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Dr. Bulman is a specialist in the field of Human Genetics in the areas of classical genetics, X-linked disorders, autosomal dominant traits and complex multifactorial diseases.
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Dr. Bulman is a specialist in the field of Human Genetics in the areas of classical genetics, X-linked disorders, autosomal dominant traits and complex multifactorial diseases.
EXPLORE >   Researchers >  Dennis E. Bulman
RESEARCH
BIOGRAPHY
KEY PUBLICATIONS
INTELLECTUAL PROPERTY
Research
The Bulmanare lab conducts high throughput genotyping as a first step towards identifying genes cause and understanding the pathophysiology of genetic disorders.

Dr. Dennis E. Bulman’s current research work involves finding the genes for Parkinson's disease, migraine, ataxia, various forms of epilepsy, Bi-cuspid Aortic Valve, Brachydactyly A-1 and myoclonus dystonia within large families which are affected by these disorders.
Researcher Information
Senior Scientist,Associate Professor
Dept of Biochemistry
Website
725 Parkdale Ave.
Ottawa, Ontario
Canada K1Y 4E9
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Biography
Dr. Bulman received his B.Sc. in Genetics and an M.Sc. in Microbiology and Immunology from the University of Western Ontario. He completed a Ph.D. in Molecular and Medical Genetics at the University of Toronto.

Dr. Bulman is a Senior Research Scientist at the Ottawa Hospital Research Institute, and an Associate Professor in the Division of Neurology, Department of Medicine at the University of Ottawa. He is a Network Scholar of the Canadian Genetic Disease Network, and a Canadian Foundation for Innovation Researcher.
Researcher Information
Senior Scientist,Associate Professor
Dept of Biochemistry
Website
725 Parkdale Ave.
Ottawa, Ontario
Canada K1Y 4E9


Key Publications
Armour CM, Bulman DE, Jarinova O,et al.
17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD).
Eur J Hum Genet. 2011
Hakimi M, Selvanantham T, Bulman DE et al.
Parkinson's disease-linked LRRK2 is expressed in circulating and tissue immune cells and upregulated following recognition of microbial structures.
J Neural Transm. 2011,118,5:795-808.
McQuibban GA, Bulman DE.
The PARLance of Parkinson disease.
Autophagy. 2011,7,7:790-2.
Shi G, Lee JR, Bulman DE., et al.
Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease.
Hum Mol Genet. 2011,20,10:1966-74.
Researcher Information
Senior Scientist,Associate Professor
Dept of Biochemistry
Website
725 Parkdale Ave.
Ottawa, Ontario
Canada K1Y 4E9


Intellectual Property

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CATEGORIES
Application Area
Human health
Disciplinary Focus
Clinical science, Experimental biology and chemistry
Research Paradigm
Large-scale projects
Core Technology
Nucleic acids: DNA sequencing, Gene expression systems, Genotyping
Proteins: Protein expression and purification, Protein sequencing, Protein-protein interaction assays
Organism
Human
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