Works matching AU Stratton, Michael R.

Results: 64

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer.

Published in:

Nucleic Acids Research, 2010, v. 38, p. D652, doi. 10.1093/nar/gkp995

By:

Forbes, Simon A.;
Tang, Gurpreet;
Bindal, Nidhi;
Bamford, Sally;
Dawson, Elisabeth;
Cole, Charlotte;
Chai Yin Kok;
Mingming Jia;
Ewing, Rebecca;
Menzies, Andrew;
Teague, Jon W.;
Stratton, Michael R.;
Futreal, P. Andrew

Publication type:

Article

Reconstructing phylogenetic trees from genome-wide somatic mutations in clonal samples.

Published in:

Nature Protocols, 2024, v. 19, n. 6, p. 1866, doi. 10.1038/s41596-024-00962-8

By:

Coorens, Tim H. H.;
Spencer Chapman, Michael;
Williams, Nicholas;
Martincorena, Inigo;
Stratton, Michael R.;
Nangalia, Jyoti;
Campbell, Peter J.

Publication type:

Article

Localisation of susceptibility genes for familial testicular germ cell tumour.

Published in:

APMIS, 2003, v. 111, n. 1, p. 128, doi. 10.1034/j.1600-0463.2003.11101171.x

By:

RAPLEY, ELIZABETH A;
CROCKFORD, GILLIAN P;
EASTON, DOUGLAS F;
STRATTON, MICHAEL R;
BISHOP, D. TIMOTHY

Publication type:

Article

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

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

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

Journeys into the genome of cancer cells.

Published in:

EMBO Molecular Medicine, 2013, v. 5, n. 2, p. 169, doi. 10.1002/emmm.201202388

By:

Stratton, Michael R.

Publication type:

Article

Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.

Published in:

Journal of Pathology, 2012, v. 227, n. 4, p. 446, doi. 10.1002/path.4042

By:

McBride, David J;
Etemadmoghadam, Dariush;
Cooke, Susanna L;
Alsop, Kathryn;
George, Joshy;
Butler, Adam;
Cho, Juok;
Galappaththige, Danushka;
Greenman, Chris;
Howarth, Karen D;
Lau, King W;
Ng, Charlotte K;
Raine, Keiran;
Teague, Jon;
Wedge, David C;
Cancer Study Group, Australian Ovarian;
Caubit, Xavier;
Stratton, Michael R;
Brenton, James D;
Campbell, Peter J

Publication type:

Article

Genetic alterations in 'normal' luminal and myoepithelial cells of the breast.

Published in:

Journal of Pathology, 1999, v. 189, n. 4, p. 496, doi. 10.1002/(SICI)1096-9896(199912)189:4<496::AID-PATH485>3.0.CO;2-D

By:

Lakhani, Sunil R.;
Chaggar, Ranbir;
Davies, Susan;
Jones, Chris;
Collins, Nadine;
Odel, Christopher;
Stratton, Michael R.;
O'Hare, Michael J.

Publication type:

Article

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

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

Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays.

Published in:

Oncogene, 2003, v. 22, n. 8, p. 1247, doi. 10.1038/sj.onc.1206247

By:

Clark, Jeremy;
Edwards, Sandra;
Feber, Andrew;
Flohr, Penny;
John, Megan;
Giddings, Ian;
Crossland, Sue;
Stratton, Michael R;
Wooster, Richard;
Campbell, Colin;
Cooper, Colin S

Publication type:

Article

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

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

Mutations of BRAF and KRAS in gastric cancer and their association with microsatellite instability(There is no commercial sponsorship or competing financial interests.).

Published in:

International Journal of Cancer, 2004, v. 108, n. 1, p. 167, doi. 10.1002/ijc.11553

By:

Wei Zhao;
Tsun Leung Chan;
Kent-Man Chu;
Annie S. Chan;
Michael R. Stratton;
Siu Tsan Yuen;
Suet Yi Leung

Publication type:

Article

The emerging landscape of breast cancer susceptibility.

Published in:

Nature Genetics, 2008, v. 40, n. 1, p. 17, doi. 10.1038/ng.2007.53

By:

Stratton, Michael R.;
Rahman, Nazneen

Publication type:

Article

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

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.

