Stephen W. Scherer
Affiliations: | Molecular and Medical Genetics | University of Toronto, Toronto, ON, Canada |
Area:
Genetics, Neuroscience Biology, Mental HealthGoogle:
"Stephen Scherer"Mean distance: 53433
Children
Sign in to add trainee| C. Giovanni Traverso | research assistant | 1994-1996 | University of Toronto (Sick Kids) (Chemistry Tree) |
| Anath C. Lionel | grad student | 2014 | University of Toronto |
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Publications
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| Scala M, Bradley CA, Howe JL, et al. (2023) Genetic variants in contribute to Autism Spectrum Disorder associated with the Xp22.11 locus. Medrxiv : the Preprint Server For Health Sciences |
| Yip S, Calli K, Qiao Y, et al. (2023) Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous Variant. Genes. 14 |
| Costa CIS, da Silva Campos G, da Silva Montenegro EM, et al. (2023) Three generation families: Analysis of de novo variants in autism. European Journal of Human Genetics : Ejhg |
| Rots D, Jakub TE, Keung C, et al. (2023) The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder. American Journal of Human Genetics |
| Trost B, Thiruvahindrapuram B, Chan AJS, et al. (2022) Genomic architecture of autism from comprehensive whole-genome sequence annotation. Cell. 185: 4409-4427.e18 |
| Chan AJS, Engchuan W, Reuter MS, et al. (2022) Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Nature Communications. 13: 6463 |
| Maihofer AX, Engchuan W, Huguet G, et al. (2022) Rare copy number variation in posttraumatic stress disorder. Molecular Psychiatry |
| Lok S, Lau TNH, Trost B, et al. (2022) Chromosomal-Level Reference Genome Assembly of the North American Wolverine (Gulo gulo luscus): A Resource for Conservation Genomics. G3 (Bethesda, Md.) |
| Teles E Silva AL, Glaser T, Griesi-Oliveira K, et al. (2022) Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder. Translational Psychiatry. 12: 234 |
| Evans DR, Qiao Y, Trost B, et al. (2022) Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous Variant. Genes. 13 |