Jean T. Pantel
Aachen, NW, Germany
Last Updated: 09/26/2026
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Found 20 publications
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: June 24, 2025
Development of an Interactive Online Course on Artificial Intelligence in Medicine: A Study on Design and Implementation.
Journal: Studies in health technology and informatics
Published: April 09, 2025
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals.
Journal: Orphanet journal of rare diseases
Published: January 28, 2025
Artificial intelligence: helpful for general practitioners?
Journal: MMW Fortschritte der Medizin
Published: November 22, 2024
Short paths to diagnosis with artificial intelligence: systematic literature review on diagnostic decision support systems
Journal: Schmerz (Berlin, Germany)
Published: November 24, 2023
Treating pain in patients with Ehlers-Danlos syndrome : Multidisciplinary management of a multisystemic disease.
Journal: Schmerz (Berlin, Germany)
Published: November 24, 2023
Understanding recessive disease risk in multi-ethnic populations with different degrees of consanguinity.
Journal: American journal of medical genetics. Part A
Published: September 30, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.
Journal: medRxiv : the preprint server for health sciences
Published: July 28, 2023
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Journal: Nature genetics
Published: July 19, 2023
Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study.
Journal: Journal of medical Internet research
Published: September 27, 2022
Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid features.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2022
Last Updated: 09/26/2026