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Tudor Groza

Showing results (21-30 of 76) with videos related to

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Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 8, 2023
A consensus score to combine inferences from multiple centresHamed Haselimashhadi, Kolawole Babalola, Robert Wilson, et al.
JCO Clinical Cancer Informatics|January 18, 2019
Cancer Care Treatment Outcome Ontology: A Novel Computable Ontology for Profiling Treatment Outcomes in Patients With Solid TumorsFrank P Lin, Tudor Groza, Simon Kocbek, et al.
Peerj|October 23, 2018
Building interpretable models for polypharmacy prediction in older chronic patients based on drug prescription recordsSimon Kocbek, Primoz Kocbek, Andraz Stozer, et al.
American Journal of Human Genetics|April 17, 2025
First steps toward building natural history of diseases computationally: Lessons learned from the Noonan syndrome use caseTudor Groza, Warittha Rayabsri, Dylan Gration, et al.
Database : the Journal of Biological Databases and Curation|October 29, 2015
PhenoMiner: from text to a database of phenotypes associated with OMIM diseasesNigel Collier, Tudor Groza, Damian Smedley, et al.
Journal of Medical Genetics|January 26, 2020
Impacts of genomics on the health and social costs of intellectual disabilityBrett Doble, Deborah Schofield, Carey-Anne Evans, et al.
Journal of Biomedical Semantics|December 14, 2016
Thematic issue of the Second combined Bio-ontologies and Phenotypes WorkshopKarin Verspoor, Anika Oellrich, Nigel Collier, et al.
Journal of Biomedical Semantics|December 19, 2015
Special issue on bio-ontologies and phenotypesLarisa N Soldatova, Nigel Collier, Anika Oellrich, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
On the limitations of large language models in clinical diagnosisJustin T Reese, Daniel Danis, J Harry Caufield, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 8, 2023
A consensus score to combine inferences from multiple centresHamed Haselimashhadi, Kolawole Babalola, Robert Wilson, et al.
JCO Clinical Cancer Informatics|January 18, 2019
Cancer Care Treatment Outcome Ontology: A Novel Computable Ontology for Profiling Treatment Outcomes in Patients With Solid TumorsFrank P Lin, Tudor Groza, Simon Kocbek, et al.
Peerj|October 23, 2018
Building interpretable models for polypharmacy prediction in older chronic patients based on drug prescription recordsSimon Kocbek, Primoz Kocbek, Andraz Stozer, et al.
American Journal of Human Genetics|April 17, 2025
First steps toward building natural history of diseases computationally: Lessons learned from the Noonan syndrome use caseTudor Groza, Warittha Rayabsri, Dylan Gration, et al.
Database : the Journal of Biological Databases and Curation|October 29, 2015
PhenoMiner: from text to a database of phenotypes associated with OMIM diseasesNigel Collier, Tudor Groza, Damian Smedley, et al.
Journal of Medical Genetics|January 26, 2020
Impacts of genomics on the health and social costs of intellectual disabilityBrett Doble, Deborah Schofield, Carey-Anne Evans, et al.
Journal of Biomedical Semantics|December 14, 2016
Thematic issue of the Second combined Bio-ontologies and Phenotypes WorkshopKarin Verspoor, Anika Oellrich, Nigel Collier, et al.
Journal of Biomedical Semantics|December 19, 2015
Special issue on bio-ontologies and phenotypesLarisa N Soldatova, Nigel Collier, Anika Oellrich, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
On the limitations of large language models in clinical diagnosisJustin T Reese, Daniel Danis, J Harry Caufield, et al.
Pageof 8