Works matching AU Stratton, Michael R.

Results: 64
    1
    2

    The cancer genome.

    Published in:
    Nature, 2009, v. 458, n. 7239, p. 719, doi. 10.1038/nature07943
    By:
    • Stratton, Michael R.;
    • Campbell, Peter J.;
    • Futreal, P. Andrew
    Publication type:
    Article
    3

    Cancer: Understanding the target.

    Published in:
    Nature, 2004, v. 430, n. 6995, p. 30, doi. 10.1038/430030a
    By:
    • Stratton, Michael R.;
    • Futreal, P. Andrew
    Publication type:
    Article
    4
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    Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells.

    Published in:
    Nucleic Acids Research, 2013, v. 41, p. D955, doi. 10.1093/nar/gks1111
    By:
    • Wanjuan Yang;
    • Soares, Jorge;
    • Greninger, Patricia;
    • Edelman, Elena J.;
    • Lightfoot, Howard;
    • Forbes, Simon;
    • Bindal, Nidhi;
    • Beare, Dave;
    • Smith, James A.;
    • Thompson, I. Richard;
    • Ramaswamy, Sridhar;
    • Futreal, P. Andrew;
    • Haber, Daniel A.;
    • Stratton, Michael R.;
    • Benes, Cyril;
    • McDermott, Ultan;
    • Garnett, Mathew J.
    Publication type:
    Article
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    Mutational landscape of normal epithelial cells in Lynch Syndrome patients.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29920-2
    By:
    • Lee, Bernard C. H.;
    • Robinson, Philip S.;
    • Coorens, Tim H. H.;
    • Yan, Helen H. N.;
    • Olafsson, Sigurgeir;
    • Lee-Six, Henry;
    • Sanders, Mathijs A.;
    • Siu, Hoi Cheong;
    • Hewinson, James;
    • Yue, Sarah S. K.;
    • Tsui, Wai Yin;
    • Chan, Annie S. Y.;
    • Chan, Anthony K. W.;
    • Ho, Siu Lun;
    • Campbell, Peter J.;
    • Martincorena, Inigo;
    • Buczacki, Simon J. A.;
    • Yuen, Siu Tsan;
    • Leung, Suet Yi;
    • Stratton, Michael R.
    Publication type:
    Article
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    CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.

    Published in:
    European Journal of Human Genetics, 2010, v. 18, n. 5, p. 544, doi. 10.1038/ejhg.2009.220
    By:
    • Hackett, Anna;
    • Tarpey, Patrick S.;
    • Licata, Andrea;
    • Cox, James;
    • Whibley, Annabel;
    • Boyle, Jackie;
    • Rogers, Carolyn;
    • Grigg, John;
    • Partington, Michael;
    • Stevenson, Roger E.;
    • Tolmie, John;
    • Yates, John R. W.;
    • Turner, Gillian;
    • Wilson, Meredith;
    • Futreal, Andrew P.;
    • Corbett, Mark;
    • Shaw, Marie;
    • Gecz, Jozef;
    • Raymond, F. Lucy;
    • Stratton, Michael R.
    Publication type:
    Article
    12
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    Mining cancer genomes in COSMIC.

    Published in:
    2012
    By:
    • Jia, Mingming;
    • Forbes, Simon A.;
    • Beare, David;
    • Bindal, Nidhi;
    • Gunasekaran, Prasad;
    • Leung, Kenric;
    • Kok, Chai Yin;
    • Bamford, Sally;
    • Cole, Charlotte;
    • Ward, Sari;
    • Teague, Jon;
    • Stratton, Michael R.;
    • Campbell, Peter;
    • Futreal, Andrew
    Publication type:
    Abstract
    15

    Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.

    Published in:
    Nature Genetics, 2010, v. 42, n. 7, p. 604, doi. 10.1038/ng.607
    By:
    • Turnbull, Clare;
    • Rapley, Elizabeth A;
    • Seal, Sheila;
    • Pernet, David;
    • Renwick, Anthony;
    • Hughes, Deborah;
    • Ricketts, Michelle;
    • Linger, Rachel;
    • Nsengimana, Jeremie;
    • Deloukas, Panagiotis;
    • Collaboration, UK Testicular Cancer;
    • Huddart, Robert A;
    • Bishop, D Timothy;
    • Easton, Douglas F;
    • Stratton, Michael R;
    • Rahman, Nazneen
    Publication type:
    Article
    16

    A genome-wide association study of testicular germ cell tumor.

