Meet the lab’s two new members

Our lab is growing! We are excited to introduce two new members who have joined the Lochmüller lab this winter.

Daniel O’Neil

Daniel holds a BSc in Biochemistry from the University of Ottawa. During his undergraduate studies, he worked with Dr. Alexandre Blais’s laboratory where he studied the role of the Six1 transcription factor in adult satellite cell proliferation. Subsequently, he completed his MSc in Neuroscience at the University of Ottawa in Dr. Ruth Slack’s laboratory. His thesis examined the role of the activator E2f transcription factors, crucial regulators of cell cycle progression, in adult neural stem cell quiescence and activation.

Daniel looks forward to applying his accumulated technical knowledge to support ongoing research projects in Dr. Lochmüller’s lab.

 

Catherine Choueiri

Catherine recently graduated with an HBSc degree in Biology from Western University in October 2020. After completing her final year, she worked as a research assistant and laboratory manager in Dr. Kathleen Hill’s lab. In her role, she contributed to projects relevant to environmental mutagenesis, mouse SNP genotyping, and the use of genomic signatures for disease screening. Under Kathleen Hill’s supervision, Catherine also completed a teaching fellowship at Western, during which she helped to redesign the Principles of Human Genetics course for online delivery.

In January 2021, Catherine began her Master’s program in Cellular and Molecular Medicine with a specialization in Human and Molecular Genetics. She is working under the supervision of Dr. Lochmüller to create a zebrafish model for riboflavin transporter deficiency to be used in therapeutic screening.

 

 

Neuromuscular junction and animal models

Read next...

New publications alert

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...
New members post - July 2026

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...
Kelly and Ofosu papers (4)

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...
PDF position with Kiran-2

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...
Adobe Express - file

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...
haleyozgefinal

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)...