Philip A. Hieter
2185 East Mall
Vancouver, BC, Canada
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 40 publications
Global partnerships in rare disease research.
Journal: Disease models & mechanisms
Published: July 28, 2025
Deep structure-function analysis of the endonuclease Mus81 with dominant mutational scanning.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 18, 2025
Synthetic cytotoxicity profiling of cohesin mutants highlights recombination-based dependencies.
Journal: DNA repair
Published: April 17, 2025
Mapping of DDX11 genetic interactions defines sister chromatid cohesion as the major dependency.
Journal: G3 (Bethesda, Md.)
Published: January 22, 2024
Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases.
Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases.
Journal: G3 (Bethesda, Md.)
Published: August 09, 2023
ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.
Journal: Human mutation
Published: September 30, 2021
Mapping Synthetic Dosage Lethal Genetic Interactions in Saccharomyces cerevisiae.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 30, 2021
A nuclear proteome localization screen reveals the exquisite specificity of Gpn2 in RNA polymerase biogenesis.
Journal: Cell cycle (Georgetown, Tex.)
Published: June 28, 2021
Paralogous synthetic lethality underlies genetic dependencies of the cancer-mutated gene STAG2.
Journal: Life science alliance
Published: April 01, 2021
Modeling DNA trapping of anticancer therapeutic targets using missense mutations identifies dominant synthetic lethal interactions.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 30, 2021
Last Updated: 09/26/2026