Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2 von Guilhamon, Paul, Eskandarpour, Malihe, Halai, Dina, Wilson, Gareth A., Feber, Andrew, Teschendorff, Andrew E., Gomez, Valenti, Hergovich, Alexander, Tirabosco, Roberto, Fernanda Amary, M., Baumhoer, Daniel, Jundt, Gernot, Ross, Mark T., Flanagan, Adrienne M., Beck, Stephan

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Undifferentiated Sarcomas Develop through Distinct Evolutionary Pathways von Steele, Christopher D., Tarabichi, Maxime, Oukrif, Dahmane, Webster, Amy P., Ye, Hongtao, Fittall, Matthew, Lombard, Patrick, Martincorena, Iñigo, Tarpey, Patrick S., Collord, Grace, Haase, Kerstin, Strauss, Sandra J., Berisha, Fitim, Vaikkinen, Heli, Dhami, Pawan, Jansen, Marnix, Behjati, Sam, Amary, M. Fernanda, Tirabosco, Roberto, Feber, Andrew, Campbell, Peter J., Alexandrov, Ludmil B., Van Loo, Peter, Flanagan, Adrienne M., Pillay, Nischalan

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Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma: characterization of five cases von Amary, M. Fernanda, O’Donnell, Paul, Berisha, Fitim, Tirabosco, Roberto, Briggs, Tim, Pollock, Rob, Flanagan, Adrienne M.

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IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours von Amary, M Fernanda, Bacsi, Krisztian, Maggiani, Francesca, Damato, Stephen, Halai, Dina, Berisha, Fitim, Pollock, Robin, O'Donnell, Paul, Grigoriadis, Anita, Diss, Tim, Eskandarpour, Malihe, Presneau, Nadège, Hogendoorn, Pancras CW, Futreal, Andrew, Tirabosco, Roberto, Flanagan, Adrienne M

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Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma von Behjati, Sam, Tarpey, Patrick S., Haase, Kerstin, Ye, Hongtao, Young, Matthew D., Alexandrov, Ludmil B., Farndon, Sarah J., Collord, Grace, Wedge, David C., Martincorena, Inigo, Cooke, Susanna L., Davies, Helen, Mifsud, William, Lidgren, Mathias, Martin, Sancha, Latimer, Calli, Maddison, Mark, Butler, Adam P., Teague, Jon W., Pillay, Nischalan, Shlien, Adam, McDermott, Ultan, Futreal, P. Andrew, Baumhoer, Daniel, Zaikova, Olga, Bjerkehagen, Bodil, Myklebost, Ola, Amary, M. Fernanda, Tirabosco, Roberto, Van Loo, Peter, Stratton, Michael R., Flanagan, Adrienne M., Campbell, Peter J.

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Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2 von Amary, M Fernanda, Damato, Stephen, Halai, Dina, Eskandarpour, Malihe, Berisha, Fitim, Bonar, Fiona, McCarthy, Stan, Fantin, Valeria R, Straley, Kimberly S, Lobo, Samira, Aston, Will, Green, Claire L, Gale, Rosemary E, Tirabosco, Roberto, Futreal, Andrew, Campbell, Peter, Presneau, Nadège, Flanagan, Adrienne M

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The driver landscape of sporadic chordoma von Tarpey, Patrick S., Behjati, Sam, Young, Matthew D., Martincorena, Inigo, Alexandrov, Ludmil B., Farndon, Sarah J., Guzzo, Charlotte, Hardy, Claire, Latimer, Calli, Butler, Adam P., Teague, Jon W., Shlien, Adam, Futreal, P. Andrew, Shah, Sohrab, Bashashati, Ali, Jamshidi, Farzad, Nielsen, Torsten O., Huntsman, David, Baumhoer, Daniel, Brandner, Sebastian, Wunder, Jay, Dickson, Brendan, Cogswell, Patricia, Sommer, Josh, Phillips, Joanna J., Amary, M. Fernanda, Tirabosco, Roberto, Pillay, Nischalan, Yip, Stephen, Stratton, Michael R., Flanagan, Adrienne M., Campbell, Peter J.

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A common single-nucleotide variant in T is strongly associated with chordoma von Pillay, Nischalan, Plagnol, Vincent, Tarpey, Patrick S, Lobo, Samira B, Presneau, Nadège, Szuhai, Karoly, Halai, Dina, Berisha, Fitim, Cannon, Stephen R, Mead, Simon, Kasperaviciute, Dalia, Palmen, Jutta, Talmud, Philippa J, Kindblom, Lars-Gunnar, Amary, M Fernanda, Tirabosco, Roberto, Flanagan, Adrienne M

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GNAS mutations are not detected in parosteal and low-grade central osteosarcomas von Salinas-Souza, Carolina, De Andrea, Carlos, Bihl, Michel, Kovac, Michal, Pillay, Nischalan, Forshew, Tim, Gutteridge, Alice, Ye, Hongtao, Amary, M Fernanda, Tirabosco, Roberto, Toledo, Silvia Regina Caminada, Baumhoer, Daniel, Flanagan, Adrienne M

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Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study von Presneau, Nadège, Shalaby, Asem, Ye, Hongtao, Pillay, Nischalan, Halai, Dina, Idowu, Bernadine, Tirabosco, Roberto, Whitwell, Duncan, Jacques, Thomas S, Kindblom, Lars-Gunnar, Brüderlein, Silke, Möller, Peter, Leithner, Andreas, Liegl, Bernadette, Amary, Fernanda M, Athanasou, Nicholas N, Hogendoorn, Pancras CW, Mertens, Fredrik, Szuhai, Karoly, Flanagan, Adrienne M

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Isocitrate dehydrogenase 1 mutations (IDH1) and p16/CDKN2A copy number change in conventional chondrosarcomas von Amary, M. Fernanda, Ye, Hongtao, Forbes, Georgina, Damato, Stephen, Maggiani, Francesca, Pollock, Robin, Tirabosco, Roberto, Flanagan, Adrienne M.

