Danielle K Bourque
9PUBLICATIONS
22CO-AUTHORS
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Publications (9)
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|Mar 23, 2026
Expanding the Phenotype of TUFM -Related Combined Oxidative Phosphorylation Deficiency 4.Noémie Villeneuve-Cloutier, Jodi Warman-Chardon, Danielle K Bourque
|Nov 12, 2025
<i>MT-ATP6</i> variant as a cause of adult-onset hereditary spastic paraparesis: A case report and literature review.Lola Er Lessard, Danielle K Bourque, Pierre J Bourque
|Sep 27, 2024
Can endogenous ethylene glycol production occur in humans? A detailed investigation of adult monozygotic twin sisters.Marc Ghannoum, Paula J Waters, Knut Erik Hovda
|Jul 20, 2024
The diagnostic yield of genetic and metabolic investigations in syndromic and nonsyndromic patients with autism spectrum disorder, global developmental delay, or intellectual disability from a dedicated neurodevelopmental disorders genetics clinic.Julianne K Postma, Mary-Ann Harrison, Stephen Kutcher
|Sep 01, 2023
The mitochondrial tRNA MT-TW m.5537_5538insT variant presents with significant intra-familial clinical variability.Lauren Strasser, Asif Doja, Jorge Davila
|Apr 19, 2021
Gastroschisis in Ontario, Canada: 2012-2018.Danielle K Bourque, Lynn Meng, Shelley Dougan
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Frequent Collaborators
2 joint publications
Jodi Warman-Chardon
1 joint publications
Kym M Boycott
1 joint publications
Inara Chacon Fonseca
1 joint publications
David Chitayat
1 joint publications
Lynn Meng
1 joint publications
Lauren Strasser
1 joint publications
Pranesh Chakraborty
1 joint publications
Julianne K Postma
1 joint publications
Andrea C Yu
1 joint publications
Melissa T Carter
