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Author Details
Full Name
Miguel Vazquez
Affiliation
Norwegian University of Science and Technology
ORCID
Career Start Year
2008
Papers
37
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34875418
ExTRI: Extraction of transcription regulation interactions from literature.
Biochim Biophys Acta Gene Regul Mech
2022
34664389
COVID19 Disease Map, a computational knowledge repository of virus-host interaction mechanisms.
Mol Syst Biol
2021
33743482
Immune analysis of lymph nodes in relation to the presence or absence of tumor infiltrating lymphocytes in triple-negative breast cancer.
Eur J Cancer
2021
33609721
Longitudinal whole-exome sequencing of cell-free DNA for tracking the co-evolutionary tumor and immune evasion dynamics: longitudinal data from a single patient.
Ann Oncol
2021
34939300
COVID-19 Disease Map, a computational knowledge repository of virus-host interaction mechanisms.
Mol Syst Biol
2021
32610166
Neoantigen prediction and computational perspectives towards clinical benefit: recommendations from the ESMO Precision Medicine Working Group.
Ann Oncol
2020
33195403
A Middle-Out Modeling Strategy to Extend a Colon Cancer Logical Model Improves Drug Synergy Predictions in Epithelial-Derived Cancer Cell Lines.
Front Mol Biosci
2020
32636365
A user guide for the online exploration and visualization of PCAWG data.
Nat Commun
2020
32848834
Strategies to Enhance Logic Modeling-Based Cell Line-Specific Drug Synergy Prediction.
Front Physiol
2020
31622330
Patient Dossier: Healthcare queries over distributed resources.
PLoS Comput Biol
2019
28549153
ChiPPI: a novel method for mapping chimeric protein-protein interactions uncovers selection principles of protein fusion events in cancer.
Nucleic Acids Res
2017
28444126
CImbinator: a web-based tool for drug synergy analysis in small- and large-scale datasets.
Bioinformatics
2017
27103312
Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal Nevi.
J Invest Dermatol
2016
26443060
wKinMut-2: Identification and Interpretation of Pathogenic Variants in Human Protein Kinases.
Hum Mutat
2016
27357839
KinMutRF: a random forest classifier of sequence variants in the human protein kinase superfamily.
BMC Genomics
2016
27542845
The Markyt visualisation, prediction and benchmark platform for chemical and gene entity recognition at BioCreative/CHEMDNER challenge.
Database (Oxford)
2016
25740935
Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolution.
G3 (Bethesda)
2015
26125594
Pathway and network analysis of cancer genomes.
Nat Methods
2015
25765346
Structure-PPi: a module for the annotation of cancer-related single-nucleotide variants at protein-protein interfaces.
Bioinformatics
2015
25810773
The CHEMDNER corpus of chemicals and drugs and its annotation principles.
J Cheminform
2015
25810766
CHEMDNER: The drugs and chemical names extraction challenge.
J Cheminform
2015
24227678
CheNER: chemical named entity recognizer.
Bioinformatics
2014
23671335
3DEM Loupe: Analysis of macromolecular dynamics using structures from electron microscopy.
Nucleic Acids Res
2013
24289158
wKinMut: an integrated tool for the analysis and interpretation of mutations in human protein kinases.
BMC Bioinformatics
2013
24121791
Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy.
Nat Genet
2013
23900255
Computational approaches to identify functional genetic variants in cancer genomes.
Nat Methods
2013
22348024
Quantification of miRNA-mRNA interactions.
PLoS One
2012
23300415
Chapter 14: Cancer genome analysis.
PLoS Comput Biol
2012
22759651
Prioritization of pathogenic mutations in the protein kinase superfamily.
BMC Genomics
2012
22438567
How to link ontologies and protein-protein interactions to literature: text-mining approaches and the BioCreative experience.
Database (Oxford)
2012
22151929
The Protein-Protein Interaction tasks of BioCreative III: classification/ranking of articles and linking bio-ontology concepts to full text.
BMC Bioinformatics
2011
27467152
Text Mining for Drugs and Chemical Compounds: Methods, Tools and Applications.
Mol Inform
2011
22158541
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.
Nat Genet
2011
20513648
MARQ: an online tool to mine GEO for experiments with similar or opposite gene expression signatures.
Nucleic Acids Res
2010
19458159
SENT: semantic features in text.
Nucleic Acids Res
2009
19465387
GeneCodis: interpreting gene lists through enrichment analysis and integration of diverse biological information.
Nucleic Acids Res
2009
18515346
bioNMF: a web-based tool for nonnegative matrix factorization in biology.
Nucleic Acids Res
2008
1 - 37 of 37
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