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Genetics of complex disease, genomic variation, genomic technologies. Genetics of Autism Spectrum Disorder.
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Researcher Information
Assistant Director, TCAG
The Centre for Applied Genomics (TCAG)
Website
MaRS Centre TMDT, Room 14-707
101 College St.
Toronto, Ontario
Canada M5G 1L7
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Dr. Wintle completed a PhD in the Department of Molecular and Medical Genetics at the University of Toronto, studying the organization of antibody heavy chain genes. His postdoctoral work at the Centre for Addiction and Mental Health (Toronto) involved the study of neurotransmitter signaling in the nervous system of the nematode C. elegans. He then worked with two startup biotechnology companies, in the areas of laboratory operations and scientific project management, including managing a multi-million dollar research initiative on the genetics of inflammatory and other complex diseases.
Currently, he is the Assistant Director of The Centre for Applied Genomics at SickKids hospital in Toronto. TCAG is core facility employing over 70 people, and providing services in cutting-edge genomic laboratory experimentation, project consultation and bioinformatic and computational support to over 1,300 laboratories in Ontario, the rest of Canada, and worldwide.
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Researcher Information
Assistant Director, TCAG
The Centre for Applied Genomics (TCAG)
Website
MaRS Centre TMDT, Room 14-707
101 College St.
Toronto, Ontario
Canada M5G 1L7
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Wintle, R.F., T.G. Nygaard, J.S. Herbrick K. Kvaløy and D.W. Cox. Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q. Genomics 1997, 40:409-414
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Sanyal, S., R.F. Wintle (co-first authors), K.S. Kindt, W.M. Nuttley, R. Arvand, P. Fitzmaurice, E. Bigras, D.C. Merz, T.E. Hebert, D. van der Kooy, W.R. Schafer, J.G. Culotti and H.H.M. Van Tol. Dopamine modulates the plasticity of mechanosensory responses in C. elegans. EMBO J. 2004, 23(2):473-82
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Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nature Genet. 2004, 36(5):471-75
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Feuk, L., C.R. Marshall, R.F. Wintle and S.W. Scherer. Structural variants: changing the landscape of chromosomes and design of disease studies. Hum. Molec. Genet. 2006, 15:R57-R66
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Goobie S, Knijnenburg J, Fitzpatrick D, Sharkey FH, Lionel AC, Marshall CR, Azam T, Shago M, Chong K, Mendoza-Londono R, den Hollander NS, Ruivenkamp C, Maher E, Tanke HJ, Szuhai K, Wintle RF, Scherer SW. Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenet Genome Res. 2008;123(1-4):65-78
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Researcher Information
Assistant Director, TCAG
The Centre for Applied Genomics (TCAG)
Website
MaRS Centre TMDT, Room 14-707
101 College St.
Toronto, Ontario
Canada M5G 1L7
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ORGANIZATIONS
PROJECTS
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YOU MAY ALSO BE INTERESTED IN:
CATEGORIES
Application Area
Human health,
Instrumentation and tools
Disciplinary Focus
Experimental biology and chemistry,
Informatics, theoretical biology and computer science
Research Paradigm
Focused-scope projects,
Large-scale projects,
Technology development
Core Technology
statistical genetics
Cells and tissues:
Biobanking,
Cell imaging
Nucleic acids:
Cytogenomics,
DNA sequencing,
Gene expression systems,
Genotyping,
Microarrays,
RNA technologies
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