Maxime Cadieux-Dion
5PUBLICATIONS
32CO-AUTHORS
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Publications (5)
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|Mar 03, 2023
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.Zeineb Bakey, Oscar A Cabrera, Julia Hoefele
|Feb 04, 2020
Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer.Kezhi Yan, Justine Rousseau, Keren Machol
|Jan 11, 2020
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing.Ivana Jedličková, Maxime Cadieux-Dion, Anna Přistoupilová
|Apr 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencing.Jean Monlong, Simon L Girard, Caroline Meloche
|Mar 11, 2018
Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report.Maxime Cadieux-Dion, Nicole P Safina, Kendra Engleman
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Frequent Collaborators
2 joint publications
Isabelle Thiffault
1 joint publications
Jean Monlong
1 joint publications
Simon L Girard
1 joint publications
Jakub Sikora
1 joint publications
Kezhi Yan
1 joint publications
Keren Machol
1 joint publications
Anne Goverde
1 joint publications
Hannah Verdin
1 joint publications
Natacha Esber
1 joint publications
Alan F Riley
