Christine M. Armour
University of Ottawa(CA)Children's Hospital of Eastern Ontario(CA)Agricultural Research Institute of Ontario(CA)Newborn Screening Ontario(CA)Ontario Stroke Network(CA)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Fetal and Pediatric Neurological Disorders, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes(2012)745 cited
- → The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists(2015)234 cited
- → Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing(2017)145 cited
- → RETIRED: No. 348-Joint SOGC-CCMG Guideline: Update on Prenatal Screening for Fetal Aneuploidy, Fetal Anomalies, and Adverse Pregnancy Outcomes(2017)143 cited
- → Further delineation of cardio-facio-cutaneous syndrome: clinical features of 38 individuals with proven mutations(2007)124 cited
- → Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations(2016)122 cited