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Author Details
Full Name
Abel Gonzalez-Perez
Affiliation
Universitat Pompeu Fabra
ORCID
Career Start Year
2005
Papers
69
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36928603
Multiomic analysis of malignant pleural mesothelioma identifies molecular axes and specialized tumor profiles driving intertumor heterogeneity.
Nat Genet
2023
36697832
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.
Nature
2023
36780550
Copy number footprints of platinum-based anticancer therapies.
PLoS Genet
2023
34718417
DeepMP: a deep learning tool to detect DNA base modifications on Nanopore sequencing data.
Bioinformatics
2022
35871184
Discovering the drivers of clonal hematopoiesis.
Nat Commun
2022
36071033
High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER<sup>+</sup> breast cancer.
Nat Commun
2022
36264838
Ten simple rules for a successful international consortium in big data omics.
PLoS Comput Biol
2022
36376284
Author Correction: High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER<sup>+</sup> breast cancer.
Nat Commun
2022
33347579
Variable interplay of UV-induced DNA damage and repair at transcription factor binding sites.
Nucleic Acids Res
2021
34493867
Genomic and evolutionary classification of lung cancer in never smokers.
Nat Genet
2021
34376657
The evolution of hematopoietic cells under cancer therapy.
Nat Commun
2021
34321661
In silico saturation mutagenesis of cancer genes.
Nature
2021
31462706
LOXL2-mediated H3K4 oxidation reduces chromatin accessibility in triple-negative breast cancer cells.
Oncogene
2020
35121836
Systematic analysis of alterations in the ubiquitin proteolysis system reveals its contribution to driver mutations in cancer.
Nat Cancer
2020
33225950
The evolution of relapse of adult T cell acute lymphoblastic leukemia.
Genome Biol
2020
33128047
Are carcinogens direct mutagens?
Nat Genet
2020
32592465
BnpC: Bayesian non-parametric clustering of single-cell mutation profiles.
Bioinformatics
2020
32778778
A compendium of mutational cancer driver genes.
Nat Rev Cancer
2020
30523021
NK Cell Infiltrates and HLA Class I Expression in Primary HER2<sup>+</sup> Breast Cancer Predict and Uncouple Pathological Response and Disease-free Survival.
Clin Cancer Res
2019
31740835
The mutational footprints of cancer therapies.
Nat Genet
2019
31491604
Dynamic clonal remodelling in breast cancer metastases is associated with subtype conversion.
Eur J Cancer
2019
31228182
OncodriveCLUSTL: a sequence-based clustering method to identify cancer drivers.
Bioinformatics
2019
31369060
OncodriveCLUSTL: a sequence-based clustering method to identify cancer drivers.
Bioinformatics
2019
30901533
Local Determinants of the Mutational Landscape of the Human Genome.
Cell
2019
29023197
Mutational landscape of RNA-binding proteins in human cancers.
RNA Biol
2018
29973711
Author Correction: Reduced mutation rate in exons due to differential mismatch repair.
Nat Genet
2018
30096302
Comprehensive Characterization of Cancer Driver Genes and Mutations.
Cell
2018
30041662
Frequency and clinical impact of CDKN2A/ARF/CDKN2B gene deletions as assessed by in-depth genetic analyses in adult T cell acute lymphoblastic leukemia.
J Hematol Oncol
2018
30065304
Manic Fringe deficiency imposes Jagged1 addiction to intestinal tumor cells.
Nat Commun
2018
30137196
A framework to rank genomic alterations as targets for cancer precision medicine: the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT).
Ann Oncol
2018
30319692
Network, Transcriptomic and Genomic Features Differentiate Genes Relevant for Drug Response.
Front Genet
2018
30388444
Somatic and Germline Mutation Periodicity Follow the Orientation of the DNA Minor Groove around Nucleosomes.
Cell
2018
29666300
A Pan-cancer Landscape of Interactions between Solid Tumors and Infiltrating Immune Cell Populations.
Clin Cancer Res
2018
29625053
Comprehensive Characterization of Cancer Driver Genes and Mutations.
Cell
2018
29592813
Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations.
Genome Med
2018
29106418
Reduced mutation rate in exons due to differential mismatch repair.
Nat Genet
2017
27075101
Nucleotide excision repair is impaired by binding of transcription factors to DNA.
Nature
2016
27716338
Rational design of cancer gene panels with OncoPaD.
Genome Med
2016
27404455
Non-canonical NF-κB pathway activation predicts outcome in borderline oestrogen receptor positive breast carcinoma.
Br J Cancer
2016
27311963
OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations.
Genome Biol
2016
27095575
Altered oncomodules underlie chromatin regulatory factors driver mutations.
Oncotarget
2016
26792175
Circuits of cancer drivers revealed by convergent misregulation of transcription factor targets across tumor types.
Genome Med
2016
27080396
Uncovering disease mechanisms through network biology in the era of Next Generation Sequencing.
Sci Rep
2016
25501392
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes.
Nat Genet
2015
26125594
Pathway and network analysis of cancer genomes.
Nat Methods
2015
25759023
In silico prescription of anticancer drugs to cohorts of 28 tumor types reveals targeting opportunities.
Cancer Cell
2015
25823659
Cytoplasmic accumulation of NCoR in malignant melanoma: consequences of altered gene repression and prognostic significance.
Oncotarget
2015
24265505
Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia.
Genome Res
2014
25161246
OncodriveROLE classifies cancer driver genes in loss of function and activating mode of action.
Bioinformatics
2014
23363777
Visualizing multidimensional cancer genomics data.
Genome Med
2013
1 - 50 of 69
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Institute for Research in Biomedicine
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