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Simon A Forbes
Simon A Forbes
Verified email at sanger.ac.uk
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Year
COSMIC: the catalogue of somatic mutations in cancer
JG Tate, S Bamford, HC Jubb, Z Sondka, DM Beare, N Bindal, ...
Nucleic acids research 47 (D1), D941-D947, 2019
37182019
Patterns of somatic mutation in human cancer genomes
C Greenman, P Stephens, R Smith, GL Dalgliesh, C Hunter, G Bignell, ...
Nature 446 (7132), 153-158, 2007
37142007
Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells
W Yang, J Soares, P Greninger, EJ Edelman, H Lightfoot, S Forbes, ...
Nucleic acids research 41 (D1), D955-D961, 2012
28072012
COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
SA Forbes, N Bindal, S Bamford, C Cole, CY Kok, D Beare, M Jia, ...
Nucleic acids research 39 (suppl_1), D945-D950, 2010
26702010
COSMIC: exploring the world's knowledge of somatic mutations in human cancer
SA Forbes, D Beare, P Gunasekaran, K Leung, N Bindal, H Boutselakis, ...
Nucleic acids research 43 (D1), D805-D811, 2015
26062015
COSMIC: somatic cancer genetics at high-resolution
SA Forbes, D Beare, H Boutselakis, S Bamford, N Bindal, J Tate, CG Cole, ...
Nucleic acids research 45 (D1), D777-D783, 2017
19762017
Clinical and biological implications of driver mutations in myelodysplastic syndromes
E Papaemmanuil, M Gerstung, L Malcovati, S Tauro, G Gundem, ...
Blood, The Journal of the American Society of Hematology 122 (22), 3616-3627, 2013
19702013
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website
S Bamford, E Dawson, S Forbes, J Clements, R Pettett, A Dogan, ...
British journal of cancer 91 (2), 355-358, 2004
13612004
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes
GL Dalgliesh, K Furge, C Greenman, L Chen, G Bignell, A Butler, ...
Nature 463 (7279), 360-363, 2010
13452010
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers
Z Sondka, S Bamford, CG Cole, SA Ward, I Dunham, SA Forbes
Nature Reviews Cancer 18 (11), 696-705, 2018
11532018
Intragenic ERBB2 kinase mutations in tumours
P Stephens, C Hunter, G Bignell, S Edkins, H Davies, J Teague, ...
Nature 431 (7008), 525-526, 2004
9432004
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer
G Van Haaften, GL Dalgliesh, H Davies, L Chen, G Bignell, C Greenman, ...
Nature genetics 41 (5), 521-523, 2009
9252009
COSMIC: high‐resolution cancer genetics using the catalogue of somatic mutations in cancer
SA Forbes, D Beare, N Bindal, S Bamford, S Ward, CG Cole, M Jia, C Kok, ...
Current protocols in human genetics 91 (1), 10.11. 1-10.11. 37, 2016
8822016
Complete sequence and gene map of a human major histocompatibility complex
MHC Sequencing Consortium
Nature 401 (6756), 921-923, 1999
8481999
The BioMart community portal: an innovative alternative to large, centralized data repositories
D Smedley, S Haider, S Durinck, L Pandini, P Provero, J Allen, O Arnaiz, ...
Nucleic acids research 43 (W1), W589-W598, 2015
7862015
COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer
SA Forbes, G Tang, N Bindal, S Bamford, E Dawson, C Cole, CY Kok, ...
Nucleic acids research 38 (suppl_1), D652-D657, 2010
6432010
Somatic mutations of the protein kinase gene family in human lung cancer
H Davies, C Hunter, R Smith, P Stephens, C Greenman, G Bignell, ...
Cancer research 65 (17), 7591-7595, 2005
5772005
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
I Lemmens, WJM Van de Ven, K Kas, CX Zhang, S Giraud, V Wautot, ...
Human molecular genetics 6 (7), 1177-1183, 1997
5441997
Characterization of mutations in patients with multiple endocrine neoplasia type 1
JHD Bassett, SA Forbes, AAJ Pannett, SE Lloyd, PT Christie, C Wooding, ...
The American Journal of Human Genetics 62 (2), 232-244, 1998
5141998
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set
ON Ikediobi, H Davies, G Bignell, S Edkins, C Stevens, S O'Meara, ...
Molecular cancer therapeutics 5 (11), 2606-2612, 2006
4932006
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