Paul F. Lasko
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 61 publications
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.
Journal: Nature genetics
Published: October 21, 2024
Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe).
Journal: Lab animal
Published: June 24, 2024
An EpCAM/Trop2 mechanostat differentially regulates collective behaviour of human carcinoma cells.
Journal: The EMBO journal
Published: April 08, 2024
Remodeling of cadherin contacts in embryonic mesenchymal tissues during differential cell migration.
Remodeling of cadherin contacts in embryonic mesenchymal tissues during differential cell migration.
Journal: Developmental cell
Published: April 20, 2023
Functional analysis of the AUG initiator codon context reveals novel conserved sequences that disfavor mRNA translation in eukaryotes.
Journal: Nucleic acids research
Published: February 22, 2023
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.
Journal: American journal of human genetics
Published: May 15, 2022
Eukaryotic translation initiation factor eIF4E-5 is required for spermiogenesis in Drosophila melanogaster.
Journal: Development (Cambridge, England)
Published: December 20, 2021
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.
Journal: Clinical genetics
Published: July 14, 2021
Transgenes of genetically modified animals detected non-invasively via environmental DNA.
Journal: PloS one
Published: March 14, 2021
Investigating rare and ultrarare epilepsy syndromes with Drosophila models.
Journal: Faculty reviews
Published: March 04, 2021
Last Updated: 09/26/2026