A. Vaags

发表

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

D. Pinto, S. Scherer, D. Collier, 2012, American journal of human genetics.

Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository

Matthew S. Lebo, C. Marshall, H. Feilotter, 2021, Journal of Medical Genetics.

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

D. Pinto, S. Scherer, D. Collier, 2015, Human mutation.

eNOS overexpressing bone marrow cells are safe and effective in a porcine model of myocardial regeneration following acute myocardial infarction.

M. Ward, D. Stewart, M. R. Hough, 2013, Cardiovascular therapeutics.

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

M. DeMarco, A. Mattman, M. Speevak, 2020, Clinical biochemistry.

Identification of two novel mutations, L105R and C342R, in Type I Gaucher disease

B. Fernandez, A. Vaags, K. Wong, 2002, Clinical genetics.

Migration of Cells From the Yolk Sac to Hematopoietic Tissues After In Utero Transplantation of Early and Mid Gestation Canine Fetuses

M. R. Hough, A. Dick, W. Foltz, 2011, Transplantation.

HIV TAT variants differentially influence the production of glucocerebrosidase in Sf9 cells.

A. Vaags, F. Choy, T. Campbell, 2005, Genetics and molecular research : GMR.

Development of a comprehensive approach to adult hereditary cancer testing in Ontario

H. Feilotter, A. Pollett, A. Eisen, 2022, Journal of Medical Genetics.

Adult and Embryonic Stem Cell Sources for Use in a Canine Model of In Utero Transplantation

A. Vaags, 2012 .

Derivation and Characterization of Canine Embryonic Stem Cell Lines with In Vitro and In Vivo Differentiation Potential

M. R. Hough, A. Vaags, S. Kruth, 2009, Stem cells.

Practice guidelines for BRCA1/2 tumour testing in ovarian cancer

D. Butcher, D. Grafodatskaya, T. Stockley, 2022, Journal of Medical Genetics.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

John Wei, S. Scherer, J. Rosenfeld, 2014, Human molecular genetics.

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

S. Scherer, A. C. Lionel, C. Marshall, 2014, Journal of Neurodevelopmental Disorders.

Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

J. Rosenfeld, D. Merico, A. C. Lionel, 2013 .

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

S. Scherer, G. Kirov, D. Merico, 2013, Human molecular genetics.

Ectopic TLX1 Expression Accelerates Malignancies in Mice Deficient in DNA-PK

M. R. Hough, Edwin Chen, Valentina Evdokimova, 2014, PloS one.

Autism Spectrum Disorder

D. Pinto, S. Scherer, P. Bolton, 2018, Sleep in Children with Neurodevelopmental Disabilities.

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

S. Scherer, J. Rosenfeld, L. Shaffer, 2013, Journal of Medical Genetics.

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

H. Feilotter, D. Demetrick, D. Grafodatskaya, 2021, JTO clinical and research reports.

Long-term tracking of bone marrow progenitor cells following intracoronary injection post-myocardial infarction in swine using MRI.

G. Wright, M. Ward, D. Stewart, 2010, American journal of physiology. Heart and circulatory physiology.

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

M. R. Hough, A. Dick, W. Foltz, 2011 .

Absent CNKSR2 causes seizures and intellectual, attention, and language deficits

S. Scherer, C. Marshall, S. Walker, 2014, Annals of neurology.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

John Wei, S. Scherer, J. Rosenfeld, 2014, Human molecular genetics.