Grants and funders

We are grateful for the support of numerous funders who make the work of the Lochmüller Lab possible.

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Hanns holds the Canada Research Chair in Neuromuscular Genomics and Health and our lab’s work is supported by funding from the Canada Research Chairs program.

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CFI_CMYK

The Canada Foundation for Innovation (CFI) supports equipment in our lab as part of the CRC award.

Canada First Research fund
New frontiers in research fund
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The New Frontiers in Research Fund and European Commission supports the Accelerating drug repurposing for rare neurological, neurometabolic and neuromuscular diseases by exploiting SIMilarities in clinical and molecular PATHology (SIMPATHIC).

EJPRD

Funding from the European Joint Programme for Rare Diseases (EJP-RD) supports the PROMOT network: Performing a Rare Disease-Oriented Master Observational Trial to decipher complexity and optimize trial readiness (with Canadian funding contributed by the CIHR), and ProdGNE: Novel therapeutic approaches to target GNE Myopathy (with Canadian funding contributed by the CIHR). 

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We are supported by Muscular Dystrophy Canada with a Network Grant in Muscular Dystrophy for NMD4C, a neuromuscular network for Canada (jointly funded by CIHR).

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Stephen Holland is the recipient of a Scholarship in Translational Research (STaR) Award from the Dr. Eric Poulin Centre for Neuromuscular Disease (CNMD) in partnership with the University of Ottawa Brain and Mind Research Institute (uOBMRI). This award supports Stephen’s research over 2024-2025. 

Kaela O'Connor is the recipient of a Queen Elizabeth II scholarship award, which will allow her to continue her research for the 2023-2024 academic year. 

support

Read next...

Text reading: Solve-RD publication: Solve-RD flagship publication: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses. Photos of Dr Kiran Polavarapu, Dr Rachel Thompson, Dr Hanns Lochmüller.

Solve-RD flagship publication in Nature Medicine: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses

Patients and families with rare disorders often remain without a genetic diagnosis despite modern advances in diagnostic testing. Due to the rarity and global distribution of these diseases, data sharing...
New publication: Identifies Novel ATP2A2 Variant as Genetic Cause of Dominant Rhabdomyolysis . Author's photos on the right, diagram from paper underneath title.

New Lab Publication Identifies Novel ATP2A2 Variant as Genetic Cause of Dominant Rhabdomyolysis

Rhabdomyolysis is an acute failure of cellular homeostasis characterized by acute skeletal muscle damage triggered by trauma, infection, drugs, or strenuous exercise. Recurrent rhabdomyolysis is a complication in several neuromuscular...
New lab publication on riboflavin transporter deficiency model

New Publication: Development of a riboflavin-responsive model of riboflavin transporter deficiency in zebrafish

Riboflavin transporter deficiency (RTD) is a rare genetic disorder in children, characterised by progressive sensorimotor and cranial neuronopathy caused by mutations in riboflavin transporter protein-encoding genes. It often results in...
Congratulations CNMD Ottawa on 25 years of neuromuscular research. Photo of all former and current directors of the Centre.

uOttawa Eric Poulin Centre for Neuromuscular Disease Celebrates 25 Years of Neuromuscular Research

New co-directors Dr Mireille Khacho and Dr Hanns Lochmüller begin their tenure On November 25th the University of Ottawa Eric Poulin Centre for Neuromuscular Disease (CNMD) welcomed researchers, trainees and...
Clinical trial update - Canadian Patient First in the World to Receive Trial Drug in Argenx DOK7-CMS Study

Canadian Patient Dosed in Argenx DOK7-CMS Study

Our clinical research team at the NeuroMuscular centre of The Ottawa Hospital is excited to share that a Canadian patient affected by DOK-7 Congenital Myasthenic Syndrome (CMS) is the first...
New lab publication - Brain malformations and seizures by impaired chaperonin function of TRiC

New Publication: Brain malformations and seizures by impaired chaperonin function of TRiC

We are excited to share a new publication from our research team! The study “Brain malformations and seizures by impaired chaperonin function of TRiC” uncovers critical genetic mutations linked to...