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IDH1 mutations are not found in cartilaginous tumours other than central and periosteal chondrosarcomas and enchondromas von Damato, Stephen, Alorjani, Mohammed, Bonar, Fiona, McCarthy, Stanley W, Cannon, Stephen R, O'Donnell, Paul, Tirabosco, Roberto, Amary, M Fernanda, Flanagan, Adrienne M

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P63 does not regulate brachyury expression in human chordomas and osteosarcomas von Pillay, Nischalan, Amary, Fernanda M, Berisha, Fitim, Tirabosco, Roberto, Flanagan, Adrienne M

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Gout‐mimicking sarcoma recurrence at a prosthesis bone interface remote from any joint von Ogunwale, Bamikole Busayo Kenneth, Amary, M Fernanda, Skinner, John Andrew Mcinnes, Green, Ruth Amanda Rachel

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In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets von Arbajian, Elsa, Puls, Florian, Antonescu, Cristina R, Amary, Fernanda, Sciot, Raf, Debiec-Rychter, Maria, Sumathi, Vaiyapuri P, Järås, Marcus, Magnusson, Linda, Nilsson, Jenny, Hofvander, Jakob, Mertens, Fredrik

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Clinical outcome in patients with peripherally‐sited atypical lipomatous tumours and dedifferentiated liposarcoma von Kalimuthu, Sangeetha N, Tilley, Charles, Forbes, Georgina, Ye, Hongtao, Lehovsky, Katie, Pillay, Nischalan, Seddon, Beatrice M, O'Donnell, Paul, Pollock, Robin, Tirabosco, Roberto, Amary, M Fernanda, Flanagan, Adrienne M.

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Corrigendum: distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone von Behjati, Sam, Tarpey, Patrick S, Presneau, Nadege, Scheipl, Susanne, Pillay, Nischalan, Van Loo, Peter, Wedge, David C, Cooke, Susanna L, Gundem, Gunes, Davies, Helen, Nik-Zainal, Serena, Martin, Sancha, McLaren, Stuart, Goodie, Victoria, Robinson, Ben, Butler, Adam, Teague, Jon W, Halai, Dina, Khatri, Bhavisha, Myklebost, Ola, Baumhoer, Daniel, Jundt, Gernot, Hamoudi, Rifat, Tirabosco, Roberto, Amary, M. Fernanda, Futreal, P. Andrew, Stratton, Michael R, Campbell, Peter J, Flanagan, Adrienne M

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Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone von Behjati, Sam, Tarpey, Patrick S, Presneau, Nadege, Scheipl, Susanne, Pillay, Nischalan, Van Loo, Peter, Wedge, David C, Cooke, Susanna L, Gundem, Gunes, Davies, Helen, Nik-Zainal, Serena, Martin, Sancha, McLaren, Stuart, Goodie, Victoria, Robinson, Ben, Butler, Adam, Teague, Jon W, Halai, Dina, Khatri, Bhavisha, Myklebost, Ola, Baumhoer, Daniel, Jundt, Gernot, Hamoudi, Rifat, Tirabosco, Roberto, Amary, M. Fernanda, Futreal, P. Andrew, Stratton, Michael R, Campbell, Peter J, Flanagan, Adrienne M

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Distinct H3F3A and H3F3B driver variants define chondroblastoma and giant cell tumour of bone von Behjati, Sam, Tarpey, Patrick S, Presneau, Nadège, Scheipl, Susanne, Pillay, Nischalan, Van Loo, Peter, Wedge, David C, Cooke, Susanna L, Gundem, Gunes, Davies, Helen, Nik-Zainal, Serena, Martin, Sancha, McLaren, Stuart, Goodie, Victoria, Robinson, Ben, Butler, Adam, Teague, Jon W, Halai, Dina, Khatri, Bhavisha, Myklebost, Ola, Baumhoer, Daniel, Jundt, Gernot, Hamoudi, Rifat, Tirabosco, Roberto, Amary, M Fernanda, Futreal, P Andrew, Stratton, Michael R, Campbell, Peter J, Flanagan, Adrienne M

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Clear cell sarcoma of the mediastinum von Tirabosco, Roberto, MD, Lang-Lazdunski, Loic, MD, PhD, FRCS, Diss, Timothy C., PhD, Amary, Maria Fernanda C., MD, PhD, Rodriguez-Justo, Manuel, MD, Landau, David, FRCP, Lorenzi, Will, MD, Flanagan, Adrienne M., MD, PhD, FRCPath

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