Fitim Berisha
Publications by Year
Research Areas
Sarcoma Diagnosis and Treatment, Bone Tumor Diagnosis and Treatments, Cancer-related molecular mechanisms research, Oral and Maxillofacial Pathology, Soft tissue tumor case studies
Most-Cited Works
- → IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours(2011)979 cited
- → Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2(2011)429 cited
- → H3F3A (Histone 3.3) G34W Immunohistochemistry(2017)215 cited
- → Detection of SS18-SSX fusion transcripts in formalin-fixed paraffin-embedded neoplasms: analysis of conventional RT-PCR, qRT-PCR and dual color FISH as diagnostic tools for synovial sarcoma(2007)177 cited
- → Recurrent rearrangements of FOS and FOSB define osteoblastoma(2018)146 cited
- → The H3F3 K36M mutant antibody is a sensitive and specific marker for the diagnosis of chondroblastoma(2016)134 cited
- → A common single-nucleotide variant in T is strongly associated with chordoma(2012)129 cited
- → Undifferentiated Sarcomas Develop through Distinct Evolutionary Pathways(2019)128 cited
- → The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target(2010)115 cited
- → Synovial chondromatosis and soft tissue chondroma: extraosseous cartilaginous tumor defined by FN1 gene rearrangement(2019)101 cited