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American Journal of Obstetrics and Gynecology|January 10, 2023
Cytogenetic outcomes following a failed cell-free DNA screen: a population-based retrospective cohort study of 35,146 singleton pregnanciesKara Bellai-Dussault, Lynn Meng, Heather Howley, et al.Molecular and Cellular Biology|February 6, 2013
A high-confidence interaction map identifies SIRT1 as a mediator of acetylation of USP22 and the SAGA coactivator complexSean M Armour, Eric J Bennett, Craig R Braun, et al.CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 4, 2021
Performance of a universal prenatal screening program incorporating cell-free fetal DNA analysis in Ontario, CanadaShelley D Dougan, Nan Okun, Kara Bellai-Dussault, et al.Plos One|June 18, 2024
CAManim: Animating end-to-end network activation mapsEmily Kaczmarek, Olivier X Miguel, Alexa C Bowie, et al.Clinical Biochemistry|June 9, 2023
First and second trimester maternal serum markers for prenatal aneuploidy screening: An update on the adjustment factors for race, smoking, and insulin dependent diabetes mellitusTianhua Huang, Kara Bellai-Dussault, Lynn Meng, et al.Scientific Reports|March 30, 2026
MetaCAM as an ensemble-based class activation mapping framework improves model explainabilityKevin Dick, Emily Kaczmarek, Olivier X Miguel, et al.Journal of Community Genetics|April 28, 2018
Primary care providers' lived experiences of genetics in practiceBrittany Harding, Colleen Webber, Lucia Ruhland, et al.American Journal of Medical Genetics. Part A|May 3, 2016
Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple eventsChristine M Armour, Amanda Smith, Taila Hartley, et al.Acta Obstetricia Et Gynecologica Scandinavica|September 29, 2024
Outcomes of pregnancies with varying levels of nuchal translucency measurements: A population-based retrospective study in Ontario, CanadaKara Bellai-Dussault, Shelley D Dougan, Deshayne B Fell, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2019
The value of diagnostic testing for parents of children with rare genetic diseasesDeborah A Marshall, Karen V MacDonald, Sebastian Heidenreich, et al.Pageof 11