Nadège Presneau
University of Westminster(GB)
Publications by Year
Research Areas
BRCA gene mutations in cancer, Sarcoma Diagnosis and Treatment, Genetic Associations and Epidemiology, Bone Tumor Diagnosis and Treatments, Bioinformatics and Genomic Networks
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
- → Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone(2013)845 cited
- → Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas(2006)581 cited
- → Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2(2011)429 cited
- → Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional‐based study(2010)194 cited
- → Diagnostic value of H3F3A mutations in giant cell tumour of bone compared to osteoclast‐rich mimics(2015)160 cited
- → A common single-nucleotide variant in T is strongly associated with chordoma(2012)129 cited
- → A molecular map of mesenchymal tumors(2005)127 cited
- → Potential therapeutic targets for chordoma: PI3K/AKT/TSC1/TSC2/mTOR pathway(2009)118 cited
- → The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target(2010)115 cited