Matthew M. Osmond
Ottawa, ON, Canada
Last Updated: 09/26/2026
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Found 58 publications
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants.
Journal: Clinical genetics
Published: May 12, 2026
When Does the Probability of Evolutionary Rescue Increase with the Strength of Selection despite a Potential Demographic Cost?
Journal: The American naturalist
Published: April 23, 2026
How Genotype-by-Environment Interactions Can Maintain Variation in Mutualisms.
Journal: The American naturalist
Published: February 06, 2026
The promise and challenge of spatial inference with the full ancestral recombination graph under Brownian motion.
Journal: bioRxiv : the preprint server for biology
Published: March 03, 2025
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient Matchmaking.
Journal: Human mutation
Published: January 28, 2025
NUBP2 deficiency disrupts the centrosome-check point in the brain and causes primary microcephaly.
Journal: medRxiv : the preprint server for health sciences
Published: January 27, 2025
Mainstreaming of clinical genetic testing: A conceptual framework.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 15, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.
Journal: Nature genetics
Published: October 02, 2024
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations.
Journal: BMJ open
Published: September 04, 2024
De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features.
Journal: American journal of human genetics
Published: May 15, 2024
Last Updated: 09/26/2026