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Dylan Gration

Showing results (1-10 of 11) with videos related to

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Bioinformatics (Oxford, England)|June 24, 2024
FastHPOCR: pragmatic, fast, and accurate concept recognition using the human phenotype ontologyTudor Groza, Dylan Gration, Gareth Baynam, et al.
Pediatric Dermatology|September 19, 2019
Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumabCathryn Poulton, Dylan Gration, Kevin Murray, et al.
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, 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.
Pharmacoepidemiology and Drug Safety|June 3, 2024
Use of privacy-preserving record linkage to examine the dispensing of pharmaceutical benefits scheme medicines to pregnant women in Western AustraliaErin Kelty, Michele Hansen, Sean Randall, et al.
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.
Clinical Genetics|June 1, 2022
Further evidence for distinct traits associated with RBM10 missense variantsCathryn Poulton, Gareth Baynam, Kye Pugh, et al.
American Journal of Medical Genetics. Part A|August 29, 2018
Silver Russel syndrome in an aboriginal patient from AustraliaCathryn Poulton, Dimitar Azmanov, Vanessa Atkinson, et al.
Neurology. Genetics|February 12, 2020
Defining and expanding the phenotype of <i>QARS</i>-associated developmental epileptic encephalopathyKatrine M Johannesen, Diana Mitter, Robert Janowski, et al.
Frontiers in Genetics|August 17, 2019
Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva InitiativeChristoffer Nellåker, Fowzan S Alkuraya, Gareth Baynam, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|June 24, 2024
FastHPOCR: pragmatic, fast, and accurate concept recognition using the human phenotype ontologyTudor Groza, Dylan Gration, Gareth Baynam, et al.
Pediatric Dermatology|September 19, 2019
Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumabCathryn Poulton, Dylan Gration, Kevin Murray, et al.
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, 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.
Pharmacoepidemiology and Drug Safety|June 3, 2024
Use of privacy-preserving record linkage to examine the dispensing of pharmaceutical benefits scheme medicines to pregnant women in Western AustraliaErin Kelty, Michele Hansen, Sean Randall, et al.
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.
Clinical Genetics|June 1, 2022
Further evidence for distinct traits associated with RBM10 missense variantsCathryn Poulton, Gareth Baynam, Kye Pugh, et al.
American Journal of Medical Genetics. Part A|August 29, 2018
Silver Russel syndrome in an aboriginal patient from AustraliaCathryn Poulton, Dimitar Azmanov, Vanessa Atkinson, et al.
Neurology. Genetics|February 12, 2020
Defining and expanding the phenotype of <i>QARS</i>-associated developmental epileptic encephalopathyKatrine M Johannesen, Diana Mitter, Robert Janowski, et al.
Frontiers in Genetics|August 17, 2019
Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva InitiativeChristoffer Nellåker, Fowzan S Alkuraya, Gareth Baynam, et al.
Pageof 2