Grants
Molecular Characterization of Skeletal Disorders in Manitoba Patients, Manitoba Institute of Child Health, Principal Investigator
Phenotypic and Genotypic Characterization of Ritscher-Schinzel Syndrome Patients, Manitoba Medical Services Foundation, Principal Investigator
GenCOUNSEL: Optimization of genetic counselling with clinical implementation of genome-wide sequencing, Genome Canada
RAPIDOMICS: Rapid sequencing in the neonatal intensive care unit, Genome BC
Honours &
Awards
Top poster award 2016 David W. Smith Meeting on Malformations of Morphogenesis (Elliott, When Developmental Fields are not Respected: The case of monodactylous split hand foot malformation (SHFM))
Top abstract award 2017 American Clinical Genetics and Genomics Meeting (Elliott et al., Interpreting the Interpretation: The CAUSES Research Clinic Experience), a study that investigated the discrepancies between laboratory reporting and research classifications in patients who have undergone genome-wide sequencing.
Reviewer’s Choice abstract award 2018 American Society of Human Genetics Annual Meeting (Elliott et al., Blended Phenotypes: An Interesting subset of the first 400 patients of the CAUSES Research Study).
2018 Canadian Association of Genetic Counsellors National Award: Professional Practice, Innovation and Advocacy Leadership Award