Understanding the genetic causes of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting motor neurons and leading to paralysis and premature death. Although more than 40 ALS-associated genes have been identified, a large proportion of cases—particularly sporadic ALS—remain genetically unexplained. Increasing evidence shows that genetic defects, including rare variants, oligogenic inheritance, and non-coding or structural genomic alterations, play a central role even in sporadic disease.
This PhD project aims to uncover novel genetic contributors to ALS using whole genome sequencing (WGS). You will work with a unique biobank of 250 well-characterized ALS patients established in the Slachtova Lab and integrate genomic data with detailed clinical information. Your work will help reveal disease mechanisms and contribute to future precision medicine approaches for patients with ALS.
Head of the Department
Lenka Šlachtová, PhD
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Tagged as: Life Sciences
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ApplyPlease send your application to lenka.slachtova@iem.cas.cz
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