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. 

Caroline Part is the recipient of a Scholarship in Translational Research (STaR) Award from 2025-2026.

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...

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New Publications Alert!

Our group has recently published two new papers with the first providing insights on the impact of GFPT1 loss in cellular models and the second highlighting importance of reanalysis in...
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Meet The Lochmüller group’s Newest Members!

Our group is growing! We are excited to introduce two new members who have recently joined the Lochmüller group. Claudia Wyld Clinical Research Assistant Claudia joined Dr. Lochmüller's clinical research...
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New Publication: Gene-specific response to muscle specific kinase agonist antibody in the treatment of congenital myasthenic syndromes

Congenital myasthenic syndromes (CMS) are a group of rare inherited neuromuscular disorders. Although many forms of CMS appear similar clinically, the disease can be caused by mutations in more than...
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We are recruiting: Postdoctoral Fellow in Rare Disease Bioinformatics

The Polavarapu research group is recruiting a Postdoctoral Fellow in Rare Disease Bioinformatics. Working within a multidisciplinary and collaborative research environment, the postholder will provide computational and bioinformatic expertise to...
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Oral Platform Presentation (Undergraduate) Category Winner!

We are thrilled to share that Katerina was the winner of Undergraduate Category for her presentation titled “Novel gene discovery in congenital myasthenic syndromes using optogenetic zebrafish models” at the 2026 annual...
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Two Research Lab Members Receive CIHR Funding Awards!

We are excited to share that two of our research team members have received competitive funding awards from the Canadian Institutes of Health Research (CIHR) to support their projects. Academic...