Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts von Papaemmanuil, E, Cazzola, M, Boultwood, J, Malcovati, L, Vyas, P, Bowen, D, Pellagatti, A, Wainscoat, J.S, Hellstrom-Lindberg, E, Gambacorti-Passerini, C, Godfrey, A.L, Rapado, I, Cvejic, A, Rance, R, McGee, C, Ellis, P, Mudie, L.J, Stephens, P.J, McLaren, S, Massie, C.E, Tarpey, P.S, Varela, I, Nik-Zainal, S, Davies, H.R, Shlien, A, Jones, D, Raine, K, Hinton, J, Butler, A.P, Teague, J.W, Baxter, E.J, Score, J, Galli, A, Della Porta, M.G, Travaglino, E, Groves, M, Tauro, S, Munshi, N.C, Anderson, K.C, El-Naggar, A, Fischer, A, Mustonen, V, Warren, A.J, Cross, N.C.P, Green, A.R, Futreal, P.A, Stratton, M.R, Campbell, P.J

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High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes von Reid, Alistair G., Tarpey, Patrick S., Nacheva, Ellie P.

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Amino acid sequence and the cellular location of the Na(+)-dependent D-glucose symporters (SGLT1) in the ovine enterocyte and the parotid acinar cell von Tarpey, P S, Wood, I S, Shirazi-Beechey, S P, Beechey, R B

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Epithelial phosphate transport in ruminants, mechanisms and regulation von Shirazi-Beechey, Soraya P., Penny, Jeffery I., Dyer, Jane, Wood, I. Stuart, Tarpey, Patrick S., Scott, Dennis, Buchan, William

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Undifferentiated Sarcomas Develop through Distinct Evolutionary Pathways von Steele, CD, Tarabichi, M, Oukrif, D, Webster, AP, Ye, H, Fittall, M, Lombard, P, Martincorena, I, Tarpey, PS, Collord, G, Haase, K, Strauss, SJ, Berisha, F, Vaikkinen, H, Dhami, P, Jansen, M, Behjati, S, Amary, MF, Tirabosco, R, Feber, A, Campbell, PJ, Alexandrov, LB, Van Loo, P, Flanagan, AM, Pillay, N

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Embryonal precursors of Wilms tumor von Coorens, THH, Treger, TD, Al-Saadi, R, Moore, L, Tran, MGB, Mitchell, TJ, Tugnait, S, Thevanesan, C, Young, MD, Oliver, TRW, Oostveen, M, Collord, G, Tarpey, PS, Cagan, A, Hooks, Y, Brougham, M, Reynolds, BC, Barone, G, Anderson, J, Jorgensen, M, Burke, GAA, Visser, J, Nicholson, JC, Smeulders, N, Mushtaq, I, Stewart, GD, Campbell, PJ, Wedge, DC, Martincorena, I, Rampling, D, Hook, L, Warren, AY, Coleman, N, Chowdhury, T, Sebire, N, Drost, J, Saeb-Parsy, K, Stratton, MR, Straathof, K, Pritchard-Jones, K, Behjati, S

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Recurrent rearrangements of FOS and FOSB define osteoblastoma von Fittall, MW, Mifsud, W, Pillay, N, Ye, H, Strobl, A-C, Verfaillie, A, Demeulemeester, J, Zhang, L, Berisha, F, Tarabichi, M, Young, MD, Miranda, E, Tarpey, PS, Tirabosco, R, Amary, F, Grigoriadis, AE, Stratton, MR, Van Loo, P, Antonescu, CR, Campbell, PJ, Flanagan, AM, Behjati, S

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The driver landscape of sporadic chordoma von Tarpey, PS, Behjati, S, Young, MD, Martincorena, I, Alexandrov, LB, Farndon, SJ, Guzzo, C, Hardy, C, Latimer, C, Butler, AP, Teague, JW, Shlien, A, Futreal, PA, Shah, S, Bashashati, A, Jamshidi, F, Nielsen, TO, Huntsman, D, Baumhoer, D, Brandner, S, Wunder, J, Dickson, B, Cogswell, P, Sommer, J, Phillips, JJ, Amary, MF, Tirabosco, R, Pillay, N, Yip, S, Stratton, MR, Flanagan, AM, Campbell, PJ

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Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma von Behjati, S, Tarpey, PS, Haase, K, Ye, H, Young, MD, Alexandrov, LB, Farndon, SJ, Collord, G, Wedge, DC, Martincorena, I, Cooke, SL, Davies, H, Mifsud, W, Lidgren, M, Martin, S, Latimer, C, Maddison, M, Butler, AP, Teague, JW, Pillay, N, Shlien, A, McDermott, U, Futreal, PA, Baumhoer, D, Zaikova, O, Bjerkehagen, B, Myklebost, O, Amary, MF, Tirabosco, R, Van Loo, P, Stratton, MR, Flanagan, AM, Campbell, PJ

