Laura I. Furlong

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 20

Top Topics

Expert Knowledge

Top Venues

Database J. Biol. Databases Curation

Nucleic Acids Res.

Publications

Piotr Gawron, David Hoksza, Janet Piñero, María Peña-Chilet, Marina Esteban-Medina, Jose Luis Fernandez-Rueda, Vincenza Colonna, Ewa Smula, Laurent Heirendt, François Ancien, Valentin Grouès, Venkata P. Satagopam, Reinhard Schneider, Joaquín Dopazo, Laura I. Furlong, Marek Ostaszewski
Visualization of automatically combined disease maps and pathway diagrams for rare diseases. Frontiers Bioinform. 3 (2023)
Alexia Giannoula, Emilio Centeno, Miguel Angel Mayer, Ferran Sanz, Laura I. Furlong
A system-level analysis of patient disease trajectories based on clinical, phenotypic and molecular similarities. Bioinform. 37 (10) (2021)
Janet Piñero González, Juan Manuel Ramírez-Anguita, Josep Saüch-Pitarch, Francesco Ronzano, Emilio Centeno, Ferran Sanz, Laura I. Furlong
The DisGeNET knowledge platform for disease genomics: 2019 update. Nucleic Acids Res. 48 (Database-Issue) (2020)
Angela Leis, Miguel Angel Mayer, Francesco Ronzano, Marta Torrens, Claudio Castillo, Laura I. Furlong, Ferran Sanz
Clinical-Based and Expert Selection of Terms Related to Depression for Twitter Streaming and Language Analysis. MIE (2020)
David Salgado, Irina M. Armean, Michael Baudis, Sergi Beltran, Salvador Capella-Gutiérrez, Denise Carvalho-Silva, Victoria Dominguez Del Angel, Joaquín Dopazo, Laura I. Furlong, Bo Gao, Leyla Jael García Castro, Dietlind Gerloff, Ivo Gut, Attila Gyenesei, Nina Habermann, John M. Hancock, Marc Hanauer, Eivind Hovig, Lennart F. Johansson, Thomas Keane, Jan Korbel, Katharina B. Lauer, Steve Laurie, Brane Leskosek, David Lloyd, Tomàs Marquès-Bonet, Hailiang Mei, Katalin Monostory, Janet Piñero, Krzysztof Poterlowicz, Ana Rath, Pubudu Samarakoon, Ferran Sanz, Gary Saunders, Daoud Sie, Morris A. Swertz, Kirill Tsukanov, Alfonso Valencia, Marko Vidak, Cristina Yenyxe González, Bauke Ylstra, Christophe Béroud
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. F1000Research 9 (2020)
Francesco Ronzano, Alba Gutiérrez-Sacristán, Laura I. Furlong
Comorbidity4j: a tool for interactive analysis of disease comorbidities over large patient datasets. Bioinform. 35 (18) (2019)
Lluís Domínguez-Mas, Francesco Ronzano, Laura I. Furlong
Supervised Learning Approaches to Detect Negation Cues in Spanish Reviews. IberLEF@SEPLN (2019)
Francesco Ronzano, Emilio Centeno, Judith Pérez-Granado, Laura I. Furlong
IBI at TREC 2018: Precision Medicine Track. TREC (2018)
Tobias Kuhn, Albert Meroño-Peñuela, Alexander Malic, Jorrit H. Poelen, Allen H. Hurlbert, Emilio Centeno, Laura I. Furlong, Núria Queralt-Rosinach, Christine Chichester, Juan M. Banda, Egon L. Willighagen, Friederike Ehrhart, Chris T. A. Evelo, Tareq B. Malas, Michel Dumontier
Nanopublications: A Growing Resource of Provenance-Centric Scientific Linked Data. CoRR (2018)
