Professor Claude Bh茅rer and her team are studying the genomes of founder populations and their genetic diseases
In a recent article published by the 平特五不中 Reporter, we learn about Claude Bh茅rer's journey from biological anthropology to population genetics. Following her nephew's sudden death from lactic acidosis, Bh茅rer delved into genetic research, uncovering prevalent hereditary diseases. Her team's systematic analysis has revealed over 100 genetic variants unique to Quebec, prompting investigations into potential therapies. Bh茅rer's research extends to digital health platforms for real-time data collection and Equity, Diversity, and Inclusion (EDI) initiatives in genomics. With a focus on improving understanding and treatment of rare diseases, Bh茅rer's work holds promise for future therapies and enhanced genomic diversity awareness.
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