| |
Investigator |
Affiliation |
Projects |
| |
Clarke, Lorne |
Investigator |
Gene therapy strategies in a murine model
for mucopolysaccharidosis type 1 |
 |
| |
Cox, Diane |
Investigator |
Genetic factors in liver disease |
|
| |
Danska, Jayne |
Core |
Mouse Cytogenomics Core Facility |
|
| |
Danska, Jayne |
Investigator |
Genetics of Type 1 diabetes |
|
| |
Dick, John |
Investigator |
Preclinical model for retrovirus-mediated
gene therapy into human stem cells |
|
| |
Drouin, Regen |
Core |
In vivo DNA analysis Core Facility |
|
| |
Field Leigh |
Investigator |
Genetics of Phonological Coding dyslexia (PCD), Genetic susceptibility to IDDM |
|
| |
Foulkes, William |
Investigator |
Clinicopathologic features of hereditary breast cancer |
|
| |
Gallie, Brenda |
Investigator |
Non-coding conserved regions in RB1 gene regulation and initiation of retinoblastoma; Mutation identification in health care |
|
| |
Glerum, Moira |
Investigator |
Analysis of mtDNA mutations in cancer. |
|
| |
Gravel, Roy |
Investigator |
Pathogenesis of neuron death in Tay-Sachs and Sandhoff disease |
|
| |
Gros, Phillippe |
Investigator |
Genetic control of susceptibility to infection |
|
| |
Hayden, Michael |
Core |
DNA Sequencing Core Facility |
|
| |
Hayden, Michael |
Investigator |
Identification of genes contributing to HDL levels in humans; Neurodegeneration in Huntington disease; Gene therapy for LPL deficiency |
|
| |
Hegele, Rob |
Investigator |
Genetic determinants of diabetes and atherosclerosis |
|
| |
Heon, Elise |
Investigator |
Molecular characterization of corneal
dystrophies: VSX1 and beyond |
|
| |
Hicks, Geoff |
Investigator, Core |
Functional genomics core facility |
|
| |
Hudson, Tom |
Core |
Genotyping core facility |
|
| |
Hudson, Tom |
Core |
Microarray Analysis Core Facility |
|
| |
Hudson, Tom |
Investigator |
Expression studies using high-density arrays |
|
| |
Jirik, Frank |
Investigator |
Fanconi anemia |
|
| |
Korneluk, Bob |
Investigator |
Myotonic dystrophy; Apoptosis |
|
| |
Leavitt, Blair |
Core |
Transgenic Mouse Core Facility |
|
| |
Leavitt, Blair |
Investigator |
Gene therapy in transgenic mouse models of human genetic disease |
|
| |
Lobe, Corrinne |
Core |
ES cell-mediated genome alterations |
|
| |
Mackenzie, Alex |
Investigator |
Spinal muscular atrophy and other inherited neuromuscular disorders |
|
| |
Maclennan, David |
Investigator |
Calcium signalling and muscle diseases |
|
| |
McInnes, Rod |
Investigator |
Inherited retinal degeneration; Inherited epilepsy |
|
| |
Mitchell, Grant |
Investigator |
The biological roles of hormone sensitive
lipase |
|
| |
Morgan, Ken |
Investigator |
Gene identification relevant to common diseases |
|
| |
Nadon, Robert |
Core |
Microarray Analysis Core Facility |
|
| |
Narod, Steven |
Investigator |
Risk modifiers in hereditary breast cancer |
|
| |
Ouellette, Francis |
Core |
Bioinformatics Core Facility |
|
| |
Ouellette, Francis |
Investigator |
Integrated bioinformatics and clinical
approach identify novel disease gene associations: Mining the
genome for GeMS |
|
| |
Peterson, Alan |
Core |
HPRT Targeted Transgenesis Core Facility |
|
| |
Robinson, Brian |
Investigator |
Cytochrome oxidase deficiency; Genes involved in protection against oxygen free radicals |
|
| |
Rommens, Johanna |
Investigator |
Identification of Cobalamin Group C deficiency |
|
| |
Rouleau, Guy |
Investigator |
Pure autosomal recessive ataxia |
|
| |
Rousseau, Francois |
Investigator |
Inherited mental retardation
and the FMRI gene |
|
| |
Rozen, Rima |
Investigator |
Investigation of folate metabolism
in intestinal neoplasia |
|
| |
Scherer, Stephen |
Core |
DNA Sequencing Core Facility
|
|
| |
Scherer, Stephen |
Core |
Mouse Cytogenomics Core Facility |
|
| |
Scherer, Stephen |
Investigator |
Identification of genes involved
in autism |
|
| |
Schurr, Erwin |
Investigator |
Genetic factors and infectious
disease |
|
| |
Scriver, Charles |
Investigator |
Mutation database |
|
| |
Siminovitch, Kathy |
Investigator |
Genes involved in inflammatory bowel disease; Genes involved in rheumatoid arthritis |
|
| |
Skamene, Emil |
Investigator |
Complex trait analysis in mice |
|
| |
Shoubridge, Eric |
Investigator |
Nuclear control of mtDNA & the structure of the mtDNA nucleoid |
|
| |
St.George Hyslop, Peter |
Investigator |
Genetics of Dementia; Presenilins |
|
| |
Triggs-Raine, Barbara |
Investigator |
Type II diabetes and insulin signaling |
|
| |
Tsui, Lap-Chee |
Investigator |
Molecular genetics of cystic fibrosis; Systematic mutation detection in cystic fibrosis and related diseases |
|
| |
Walter, Michael |
Investigator |
Genetic Basis of common diseases - ocular diseases |
|
| |
Wasserman, Wyeth |
Investigator |
Analysis of regulatory sequences in the human genome |
