M

Marco Tartaglia

Université de Bordeaux

ORCID: 0000-0001-7736-9672

Publishes on Protein Tyrosine Phosphatases, Galectins and Cancer Biology, Genomics and Rare Diseases. 676 papers and 26.9k citations.

676Publications

26.9kTotal Citations

Protein Tyrosine Phosphatases Galectins and Cancer Biology Genomics and Rare Diseases RNA modifications and cancer Genetics and Neurodevelopmental Disorders

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Top publicationsby citations

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg et al.|Nature Genetics|2001

Cited by 1.7k

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

Marco Tartaglia, Charlotte M. Niemeyer, Alessandra Fragale et al.|Nature Genetics|2003

Cited by 1k

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

Marco Tartaglia, Kamini Kalidas, Adam Shaw et al.|The American Journal of Human Genetics|2002

Cited by 795Open Access

Noonan syndrome

Amy E. Roberts, Judith Allanson, Marco Tartaglia et al.|The Lancet|2013

Cited by 767Open Access

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

Bhaswati Pandit, Anna Sárközy, L Pennacchio et al.|Nature Genetics|2007

Cited by 699