Kirsley Chennen

6PUBLICATIONS
40CO-AUTHORS
Data qualityNeonatologyBiomechanicsGene expression (incl. microarray and other genome-wide approaches)Data mining and knowledge discovery
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Publications (6)

|Aug 26, 2026
Building a National Interoperable Rare Eye Disease Data Warehouse: Methodological Framework and Implementation Report From the French Rare Eye Disease Database (FREDD) Initiative.

|May 26, 2026
Interoperable Integration of a National Rare Disease Registry Into a Rare Eye Disease Data Warehouse: Implementation Study.

|Mar 23, 2026
Novel PCDH12 pathogenic missense variants cause neurodevelopmental disorders with ocular malformation.

Jennifer Rakotomamonjy, Lucas Fares-Taie, Raman Kumar

|Jul 29, 2025
Knee Osteoarthritis Diagnosis: Future and Perspectives.

Henri Favreau, Kirsley Chennen, Sylvain Feruglio

|Aug 01, 2020
MISTIC: A prediction tool to reveal disease-relevant deleterious missense variants.

Kirsley Chennen, Thomas Weber, Xavière Lornage

|Jun 18, 2017
MyGeneFriends: A Social Network Linking Genes, Genetic Diseases, and Researchers.

Alexis Allot, Kirsley Chennen, Yannis Nevers

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Frequent Collaborators

2 joint publications

Matthieu Stoll

2 joint publications

Hélène Dollfus

2 joint publications

Laura Ratenet

2 joint publications

Olivier Poch