Ania C. Muntau

7.3k total citations · 1 hit paper
116 papers, 4.3k citations indexed

About

Ania C. Muntau is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Ania C. Muntau has authored 116 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 67 papers in Clinical Biochemistry and 38 papers in Physiology. Recurrent topics in Ania C. Muntau's work include Metabolism and Genetic Disorders (67 papers), Mitochondrial Function and Pathology (39 papers) and Diet and metabolism studies (27 papers). Ania C. Muntau is often cited by papers focused on Metabolism and Genetic Disorders (67 papers), Mitochondrial Function and Pathology (39 papers) and Diet and metabolism studies (27 papers). Ania C. Muntau collaborates with scholars based in Germany, United States and France. Ania C. Muntau's co-authors include Adelbert A. Roscher, Søren W. Gersting, Wulf Röschinger, Alberto Burlina, François Feillet, Nenad Blau, Francjan J. van Spronsen, Anita MacDonald, Maria Giżewska and Christian P. Sommerhoff and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Ania C. Muntau

113 papers receiving 4.2k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The complete European guidelines on phenylketonuria: diagnosis and treatment

2017 531 citations Annemiek M. J. van Wegberg, Anita MacDonald et al. Orphanet Journal of Rare Diseases profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ania C. Muntau Germany	38	2.6k	2.6k	1.4k	560	533	116	4.3k
William J. Rhead United States	36	2.6k 1.0×	2.5k 1.0×	1.3k 0.9×	560 1.0×	657 1.2×	111	4.5k
Johannes Häberle Switzerland	36	2.9k 1.1×	2.5k 1.0×	657 0.5×	568 1.0×	974 1.8×	194	4.9k
R. J. Pollitt United Kingdom	32	2.1k 0.8×	2.0k 0.8×	748 0.5×	391 0.7×	574 1.1×	158	3.9k
Anibh M. Das Germany	31	1.1k 0.4×	1.6k 0.6×	1.0k 0.7×	321 0.6×	340 0.6×	143	3.5k
Mendel Tuchman United States	39	2.4k 0.9×	2.6k 1.0×	570 0.4×	399 0.7×	868 1.6×	151	4.9k
James Pitt Australia	31	1.1k 0.4×	1.7k 0.7×	317 0.2×	311 0.6×	304 0.6×	104	2.8k
Derek A. Applegarth Canada	26	1.1k 0.4×	1.2k 0.5×	543 0.4×	269 0.5×	306 0.6×	131	2.5k
Cécile Acquaviva France	29	807 0.3×	1.5k 0.6×	295 0.2×	245 0.4×	463 0.9×	110	2.7k
Timothy A. Garrow United States	32	763 0.3×	1.4k 0.6×	246 0.2×	2.1k 3.7×	437 0.8×	78	3.3k
Robert Guthrie United States	22	1.3k 0.5×	1.2k 0.5×	381 0.3×	268 0.5×	578 1.1×	59	3.0k

Countries citing papers authored by Ania C. Muntau

Since Specialization

Citations

This map shows the geographic impact of Ania C. Muntau'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 Ania C. Muntau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ania C. Muntau more than expected).

Fields of papers citing papers by Ania C. Muntau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ania C. Muntau. 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 Ania C. Muntau. The network helps show where Ania C. Muntau may publish in the future.

Co-authorship network of co-authors of Ania C. Muntau

This figure shows the co-authorship network connecting the top 25 collaborators of Ania C. Muntau. A scholar is included among the top collaborators of Ania C. Muntau 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 Ania C. Muntau. Ania C. Muntau is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Гундорова, П., et al.. (2025). Personalized Genotype‐Based Approach for Treatment of Phenylketonuria. Journal of Inherited Metabolic Disease. 48(5). e70067–e70067. 1 indexed citations

Feillet, François, Jean‐Baptiste Arnoux, Alberto Burlina, et al.. (2024). Long‐term safety of sapropterin in paediatric and adult individuals with phenylalanine hydroxylase deficiency: Final results of the Kuvan® Adult Maternal Paediatric European Registry multinational observational study. Journal of Inherited Metabolic Disease. 48(1). e12796–e12796. 1 indexed citations

Rocha, Júlio César, Á. Hermida Ameijeiras, Sarah Rose, et al.. (2024). Meta-analysis of bone mineral density in adults with phenylketonuria. Orphanet Journal of Rare Diseases. 19(1). 338–338. 1 indexed citations