Tobias Kuhn, Albert Meroño-Peñuela, Alexander Malic, Jorrit H. Poelen, Allen H. Hurlbert, Emilio Centeno Ortiz, Laura I. Furlong, Núria Queralt-Rosinach, Christine Chichester, Juan M. Banda, Egon L. Willighagen, Friederike Ehrhart, Chris T. A. Evelo, Tareq B. Malas, Michel Dumontier
Nanopublications: A Growing Resource of Provenance-Centric Scientific Linked Data. eScience (2018)
Tobias Kuhn, Egon L. Willighagen, Chris T. A. Evelo, Núria Queralt-Rosinach, Emilio Centeno, Laura I. Furlong
Reliable Granular References to Changing Linked Data. ISWC (1) (2017)
Tobias Kuhn, Egon L. Willighagen, Chris T. A. Evelo, Núria Queralt-Rosinach, Emilio Centeno, Laura I. Furlong
Reliable Granular References to Changing Linked Data. CoRR (2017)
Janet Piñero González, Àlex Bravo, Núria Queralt-Rosinach, Alba Gutiérrez-Sacristán, Jordi Deu-Pons, Emilio Centeno, Javier García-García, Ferran Sanz, Laura I. Furlong
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants. Nucleic Acids Res. 45 (Database-Issue) (2017)
Alba Gutiérrez-Sacristán, Àlex Bravo, Marta Portero-Tresserra, Olga Valverde, Antonio Armario, M. C. Blanco-Gandía, Adriana Farré, Lierni Fernández-Ibarrondo, Francina Fonseca, Jesús Giraldo, Angela Leis, Anna Mané, Miguel Angel Mayer, Sandra Montagud-Romero, Roser Nadal, Jordi Ortiz, Francisco Javier Pavon, Ezequiel Perez, Marta Rodríguez-Arias, Antonia Serrano, Marta Torrens, Vincent Warnault, Ferran Sanz, Laura I. Furlong
Text mining and expert curation to develop a database on psychiatric diseases and their genes. Database J. Biol. Databases Curation 2017 (2017)
Núria Queralt-Rosinach, Janet Piñero González, Àlex Bravo, Ferran Sanz, Laura I. Furlong
DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases. Bioinform. 32 (14) (2016)
Àlex Bravo, Tong Shu Li, Andrew I. Su, Benjamin M. Good, Laura I. Furlong
Combining machine learning, crowdsourcing and expert knowledge to detect chemical-induced diseases in text. Database J. Biol. Databases Curation 2016 (2016)
Alba Gutiérrez-Sacristán, Àlex Bravo, Marta Portero-Tresserra, Olga Valverde, Antonio Armario, M. C. Blanco-Gandía, Adriana Farré, Lierni Fernández-Ibarrondo, Francina Fonseca, Jesús Giraldo, Angela Leis, Anna Mané, Miguel Angel Mayer, Sandra Montagud-Romero, Roser Nadal, Jordi Ortiz, Francisco Javier Pavon, Ezequiel Perez, Marta Rodríguez-Arias, Antonia Serrano, Marta Torrens, Vincent Warnault, Ferran Sanz, Laura I. Furlong
Text Mining and Expert Curation to Develop a Database on Psychiatric Diseases and their Genes. SMBM (2016)
Núria Queralt-Rosinach, Tobias Kuhn, Christine Chichester, Michel Dumontier, Ferran Sanz, Laura I. Furlong
Publishing DisGeNET as nanopublications. Semantic Web 7 (5) (2016)
Tong Shu Li, Àlex Bravo, Laura I. Furlong, Benjamin M. Good, Andrew I. Su
A crowdsourcing workflow for extracting chemical-induced disease relations from free text. Database J. Biol. Databases Curation 2016 (2016)
Mélanie Courtot, Alex L. Mitchell, Maxim Scheremetjew, Janet Piñero González, Laura I. Furlong, Robert D. Finn, Helen E. Parkinson
Slim-o-matic: a Semi-Automated Way to Generate Gene Ontology Slims. SWAT4LS (2016)