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| The repertoire of mutational signatures in human cancer LB Alexandrov, J Kim, NJ Haradhvala, MN Huang, AWT Ng, Y Wu, A Boot, ... Nature 578 (7793), 94-101, 2020 | 3045 | 2020 |
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| Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin KA Hoadley, C Yau, DM Wolf, AD Cherniack, D Tamborero, S Ng, ... Cell 158 (4), 929-944, 2014 | 1606 | 2014 |
| Whole-genome landscapes of major melanoma subtypes NK Hayward, JS Wilmott, N Waddell, PA Johansson, MA Field, K Nones, ... Nature 545 (7653), 175-180, 2017 | 1414 | 2017 |
| Non-coding recurrent mutations in chronic lymphocytic leukaemia XS Puente, S Beà, R Valdés-Mas, N Villamor, J Gutiérrez-Abril, ... Nature 526 (7574), 519-524, 2015 | 1074 | 2015 |
| A compendium of mutational cancer driver genes F Martínez-Jiménez, F Muiños, I Sentís, J Deu-Pons, I Reyes-Salazar, ... Nature Reviews Cancer 20 (10), 555-572, 2020 | 1033 | 2020 |
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| Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel A González-Pérez, N López-Bigas The American Journal of Human Genetics 88 (4), 440-449, 2011 | 914 | 2011 |
| Expansion of the BioCyc collection of pathway/genome databases to 160 genomes PD Karp, CA Ouzounis, C Moore-Kochlacs, L Goldovsky, P Kaipa, ... Nucleic acids research 33 (19), 6083-6089, 2005 | 774 | 2005 |
| A framework to rank genomic alterations as targets for cancer precision medicine: the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT) J Mateo, D Chakravarty, R Dienstmann, S Jezdic, A Gonzalez-Perez, ... Annals of Oncology 29 (9), 1895-1902, 2018 | 643 | 2018 |
| Analyses of non-coding somatic drivers in 2,658 cancer whole genomes E Rheinbay, MM Nielsen, F Abascal, JA Wala, O Shapira, G Tiao, ... Nature 578 (7793), 102-111, 2020 | 621 | 2020 |
| IntOGen-mutations identifies cancer drivers across tumor types A Gonzalez-Perez, C Perez-Llamas, J Deu-Pons, D Tamborero, ... Nature methods 10 (11), 1081-1082, 2013 | 600 | 2013 |
| CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer M Griffith, NC Spies, K Krysiak, JF McMichael, AC Coffman, AM Danos, ... Nature genetics 49 (2), 170-174, 2017 | 591 | 2017 |
| Comprehensive identification of mutational cancer driver genes across 12 tumor types D Tamborero, A Gonzalez-Perez, C Perez-Llamas, J Deu-Pons, ... Scientific reports 3 (1), 2650, 2013 | 562 | 2013 |
| Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations D Tamborero, C Rubio-Perez, J Deu-Pons, MP Schroeder, A Vivancos, ... Genome medicine 10, 1-8, 2018 | 529 | 2018 |
| Are splicing mutations the most frequent cause of hereditary disease? N López-Bigas, B Audit, C Ouzounis, G Parra, R Guigó FEBS letters 579 (9), 1900-1903, 2005 | 515 | 2005 |
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| OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes D Tamborero, A Gonzalez-Perez, N Lopez-Bigas Bioinformatics 29 (18), 2238-2244, 2013 | 493 | 2013 |
Abel Gonzalez-PerezInstitut de Recerca Biomedica BarcelonaVerified email at irbbarcelona.org