Barroso, Madalena, Ingrid Goebel, Karl Kuchler, et al.. (2024). Use of the Novel Site-Directed Enzyme Enhancement Therapy (SEE-Tx) Drug Discovery Platform to Identify Pharmacological Chaperones for Glutaric Acidemia Type 1. Journal of Medicinal Chemistry. 67(19). 17087–17100. 1 indexed citations

Zazara, Dimitra E., Anastasios D. Giannou, Maike Pincus, et al.. (2024). Fetal lung growth predicts the risk for early-life respiratory infections and childhood asthma. World Journal of Pediatrics. 20(5). 481–495. 5 indexed citations

Barroso, Madalena, et al.. (2023). Glutaryl-CoA Dehydrogenase Misfolding in Glutaric Acidemia Type 1. International Journal of Molecular Sciences. 24(17). 13158–13158. 3 indexed citations

Armann, Jakob, Uta Behrends, Reinhard Berner, et al.. (2023). Comparing SARS-CoV-2 variants among children and adolescents in Germany: relative risk of COVID-19-related hospitalization, ICU admission and mortality. Infection. 51(5). 1357–1367. 9 indexed citations

Rocha, Júlio César, Kirsten Ahring, Deborah A. Bilder, et al.. (2023). Expert Consensus on the Long-Term Effectiveness of Medical Nutrition Therapy and Its Impact on the Outcomes of Adults with Phenylketonuria. Nutrients. 15(18). 3940–3940. 3 indexed citations

Paul, Kevin, Maya Merabishvili, Ronen Hazan, et al.. (2021). Bacteriophage Rescue Therapy of a Vancomycin-Resistant Enterococcus faecium Infection in a One-Year-Old Child following a Third Liver Transplantation. Viruses. 13(9). 1785–1785. 47 indexed citations

10.

Muntau, Ania C., Darius J. Adams, Amaya Bélanger-Quintana, et al.. (2019). International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria. Molecular Genetics and Metabolism. 127(1). 1–11. 43 indexed citations

11.

Eichinger, Anna, et al.. (2018). Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism. Human Molecular Genetics. 27(10). 1732–1742. 19 indexed citations

12.

Wegberg, Annemiek M. J. van, Anita MacDonald, Kirsten Ahring, et al.. (2017). The complete European guidelines on phenylketonuria: diagnosis and treatment. Orphanet Journal of Rare Diseases. 12(1). 162–162. 531 indexed citations breakdown →

13.

Schmiesing, Jessica, Michaela Schweizer, Henning Tidow, et al.. (2016). Disease-causing mutations affecting surface residues of mitochondrial glutaryl-CoA dehydrogenase impair stability, heteromeric complex formation and mitochondria architecture. Human Molecular Genetics. 26(3). ddw411–ddw411. 17 indexed citations

14.

Trefz, Friedrich K., Nenad Blau, Ania C. Muntau, et al.. (2015). Tetrahydrobiopterin (BH4) responsiveness in neonates with hyperphenylalaninemia: A semi-mechanistically-based, nonlinear mixed-effect modeling. Molecular Genetics and Metabolism. 114(4). 564–569. 7 indexed citations

15.

Roth, Susanne, Andrea Rottach, Amelie S. Lotz‐Havla, et al.. (2014). Rad50-CARD9 interactions link cytosolic DNA sensing to IL-1β production. Nature Immunology. 15(6). 538–545. 117 indexed citations

16.

Vizoso-Pinto, María Guadalupe, Venkata Raveendra Pothineni, Rudolf Haase, et al.. (2011). Varicella Zoster Virus ORF25 Gene Product: An Essential Hub Protein Linking Encapsidation Proteins and the Nuclear Egress Complex. Journal of Proteome Research. 10(12). 5374–5382. 20 indexed citations

17.

Santer, René, Johannes Rischewski, Sonja Schneppenheim, et al.. (2005). The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe. Human Mutation. 25(6). 594–594. 46 indexed citations

18.

Hoffmann, Georg F., Martin Lindner, Andreas Schulze, et al.. (2004). Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany. European Journal of Pediatrics. 163(2). 76–80. 44 indexed citations

19.

Albert, Michael H., Friedhelm R. Schuster, Christina Peters, et al.. (2003). T-cell-depleted peripheral blood stem cell transplantation for α-mannosidosis. Bone Marrow Transplantation. 32(4). 443–446. 12 indexed citations

20.

Henry, Hugues, Jean‐Daniel Tissot, M. Markert, et al.. (1997). Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: Apparent deficiencies in clusterin and serum amyloid P. Journal of Laboratory and Clinical Medicine. 129(4). 412–421. 31 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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