Laura Inés Furlong

Orcid: 0000-0002-9383-528X

Affiliations:
  • Pompeu Fabra University, Research Programme on Biomedical Informatics, Barcelona, Spain


According to our database1, Laura Inés Furlong authored at least 43 papers between 2006 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
Visualization of automatically combined disease maps and pathway diagrams for rare diseases.
Frontiers Bioinform., May, 2023

2021
A system-level analysis of patient disease trajectories based on clinical, phenotypic and molecular similarities.
Bioinform., 2021

2020
The DisGeNET knowledge platform for disease genomics: 2019 update.
Nucleic Acids Res., 2020

The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.
F1000Research, 2020

Clinical-Based and Expert Selection of Terms Related to Depression for Twitter Streaming and Language Analysis.
Proceedings of the Digital Personalized Health and Medicine - Proceedings of MIE 2020, Medical Informatics Europe, Geneva, Switzerland, April 28, 2020

2019
Comorbidity4j: a tool for interactive analysis of disease comorbidities over large patient datasets.
Bioinform., 2019

ResMarkerDB: a database of biomarkers of response to antibody therapy in breast and colorectal cancer.
Database J. Biol. Databases Curation, 2019

Supervised Learning Approaches to Detect Negation Cues in Spanish Reviews.
Proceedings of the Iberian Languages Evaluation Forum co-located with 35th Conference of the Spanish Society for Natural Language Processing, 2019

2018
comoRbidity: an R package for the systematic analysis of disease comorbidities.
Bioinform., 2018

Rcupcake: an R package for querying and analyzing biomedical data through the BD2K PIC-SURE RESTful API.
Bioinform., 2018

IBI at TREC 2018: Precision Medicine Track.
Proceedings of the Twenty-Seventh Text REtrieval Conference, 2018

Nanopublications: A Growing Resource of Provenance-Centric Scientific Linked Data.
Proceedings of the 14th IEEE International Conference on e-Science, 2018

2017
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants.
Nucleic Acids Res., 2017

psygenet2r: a R/Bioconductor package for the analysis of psychiatric disease genes.
Bioinform., 2017

Text mining and expert curation to develop a database on psychiatric diseases and their genes.
Database J. Biol. Databases Curation, 2017

IBI-UPF at BARR-2017: Learning to Identify Abbreviations in Biomedical Literature System description.
Proceedings of the Second Workshop on Evaluation of Human Language Technologies for Iberian Languages (IberEval 2017) co-located with 33th Conference of the Spanish Society for Natural Language Processing (SEPLN 2017), 2017

Reliable Granular References to Changing Linked Data.
Proceedings of the Semantic Web - ISWC 2017, 2017

2016
Publishing DisGeNET as nanopublications.
Semantic Web, 2016

CDH1/E-cadherin and solid tumors. An updated gene-disease association analysis using bioinformatics tools.
Comput. Biol. Chem., 2016

DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases.
Bioinform., 2016

A crowdsourcing workflow for extracting chemical-induced disease relations from free text.
Database J. Biol. Databases Curation, 2016

Combining machine learning, crowdsourcing and expert knowledge to detect chemical-induced diseases in text.
Database J. Biol. Databases Curation, 2016

Slim-o-matic: a Semi-Automated Way to Generate Gene Ontology Slims.
Proceedings of the 9th International Conference Semantic Web Applications and Tools for Life Sciences, 2016

2015
On Reasoning with RDF Statements about Statements using Singleton Property Triples.
CoRR, 2015

Extraction of relations between genes and diseases from text and large-scale data analysis: implications for translational research.
BMC Bioinform., 2015

PsyGeNET: a knowledge platform on psychiatric disorders and their genes.
Bioinform., 2015

DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes.
Database J. Biol. Databases Curation, 2015

Exposing Provenance Metadata Using Different RDF Models.
Proceedings of the 8th Semantic Web Applications and Tools for Life Sciences International Conference, 2015

Reuse of EHRs to Support Clinical Research in a Hospital of Reference.
Proceedings of the Digital Healthcare Empowering Europeans, 2015

2014
The Semanticscience Integrated Ontology (SIO) for biomedical research and knowledge discovery.
J. Biomed. Semant., 2014

2013
DisGeNET RDF: A Gene-Disease Association Linked Open Data Resource.
Proceedings of the 6th International Workshop on Semantic Web Applications and Tools for Life Sciences, 2013

2012
Automatic Filtering and Substantiation of Drug Safety Signals.
PLoS Comput. Biol., 2012

The EU-ADR corpus: Annotated drugs, diseases, targets, and their relationships.
J. Biomed. Informatics, 2012

DisGeNET: from MySQL to Nanopublication, Modelling Gene-Disease Associations for the Semantic Web.
Proceedings of the 5th International Workshop on Semantic Web Applications and Tools for Life Sciences, 2012

2011
Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers.
BMC Bioinform., 2011

Assessment of NER solutions against the first and second CALBC Silver Standard Corpus.
J. Biomed. Semant., 2011

2010
DisGeNET: a Cytoscape plugin to visualize, integrate, search and analyze gene-disease networks.
Bioinform., 2010

Digging for knowledge with information extraction: a case study on human gene-disease associations.
Proceedings of the 19th ACM Conference on Information and Knowledge Management, 2010

2009
From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways.
BMC Bioinform., 2009

Identification of Sequence Variants of Genes from Biomedical Literature.
Proceedings of the Information Retrieval in Biomedicine, 2009

2008
OSIRISv1.2: A named entity recognition system for sequence variants of genes in biomedical literature.
BMC Bioinform., 2008

2007
Identifying gene-Specific Variations in Biomedical Text.
J. Bioinform. Comput. Biol., 2007

2006
OSIRIS: a tool for retrieving literature about sequence variants.
Bioinform., 2006


  Loading...