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Laura Inés Furlong
2010 – today
- 2012
[j8]Erik M. van Mulligen, Annie Fourrier-Réglat, David Gurwitz, Mariam Molokhia, Ainhoa Nieto, Gianluca Trifirò, Jan A. Kors, Laura Inés Furlong: The EU-ADR corpus: Annotated drugs, diseases, targets, and their relationships. Journal of Biomedical Informatics 45(5): 879-884 (2012)- [j7]Anna Bauer-Mehren, Erik M. van Mulligen, Paul Avillach, María del Carmen Carrascosa, Ricard García-Serna, Janet Piñero, Bharat Singh, Pedro Lopes, José Luís Oliveira, Gayo Diallo, Ernst Ahlberg Helgee, Scott Boyer, Jordi Mestres, Ferran Sanz, Jan A. Kors, Laura Inés Furlong: Automatic Filtering and Substantiation of Drug Safety Signals. PLoS Computational Biology 8(4) (2012)
- [c3]Núria Queralt-Rosinach, Laura Inés Furlong: DisGeNET: from MySQL to Nanopublication, Modelling Gene-Disease Associations for the Semantic Web. SWAT4LS 2012
- 2011
- [j6]Philippe E. Thomas, Roman Klinger, Laura Inés Furlong, Martin Hofmann-Apitius, Christoph M. Friedrich: Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers. BMC Bioinformatics 12(S-4): S4 (2011)
- 2010
- [j5]Anna Bauer-Mehren, Michael Rautschka, Ferran Sanz, Laura Inés Furlong: DisGeNET: a Cytoscape plugin to visualize, integrate, search and analyze gene-disease networks. Bioinformatics 26(22): 2924-2926 (2010)
- [c2]Markus Bundschus, Anna Bauer-Mehren, Volker Tresp, Laura Inés Furlong, Hans-Peter Kriegel: Digging for knowledge with information extraction: a case study on human gene-disease associations. CIKM 2010: 1845-1848
- [c1]Dietrich Rebholz-Schuhmann, Antonio Jimeno-Yepes, Chen Li, Senay Kafkas, Ian Lewin, Ning Kang, Peter Corbett, David Milward, Ekaterina Buyko, Elena Beisswanger, Kerstin Hornbostel, Alexandre Kouznetsov, René Witte, Jonas B. Laurila, Christopher J. O. Baker, Cheng-Ju Kuo, Simon Clematide, Fabio Rinaldi, Richárd Farkas, György Móra, Kazuo Hara, Laura Inés Furlong, Michael Rautschka, Mariana L. Neves, Alberto D. Pascual-Montano, Qi Wei, Nigel Collier, Md. Faisal Mahbub Chowdhury, Alberto Lavelli, Rafael Berlanga Llavori, Roser Morante, Vincent Van Asch, Walter Daelemans, José Luís Marina, Erik M. van Mulligen, Jan A. Kors, Udo Hahn: Assessment of NER solutions against the first and second CALBC silver standard corpus. Semantic Mining in Biomedicine 2010
2000 – 2009
- 2009
- [j4]Anna Bauer-Mehren, Laura Inés Furlong, Michael Rautschka, Ferran Sanz: From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways. BMC Bioinformatics 10(S-8): 6 (2009)
- 2008
- [j3]Laura Inés Furlong, Holger Dach, Martin Hofmann-Apitius, Ferran Sanz: OSIRISv1.2: A named entity recognition system for sequence variants of genes in biomedical literature. BMC Bioinformatics 9 (2008)
- 2007
- [j2]Roman Klinger, Christoph M. Friedrich, Heinz-Theodor Mevissen, Juliane Fluck, Martin Hofmann-Apitius, Laura Inés Furlong, Ferran Sanz: Identifying gene-Specific Variations in Biomedical Text. J. Bioinformatics and Computational Biology 5(6): 1277-1296 (2007)
- 2006
- [j1]Julio Bonis, Laura Inés Furlong, Ferran Sanz: OSIRIS: a tool for retrieving literature about sequence variants. Bioinformatics 22(20): 2567-2569 (2006)
Coauthor Index
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last updated on 2013-02-09 20:45 CET by the dblp team