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A methodology for a minimum data set for rare diseases to support national centers of excellence for healthcare and research

Journal of the American Medical Informatics Association : JAMIA, 2015-01, Vol.22 (1), p.76-85

2015

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EULAR points to consider for the use of big data in rheumatic and musculoskeletal diseases

Annals of the rheumatic diseases, 2020-01, Vol.79 (1), p.69-76

2020

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Federating patients identities: the case of rare diseases

Orphanet journal of rare diseases, 2018-11, Vol.13 (1), p.199-199, Article 199

2018

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National Registries of Rare Diseases in Europe: An Overview of the Current Situation and Experiences

Public health genomics, 2015-01, Vol.18 (1), p.20-25

2015

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Real-World Evidence to Reinforce Clinical Trial Evidence in Health Technology Assessment: A Critical Review of Real-World Evidence Requirements from Seven Countries and Recommendations to Improve Acceptance

Journal of market access & health policy, 2024-06, Vol.12 (2), p.105-117

2024

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Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study

Orphanet journal of rare diseases, 2017-05, Vol.12 (1), p.94-13, Article 94

2017

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Current status of use of big data and artificial intelligence in RMDs: a systematic literature review informing EULAR recommendations

Rheumatic & musculoskeletal diseases open, 2019, Vol.5 (2), p.e001004-e001004

2019

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Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databases

Orphanet journal of rare diseases, 2017-06, Vol.12 (1), p.123-123, Article 123

2017

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X-Warehousing: An XML-Based Approach for Warehousing Complex Data

Advances in Databases and Information Systems, 2006, p.39-54

2006

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Formalizing mappings to optimize automated schema alignment: application to rare diseases

Studies in health technology and informatics, 2014, Vol.205, p.283

2014

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Interoperability driven integration of biomedical data sources

Studies in health technology and informatics, 2011, Vol.169, p.185

2011

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LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems

AMIA ... Annual Symposium proceedings, 2015-01, Vol.2015, p.434-440

2015

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An ontological approach for the exploitation of clinical data

Studies in health technology and informatics, 2013, Vol.192, p.142

2013

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Biomedical data management: a proposal framework

Studies in health technology and informatics, 2009, Vol.150, p.175

2009

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Data Definition Ontology for clinical data integration and querying

Studies in health technology and informatics, 2012, Vol.180, p.38

2012

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The Information Quality Triangle: a methodology to assess clinical information quality

Studies in health technology and informatics, 2010, Vol.160 (Pt 1), p.699

2010

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Ensuring HL7-based information model requirements within an ontology framework

Studies in health technology and informatics, 2010, Vol.160 (Pt 2), p.912

2010

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Semantic interoperability challenges to process large amount of data perspectives in forensic and legal medicine

Journal of forensic and legal medicine, 2018-07, Vol.57, p.19-23

2018

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Sujet d’avenir: La rhumatologie à l’heure de l’e-santé: objets connectés

Revue du rhumatisme (Ed. française : 1993), 2018-11, Vol.85, p.A37-A38

Choquet, Rémy

2018

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Assessing the real-world effectiveness of 8 major metastatic breast cancer drugs using target trial emulation

European journal of cancer (1990), 2024-12, Vol.213, p.115072, Article 115072

2024

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The French national registry for rare diseases: an integrated model from care to epidemiology and research

Orphanet journal of rare diseases, 2014-11, Vol.9 (9042), p.O7-O7

2014

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The DebugIT core ontology: semantic integration of antibiotics resistance patterns

Studies in health technology and informatics, 2010, Vol.160 (Pt 2), p.1060

2010

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Semantic interoperability challenges to process large amount of data perspectives in forensic and legal medicine

Journal of forensic and legal medicine, 2018-07, Vol.57, p.19-23

2018

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Towards data integration automation for the French rare disease registry

AMIA ... Annual Symposium proceedings, 2015, Vol.2015, p.880-885

2015

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Prévalence de la cystinose en France, observance du traitement et coûts directs pour l’assurance maladie : base de données de l’assurance maladie (SNIIRAM) et BNDMR

Revue d'épidémiologie et de santé publique, 2016-10, Vol.64, p.S273-S273

2016

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A methodology for a minimum data set for rare diseases to support national centers of excellence for healthcare and research

EULAR points to consider for the use of big data in rheumatic and musculoskeletal diseases

Federating patients identities: the case of rare diseases

National Registries of Rare Diseases in Europe: An Overview of the Current Situation and Experiences

Real-World Evidence to Reinforce Clinical Trial Evidence in Health Technology Assessment: A Critical Review of Real-World Evidence Requirements from Seven Countries and Recommendations to Improve Acceptance

Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study

Current status of use of big data and artificial intelligence in RMDs: a systematic literature review informing EULAR recommendations

Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databases

X-Warehousing: An XML-Based Approach for Warehousing Complex Data

Formalizing mappings to optimize automated schema alignment: application to rare diseases

Interoperability driven integration of biomedical data sources

LORD: a phenotype-genotype semantically integrated biomedical data tool to support rare disease diagnosis coding in health information systems

An ontological approach for the exploitation of clinical data

Biomedical data management: a proposal framework

Data Definition Ontology for clinical data integration and querying

The Information Quality Triangle: a methodology to assess clinical information quality

Ensuring HL7-based information model requirements within an ontology framework

Semantic interoperability challenges to process large amount of data perspectives in forensic and legal medicine

Sujet d’avenir: La rhumatologie à l’heure de l’e-santé: objets connectés

Assessing the real-world effectiveness of 8 major metastatic breast cancer drugs using target trial emulation

The French national registry for rare diseases: an integrated model from care to epidemiology and research

The DebugIT core ontology: semantic integration of antibiotics resistance patterns

Semantic interoperability challenges to process large amount of data perspectives in forensic and legal medicine

Towards data integration automation for the French rare disease registry

Prévalence de la cystinose en France, observance du traitement et coûts directs pour l’assurance maladie : base de données de l’assurance maladie (SNIIRAM) et BNDMR

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