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Author

Santiago González

Observed names: Gonzalez, Santiago, Santi Gonzalez, Santi González, Santiago Gonzalez
Observed institutions: Broad Institute, Institució Catalana de Recerca i Estudis Avançats, European Bioinformatics Institute, St Thomas' Hospital, Universitat Pompeu Fabra, Barcelona Supercomputing Center, Wellcome Sanger Institute, National Institute of Environmental Health Sciences, Institute for Research in Biomedicine, Vector Institute, Barcelona Institute of Science and Technology, European Molecular Biology Laboratory, Osaka International Cancer Institute, European Molecular Biology Laboratory, Institut de Biomedicina de la Universitat de Barcelona, Parc Científic de Barcelona, Universitat de Barcelona
ORCID: 0000-0001-5685-4580
Observed ORCID: 0000-0001-5685-4580
OpenAlex ID: A5066709653
The evolutionary history of 2,658 cancers
2020 · Moritz Gerstung, Clemency Jolly, et al. · Nature · 1,046
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Non-coding recurrent mutations in chronic lymphocytic leukaemia
2015 · Xose S. Puente, Silvia Beà, et al. · Nature · 829
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
2020 · Isidro Cortés-Ciriano, Jake June-Koo Lee, et al. · Nature Genetics · 712
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Genomic Evolution of Breast Cancer Metastasis and Relapse
2017 · Lucy R. Yates, Stian Knappskog, et al. · Cancer Cell · 665
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Pan-cancer computational histopathology reveals mutations, tumor composition and prognosis
2020 · Yu Fu, Alexander W. Jung, et al. · Nature Cancer · 654
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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
2020 · Esther Rheinbay, Morten Muhlig Nielsen, et al. · Nature · 602
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Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes
2021 · Stefan C. Dentro, Ignaty Leshchiner, et al. · Cell · 529
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Comprehensive molecular characterization of mitochondrial genomes in human cancers
2020 · Yuan Yuan, Young Seok Ju, et al. · Nature Genetics · 466
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The landscape of viral associations in human cancers
2020 · Marc Zapatka, Ivan Borozan, et al. · Nature Genetics · 382
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Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
2020 · Kadir C. Akdemir, Victoria T. Le, et al. · Nature Genetics · 283
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Genomic landscape and chronological reconstruction of driver events in multiple myeloma
2019 · Francesco Maura, Niccoló Bolli, et al. · Nature Communications · 275
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Mutational signatures are jointly shaped by DNA damage and repair
2020 · Nadezda V. Volkova, Bettina Meier, et al. · Nature Communications · 228
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Integrative pathway enrichment analysis of multivariate omics data
2020 · Marta Paczkowska, Jonathan Barenboim, et al. · Nature Communications · 221
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A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
2020 · Wei Jiao, Gurnit Atwal, et al. · Nature Communications · 217
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Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
2020 · Joana Carlevaro-Fita, Andrés Lanzós, et al. · Communications Biology · 187
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Divergent mutational processes distinguish hypoxic and normoxic tumours
2020 · Vinayak Bhandari, Constance H. Li, et al. · Nature Communications · 142
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Genomic footprints of activated telomere maintenance mechanisms in cancer
2020 · Lina Sieverling, Chen Hong, et al. · Nature Communications · 132
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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
2018 · Sílvia Bonàs-Guarch, Marta Guindo-Martínez, et al. · Nature Communications · 127
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Sex differences in oncogenic mutational processes
2020 · Constance H. Li, Stephenie D. Prokopec, et al. · Nature Communications · 126
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Pathway and network analysis of more than 2500 whole cancer genomes
2020 · Matthew A. Reyna, David Haan, et al. · Nature Communications · 112
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Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads
2014 · Valentí Moncunill, Santi Gonzalez, et al. · Nature Biotechnology · 93
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Human PGBD5 DNA transposase promotes site-specific oncogenic mutations in rhabdoid tumors
2017 · Anton G Henssen, Richard Koche, et al. · Nature Genetics · 89
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Combined burden and functional impact tests for cancer driver discovery using DriverPower
2020 · Shimin Shuai, PCAWG Drivers and Functional Interpretation Working Group, et al. · Nature Communications · 59
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Inferring structural variant cancer cell fraction
2020 · Marek Cmero, Ke Yuan, et al. · Nature Communications · 56
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The evolutionary history of 2,658 cancers
2017 · Moritz Gerstung, Clemency Jolly, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 51
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Works count: 58
Citation count: 8,590
H-index: 29
I10-index: 36
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