Ulrike Mütze

1.4k total citations
47 papers, 750 citations indexed

About

Ulrike Mütze is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ulrike Mütze has authored 47 papers receiving a total of 750 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Clinical Biochemistry, 20 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ulrike Mütze's work include Metabolism and Genetic Disorders (37 papers), Mitochondrial Function and Pathology (11 papers) and Diet and metabolism studies (11 papers). Ulrike Mütze is often cited by papers focused on Metabolism and Genetic Disorders (37 papers), Mitochondrial Function and Pathology (11 papers) and Diet and metabolism studies (11 papers). Ulrike Mütze collaborates with scholars based in Germany, United States and Singapore. Ulrike Mütze's co-authors include Skadi Beblo, Stefan Kölker, Uta Ceglarek, Wieland Kieß, Carmen Rohde, Joachim Thiery, Alena Gerlinde Thiele, Georg F. Hoffmann, Christoph Baerwald and Florian Gleich and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Cell Metabolism.

In The Last Decade

Ulrike Mütze

43 papers receiving 735 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ulrike Mütze Germany 18 491 321 252 175 172 47 750
François Feillet France 15 251 0.5× 248 0.8× 212 0.8× 98 0.6× 152 0.9× 45 685
Shawn E. McCandless United States 17 604 1.2× 495 1.5× 372 1.5× 299 1.7× 277 1.6× 34 1.2k
Susan Winter United States 19 525 1.1× 442 1.4× 139 0.6× 161 0.9× 156 0.9× 31 859
Serena Gasperini Italy 16 185 0.4× 223 0.7× 443 1.8× 110 0.6× 83 0.5× 64 880
M A Preece United Kingdom 14 420 0.9× 270 0.8× 160 0.6× 145 0.8× 121 0.7× 26 710
Dorothea Möslinger Austria 14 358 0.7× 274 0.9× 177 0.7× 98 0.6× 76 0.4× 31 572
Sema Kalkan Uçar Türkiye 14 113 0.2× 205 0.6× 203 0.8× 56 0.3× 88 0.5× 86 632
Carol L. Clow Canada 14 319 0.6× 218 0.7× 123 0.5× 194 1.1× 141 0.8× 23 731
Drago Bratkovic Australia 14 131 0.3× 200 0.6× 157 0.6× 40 0.2× 87 0.5× 48 419
Gaetano Sabetta Italy 10 402 0.8× 340 1.1× 125 0.5× 174 1.0× 62 0.4× 11 631

Countries citing papers authored by Ulrike Mütze

Since Specialization
Citations

This map shows the geographic impact of Ulrike Mütze's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ulrike Mütze with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ulrike Mütze more than expected).

Fields of papers citing papers by Ulrike Mütze

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ulrike Mütze. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ulrike Mütze. The network helps show where Ulrike Mütze may publish in the future.

