Demo Data from EDBT 2026 / reviewers in the wild / expert
Stephen L. Mathias
dblp:146/3307
· DBLP profile ↗
5ranked-venue papers
0as first author
1since 2021 · last 2021
0000-0002-7255-370XORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 5 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
2 papers |
Bioinformatics and computational biology · 86% Computational social science and digital humanities · 14% |
Topics — the 5 heaviest of 5, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
drug discovery |
0.5 | 1 | 2021 | TIGA: target illumination GWAS analytics · Bioinform. 2021 |
Bioinformatics and computational biology › drug discovery › target identification
drug target prioritization |
0.5 | 1 | 2021 | TIGA: target illumination GWAS analytics · Bioinform. 2021 |
Bioinformatics and computational biology › genomics
genome-wide association study |
0.5 | 1 | 2021 | TIGA: target illumination GWAS analytics · Bioinform. 2021 |
Computational social science and digital humanities › scientometrics
bibliometric analysis |
0.3 | 1 | 2017 | TIN-X: target importance and novelty explorer · Bioinform. 2017 |
Bioinformatics and computational biology
biomedical text mining |
0.3 | 1 | 2017 | TIN-X: target importance and novelty explorer · Bioinform. 2017 |
Methods — techniques the papers use, named apart from their topics
relative citation ratio · 0.5bibliometric analysis · 0.5text mining · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2021 | TIGA: target illumination GWAS analyticsabstractMOTIVATION: Genome-wide association studies can reveal important genotype-phenotype associations; however, data quality and interpretability issues must be addressed. For drug discovery scientists seeking to prioritize targets based on the available evidence, these issues go beyond the single study. RESULTS: Here, we describe rational ranking, filtering and interpretation of inferred gene-trait associations and data aggregation across studies by leveraging existing curation and harmonization efforts. Each gene-trait association is evaluated for confidence, with scores derived solely from aggregated statistics, linking a protein-coding gene and phenotype. We propose a method for assessing confidence in gene-trait associations from evidence aggregated across studies, including a bibliometric assessment of scientific consensus based on the iCite relative citation ratio, and meanRank scores, to aggregate multivariate evidence.This method, intended for drug target hypothesis generation, scoring and ranking, has been implemented as an analytical pipeline, available as open source, with public datasets of results, and a web application designed for usability by drug discovery scientists. AVAILABILITY AND IMPLEMENTATION: Web application, datasets and source code via https://unmtid-shinyapps.net/tiga/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Jeremy J. Yang, Dhouha Grissa, Christophe G. Lambert, Cristian Bologa, Stephen L. Mathias, Anna Waller, David J. Wild 0001, Lars Juhl Jensen, Tudor I. Oprea |
Bioinform. | 5 |
| 2017 | TIN-X: target importance and novelty explorerabstractMOTIVATION: The increasing amount of peer-reviewed manuscripts requires the development of specific mining tools to facilitate the visual exploration of evidence linking diseases and proteins. RESULTS: We developed TIN-X, the Target Importance and Novelty eXplorer, to visualize the association between proteins and diseases, based on text mining data processed from scientific literature. In the current implementation, TIN-X supports exploration of data for G-protein coupled receptors, kinases, ion channels, and nuclear receptors. TIN-X supports browsing and navigating across proteins and diseases based on ontology classes, and displays a scatter plot with two proposed new bibliometric statistics: Importance and Novelty. AVAILABILITY AND IMPLEMENTATION: http://www.newdrugtargets.org. CONTACT: [email protected]. Daniel Cannon, Jeremy J. Yang, Stephen L. Mathias, Oleg Ursu, Subramani Mani, Anna Waller, Stephan C. Schürer, Lars Juhl Jensen, Larry A. Sklar, Cristian Bologa, Tudor I. Oprea |
Bioinform. | 3 |
| 2017 | Formalizing drug indications on the road to therapeutic intentabstractTherapeutic intent, the reason behind the choice of a therapy and the context in which a given approach should be used, is an important aspect of medical practice. There are unmet needs with respect to current electronic mapping of drug indications. For example, the active ingredient sildenafil has 2 distinct indications, which differ solely on dosage strength. In progressing toward a practice of precision medicine, there is a need to capture and structure therapeutic intent for computational reuse, thus enabling more sophisticated decision-support tools and a possible mechanism for computer-aided drug repurposing. The indications for drugs, such as those expressed in the Structured Product Labels approved by the US Food and Drug Administration, appears to be a tractable area for developing an application ontology of therapeutic intent. Stuart J. Nelson, Tudor I. Oprea, Oleg Ursu, Cristian Bologa, Amrapali Zaveri, Jayme Holmes, Jeremy J. Yang, Stephen L. Mathias, Subramani Mani, Mark S. Tuttle, Michel Dumontier |
J. Am. Medical Informatics Assoc. | 8 |
| 2017 | Protein biomarker druggability profiling
Subramani Mani, Daniel Cannon, Robin Ohls, Tudor I. Oprea, Stephen L. Mathias, Karri Ballard, Oleg Ursu, Cristian Bologa |
J. Biomed. Informatics | 5 |
| 2015 | Protein Drug Target Prioritization for Illumination
Subramani Mani, Daniel Cannon, Tudor I. Oprea, Stephen L. Mathias, Oleg Ursu, Cristian Bologa |
AMIA | 4 |