    Published in:
    Nature Genetics, 2009, v. 41, n. 7, p. 807, doi. 10.1038/ng.394
    By:
    • Rapley, Elizabeth A.;
    • Turnbull, Clare;
    • Al Olama, Ali Amin;
    • Dermitzakis, Emmanouil T.;
    • Linger, Rachel;
    • Huddart, Robert A.;
    • Renwick, Anthony;
    • Hughes, Deborah;
    • Hines, Sarah;
    • Seal, Sheila;
    • Morrison, Jonathan;
    • Nsengimana, Jeremie;
    • Deloukas, Panagiotis;
    • Rahman, Nazneen;
    • Bishop, D. Timothy;
    • Easton, Douglas F;
    • Stratton, Michael R.
    Publication type:
    Article
    17
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    PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.

    Published in:
    Nature Genetics, 2007, v. 39, n. 2, p. 165, doi. 10.1038/ng1959
    By:
    • Rahman, Nazneen;
    • Seal, Sheila;
    • Thompson, Deborah;
    • Kelly, Patrick;
    • Renwick, Anthony;
    • Elliott, Anna;
    • Reid, Sarah;
    • Spanova, Katarina;
    • Barfoot, Rita;
    • Chagtai, Tasnim;
    • Jayatilake, Hiran;
    • McGuffog, Lesley;
    • Hanks, Sandra;
    • Evans, D. Gareth;
    • Eccles, Diana;
    • Easton, Douglas F.;
    • Stratton, Michael R.
    Publication type:
    Article
    19
    20

    ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.

    Published in:
    Nature Genetics, 2006, v. 38, n. 8, p. 873, doi. 10.1038/ng1837
    By:
    • Renwick, Anthony;
    • Thompson, Deborah;
    • Seal, Sheila;
    • Kelly, Patrick;
    • Chagtai, Tasnim;
    • Ahmed, Munaza;
    • North, Bernard;
    • Jayatilake, Hiran;
    • Barfoot, Rita;
    • Spanova, Katarina;
    • McGuffog, Lesley;
    • Evans, D. Gareth;
    • Eccles, Diana;
    • Easton, Douglas F.;
    • Stratton, Michael R.;
    • Rahman, Nazneen
    Publication type:
    Article
    21
    22

    Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 505, doi. 10.1038/ng.3252
    By:
    • Schulze, Kornelius;
    • Imbeaud, Sandrine;
    • Letouzé, Eric;
    • Rebouissou, Sandra;
    • Couchy, Gabrielle;
    • Meiller, Clément;
    • Shinde, Jayendra;
    • Soysouvanh, Frederic;
    • Calatayud, Anna-Line;
    • Pelletier, Laura;
    • Calvo, Fabien;
    • Nault, Jean-Charles;
    • Bioulac-Sage, Paulette;
    • Stratton, Michael R;
    • Llovet, Josep M;
    • Zucman-Rossi, Jessica;
    • Alexandrov, Ludmil B;
    • Calderaro, Julien;
    • Pinyol, Roser;
    • Balabaud, Charles
    Publication type:
    Article
    23

    Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer.

    Published in:
    Nature Genetics, 2014, v. 46, n. 5, p. 487, doi. 10.1038/ng.2955
    By:
    • Nik-Zainal, Serena;
    • Wedge, David C;
    • Alexandrov, Ludmil B;
    • Petljak, Mia;
    • Butler, Adam P;
    • Bolli, Niccolo;
    • Davies, Helen R;
    • Knappskog, Stian;
    • Martin, Sancha;
    • Papaemmanuil, Elli;
    • Ramakrishna, Manasa;
    • Shlien, Adam;
    • Simonic, Ingrid;
    • Xue, Yali;
    • Tyler-Smith, Chris;
    • Campbell, Peter J;
    • Stratton, Michael R
    Publication type:
    Article
    24

    Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.

    Published in:
    Nature Genetics, 2013, v. 45, n. 6, p. 686, doi. 10.1038/ng.2635
    By:
    • Ruark, Elise;
    • Seal, Sheila;
    • McDonald, Heather;
    • Zhang, Feng;
    • Elliot, Anna;
    • Lau, KingWai;
    • Perdeaux, Elizabeth;
    • Rapley, Elizabeth;
    • Eeles, Rosalind;
    • Peto, Julian;
    • Kote-Jarai, Zsofia;
    • Muir, Kenneth;
    • Nsengimana, Jeremie;
    • Shipley, Janet;
    • Bishop, D Timothy;
    • Stratton, Michael R;
    • Easton, Douglas F;
    • Huddart, Robert A;
    • Rahman, Nazneen;
    • Turnbull, Clare
    Publication type:
    Article
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    Evaluation of RAD50 in familial breast cancer predisposition.

