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Markus Ries

30PUBLICATIONS

60CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeonatologyCross-sectional analysisNeurogeneticsAircraft performance and flight control systems

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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 <i>STXBP1</i>.

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

Frequent Collaborators

3 joint publications

Konstantin Mechler

3 joint publications

Matthias Zielonka

3 joint publications

Christian Patry

3 joint publications

Steffen Syrbe

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