A. Micheil Innes
University of Calgary(CA)Rambam Health Care Campus(IL)Alberta Children's Hospital(CA)Royal Hobart Hospital(AU)AstraZeneca (Brazil)(BR)Alexion Pharmaceuticals (United States)(US)AstraZeneca (United States)(US)Alexion Pharma (Switzerland)(CH)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, RNA modifications and cancer, Congenital heart defects research
Most-Cited Works
- → De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes(2012)745 cited
- → G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex(2004)521 cited
- → The Role of PIEZO2 in Human Mechanosensation(2016)461 cited
- → Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care(2015)391 cited
- → The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies(2016)350 cited
- → Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling(2015)330 cited