    Published in:
    International Journal of Cancer, 2006, v. 118, n. 11, p. 2911, doi. 10.1002/ijc.21738
    By:
    • Tommiska, Johanna;
    • Seal, Sheila;
    • Renwick, Anthony;
    • Barfoot, Rita;
    • Baskcomb, Linda;
    • Jayatilake, Hiran;
    • Bartkova, Jirina;
    • Tallila, Jonna;
    • Kaare, Milja;
    • Tamminen, Anitta;
    • Heikkilä, Päivi;
    • Evans, D. Gareth;
    • Eccles, Diana;
    • Aittomäki, Kristiina;
    • Blomqvist, Carl;
    • Bartek, Jiri;
    • Stratton, Michael R.;
    • Nevanlinna, Heli;
    • Rahman, Nazneen
    Publication type:
    Article
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    A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.

    Published in:
    Nature, 1998, v. 391, n. 6663, p. 184, doi. 10.1038/34432
    By:
    • Hemminki, Akseli;
    • Markie, David;
    • Tomlinson, Ian;
    • Avizienyte, Egle;
    • Roth, Stina;
    • Loukola, Anu;
    • Bignell, Graham;
    • Warren, William;
    • Aminoff, Maria;
    • Höglund, Pia;
    • Järvinen, Heikki;
    • Kristo, Paula;
    • Pelin, Katarina;
    • Ridanpää, Maaret;
    • Salovaara, Reijo;
    • Toro, Tumi;
    • Bodmer, Walter;
    • Olschwang, Sylviane;
    • Olsen, Anne S.;
    • Stratton, Michael R.
    Publication type:
    Article
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    33

    A census of human cancer genes.

    Published in:
    Nature Reviews Cancer, 2004, v. 4, n. 3, p. 177, doi. 10.1038/nrc1299
    By:
    • Futreal, P. Andrew;
    • Coin, Lachlan;
    • Marshall, Mhairi;
    • Down, Thomas;
    • Hubbard, Timothy;
    • Wooster, Richard;
    • Rahman, Nazneen;
    • Stratton, Michael R.
    Publication type:
    Article
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    Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.

    Published in:
    Human Genetics, 2008, v. 123, n. 5, p. 469, doi. 10.1007/s00439-008-0498-4
    By:
    • Santos, Lane J. Jaeckle;
    • Chao Xing;
    • Barnes, Robert B.;
    • Ades, Lesley C.;
    • Megarbane, Andre;
    • Vidal, Christopher;
    • Xuereb, Angela;
    • Tarpey, Patrick S.;
    • Smith, RaVaella;
    • Khazab, Mahmoud;
    • Shoubridge, Cheryl;
    • Partington, Michael;
    • Futreal, Andrew;
    • Stratton, Michael R.;
    • Gecz, Jozef;
    • Zinn, Andrew R.
    Publication type:
    Article
    38
    39

    Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

    Published in:
    Oncogene, 2000, v. 19, n. 36, p. 4170, doi. 10.1038/sj.onc.1203735
    By:
    • Rahman, Nazneen;
    • Teare, M Dawn;
    • Seal, Sheila;
    • Renard, Helene;
    • Mangion, Jon;
    • Cour, Chantal;
    • Thompson, Deborah;
    • Shugart, Yin;
    • Eccles, Diana;
    • Devilee, Peter;
    • Meijers, Hanne;
    • Nathanson, Katherine L;
    • Neuhausen, Susan L;
    • Weber, Barbara;
    • Chang-Claude, Jenny;
    • Easton, Douglas F;
    • Goldgar, David;
    • Stratton, Michael R
    Publication type:
    Article
    40
    41

    COSMIC: exploring the world's knowledge of somatic mutations in human cancer.

    Published in:
    Nucleic Acids Research, 2015, v. 43, n. D1, p. D805, doi. 10.1093/nar/gku1075
    By:
    • Forbes, Simon A.;
    • Beare, David;
    • Gunasekaran, Prasad;
    • Leung, Kenric;
    • Bindal, Nidhi;
    • Boutselakis, Harry;
    • Ding, Minjie;
    • Bamford, Sally;
    • Cole, Charlotte;
    • Ward, Sari;
    • Kok, Chai Yin;
    • Jia, Mingming;
    • De, Tisham;
    • Teague, Jon W.;
    • Stratton, Michael R.;
    • McDermott, Ultan;
    • Campbell, Peter J.
    Publication type:
    Article
    42

    Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04650-6
    By:
    • Wegert, Jenny;
    • Vokuhl, Christian;
    • Collord, Grace;
    • Del Castillo Velasco-Herrera, Martin;
    • Farndon, Sarah J.;
    • Guzzo, Charlotte;
    • Jorgensen, Mette;
    • Anderson, John;
    • Slater, Olga;
    • Duncan, Catriona;
    • Bausenwein, Sabrina;
    • Streitenberger, Heike;
    • Ziegler, Barbara;
    • Furtwängler, Rhoikos;
    • Graf, Norbert;
    • Stratton, Michael R.;
    • Campbell, Peter J.;
    • Jones, David T. W.;
    • Koelsche, Christian;
    • Pfister, Stefan M.
    Publication type:
    Article
    43

    Recurrent rearrangements of FOS and FOSB define osteoblastoma.

