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From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways.

, , , and . BMC Bioinformatics, 10 (S-8): 6 (2009)

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psygenet2r: a R/Bioconductor package for the analysis of psychiatric disease genes., , , and . Bioinformatics, 33 (24): 4004-4006 (2017)OSIRISv1.2: A named entity recognition system for sequence variants of genes in biomedical literature., , , and . BMC Bioinformatics, (2008)Assessment of NER solutions against the first and second CALBC silver standard corpus., , , , , , , , , and 27 other author(s). Semantic Mining in Biomedicine, volume 714 of CEUR Workshop Proceedings, CEUR-WS.org, (2010)ResMarkerDB: a database of biomarkers of response to antibody therapy in breast and colorectal cancer., , and . Database, (2019)DisGeNET: a Cytoscape plugin to visualize, integrate, search and analyze gene-disease networks., , , and . Bioinformatics, 26 (22): 2924-2926 (2010)PsyGeNET: a knowledge platform on psychiatric disorders and their genes., , , , , , , and . Bioinformatics, 31 (18): 3075-3077 (2015)Identifying gene-Specific Variations in Biomedical Text., , , , , , and . J. Bioinformatics and Computational Biology, 5 (6): 1277-1296 (2007)Automatic Filtering and Substantiation of Drug Safety Signals., , , , , , , , , and 6 other author(s). PLoS Computational Biology, (2012)DisGeNET RDF: A Gene-Disease Association Linked Open Data Resource., and . SWAT4LS, volume 1114 of CEUR Workshop Proceedings, CEUR-WS.org, (2013)DisGeNET: from MySQL to Nanopublication, Modelling Gene-Disease Associations for the Semantic Web., and . SWAT4LS, volume 952 of CEUR Workshop Proceedings, CEUR-WS.org, (2012)