Maxime Douillet
Paris, France
Last Updated: 09/26/2026
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Found 11 publications
Enhancing Longitudinal Data Analysis with Unstructured EHRs: A Case Study of Renal Function Evaluation in Rare Disease.
Journal: Studies in health technology and informatics
Published: May 17, 2025
Objectivizing issues in the diagnosis of complex rare diseases: lessons learned from testing existing diagnosis support systems on ciliopathies.
Journal: BMC medical informatics and decision making
Published: January 30, 2024
Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome.
Journal: Scientific reports
Published: December 20, 2023
AI-based diagnosis and phenotype - Genotype correlations in syndromic craniosynostoses.
Journal: Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
Published: December 02, 2023
Artificial intelligence-based diagnosis in fetal pathology using external ear shapes.
Journal: Prenatal diagnosis
Published: October 22, 2023
The Smart Data Extractor, a Clinician Friendly Solution to Accelerate and Improve the Data Collection During Clinical Trials.
Journal: Studies in health technology and informatics
Published: May 19, 2023
AI-based diagnosis in mandibulofacial dysostosis with microcephaly using external ear shapes.
Journal: Frontiers in pediatrics
Published: February 27, 2023
The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.
Journal: Kidney international
Published: November 15, 2022
An automatic facial landmarking for children with rare diseases.
Journal: American journal of medical genetics. Part A
Published: November 02, 2022
Using Deep Learning to Improve Phenotyping from Clinical Reports.
Journal: Studies in health technology and informatics
Published: June 08, 2022
Phenotypic similarity for rare disease: Ciliopathy diagnoses and subtyping.
Journal: Journal of biomedical informatics
Published: April 01, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026