    Published in:
    Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-04530-z
    By:
    • Fittall, Matthew W.;
    • Mifsud, William;
    • Pillay, Nischalan;
    • Hongtao Ye;
    • Strobl, Anna-Christina;
    • Verfaillie, Annelien;
    • Demeulemeester, Jonas;
    • Lei Zhang;
    • Berisha, Fitim;
    • Tarabichi, Maxime;
    • Young, Matthew D.;
    • Miranda, Elena;
    • Tarpey, Patrick S.;
    • Tirabosco, Roberto;
    • Amary, Fernanda;
    • Grigoriadis, Agamemnon E.;
    • Stratton, Michael R.;
    • Van Loo, Peter;
    • Antonescu, Cristina R.;
    • Campbell, Peter J.
    Publication type:
    Article
    44

    Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01355-0
    By:
    • Cheng, Jiqiu;
    • Demeulemeester, Jonas;
    • Wedge, David C.;
    • Vollan, Hans Kristian M.;
    • Pitt, Jason J.;
    • Russnes, Hege G.;
    • Pandey, Bina P.;
    • Nilsen, Gro;
    • Nord, Silje;
    • Bignell, Graham R.;
    • White, Kevin P.;
    • Børresen-Dale, Anne-Lise;
    • Campbell, Peter J.;
    • Kristensen, Vessela N.;
    • Stratton, Michael R.;
    • Lingjærde, Ole Christian;
    • Moreau, Yves;
    • Van Loo, Peter
    Publication type:
    Article
    45
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    Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors.

    Published in:
    Genes, Chromosomes & Cancer, 2010, v. 49, n. 11, p. 1062, doi. 10.1002/gcc.20815
    By:
    • McBride, David J.;
    • Orpana, Arto K.;
    • Sotiriou, Christos;
    • Joensuu, Heikki;
    • Stephens, Philip J.;
    • Mudie, Laura J.;
    • Hämäläinen, Eija;
    • Stebbings, Lucy A.;
    • Andersson, Leif C.;
    • Flanagan, Adrienne M.;
    • Durbecq, Virginie;
    • Ignatiadis, Michail;
    • Kallioniemi, Olli;
    • Heckman, Caroline A.;
    • Alitalo, Kari;
    • Edgren, Henrik;
    • Futreal, P. Andrew;
    • Stratton, Michael R.;
    • Campbell, Peter J.
    Publication type:
    Article
    48

    GLO1-A novel amplified gene in human cancer.

    Published in:
    Genes, Chromosomes & Cancer, 2010, v. 49, n. 8, p. 711, doi. 10.1002/gcc.20784
    By:
    • Santarius, Thomas;
    • Bignell, Graham R.;
    • Greenman, Chris D.;
    • Widaa, Sara;
    • Chen, Lina;
    • Mahoney, Claire L.;
    • Butler, Adam;
    • Edkins, Sarah;
    • Waris, Sahar;
    • Thornalley, Paul J.;
    • Futreal, P. Andrew;
    • Stratton, Michael R.
    Publication type:
    Article
    49

    Cancer and genomics.

    Published in:
    Nature, 2001, v. 409, n. 6822, p. 850, doi. 10.1038/35057046
    By:
    • Futreal, P. Andrew;
    • Kasprzyk, Arek;
    • Birney, Ewan;
    • Mullikin, James C.;
    • Wooster, Richard;
    • Stratton, Michael R.
    Publication type:
    Article
    50

    Data mining using the Catalogue of Somatic Mutations in Cancer BioMart.

    Published in:
    Database: The Journal of Biological Databases & Curation, 2011, v. 2011, n. 18, p. 1
    By:
    • Shepherd, Rebecca;
    • Forbes, Simon A.;
    • Beare, David;
    • Bamford, S.;
    • Cole, Charlotte G.;
    • Ward, Sari;
    • Bindal, Nidhi;
    • Gunasekaran, Prasad;
    • Jia, Mingming;
    • Kok, Chai Yin;
    • Leung, Kenric;
    • Menzies, Andrew;
    • Butler, Adam P.;
    • Teague, Jon W.;
    • Campbell, Peter J.;
    • Stratton, Michael R.;
    • Futreal, P. Andrew
    Publication type:
    Article