Guylaine D’Amours

Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

Marc‐Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian R. Marshall et al. · PLoS Genetics · 2012 · 125 citations · Full text

Heart Failure, Cardiovascular Disease, Genetic Disorder +15

Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

Guylaine D’Amours, Zoha Kibar, Géraldine Mathonnet et al. · Clinical Genetics · 2011 · 84 citations · Full text

Genetic Testing, Genetics, Pathology +22

Refining the phenotype associated with biallelic <i>DNAJC21</i> mutations

Guylaine D’Amours, Fátima Lopes, J Gauthier et al. · Clinical Genetics · 2018 · 38 citations · Full text

Chromatin, Allelic Variant, Distinct Ibmfs +14

A variant of neonatal progeroid syndrome, or Wiedemann–Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GL

Éliane Beauregard‐Lacroix, Smrithi Salian, Hyunyun Kim et al. · European Journal of Human Genetics · 2019 · 31 citations · Full text

Neonatal Progeroid Syndrome, Autoimmune Disease, Genetic Disorder +9

Differential gene expression profiling in the mouse brain during motor skill learning: Focus on the striatum structure

Guylaine D’Amours, Geneviève Bureau, Marie-Josée Boily et al. · Behavioural Brain Research · 2011 · 20 citations

Motor Learning, Molecular Neuroscience, Cognitive Science +11