Tatiana Maroilley
Calgary, AB, Canada
Last Updated: 09/26/2026
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Found 21 publications
A course-undergraduate research experience (CURE) to explore the effect of structural variants on gene expression in C. elegans balancers.
Journal: PloS one
Published: January 27, 2026
Detection of Complex Genomic Rearrangements Using Short-Read Whole Genome Sequencing in C. elegans.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: August 30, 2025
The cost and cost trajectory of genome sequencing and bioinformatics analysis for Indigenous children with suspected rare diseases.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 28, 2025
Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique.
Journal: Epilepsia
Published: January 20, 2024
Mitogen-induced defective mitosis transforms neural progenitor cells.
Journal: Neuro-oncology
Published: May 15, 2023
Molecular basis of essential and morphological variations across 12 balancer strains in C. elegans.
Journal: microPublication biology
Published: April 28, 2023
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversion.
Journal: Life science alliance
Published: April 26, 2023
Model Organism Modifier (MOM): a user-friendly Galaxy workflow to detect modifiers from genome sequencing data using Caenorhabditis elegans.
Journal: G3 (Bethesda, Md.)
Published: April 21, 2023
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases.
Journal: Genes
Published: December 15, 2022
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach.
Journal: Epilepsia open
Published: November 03, 2022
Last Updated: 09/26/2026