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Tudor Groza

Showing results (31-40 of 76) with videos related to

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BMC Medical Informatics and Decision Making|January 31, 2024
An evaluation of GPT models for phenotype concept recognitionTudor Groza, Harry Caufield, Dylan Gration, et al.
Frontiers in Public Health|December 25, 2025
The United Nations convention on rare diseases-A framework for research prioritizationMohammed Junaid, Jenny Downs, Tudor Groza, et al.
Database : the Journal of Biological Databases and Curation|March 1, 2015
Automatic concept recognition using the human phenotype ontology reference and test suite corporaTudor Groza, Sebastian Köhler, Sandra Doelken, et al.
Bioinformatics (Oxford, England)|November 24, 2023
Term-BLAST-like alignment tool for concept recognition in noisy clinical textsTudor Groza, Honghan Wu, Marcel E Dinger, et al.
HGG Advances|December 12, 2025
A systematic assessment of large language models' knowledge of rare diseases: How much do large language models know about rare disease?Tudor Groza, Allison J Marcello, Tristan Carlisle, et al.
Journal of Paediatrics and Child Health|August 12, 2014
Phenotyping: targeting genotype's rich cousin for diagnosisGareth Baynam, Mark Walters, Peter Claes, et al.
Nucleic Acids Research|November 18, 2022
PDCM Finder: an open global research platform for patient-derived cancer modelsZinaida Perova, Mauricio Martinez, Tushar Mandloi, et al.
BMC Medical Informatics and Decision Making|June 27, 2018
CogStack - experiences of deploying integrated information retrieval and extraction services in a large National Health Service Foundation Trust hospitalRichard Jackson, Ismail Kartoglu, Clive Stringer, et al.
Human Mutation|August 14, 2015
Use of model organism and disease databases to support matchmaking for human disease gene discoveryChristopher J Mungall, Nicole L Washington, Jeremy Nguyen-Xuan, et al.
NPJ Digital Medicine|November 25, 2025
Information content as a health system screening tool for rare diseasesTudor Groza, Peter N Robinson, Weng Khong Lim, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
BMC Medical Informatics and Decision Making|January 31, 2024
An evaluation of GPT models for phenotype concept recognitionTudor Groza, Harry Caufield, Dylan Gration, et al.
Frontiers in Public Health|December 25, 2025
The United Nations convention on rare diseases-A framework for research prioritizationMohammed Junaid, Jenny Downs, Tudor Groza, et al.
Database : the Journal of Biological Databases and Curation|March 1, 2015
Automatic concept recognition using the human phenotype ontology reference and test suite corporaTudor Groza, Sebastian Köhler, Sandra Doelken, et al.
Bioinformatics (Oxford, England)|November 24, 2023
Term-BLAST-like alignment tool for concept recognition in noisy clinical textsTudor Groza, Honghan Wu, Marcel E Dinger, et al.
HGG Advances|December 12, 2025
A systematic assessment of large language models' knowledge of rare diseases: How much do large language models know about rare disease?Tudor Groza, Allison J Marcello, Tristan Carlisle, et al.
Journal of Paediatrics and Child Health|August 12, 2014
Phenotyping: targeting genotype's rich cousin for diagnosisGareth Baynam, Mark Walters, Peter Claes, et al.
Nucleic Acids Research|November 18, 2022
PDCM Finder: an open global research platform for patient-derived cancer modelsZinaida Perova, Mauricio Martinez, Tushar Mandloi, et al.
BMC Medical Informatics and Decision Making|June 27, 2018
CogStack - experiences of deploying integrated information retrieval and extraction services in a large National Health Service Foundation Trust hospitalRichard Jackson, Ismail Kartoglu, Clive Stringer, et al.
Human Mutation|August 14, 2015
Use of model organism and disease databases to support matchmaking for human disease gene discoveryChristopher J Mungall, Nicole L Washington, Jeremy Nguyen-Xuan, et al.
NPJ Digital Medicine|November 25, 2025
Information content as a health system screening tool for rare diseasesTudor Groza, Peter N Robinson, Weng Khong Lim, et al.
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