Stephen W. Scherer

April 2011 Stephen Wayne "Steve" Scherer (born January 5, 1964) is a Canadian scientist who currently serves as the Chief of Research at The Hospital for Sick Children (SickKids) and distinguished University Professor at the University of Toronto. He obtained his PhD at the University of Toronto under Professor Lap-chee Tsui. Together they founded the Centre for Applied Genomics (TCAG). He is a Senior Fellow of Massey College at the University of Toronto. In 2014, he was named an esteemed Clarivate (previously Thomson Reuters) Citation laureate in Physiology or Medicine for the “''Discovery of large-scale gene copy number variation and its association with specific diseases.''” Provided by Wikipedia
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  1. 1
    An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell Composition

    An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell Composition by Maryam Jangjoo, Sarah J. Goodman, Sanaa Choufani, Brett Trost, Brett Trost, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Elizabeth Kelley, Muhammad Ayub, Rob Nicolson, Stelios Georgiades, Jennifer Crosbie, Jennifer Crosbie, Russell Schachar, Russell Schachar, Russell Schachar, Evdokia Anagnostou, Evdokia Anagnostou, Eyal Grunebaum, Eyal Grunebaum, Eyal Grunebaum, Rosanna Weksberg, Rosanna Weksberg, Rosanna Weksberg, Rosanna Weksberg, Rosanna Weksberg

    Published 2021-04-01
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  2. 2
    Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> Variant

    Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> Variant by Silas Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W. Scherer, M. E. Suzanne Lewis

    Published 2023-11-01
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  3. 3
    SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report.

    SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report. by Xavier Estivill, Nancy J Cox, Stephen J Chanock, Pui-Yan Kwok, Stephen W Scherer, Anthony J Brookes

    Published 2008-04-01
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  4. 4
    Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data

    Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data by Luciana Bertholim-Nasciben, Luciana Bertholim-Nasciben, Marilia O. Scliar, Guilherme Debortoli, Bhooma Thiruvahindrapuram, Stephen W. Scherer, Stephen W. Scherer, Yeda A. O. Duarte, Mayana Zatz, Mayana Zatz, Guilherme Suarez-Kurtz, Esteban J. Parra, Michel S. Naslavsky, Michel S. Naslavsky, Michel S. Naslavsky

    Published 2023-05-01
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  5. 5
    Modeling neuronal consequences of autism-associated gene regulatory variants with human induced pluripotent stem cells

    Modeling neuronal consequences of autism-associated gene regulatory variants with human induced pluripotent stem cells by P. Joel Ross, Rebecca S. F. Mok, Brandon S. Smith, Deivid C. Rodrigues, Marat Mufteev, Stephen W. Scherer, James Ellis

    Published 2020-05-01
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  6. 6
    Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testing

    Predictors of empowerment in parents of children with autism and related neurodevelopmental disorders who are undergoing genetic testing by Iskra Peltekova, Afiqah Yusuf, Jennifer Frei, Tal Savion‐Lemieux, Ridha Joober, Jennifer Howe, Stephen W. Scherer, Mayada Elsabbagh

    Published 2021-11-01
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  7. 7
    Association between distress and knowledge among parents of autistic children.

    Association between distress and knowledge among parents of autistic children. by Afiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, Jennifer Frei, Ruth Bruno, Ridha Joober, Jennifer Howe, Stephen W Scherer, Mayada Elsabbagh

    Published 2019-01-01
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  8. 8
    Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies.

    Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies. by Lars Feuk, Jeffrey R MacDonald, Terence Tang, Andrew R Carson, Martin Li, Girish Rao, Razi Khaja, Stephen W Scherer

    Published 2005-10-01
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  9. 9
    Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous <i>POLR2A</i> Variant

    Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous <i>POLR2A</i> Variant by Daniel R. Evans, Ying Qiao, Brett Trost, Kristina Calli, Sally Martell, Steven J. M. Jones, Stephen W. Scherer, M. E. Suzanne Lewis

    Published 2022-03-01
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  10. 10
    Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.

    Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease. by Svetlana Frenkel, Charles N Bernstein, Michael Sargent, Qin Kuang, Wenxin Jiang, John Wei, Bhooma Thiruvahindrapuram, Elizabeth Spriggs, Stephen W Scherer, Pingzhao Hu

    Published 2019-01-01
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  11. 11
    Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy.

    Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy. by Hoh Boon-Peng, Julia Ashazila Mat Jusoh, Christian R Marshall, Fadhlina Majid, Norlaila Danuri, Fashieha Basir, Bhooma Thiruvahindrapuram, Stephen W Scherer, Khalid Yusoff

    Published 2016-01-01
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  12. 12
    Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions

    Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions by Miguel Ramirez, Yuliya Badayeva, Joanna Yeung, Joshua Wu, Ayasha Abdalla-Wyse, Erin Yang, FANTOM 5 Consortium, Brett Trost, Stephen W Scherer, Daniel Goldowitz

    Published 2022-08-01
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  13. 13
    Genome-wide copy number variant data for inflammatory bowel disease in a caucasian population

    Genome-wide copy number variant data for inflammatory bowel disease in a caucasian population by Svetlana Frenkel, Charles N. Bernstein, Yong Won Jin, Michael Sargent, Qin Kuang, Wenxin Jiang, John Wei, Bhooma Thiruvahindrapuram, Stephen W. Scherer, Pingzhao Hu

    Published 2019-08-01
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  14. 14
    Disruption of the autism-associated gene SCN2A alters synaptic development and neuronal signaling in patient iPSC-glutamatergic neurons

    Disruption of the autism-associated gene SCN2A alters synaptic development and neuronal signaling in patient iPSC-glutamatergic neurons by Chad O. Brown, Chad O. Brown, Jarryll A. Uy, Jarryll A. Uy, Nadeem Murtaza, Nadeem Murtaza, Elyse Rosa, Alexandria Alfonso, Biren M. Dave, Biren M. Dave, Savannah Kilpatrick, Savannah Kilpatrick, Annie A. Cheng, Sean H. White, Stephen W. Scherer, Stephen W. Scherer, Karun K. Singh, Karun K. Singh, Karun K. Singh

    Published 2024-01-01
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  15. 15
    Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.

    Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease. by Nancy J Butcher, Daniele Merico, Mehdi Zarrei, Lucas Ogura, Christian R Marshall, Eva W C Chow, Anthony E Lang, Stephen W Scherer, Anne S Bassett

    Published 2017-01-01
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  16. 16
    Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings

    Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings by Jasleen Dhaliwal, Ying Qiao, Kristina Calli, Sally Martell, Simone Race, Chieko Chijiwa, Armansa Glodjo, Steven Jones, Evica Rajcan-Separovic, Stephen W. Scherer, Suzanne Lewis

    Published 2021-07-01
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  17. 17
    Editorial: Secondary vs. Idiopathic Autism

    Editorial: Secondary vs. Idiopathic Autism by Manuel F. Casanova, Emily L. Casanova, Richard Eugene Frye, Carolina Baeza-Velasco, Janine M. LaSalle, Randi Jensen Hagerman, Stephen W. Scherer, Marvin R. Natowicz

    Published 2020-04-01
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  18. 18
    Mutational Landscape of Autism Spectrum Disorder Brain Tissue

    Mutational Landscape of Autism Spectrum Disorder Brain Tissue by Marc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, Nasna Nassir, Hosneara Akter, Darren D. O’Rielly, Proton Rahman, Richard F. Wintle, Stephen W. Scherer, Mohammed Uddin

    Published 2022-01-01
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  19. 19
    Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.

    Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. by Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall, Stephen W Scherer, Anne S Bassett

    Published 2012-01-01
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  20. 20
    Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay

    Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay by Yi Liu, Yuqiang Lv, Mehdi Zarrei, Rui Dong, Xiaomeng Yang, Edward J. Higginbotham, Yue Li, Dongmei Zhao, Fengling Song, Yali Yang, Haiyan Zhang, Ying Wang, Stephen W. Scherer, Zhongtao Gai

    Published 2022-01-01
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