E. Mönch

1.0k total citations
37 papers, 686 citations indexed

About

E. Mönch is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, E. Mönch has authored 37 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Clinical Biochemistry, 13 papers in Physiology and 11 papers in Molecular Biology. Recurrent topics in E. Mönch's work include Metabolism and Genetic Disorders (27 papers), Diet and metabolism studies (10 papers) and Folate and B Vitamins Research (7 papers). E. Mönch is often cited by papers focused on Metabolism and Genetic Disorders (27 papers), Diet and metabolism studies (10 papers) and Folate and B Vitamins Research (7 papers). E. Mönch collaborates with scholars based in Germany, Switzerland and Austria. E. Mönch's co-authors include Julia B. Hennermann, Barbara Vetter, D. Rating, Cornelis Jakobs, F. Hanefeld, H. Siemes, Christoph Bührer, Nenad Blau, Kurt Ullrich and M. Herrmann and has published in prestigious journals such as Journal of Nutrition, European Journal of Cancer and Journal Of Clinical Periodontology.

In The Last Decade

E. Mönch

33 papers receiving 655 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Mönch Germany 13 519 347 287 106 97 37 686
Stephen Cederbaum United States 17 682 1.3× 508 1.5× 270 0.9× 119 1.1× 164 1.7× 24 919
H. D. Bakker Netherlands 14 354 0.7× 267 0.8× 175 0.6× 122 1.2× 82 0.8× 28 556
Kathryn Moseley United States 17 672 1.3× 416 1.2× 410 1.4× 103 1.0× 137 1.4× 26 833
K. Bartholomé Germany 16 636 1.2× 441 1.3× 181 0.6× 162 1.5× 108 1.1× 27 931
Ricardo Flores Pires Brazil 15 251 0.5× 286 0.8× 338 1.2× 63 0.6× 43 0.4× 36 624
M. Blaskovics United States 12 340 0.7× 248 0.7× 146 0.5× 73 0.7× 98 1.0× 21 534
L. Kierat Switzerland 13 266 0.5× 271 0.8× 99 0.3× 63 0.6× 90 0.9× 26 496
Sara Boenzi Italy 20 524 1.0× 539 1.6× 263 0.9× 101 1.0× 136 1.4× 43 1.0k
C. R. Roe United States 9 524 1.0× 409 1.2× 164 0.6× 51 0.5× 182 1.9× 10 691
C. Jakobs Netherlands 11 230 0.4× 218 0.6× 81 0.3× 100 0.9× 76 0.8× 13 477

Countries citing papers authored by E. Mönch

Since Specialization
Citations

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

Fields of papers citing papers by E. Mönch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Mönch. 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 E. Mönch. The network helps show where E. Mönch may publish in the future.

Co-authorship network of co-authors of E. Mönch

This figure shows the co-authorship network connecting the top 25 collaborators of E. Mönch. A scholar is included among the top collaborators of E. Mönch 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 E. Mönch. E. Mönch 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.
Das, Anibh M., Diana Ballhausen, Dorothea Haas, et al.. (2024). Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German‐speaking countries. Journal of Inherited Metabolic Disease. 48(1). e12824–e12824. 3 indexed citations
2.
Löber, Ulrike, Corinna Bang, André Franke, et al.. (2024). Oral microbiota of patients with phenylketonuria: A nation‐based cross‐sectional study. Journal Of Clinical Periodontology. 51(8). 1081–1092. 1 indexed citations
3.
Pandis, Nikolaos, et al.. (2023). Dietary and metabolic effects on the oral status of patients with phenylketonuria: a nation-based cross-sectional study. Clinical Oral Investigations. 27(5). 1981–1991. 2 indexed citations
4.
5.
Mühlendahl, K. E. von, W. Lehnert, & E. Mönch. (2008). Medium-Chain-Acyl-CoA-Dehydrogenase(MCAD)-Defekt: Akute zerebrale Episoden und nicht-ketotische Hypoglykämien bei Kindern. DMW - Deutsche Medizinische Wochenschrift. 115(33). 1235–1238. 1 indexed citations
6.
Hennermann, Julia B., Christoph Bührer, Nenad Blau, Barbara Vetter, & E. Mönch. (2005). Long-term treatment with tetrahydrobiopterin increases phenylalanine tolerance in children with severe phenotype of phenylketonuria. Molecular Genetics and Metabolism. 86. 86–90. 91 indexed citations
7.
Hennermann, Julia B., A Loui, Astrid Weber, & E. Mönch. (2004). Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria. Journal of Perinatal Medicine. 32(4). 383–5. 6 indexed citations
8.
Hennermann, Julia B., Barbara Vetter, Luitgard M. Neumann, et al.. (2002). An Unexpectedly High Frequency of Hypergalactosemia in an Immigrant Bosnian Population Revealed by Newborn Screening. Pediatric Research. 51(5). 598–601. 11 indexed citations
9.
Mönch, E., et al.. (2001). Biochemical characterization of bioreactors for hybrid liver support: serum-free liver cell coculture of nonparenchymal and parenchymal cells. Transplantation Proceedings. 33(1-2). 1930–1931. 8 indexed citations
10.
Hundsdoerfer, Patrick, B. Stöver, C. Bassir, et al.. (2000). Design of a prospective neonatal cohort study of homozygous and double heterozygous Factor V Leiden and Factor II G20210A. Klinische Pädiatrie. 212(4). 159–162. 2 indexed citations
11.
Siedler, Anette, et al.. (2000). Spread of HIV infection in the general population in Germany. AIDS. 14(18). 2949–2951.
12.
Burgard, Peter, H. J. Bremer, P Bührdel, et al.. (1999). Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997. European Journal of Pediatrics. 158(1). 46–54. 109 indexed citations
13.
Mönch, E., et al.. (1996). Utilisation of amino acid mixtures in adolescents with phenylketonuria. European Journal of Pediatrics. 155(S1). S115–S120. 41 indexed citations
14.
Herrmann, M., H. Brösicke, Maren Keller, E. Mönch, & H Helge. (1994). Dependence of the utilization of a phenylalanine-free amino acid mixture on different amounts of single dose ingested. A case report. European Journal of Pediatrics. 153(7). 501–503. 30 indexed citations
15.
Wabitsch, Martin, Frank Pohlandt, D. Leupold, et al.. (1993). Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis. European Journal of Pediatrics. 152(4). 327–330. 1 indexed citations
16.
Mönch, E., et al.. (1991). Plasma Taurine Levels in Healthy Cats and Cats with Cardiac Disorders. Journal of Nutrition. 121(11 Suppl). S171–S172. 1 indexed citations
17.
Mönch, E., et al.. (1990). Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age—part 1. European Journal of Pediatrics. 149(S1). 17–24. 8 indexed citations
18.
Stuhrmann, Manfred, et al.. (1989). Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families. Clinical Genetics. 36(2). 117–121. 12 indexed citations
19.
Özalp, İ, et al.. (1989). Inherited metabolic disorders in Turkey. Journal of Inherited Metabolic Disease. 13(5). 732–738. 47 indexed citations
20.
Mönch, E., et al.. (1978). Glutaraldehyde mediated echinocyte/discocyte transformation is Ca2+ dependent.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 105(5). 672–8. 1 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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