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Mutational signatures of ionizing radiation in second malignancies von Behjati, S, Gundem, G, Wedge, DC, Roberts, ND, Tarpey, PS, Cooke, SL, Van Loo, P, Alexandrov, LB, Ramakrishna, M, Davies, H, Nik-Zainal, S, Hardy, C, Latimer, C, Raine, KM, Stebbings, L, Menzies, A, Jones, D, Shepherd, R, Butler, AP, Teague, JW, Jorgensen, M, Khatri, B, Pillay, N, Shlien, A, Futreal, PA, Badie, C, ICGC Prostate Group, McDermott, U, Bova, GS, Richardson, AL, Flanagan, AM, Stratton, MR, Campbell, PJ

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Mutational signatures of ionizing radiation in second malignancies von Behjati, S, Gundem, G, Wedge, DC, Roberts, ND, Tarpey, PS, Cooke, SL, Van Loo, P, Alexandrov, LB, Ramakrishna, M, Davies, H, Nik-Zainal, S, Hardy, C, Latimer, C, Raine, KM, Stebbings, L, Menzies, A, Jones, D, Shepherd, R, Butler, AP, Teague, JW, Jorgensen, M, Khatri, B, Pillay, N, Shlien, A, Futreal, PA, Badie, C, ICGC Prostate Group, McDermott, U, Bova, GS, Richardson, AL, Flanagan, AM, Stratton, MR, Campbell, PJ

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HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: The results of an X-chromosome exome sequencing study von Friez, MJ, Brooks, SS, Stevenson, RE, Field, M, Basehore, MJ, Adès, LC, Sebold, C, Mcgee, S, Saxon, S, Skinner, C, Craig, ME, Murray, L, Simensen, RJ, Yap, YY, Shaw, MA, Gardner, A, Corbett, M, Kumar, R, Bosshard, M, Van Loon, B, Tarpey, PS, Abidi, F, Gecz, J, Schwartz, CE

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Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells von Ju, YS, Tubio, JM, Mifsud, W, Fu, B, Davies, HR, Ramakrishna, M, Li, Y, Yates, L, Gundem, G, Tarpey, PS, Behjati, S, Papaemmanuil, E, Martin, S, Fullam, A, Gerstung, M, ICGC Prostate Cancer Working Group, ICGC Bone Cancer Working Group, ICGC Breast Cancer Working Group, Nangalia, J, Green, AR, Caldas, C, Borg, Å, Tutt, A, Lee, MT, van't Veer, LJ, Tan, BK, Aparicio, S, Span, PN, Martens, JW, Knappskog, S, Vincent-Salomon, A, Børresen-Dale, AL, Eyfjörd, JE, Flanagan, AM, Foster, C, Neal, DE, Cooper, C, Eeles, R, Lakhani, SR, Desmedt, C, Thomas, G, Richardson, AL, Purdie, CA, Thompson, AM, McDermott, U, Yang, F, Nik-Zainal, S, Campbell, PJ, Stratton, MR

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Recurrent PTPRB and PLCG1 mutations in angiosarcoma von Behjati, S, Tarpey, PS, Sheldon, H, Martincorena, I, Van Loo, P, Gundem, G, Wedge, DC, Ramakrishna, M, Cooke, SL, Pillay, N, Vollan, HK, Papaemmanuil, E, Koss, H, Bunney, TD, Hardy, C, Joseph, OR, Martin, S, Mudie, L, Butler, A, Teague, JW, Patil, M, Steers, G, Cao, Y, Gumbs, C, Ingram, D, Lazar, AJ, Little, L, Mahadeshwar, H, Protopopov, A, Al Sannaa, GA, Seth, S, Song, X, Tang, J, Zhang, J, Ravi, V, Torres, KE, Khatri, B, Halai, D, Roxanis, I, Baumhoer, D, Tirabosco, R, Amary, MF, Boshoff, C, McDermott, U, Katan, M, Stratton, MR, Futreal, PA, Flanagan, AM, Harris, A, Campbell, PJ

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Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer von Ju, YSE, Alexandrov, LB, Gerstung, M, Martincorena, I, Nik-Zainal, S, Ramakrishna, M, Davies, HR, Papaemmanuil, E, Gundem, G, Shlien, A, Bolli, N, Behjati, S, Tarpey, PS, Nangalia, J, Massie, CE, Butler, AP, Teague, JW, Vassiliou, GS, Green, AR, Du, MQ, Unnikrishnan, A, Pimanda, JE, Teh, BTE, Munshi, N, Greaves, M, Vyas, P, El-Naggar, AK, Santarius, T, Collins, VP, Grundy, R, Taylor, JA, Hayes, DN, Malkin, D, Foster, CS, Warren, AY, Whitaker, HC, Brewer, D, Eeles, R, Cooper, C, Neal, D, Visakorpi, T, Isaacs, WB, Bova, GS, Flanagan, AM, Futreal, PA, Lynch, AG, Chinnery, PF, McDermott, U, Stratton, MR, Campbell, PJ

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Validation of a croup score and its use in triaging children with croup von Jacobs, S., Shortland, G., Warner, J., Dearden, A., Gataure, P. Singh, Tarpey, J.

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