Publications by authors named "Dylan Gration"

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Mondo: Integrating Disease Terminology Across Communities.
Nicole A Vasilevsky, Sabrina Toro, Nicolas Matentzoglu, Joseph E Flack, Kathleen R Mullen, Dylan Gration

Genetics· October 2025

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First steps toward building natural history of diseases computationally: Lessons learned from the Noonan syndrome use case.
Tudor Groza, Warittha Rayabsri, Dylan Gration, Harshini Hariram, Saumya Shekhar Jamuar

Am J Hum Genet· May 2025

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FastHPOCR: pragmatic, fast, and accurate concept recognition using the human phenotype ontology.
Tudor Groza, Dylan Gration, Gareth Baynam, Peter N Robinson

Bioinformatics· July 2024

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Use of privacy-preserving record linkage to examine the dispensing of pharmaceutical benefits scheme medicines to pregnant women in Western Australia.
Erin Kelty, Michele Hansen, Sean Randall, Dylan Gration, Gareth Baynam

Pharmacoepidemiol Drug Saf· June 2024

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An evaluation of GPT models for phenotype concept recognition.
Tudor Groza, Harry Caufield, Dylan Gration, Gareth Baynam, Melissa A Haendel

BMC Med Inform Decis Mak· January 2024

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Surfacing undiagnosed disease: consideration, counting and coding.
Megan F Baxter, Michele Hansen, Dylan Gration, Tudor Groza, Gareth Baynam

Front Pediatr· October 2023

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Further evidence for distinct traits associated with RBM10 missense variants.
Cathryn Poulton, Gareth Baynam, Kye Pugh, Michael Mason, Catherine Kiraly-Borri, Dylan Gration

Clin Genet· August 2022

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Defining and expanding the phenotype of -associated developmental epileptic encephalopathy.
Katrine M Johannesen, Diana Mitter, Robert Janowski, Christian Roth, Joseph Toulouse, Dylan Gration

Neurol Genet· December 2019

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Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumab.
Cathryn Poulton, Dylan Gration, Kevin Murray, Gareth Baynam, Anne Halbert

Pediatr Dermatol· November 2019

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Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative.
Christoffer Nellåker, Fowzan S Alkuraya, Gareth Baynam, Raphael A Bernier, Francois P J Bernier, Dylan Gration

Front Genet· July 2019

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Silver Russel syndrome in an aboriginal patient from Australia.
Cathryn Poulton, Dimitar Azmanov, Vanessa Atkinson, John Beilby, Lisa Ewans, Dylan Gration

Am J Med Genet A· December 2018

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