Sofie Verbeke

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo et al. · Nature Genetics · 2011 · 546 citations · Full text

Developmental Biology, Somatic Variant, Genetic Disorder +8

Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples

Daniëlle de Jong, Sofie Verbeke, Daniëlle Meijer et al. · BMC Research Notes · 2011 · 263 citations · Full text

Long-Term Outcomes and Genetic Predictors of Response to Metastasis-Directed Therapy Versus Observation in Oligometastatic Prostate Cancer: Analysis of STOMP and ORIOLE Trials

Matthew P. Deek, Kim Van der Eecken, Philip Sutera et al. · Journal of Clinical Oncology · 2022 · 222 citations · Full text

Distinct histological features characterize primary angiosarcoma of bone

Sofie Verbeke, Franco Bertoni, Patrizia Bacchini et al. · Histopathology · 2011 · 67 citations

R132C IDH1 Mutations Are Found in Spindle Cell Hemangiomas and Not in Other Vascular Tumors or Malformations

Kyle C. Kurek, Twinkal C. Pansuriya, Maayke A.J.H. van Ruler et al. · American Journal Of Pathology · 2013 · 66 citations · Full text

Tumor Biology, Tumoral Pathology, Pathology +6