Published in:

Nature Genetics, 2006, v. 38, n. 11, p. 1239, doi. 10.1038/ng1902

By:

Seal, Sheila;
Thompson, Deborah;
Renwick, Anthony;
Elliott, Anna;
Kelly, Patrick;
Barfoot, Rita;
Chagtai, Tasnim;
Jayatilake, Hiran;
Ahmed, Munaza;
Spanova, Katarina;
North, Bernard;
McGuffog, Lesley;
Evans, D. Gareth;
Eccles, Diana;
Easton, Douglas F.;
Stratton, Michael R.;
Rahman, Nazneen

Publication type:

Article

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

Whole genome DNA copy number changes identified by high density oligonucleotide arrays.

Published in:

Human Genomics, 2004, v. 1, n. 4, p. 287, doi. 10.1186/1479-7364-1-4-287

By:

Jing Huang;
Wen Wei;
Jane Zhang;
Guoying Liu;
Bignell, Graham R.;
Stratton, Michael R.;
Futreal, P. Andrew;
Wooster, Richard;
Jones, Keith W.;
Shapero, Michael H.

Publication type:

Article

Mutagenicity of acrylamide and glycidamide in human TP53 knock-in (Hupki) mouse embryo fibroblasts.

Published in:

Archives of Toxicology, 2020, v. 94, n. 12, p. 4173, doi. 10.1007/s00204-020-02878-0

By:

Hölzl-Armstrong, Lisa;
Kucab, Jill E.;
Moody, Sarah;
Zwart, Edwin P.;
Loutkotová, Lucie;
Duffy, Veronica;
Luijten, Mirjam;
Gamboa da Costa, Gonçalo;
Stratton, Michael R.;
Phillips, David H.;
Arlt, Volker M.

Publication type:

Article

A census of amplified and overexpressed human cancer genes.

Published in:

2010

By:

Santarius, Thomas;
Shipley, Janet;
Brewer, Daniel;
Stratton, Michael R.;
Cooper, Colin S.

Publication type:

research

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

Statistical Analysis of Pathogenicity of Somatic Mutations in Cancer.

Published in:

Genetics, 2006, v. 173, n. 4, p. 2187, doi. 10.1534/genetics.105.044677

By:

Greenman, Chris;
Wooster, Richard;
Futreal, P. Andrew;
Stratton, Michael R.;
Easton, Douglas F.

Publication type:

Article

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

Published in:

Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08512-7

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

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

Published in:

Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07842-2

By:

Jiqiu Cheng;
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

High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma.

Published in:

Nature Medicine, 2015, v. 21, n. 1, p. 81, doi. 10.1038/nm.3773

By:

Linnemann, Carsten;
van Buuren, Marit M;
Bies, Laura;
Verdegaal, Els M E;
Schotte, Remko;
Calis, Jorg J A;
Behjati, Sam;
Velds, Arno;
Hilkmann, Henk;
Atmioui, Dris el;
Visser, Marten;
Stratton, Michael R;
Haanen, John B A G;
Spits, Hergen;
van der Burg, Sjoerd H;
Schumacher, Ton N M

Publication type:

Article

Genome sequencing of normal cells reveals developmental lineages and mutational processes.

Published in:

Nature, 2014, v. 513, n. 7518, p. 422, doi. 10.1038/nature13448

By:

Behjati, Sam;
Huch, Meritxell;
van Boxtel, Ruben;
Karthaus, Wouter;
Wedge, David C.;
Martincorena, Iñigo;
Petljak, Mia;
Alexandrov, Ludmil B.;
Gundem, Gunes;
Tarpey, Patrick S.;
Roerink, Sophie;
Maddison, Mark;
Mudie, Laura;
Robinson, Ben;
Campbell, Peter;
Stratton, Michael R.;
Tamuri, Asif U.;
Goldman, Nick;
Blokker, Joyce;
van de Wetering, Marc

Publication type:

Article

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

Published in:

1999

By:

Peto, Julian;
Collins, Nadine;
Barfoot, Rita;
Seal, Sheila;
Warren, William;
Rahman, Nazneen;
Easton, Douglas F.;
Evans, Christopher;
Deacon, Judith;
Stratton, Michael R.;
Peto, J;
Collins, N;
Barfoot, R;
Seal, S;
Warren, W;
Rahman, N;
Easton, D F;
Evans, C;
Deacon, J;
Stratton, M R

Publication type:

journal article

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

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

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

Recurrent histone mutations in T‐cell acute lymphoblastic leukaemia.

