Publications by authors named "G Rudolf"

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Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis.
Maria Victoria Hinckelmann, Aline Dubos, Victorine Artot, Gabrielle Rudolf, Thu Lan Nguyen

Mol Psychiatry· November 2025

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Molecular and Phenotypic Characterization of the -Related Disorder.
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, Tiziana Pisano, Laloe Monteiro, Gabrielle Rudolf

Neurology· January 2024

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Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy.
Anja Kovanda, Luca Lovrečić, Gorazd Rudolf, Ivana Babic Bozovic, Helena Jaklič

Genes (Basel)· November 2023

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Author Correction: A prospective observational study of post-COVID-19 chronic fatigue syndrome following the first pandemic wave in Germany and biomarkers associated with symptom severity.
Claudia Kedor, Helma Freitag, Lil Meyer-Arndt, Kirsten Wittke, Leif G Hanitsch, Gordon Rudolf

Nat Commun· October 2022

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A prospective observational study of post-COVID-19 chronic fatigue syndrome following the first pandemic wave in Germany and biomarkers associated with symptom severity.
Claudia Kedor, Helma Freitag, Lil Meyer-Arndt, Kirsten Wittke, Leif G Hanitsch, Gordon Rudolf

Nat Commun· August 2022

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