Ulrike Mütze

19PUBLICATIONS
44CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Nutritional epidemiologyNeurogeneticsNeonatologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (19)

|Oct 08, 2026
Parental reactions to and preferences for genomic newborn screening in Germany: findings from a scenario-based survey experiment.

|Jun 08, 2026
Prevalence, Disease Onset and Clinical Outcome in Arginase 1 Deficiency: Cross-Border Surveillance in Germany, Austria, and Switzerland.

|Mar 01, 2026
A multi-dimensional framework for establishing and managing a genomic newborn screening program.

Elena Schnabel-Besson, Nicola Dikow, Karla Alex

|Feb 17, 2026
Direct Prediction of VLCADD Severity Using Newborn Screening Analyte Data.

Marit Schwantje, Rose E Maase, Eugenie Dekkers

|Oct 24, 2025
Trial Readiness: Understanding the Natural History of Rare Diseases.

Thomas Opladen, Ulrike Mütze, Florian Gleich

|Dec 27, 2024
Digital-Tier Strategy Improves Newborn Screening for Glutaric Aciduria Type 1.

Elaine Zaunseder, Julian Teinert, Nikolas Boy

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Frequent Collaborators

6 joint publications

Sven F Garbade

5 joint publications

Stefan Kölker

4 joint publications

Elena Schnabel-Besson

3 joint publications

Heiko Brennenstuhl