Ulrike Mütze

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 25

Top Venues

Journal of inherited metabolic disease

Annals of clinical and translational neurology

PloS one

Metabolites

This page only lists publications with an associated author ORCID identifier.

Publications

Elena Schnabel-Besson, Ulrike Mütze, Nicola Dikow, Friederike Hörster, Marina A Morath, Karla Alex, Heiko Brennenstuhl, Sascha Settegast, Jürgen G Okun, Christian Patrick Schaaf, Eva C Winkler, Stefan Kölker
Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century? International journal of neonatal screening 10 (3) (2024)
Anna Theresa Reischl, Elena Schnabel, Florian Gleich, Katharina Mengler, Martin Lindner, Peter Burgard, Roland Posset, Svenja Lommer-Steinhoff, Sarah C Grünert, Eva Thimm, Peter Freisinger, Julia B Hennermann, Johannes Krämer, Gwendolyn Gramer, Dominic Lenz, Stine Christ, Friederike Hörster, Georg F Hoffmann, Sven F Garbade, Stefan Kölker, Ulrike Mütze
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias. Journal of inherited metabolic disease 47 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Anna Theresa Reischl, Elena Schnabel, Florian Gleich, Katharina Mengler, Martin Lindner, Peter Burgard, Roland Posset, Svenja Lommer-Steinhoff, Sarah C Grünert, Eva Thimm, Peter Freisinger, Julia B Hennermann, Johannes Krämer, Gwendolyn Gramer, Dominic Lenz, Stine Christ, Friederike Hörster, Georg F Hoffmann, Sven F Garbade, Stefan Kölker, Ulrike Mütze
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias. Journal of inherited metabolic disease (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Elena Schnabel-Besson, Sven F Garbade, Florian Gleich, Sarah C Grünert, Johannes Krämer, Eva Thimm, Julia B Hennermann, Peter Freisinger, Peter Burgard, Gwendolyn Gramer, Marina A Morath, A Tunç Tuncel, Svenja Keßler, Georg F Hoffmann, Stefan Kölker, Ulrike Mütze
Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening. Journal of inherited metabolic disease (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Anna Theresa Reischl, Elena Schnabel, Florian Gleich, Katharina Mengler, Martin Lindner, Peter Burgard, Roland Posset, Svenja Lommer-Steinhoff, Sarah C Grünert, Eva Thimm, Peter Freisinger, Julia B Hennermann, Johannes Krämer, Gwendolyn Gramer, Dominic Lenz, Stine Christ, Friederike Hörster, Georg F Hoffmann, Sven F Garbade, Stefan Kölker, Ulrike Mütze
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias. Journal of inherited metabolic disease 47 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology 11 (4) (2024)
Ulrike Mütze, Alina Ottenberger, Florian Gleich, Esther M Maier, Martin Lindner, Ralf A Husain, Katja Palm, Skadi Beblo, Peter Freisinger, René Santer, Eva Thimm, Stephan Vom Dahl, Natalie Weinhold, Karina Grohmann-Held, Claudia Haase, Julia B Hennermann, Alexandra Hörbe-Blindt, Clemens Kamrath, Iris Marquardt, Thorsten Marquardt, Robert Behne, Dorothea Haas, Ute Spiekerkoetter, Georg F Hoffmann, Sven F Garbade, Sarah Catharina Grünert, Stefan Kölker
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders. Annals of clinical and translational neurology (2024)
Elena Schnabel-Besson, Stefan Kölker, Florian Gleich, Patrik Feyh, Friederike Hörster, Dorothea Haas, Junmin Fang-Hoffmann, Marina Morath, Gwendolyn Gramer, Wulf Röschinger, Sven F Garbade, Georg F Hoffmann, Jürgen G Okun, Ulrike Mütze
Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria. Nutrients 15 (15) (2023)
Elaine Zaunseder, Ulrike Mütze, Sven F Garbade, Saskia Haupt, Patrik Feyh, Georg F Hoffmann, Vincent Heuveline, Stefan Kölker
Machine Learning Methods Improve Specificity in Newborn Screening for Isovaleric Aciduria. Metabolites 13 (2) (2023)
Rafael Tesorero, Joachim Janda, Friederike Hörster, Patrik Feyh, Ulrike Mütze, Jana Hauke, Kathrin Schwarz, Joachim B Kunz, Georg F Hoffmann, Jürgen G Okun
A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry. PloS one 18 (3) (2023)
Rafael Tesorero, Joachim Janda, Friederike Hörster, Patrik Feyh, Ulrike Mütze, Jana Hauke, Kathrin Schwarz, Joachim B Kunz, Georg F Hoffmann, Jürgen G Okun