Co-authorship network of co-authors of Ulrike Mütze

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrike Mütze. A scholar is included among the top collaborators of Ulrike Mütze based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ulrike Mütze. Ulrike Mütze is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Mütze, Ulrike, et al.. (2025). Newborn screening for neuro-metabolic disorders: Strategies, clinical benefits, and prerequisites for program expansion. European Journal of Paediatric Neurology. 56. 84–96.
2.
Mütze, Ulrike, Florian Gleich, Sarah C. Grünert, et al.. (2025). Long-Term Outcomes of Adolescents and Young Adults Identified by Metabolic Newborn Screening. PEDIATRICS. 155(4). 2 indexed citations
3.
Mütze, Ulrike, Florian Gleich, Dorothea Haas, et al.. (2024). Vitamin B12 Deficiency Newborn Screening. PEDIATRICS. 154(2). 2 indexed citations
4.
Boy, Nikolas, Sven F. Garbade, Saskia Haupt, et al.. (2024). Digital-Tier Strategy Improves Newborn Screening for Glutaric Aciduria Type 1. International Journal of Neonatal Screening. 10(4). 83–83.
5.
Okun, Jürgen G., Dirk Kohlmüller, Georgi Manukjan, et al.. (2024). Newborn screening for aromatic l-amino acid decarboxylase deficiency – Strategies, results, and implication for prevalence calculations. Molecular Genetics and Metabolism. 141(3). 108148–108148. 3 indexed citations
6.
Schnabel‐Besson, Elena, et al.. (2024). Impact of early diagnosis, disease variant, and quality of care on the neurocognitive outcome in maple syrup urine disease: A meta-analysis. Genetics in Medicine. 27(1). 101303–101303. 2 indexed citations
7.
Schnabel‐Besson, Elena, Sven F. Garbade, Florian Gleich, et al.. (2024). Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening. Journal of Inherited Metabolic Disease. 48(1). e12784–e12784. 4 indexed citations
8.
Mütze, Ulrike, Jürgen G. Okun, Georg F. Hoffmann, et al.. (2024). Personalized metabolic whole-body models for newborns and infants predict growth and biomarkers of inherited metabolic diseases. Cell Metabolism. 36(8). 1882–1897.e7. 10 indexed citations
9.
Mütze, Ulrike & Stefan Kölker. (2023). Evaluierung und Optimierung des Neugeborenenscreenings mittels strukturierter Langzeitbeobachtung – am Beispiel der angeborenen Stoffwechselerkrankungen. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 66(11). 1249–1258. 4 indexed citations
10.
Schnabel‐Besson, Elena, Stefan Kölker, Florian Gleich, et al.. (2023). Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria. Nutrients. 15(15). 3355–3355. 15 indexed citations
11.
Janda, Joachim, Friederike Hörster, Patrik Feyh, et al.. (2023). A high-throughput newborn screening approach for SCID, SMA, and SCD combining multiplex qPCR and tandem mass spectrometry. PLoS ONE. 18(3). e0283024–e0283024. 15 indexed citations
12.
Mütze, Ulrike, Uta Nennstiel, Claudia M. Haase, et al.. (2022). Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening. European Journal of Pediatrics. 181(6). 2415–2422. 10 indexed citations
13.
14.
Mütze, Ulrike, Sven F. Garbade, Gwendolyn Gramer, et al.. (2020). Long-term Outcomes of Individuals With Metabolic Diseases Identified Through Newborn Screening. PEDIATRICS. 146(5). 43 indexed citations
15.
Gramer, Gwendolyn, Junmin Fang‐Hoffmann, Patrik Feyh, et al.. (2019). Newborn Screening for Vitamin B12 Deficiency in Germany—Strategies, Results, and Public Health Implications. The Journal of Pediatrics. 216. 165–172.e4. 54 indexed citations
16.
Mütze, Ulrike, Alena Gerlinde Thiele, Christoph Baerwald, et al.. (2016). Ten years of specialized adult care for phenylketonuria – a single-centre experience. Orphanet Journal of Rare Diseases. 11(1). 27–27. 34 indexed citations
17.
Thiele, Alena Gerlinde, Carmen Rohde, Ulrike Mütze, et al.. (2015). The challenge of long-term tetrahydrobiopterin (BH4) therapy in phenylketonuria: Effects on metabolic control, nutritional habits and nutrient supply. SHILAP Revista de lepidopterología. 4. 62–67. 18 indexed citations
18.
Becker, Stefan, Dorothea Haas, Klaus Mohnike, et al.. (2015). LC–MS/MS-based quantification of cholesterol and related metabolites in dried blood for the screening of inborn errors of sterol metabolism. Analytical and Bioanalytical Chemistry. 407(17). 5227–5233. 26 indexed citations
19.
Kortüm, Fanny, Sigrid Fuchs, Beate Albrecht, et al.. (2011). Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies. Molecular Syndromology. 2(1). 27–34. 7 indexed citations
20.
Mütze, Ulrike, et al.. (2010). Transient Hyperammonemia Due to L -Asparaginase Therapy in Children with Acute Lymphoblastic Leukemia or Non-Hodgkin Lymphoma. Pediatric Hematology and Oncology. 28(1). 3–9. 33 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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