Anath C. Lionel, Ph.D.
Affiliations: | 2014 | Molecular and Medical Genetics | University of Toronto, Toronto, ON, Canada |
Area:
Genetics, Neuroscience Biology, Mental HealthGoogle:
"Anath Lionel"Mean distance: 53433
Parents
Sign in to add mentor| Stephen W. Scherer | grad student | 2014 | University of Toronto | |
| (Copy Number Variation in Neurodevelopmental Disorders.) | ||||
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Publications
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| Deneault E, White SH, Rodrigues DC, et al. (2019) Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons. Stem Cell Reports. 12: 427-429 |
| Deneault E, White SH, Rodrigues DC, et al. (2018) Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons. Stem Cell Reports |
| Lowther C, Merico D, Costain G, et al. (2017) Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Genome Medicine. 9: 105 |
| Ejaz R, Lionel AC, Blaser S, et al. (2017) De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay. American Journal of Medical Genetics. Part A |
| Lionel AC, Costain G, Monfared N, et al. (2017) Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Mosca SJ, Langevin LM, Dewey D, et al. (2016) Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder. Journal of Medical Genetics |
| Lionel AC, Monfared N, Scherer SW, et al. (2016) MED23-associated refractory epilepsy successfully treated with the ketogenic diet. American Journal of Medical Genetics. Part A |
| Lowther C, Speevak M, Armour CM, et al. (2016) Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Costain G, Lionel AC, Ogura L, et al. (2015) Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International Journal of Cardiology. 204: 115-121 |
| Tammimies K, Fernandez BA, Walker S, et al. (2015) High resolution genomic analyses of a clinically defined autism spectrum disorder cohort. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 76 |