A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry. PloS one 18 (3) (2023)
Ulrike Mütze, Lucy Henze, Julian Schröter, Florian Gleich, Martin Lindner, Sarah C Grünert, Ute Spiekerkoetter, René Santer, Eva Thimm, Regina Ensenauer, Johannes Weigel, Skadi Beblo, Maria Arélin, Julia B Hennermann, Iris Marquardt, Peter Freisinger, Johannes Krämer, Andrea Dieckmann, Natalie Weinhold, Katharina A Schiergens, Esther M Maier, Georg F Hoffmann, Sven F Garbade, Stefan Kölker
Isovaleric aciduria identified by newborn screening: Strategies to predict disease severity and stratify treatment. Journal of inherited metabolic disease (2023)
Elaine Zaunseder, Ulrike Mütze, Sven F Garbade, Saskia Haupt, Patrik Feyh, Georg F Hoffmann, Vincent Heuveline, Stefan Kölker
Machine Learning Methods Improve Specificity in Newborn Screening for Isovaleric Aciduria. Metabolites 13 (2) (2023)
Rafael Tesorero, Joachim Janda, Friederike Hörster, Patrik Feyh, Ulrike Mütze, Jana Hauke, Kathrin Schwarz, Joachim B Kunz, Georg F Hoffmann, Jürgen G Okun
A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry. PloS one 18 (3) (2023)
Elaine Zaunseder, Ulrike Mütze, Sven F Garbade, Saskia Haupt, Patrik Feyh, Georg F Hoffmann, Vincent Heuveline, Stefan Kölker
Machine Learning Methods Improve Specificity in Newborn Screening for Isovaleric Aciduria. Metabolites 13 (2) (2023)
Elaine Zaunseder, Ulrike Mütze, Sven F Garbade, Saskia Haupt, Patrik Feyh, Georg F Hoffmann, Vincent Heuveline, Stefan Kölker
Machine Learning Methods Improve Specificity in Newborn Screening for Isovaleric Aciduria. Metabolites 13 (2) (2023)
Rafael Tesorero, Joachim Janda, Friederike Hörster, Patrik Feyh, Ulrike Mütze, Jana Hauke, Kathrin Schwarz, Joachim B Kunz, Georg F Hoffmann, Jürgen G Okun
A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry. PloS one 18 (3) (2023)
Ulrike Mütze, Uta Nennstiel, Birgit Odenwald, Claudia Haase, Uta Ceglarek, Nils Janzen, Sven F Garbade, Georg F Hoffmann, Stefan Kölker, Dorothea Haas
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening. European journal of pediatrics 181 (6) (2022)
Ulrike Mütze, Florian Gleich, Sven F Garbade, Céline Plisson, Luis Aldámiz-Echevarría, Francisco Arrieta, Diana Ballhausen, Matthias Zielonka, Danijela Petković Ramadža, Matthias R Baumgartner, Aline Cano, María Concepción García Jiménez, Carlo Dionisi-Vici, Pavel Ješina, Henk J Blom, Maria Luz Couce, Silvia Meavilla Olivas, Karine Mention, Fanny Mochel, Andrew A M Morris, Helen Mundy, Redonnet-Vernhet Isabelle, Saikat Santra, Manuel Schiff, Aude Servais, Isidro Vitoria, Martina Huemer, Viktor Kožich, Stefan Kölker
Postauthorization safety study of betaine anhydrous. Journal of inherited metabolic disease 45 (4) (2022)
Ulrike Mütze, Sven F Garbade, Florian Gleich, Martin Lindner, Peter Freisinger, Julia B Hennermann, Eva Thimm, Gwendolyn Gramer, Roland Posset, Johannes Krämer, Sarah C Grünert, Georg F Hoffmann, Stefan Kölker
Long-term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening. Journal of inherited metabolic disease (2022)
Ulrike Mütze, Katharina Mengler, Nikolas Boy, Florian Gleich, Thomas Opladen, Sven F Garbade, Stefan Kölker
How longitudinal observational studies can guide screening strategy for rare diseases. Journal of inherited metabolic disease 45 (5) (2022)
Ulrike Mütze, Lucy Henze, Florian Gleich, Martin Lindner, Sarah C Grünert, Ute Spiekerkoetter, René Santer, Holger Blessing, Eva Thimm, Regina Ensenauer, Johannes Weigel, Skadi Beblo, Maria Arélin, Julia B Hennermann, Thorsten Marquardt, Iris Marquardt, Peter Freisinger, Johannes Krämer, Andrea Dieckmann, Natalie Weinhold, Mareike Keller, Magdalena Walter, Katharina A Schiergens, Esther M Maier, Georg F Hoffmann, Sven F Garbade, Stefan Kölker
Newborn screening and disease variants predict neurological outcome in isovaleric aciduria. Journal of inherited metabolic disease 44 (4) (2021)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ulrike Mütze