Project MinE

Printer-friendly version

“Why have I been diagnosed with ALS when so many other people have not?”
This is an all-too-common question of people living with the devastation of an ALS diagnosis, and the ALS Society of Canada (ALS Canada) wants to help answer it. We are leading Canada’s fundraising efforts for Project MinE to support the mapping and analysis of up to 1,000 DNA profiles.
Project MinE is a multi-national initiative with more than 15 participating countries. It will map the full DNA profiles of 15,000 people with ALS and 7,500 control subjects, establishing a global resource of human data that will enable scientists worldwide to understand the genetic signature that leads someone to develop ALS.
By accumulating such a large amount of data that no one country could achieve alone, it is expected that Project MinE will identify new genetic causes of the disease that will significantly accelerate our ability to advance treatment possibilities that will slow down or stop ALS.
Who else is involved?
Research team
The Canadian component of Project MinE brings together four of Canada’s leading ALS geneticists in Vancouver, Toronto, Montreal and Quebec City for their first ever cross-country collaboration. Each has led or been part of international consortia that have resulted in some of the most important genetic discoveries in the field. They also represent a geographical balance that provides a collaborative set of Canadian samples representative of ALS cases across the country.
• Dr. Nicolas Dupré
• Dr. Ian Mackenzie
• Dr. Ekaterina Rogaeva
• Dr. Guy Rouleau
ALS Clinics
Other collaborators in Canada’s Project MinE effort are the ALS clinics who will collect and in some cases store the blood samples being used for the initiative. Potential ALS clinic partners that have been identified to date are the GF Strong Rehabilitation Centre’s ALS Centre in Vancouver, the Sunnybrook Health Sciences Centre ALS Clinic in Toronto, the ALS Program at the Montreal Neurological Institute and Hospital, and the ALS Clinic at the CHU de Québec.
ALS Canada ambassador: Chris McCauley Social worker, policy research analyst and ALS patient 
Months after celebrating his first wedding anniversary in 2014, Chris McCauley noticed some unusual twitching in his arms and legs while vacationing with his wife in Costa Rica. Shortly thereafter, he was diagnosed with ALS at the age of 52. “Instead of looking forward to establishing a home and thriving in career and community, we were doing our best not to deny the opposite reality,” he says.
Since then, Chris – a policy research analyst and social worker – has become keenly interested in ALS research. Given the multiple causes, numerous disease pathways, and the different ways and rates at which ALS progresses and the variations in survival, he has been struck by the immense challenges researchers face in developing a treatment or cure for the disease.
To Chris, Project MinE holds tremendous promise as it will make ALS easier to study and has great potential to lead to effective treatments. He is bringing his voice to Project MinE in Canada so he can help make things better for people who will be diagnosed with ALS in the future. As he puts it, “I think of others who will come after me and like me, lose the blossom of their health so insidiously. I want to do something to make it better.”

Dr. Nicolas Dupré
Neurologist; Assistant Professor, Faculty of Medicine, Université Laval; Clinician-Scientist, Axe Neurosciences, CHU de Québec - U Laval
Dr. Dupré has made major contributions both locally and internationally to the fields of neuromuscular and neurogenetic medicine, and has published more than 100 peer-reviewed papers and five book chapters.  He is currently the director of the Neuromuscular & Neurogenetic Disease Clinic of the CHU de Québec - U Laval, taking care of thousands of patients from the Eastern Quebec area afflicted with rare and common diseases of the nervous system.   Dr. Dupré was involved in the 2008 discovery that the gene TDP-43 is involved in ALS. He also helped to establish the ALS clinic at the CHU de Québec, providing care to patients in Eastern Quebec.

Dr. Ian Mackenzie, Professor
University of British Columbia; Staff Neuropathologist, Vancouver Coastal Health; Consultant Neuropathologist, BC Cancer Agency
Dr. Mackenzie is Professor of Pathology and Laboratory Medicine at The University of British Columbia, Consultant Neuropathologist of Vancouver Acute and BC Cancer Agency, and Head of the Neuropathology Division at Vancouver Acute.
Dr. Mackenzie has broad expertise in neuropathology and the use of brain tissue banks in the care of patients with neurological disorders. His research program centers on neuropathology and the molecular genetics of neurodegenerative disease, particularly dementias. He is currently the Canadian representative to the International Society of Neuropathology and is an editorial board member for a number of neuropathology journals.

Dr. Ekaterina Rogaeva
Chair in Research on Dementia with Lewy Bodies at Tanz Centre for Research in Neurodegenerative Disease; Professor, Department of Neurology, Faculty of Medicine, University of Toronto, Department of Medicine
For the past 20 years, Dr. Rogaeva has contributed substantially to the development of effective genetic testing of different forms of dementia and movement disorders in her clinical practice, with a strong focus on Parkinson's Disease, Alzheimer's Disease, amyotrophic lateral sclerosis (ALS), and frontotemporal lobar degeneration.
Dr. Rogaeva played a central role in the discovery and characterization of the two presenilin genes responsible for the most aggressive form of early-onset Alzheimer’s Disease, as well as the SORL1 gene associated with common late-onset forms of Alzheimer’s Disease. Dr. Rogaeva's current focus is on genetic and epigenetic studies of C9orf72.
Dr. Rogaeva is the author of ~225 peer-reviewed publications and is listed among the top 10 Canadian neuroscientists, based on the highest impact papers published in 2013-2014.

Dr. Guy Rouleau
Director, Montreal Neurological Institute and Hospital and Department of Neurology and Neurosurgery, McGill University
Dr. Rouleau’s landmark achievements are his contributions to the identification of dozens of disease-causing genes and his discovery of new mutational mechanisms. Over the last 25 years, Dr. Rouleau and his team have focused on understanding the genetic basis for diseases and identifying genes causing neurological and psychiatric diseases including amyotrophic lateral sclerosis, stroke, Essential Tremor, familial aneurysms, cavernous angiomas, epilepsy, spinocerebellar ataxia, spastic paraplegia, autism, Tourette syndrome, restless legs syndrome, schizophrenia and bipolar disorder. Specifically for ALS, he has been investigating the genetic basis of this disease since 1986 and has contributed to the identification of many of the genes currently known to predispose to this disease.  He has published more than 700 articles in top peer-reviewed journals such as The Lancet, Cell, and Nature, as well as 50 review articles and book chapters. His work has been cited over 50,000 times.