Ulrike Mütze

18PUBLICATIONS
42CO-AUTHORS
Nutritional epidemiologyNeurogeneticsNeonatologyEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (18)

|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

|Sep 23, 2024
Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century?

Elena Schnabel-Besson, Ulrike Mütze, Nicola Dikow

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Frequent Collaborators

6 joint publications

Sven F Garbade

5 joint publications

Stefan Kölker

4 joint publications

Elena Schnabel-Besson

2 joint publications

Martina Huemer