Esther van Dam

915 total citations
21 papers, 513 citations indexed

About

Esther van Dam is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Esther van Dam has authored 21 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Clinical Biochemistry, 16 papers in Physiology and 7 papers in Molecular Biology. Recurrent topics in Esther van Dam's work include Metabolism and Genetic Disorders (17 papers), Diet and metabolism studies (15 papers) and Mitochondrial Function and Pathology (5 papers). Esther van Dam is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Diet and metabolism studies (15 papers) and Mitochondrial Function and Pathology (5 papers). Esther van Dam collaborates with scholars based in Netherlands, United Kingdom and Germany. Esther van Dam's co-authors include Anita MacDonald, Júlio César Rocha, Amaya Bélanger-Quintana, Francjan J. van Spronsen, Kirsten Ahring, Hülya Gökmen-Özel, M. Rebecca Heiner‐Fokkema, Anna Maria Lammardo, Katharina Dokoupil and Manuela Almeida and has published in prestigious journals such as Cell Metabolism, Nutrients and Neurobiology of Disease.

In The Last Decade

Esther van Dam

21 papers receiving 503 citations

Peers

Esther van Dam
Viruna Neergheen United Kingdom
Marieke Hoeksma Netherlands
A. Hodson United States
Mandar Joshi United States
W. Ruitenbeek Netherlands
Viruna Neergheen United Kingdom
Esther van Dam
Citations per year, relative to Esther van Dam Esther van Dam (= 1×) peers Viruna Neergheen

Countries citing papers authored by Esther van Dam

Since Specialization
Citations

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

Fields of papers citing papers by Esther van Dam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Esther van Dam. 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 Esther van Dam. The network helps show where Esther van Dam may publish in the future.

Co-authorship network of co-authors of Esther van Dam

This figure shows the co-authorship network connecting the top 25 collaborators of Esther van Dam. A scholar is included among the top collaborators of Esther van Dam 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 Esther van Dam. Esther van Dam 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.
Pinto, Alex, Sharon Evans, Esther van Dam, et al.. (2023). Phenylalanine Tolerance over Time in Phenylketonuria: A Systematic Review and Meta-Analysis. Nutrients. 15(16). 3506–3506. 8 indexed citations
2.
Rossi, Alessandro, Foekje de Boer, Esther van Dam, et al.. (2021). A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single‐center study and the generation of www.emergencyprotocol.net. Journal of Inherited Metabolic Disease. 44(5). 1124–1135. 13 indexed citations
3.
Wegberg, Annemiek M. J. van, et al.. (2021). Effect of BH4 on blood phenylalanine and tyrosine variations in patients with phenylketonuria. Molecular Genetics and Metabolism. 133(1). 49–55. 8 indexed citations
4.
Rocha, Júlio César, Amaya Bélanger-Quintana, Laurie Bernstein, et al.. (2021). Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase. Molecular Genetics and Metabolism Reports. 28. 100771–100771. 16 indexed citations
5.
Dam, Esther van, et al.. (2020). Dried blood spot versus venous blood sampling for phenylalanine and tyrosine. Orphanet Journal of Rare Diseases. 15(1). 82–82. 22 indexed citations
6.
Dam, Esther van, Joel James, Lena Best, et al.. (2020). Sugar-Induced Obesity and Insulin Resistance Are Uncoupled from Shortened Survival in Drosophila. Cell Metabolism. 31(4). 710–725.e7. 81 indexed citations
7.
Blaauw, Pim de, et al.. (2020). Aspartame and Phe-Containing Degradation Products in Soft Drinks across Europe. Nutrients. 12(6). 1887–1887. 13 indexed citations
8.
Wegberg, Annemiek M. J. van, Esther van Dam, Maaike C. de Vries, et al.. (2019). Does the 48-hour BH4 loading test miss responsive PKU patients?. Molecular Genetics and Metabolism. 129(3). 186–192. 7 indexed citations
9.
Rocha, Júlio César, Esther van Dam, Kirsten Ahring, et al.. (2019). A series of three case reports in patients with phenylketonuria performing regular exercise: first steps in dietary adjustment. Journal of Pediatric Endocrinology and Metabolism. 32(6). 635–641. 10 indexed citations
10.
Wegberg, Annemiek M. J. van, et al.. (2019). The first European guidelines on phenylketonuria: Usefulness and implications for BH4 responsiveness testing. Journal of Inherited Metabolic Disease. 43(2). 244–250. 12 indexed citations
11.
Wegberg, Annemiek M. J. van, et al.. (2018). Anthropomorphic measurements and nutritional biomarkers after 5 years of BH 4 treatment in phenylketonuria patients. Molecular Genetics and Metabolism. 124(4). 238–242. 6 indexed citations
12.
Dam, Esther van, Anne Daly, Margreet van Rijn, et al.. (2017). What Is the Best Blood Sampling Time for Metabolic Control of Phenylalanine and Tyrosine Concentrations in Tyrosinemia Type 1 Patients?. JIMD Reports. 36. 49–57. 11 indexed citations
13.
Daly, Anne, Esther van Dam, Anita MacDonald, et al.. (2017). Daily variation of NTBC and its relation to succinylacetone in tyrosinemia type 1 patients comparing a single dose to two doses a day. Journal of Inherited Metabolic Disease. 41(2). 181–186. 12 indexed citations
14.
Almeida, Manuela, Esther van Dam, Kirsten Ahring, et al.. (2016). Protein substitutes for phenylketonuria in Europe: access and nutritional composition. European Journal of Clinical Nutrition. 70(7). 785–789. 35 indexed citations
15.
Almeida, Manuela, Esther van Dam, Kirsten Ahring, et al.. (2015). Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile. Orphanet Journal of Rare Diseases. 10(1). 52 indexed citations
16.
Rocha, Júlio César, Margreet van Rijn, Esther van Dam, et al.. (2015). Weight Management in Phenylketonuria: What Should Be Monitored?. Annals of Nutrition and Metabolism. 68(1). 60–65. 31 indexed citations
17.
Vaikath, Nishant N., Nour K. Majbour, Katerina E. Paleologou, et al.. (2015). Generation and characterization of novel conformation-specific monoclonal antibodies for α-synuclein pathology. Neurobiology of Disease. 79. 81–99. 100 indexed citations
18.
Vliet, Danique van, Esther van Dam, Margreet van Rijn, et al.. (2014). Infants with Tyrosinemia Type 1: Should phenylalanine be supplemented?. JIMD Reports. 18. 117–124. 27 indexed citations
19.
Putter, Sander de, Lambert Speelman, Frans Gerritsen, et al.. (2008). Towards patient-specific risk assessment of abdominal aortic aneurysm. Medical & Biological Engineering & Computing. 46(11). 1085–1095. 24 indexed citations
20.
Linssen, J.P.H., et al.. (1995). Flavour of brewed coffee.. Socio-Environmental Systems Modeling. 489–501. 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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