Ferdinand Dhombres

Orcid: 0000-0003-3246-8727

According to our database1, Ferdinand Dhombres authored at least 20 papers between 2010 and 2024.

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

Timeline

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Bibliography

2024
Prior-Guided Attribution of Deep Neural Networks for Obstetrics and Gynecology.
IEEE J. Biomed. Health Informatics, February, 2024

2022
Pattern-Based Logical Definitions of Prenatal Disorders Grounded on Dispositions.
Proceedings of the Challenges of Trustable AI and Added-Value on Health, 2022

Privileged Attribution Constrained Deep Networks for Facial Expression Recognition.
Proceedings of the 26th International Conference on Pattern Recognition, 2022

2021
Modeling Logical Definitions in Biomedical Ontologies by Reusing Ontology Design Patterns.
Proceedings of the International Conference on Biomedical Ontologies 2021 co-located with the Workshop on Ontologies for the Behavioural and Social Sciences (OntoBess 2021) as part of the Bolzano Summer of Knowledge (BOSK 2021), 2021

2017
Developing a knowledge base to support the annotation of ultrasound images of ectopic pregnancy.
J. Biomed. Semant., 2017

"Hybrid Topics" - Facilitating the Interpretation of Topics Through the Addition of MeSH Descriptors to Bags of Words.
Proceedings of the MEDINFO 2017: Precision Healthcare through Informatics, 2017

Trends in Fetal Medicine: A 10-Year Bibliometric Analysis of Prenatal Diagnosis.
Proceedings of the MEDINFO 2017: Precision Healthcare through Informatics, 2017

2016
Searching for rare diseases in PubMed: a blind comparison of Orphanet expert query and query based on terminological knowledge.
BMC Medical Informatics Decis. Mak., 2016

Interoperability between phenotypes in research and healthcare terminologies - Investigating partial mappings between HPO and SNOMED CT.
J. Biomed. Semant., 2016

Assessing the potential risk in drug prescriptions during pregnancy.
Proceedings of the AMIA 2016, 2016

2015
Extending the coverage of phenotypes in SNOMED CT through post-coordination.
Proceedings of the MEDINFO 2015: eHealth-enabled Health, 2015

LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems.
Proceedings of the AMIA 2015, 2015

2014
Un outil de visualisation de classifications et d'intégration de données phénotypiques et génétiques pour faciliter le codage des maladies rares.
Proceedings of the Actes des / Proceedings of 15es Journées francophones d'informatique médicale co-organisées avec / co-located with 2e Congrès National d'Informatique Médicale (CNIM 2014), 2014

2012
OntoMénélas. Motivations et retours d'expérience sur l'élaboration d'une ontologie noyau de la médecine.
Tech. Sci. Informatiques, 2012

Rare diseases knowledge management: the contribution of proximity measurements in OntoOrpha and OMIM.
Proceedings of the Quality of Life through Quality of Information, 2012

Construire une ontologie médicale pour la recherche d'information : problématiques terminologiques et de modélisation.
Proceedings of the IC 2012 : 23es journées Ingénierie des Connaissances (Proceedings of the 23rd French Knowledge Engineering Conference), 2012

2011
Biomedical Analyses: OWL Model Based Edition.
Proceedings of the 2nd International Conference on Biomedical Ontology, 2011

OntoOrpha: An Ontology to Support Edition and Audit of Knowledge of Rare Diseases in ORPHANET.
Proceedings of the 2nd International Conference on Biomedical Ontology, 2011

Projet OrphaOnto - Première étape de l'ontologisation des bases de connaissances d'Orphanet.
Proceedings of the IC 2011 : 22es journées Ingénierie des Connaissances (Proceedings of the 22nd French Knowledge Engineering Conference), 2011

2010
Choix méthodologiques pour la construction d'une ontologie de domaine en médecine prénatale.
Proceedings of the IC 2010 : 21es Journées Ingénierie des Connaissances 2010 (Proceedings of the 21st French Knowledge Engineering Conference), 2010


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