum: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome (Journal of Vascular Technology (2001) 29 (465-468))(2001)