Published in:

British Journal of Haematology, 2019, v. 184, n. 4, p. 676, doi. 10.1111/bjh.15155

By:

Collord, Grace;
Martincorena, Inigo;
Young, Matthew D.;
Foroni, Letizia;
Bolli, Niccolo;
Stratton, Michael R.;
Vassiliou, George S.;
Campbell, Peter J.;
Behjati, Sam

Publication type:

Article

SigProfilerMatrixGenerator: a tool for visualizing and exploring patterns of small mutational events.

Published in:

BMC Genomics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12864-019-6041-2

By:

Bergstrom, Erik N.;
Huang, Mi Ni;
Mahto, Uma;
Barnes, Mark;
Stratton, Michael R.;
Rozen, Steven G.;
Alexandrov, Ludmil B.

Publication type:

Article

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

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

Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignment.

Published in:

Bioinformatics, 2023, v. 39, n. 12, p. 1, doi. 10.1093/bioinformatics/btad756

By:

Díaz-Gay, Marcos;
Vangara, Raviteja;
Barnes, Mark;
Wang, Xi;
Islam, S M Ashiqul;
Vermes, Ian;
Duke, Stephen;
Narasimman, Nithish Bharadhwaj;
Yang, Ting;
Jiang, Zichen;
Moody, Sarah;
Senkin, Sergey;
Brennan, Paul;
Stratton, Michael R;
Alexandrov, Ludmil B

Publication type:

Article

The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.

Published in:

Oncogene, 1997, v. 14, n. 25, p. 3099, doi. 10.1038/sj.onc.1201107

By:

Rahman, Nazneen;
Arbour, Laura;
Tonin, Patricia;
Baruchel, Sylvain;
Pritchard-Jones, Kathryn;
Narod, Steven A;
Stratton, Michael R

Publication type:

Article

Short inverted repeats contribute to localized mutability in human somatic cells.

Published in:

Nucleic Acids Research, 2017, v. 45, n. 19, p. 11213, doi. 10.1093/nar/gkx731

By:

Xueqing Zou;
Morganella, Sandro;
Glodzik, Dominik;
Davies, Helen;
Yilin Li;
Stratton, Michael R.;
Nik-Zainal, Serena

Publication type:

Article

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

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

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.

Published in:

Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D945, doi. 10.1093/nar/gkq929

By:

Forbes, Simon A.;
Bindal, Nidhi;
Bamford, Sally;
Cole, Charlotte;
Kok, Chai Yin;
Beare, David;
Jia, Mingming;
Shepherd, Rebecca;
Leung, Kenric;
Menzies, Andrew;
Teague, Jon W.;
Campbell, Peter J.;
Stratton, Michael R.;
Futreal, P. Andrew

Publication type:

Article

Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance.

Published in:

Nucleic Acids Research, 2010, v. 38, n. 16, p. 5432, doi. 10.1093/nar/gkq306

By:

Thornalley, Paul J.;
Waris, Sahar;
Fleming, Thomas;
Santarius, Thomas;
Larkin, Sarah J.;
Winklhofer-Roob, Brigitte M.;
Stratton, Michael R.;
Rabbani, Naila

Publication type:

Article

A mutational signature in gastric cancer suggests therapeutic strategies.

Published in:

Nature Communications, 2015, v. 6, n. 10, p. 8683, doi. 10.1038/ncomms9683

By:

Alexandrov, Ludmil B.;
Nik-Zainal, Serena;
Siu, Hoi Cheong;
Leung, Suet Yi;
Stratton, Michael R

Publication type:

Article

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

Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1010, doi. 10.1038/ejhg.2012.114

By:

Rujirabanjerd, Sinitdhorn;
Nelson, John;
Tarpey, Patrick S;
Hackett, Anna;
Edkins, Sarah;
Raymond, F Lucy;
Schwartz, Charles E;
Turner, Gillian;
Iwase, Shigeki;
Shi, Yang;
Futreal, P Andrew;
Stratton, Michael R;
Gecz, Jozef

Publication type:

Article

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

Corrigendum to: CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.

Published in:

2010

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:

Correction Notice

Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 3, p. 330, doi. 10.1038/ejhg.2009.175

By:

Rujirabanjerd, Sinitdhorn;
Nelson, John;
Tarpey, Patrick S.;
Hackett, Anna;
Edkins, Sarah;
Raymond, F Lucy;
Schwartz, Charles E.;
Turner, Gillian;
Iwase, Shigeki;
Yang Shi;
Futreal, P. Andrew;
Stratton, Michael R.;
Gecz, Jozef

Publication type:

Article

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