Maria Fernanda Amary

<i>IDH1</i> and <i>IDH2</i> mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours

Maria Fernanda Amary, Krisztian Bacsi, Francesca Maggiani et al. · The Journal of Pathology · 2011 · 966 citations · Full text

Cartilaginous Tumours, Genetics, Pathology +25

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

Sam Behjati, Patrick Tarpey, Nadège Presneau et al. · Nature Genetics · 2013 · 836 citations · Full text

Tumor Biology, Distinct H3f3a, Bone Morphogenic Protein +7

Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2

Maria Fernanda Amary, Stephen Damato, Dina Halai et al. · Nature Genetics · 2011 · 424 citations

Somatic Variant, Mendelian Disorder, Ollier Disease +10

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

Sam Behjati, Patrick Tarpey, Helen Sheldon et al. · Nature Genetics · 2014 · 311 citations · Full text

Medicine, Recurrent Ptprb, Genetics +5

Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma

Sam Behjati, Patrick Tarpey, Kerstin Haase et al. · Nature Communications · 2017 · 250 citations · Full text