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Andrea K. Vaags

University of Toronto

20

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541

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A Pan-Canadian Validation Study for the Detection of EGFR T790M Mutation Using Circulating Tumor DNA From Peripheral Blood.

2021
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Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparison.

2020 Clinical Biochemistry
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Microdeletions of ELP4 are associated with language impairment, autism spectrum disorder and epilepsy

2015 Human Mutation
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Absent CNKSR2 causes seizures and intellectual, attention, and language deficits

2014 Annals of Neurology
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Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

2014 Human Molecular Genetics
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Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

2013 Human Molecular Genetics
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Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

2013
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Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

2013 Journal of Medical Genetics
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Migration of Cells From the Yolk Sac to Hematopoietic Tissues After Transplantation of Early and Mid Gestation Canine Fetuses

2011 Transplantation
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Migration of cells from the yolk sac to hematopoietic tissues after in utero transplantation of early and mid gestation canine fetuses.

2011 Transplantation
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