Magdalena Krygier

13PUBLICATIONS
51CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesToxicology (incl. clinical toxicology)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (13)

|Jul 09, 2026
Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omics.

|May 27, 2026
Prominent Movement Disorders in RNU2-2-Related Spliceosomopathy.

|Jan 19, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen

|Jun 16, 2025
The Attenuated Phenotype of CNTNAP1-Related Neuropathy Mimics Spastic-Dystonic Cerebral Palsy.

Magdalena Krygier, Michael Zech, Magdalena Chylińska

|Apr 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.

Philip Harrer, Magdalena Krygier, Martin Krenn

|Feb 18, 2025
Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study.

Matthias De Wachter, Charissa Millevert, Joost Nicolai

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Frequent Collaborators

8 joint publications

Maria Mazurkiewicz-Bełdzińska

6 joint publications

Marta Zawadzka

5 joint publications

Michael Zech

2 joint publications

Karol Chojnowski