Markus Ries
30PUBLICATIONS
60CO-AUTHORS
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Publications (30)
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|Jul 12, 2025
Unraveling the Genomic Architecture of Supernumerary (Iso-)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature-Based Study.Sebastian Burkart, Markus Ries, Verena Romero
|Jun 18, 2025
Phenotypical and Genotypical Expansion of Autosomal-Dominant KDM1A -Related Neurodevelopmental Disorder Spectrum: A Case Report.Sebastian Burkart, Melanie Spanjaard, Lilian Kaufmann
|Dec 05, 2024
Systematic quantitative modeling of the natural history of Aicardi syndrome: A cross sectional study of 245 published cases.Oliver Y Urban, Jan H Driedger, Sven F Garbade
|Jul 05, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1.Kim M Thalwitzer, Jan H Driedger, Julie Xian
|Sep 15, 2022
Orphan drug development in alpha-1 antitypsin deficiency.Franziska C Trudzinski, Maria Ada Presotto, Emanuel Buck
|Apr 23, 2022
Missing trial results: analysis of the current publication rate of studies in pediatric dialysis from 2003 to 2020.Christian Patry, Alexander Fichtner, Britta Höcker
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Frequent Collaborators
3 joint publications
Konstantin Mechler
3 joint publications
Matthias Zielonka
3 joint publications
Christian Patry
3 joint publications
Steffen Syrbe
2 joint publications
Sven F Garbade
2 joint publications
Burkhard Tönshoff
2 joint publications
Christian P Schaaf
2 joint publications
Sebastian Burkart
2 joint publications
Britta Höcker
2 joint publications
Afshin Saffari
