Hillary Elrick

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 5

Top Topics

Acute Myeloid Leukemia

Health Insurance

Cross Sectional

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

David O'Connor, Jose Espejo Valle-Inclan, Lucia Conde, Gianna Bloye, Sunniyat Rahman, Joana R Costa, Jack Bartram, Stuart Paul Adams, Gary Wright, Hillary Elrick, Kerry Wall, Sara Dyer, Christopher Howell, Galina Jigoulina, Javier Herrero, Isidro Cortes-Ciriano, Anthony V Moorman, Marc R Mansour
Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL. Blood 143 (10) (2024)
David O'Connor, Jose Espejo Valle-Inclan, Lucia Conde, Gianna Bloye, Sunniyat Rahman, Joana R Costa, Jack Bartram, Stuart Paul Adams, Gary Wright, Hillary Elrick, Kerry Wall, Sara Dyer, Christopher Howell, Galina Jigoulina, Javier Herrero, Isidro Cortes-Ciriano, Anthony V Moorman, Marc R Mansour
Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL. Blood 143 (10) (2024)
David O'Connor, Jose Espejo Valle-Inclan, Lucia Conde, Gianna Bloye, Sunniyat Rahman, Joana R Costa, Jack Bartram, Stuart Paul Adams, Gary Wright, Hillary Elrick, Kerry Wall, Sara Dyer, Christopher Howell, Galina Jigoulina, Javier Herrero, Isidro Cortes-Ciriano, Anthony V Moorman, Marc R Mansour
Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL. Blood 143 (10) (2024)
David O'Connor, Jose Espejo Valle-Inclan, Lucia Conde, Gianna Bloye, Sunniyat Rahman, Joana R Costa, Jack Bartram, Stuart Paul Adams, Gary Wright, Hillary Elrick, Kerry Wall, Sara A Dyer, Christopher Howell, Galina Jigoulina, Javier Herrero, Isidro Cortes-Ciriano, Anthony V Moorman, Marc R Mansour
Non-coding mutations drive persistence of a founder pre-leukemic clone which initiates late relapse in T-ALL. Blood (2024)
Hannah G Driver, Taila Hartley, E Magda Price, Andrei L Turinsky, Orion J Buske, Matthew Osmond, Arun K Ramani, Emily Kirby, Kristin D Kernohan, Madeline Couse, Hillary Elrick, Kevin Lu, Pouria Mashouri, Aarthi Mohan, Delvin So, Conor Klamann, Hannah G B H Le, Andrea Herscovich, Christian R Marshall, Andrew Statia, Care Rare Canada Consortium, Bartha Maria Knoppers, Michael Brudno, Kym M Boycott
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery. Human mutation 43 (6) (2022)