F. J. van Spronsen

722 total citations
27 papers, 504 citations indexed

About

F. J. van Spronsen is a scholar working on Clinical Biochemistry, Physiology and Biochemistry. According to data from OpenAlex, F. J. van Spronsen has authored 27 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 10 papers in Physiology and 8 papers in Biochemistry. Recurrent topics in F. J. van Spronsen's work include Metabolism and Genetic Disorders (20 papers), Amino Acid Enzymes and Metabolism (8 papers) and Diet and metabolism studies (7 papers). F. J. van Spronsen is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Amino Acid Enzymes and Metabolism (8 papers) and Diet and metabolism studies (7 papers). F. J. van Spronsen collaborates with scholars based in Netherlands, United States and Poland. F. J. van Spronsen's co-authors include P.H. Verkerk, G. P. A. Smit, Annet M. Bosch, M. van Rijn, H. S. A. Heymans, Frits A. Wijburg, J. Huisman, Maria Giżewska, J.J. Van der Meere and François Feillet and has published in prestigious journals such as The Journal of Pediatrics, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Archives of Disease in Childhood.

In The Last Decade

F. J. van Spronsen

23 papers receiving 482 citations

Peers

Countries citing papers authored by F. J. van Spronsen

Since Specialization

Citations

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

Fields of papers citing papers by F. J. van Spronsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. J. van Spronsen. 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 F. J. van Spronsen. The network helps show where F. J. van Spronsen may publish in the future.

Co-authorship network of co-authors of F. J. van Spronsen

This figure shows the co-authorship network connecting the top 25 collaborators of F. J. van Spronsen. A scholar is included among the top collaborators of F. J. van Spronsen 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 F. J. van Spronsen. F. J. van Spronsen 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

#	Work	Indexed citations
1	Inter-individuality in the transport and effect of phenylalanine in the brain: A double case report of two ‘unusual’ phenylketonuria patients 2025 ·Molecular Genetics and Metabolism ·(unknown), Stephan C. J. Huijbregts, (unknown), M. Rebecca Heiner‐Fokkema, Alexander J. Rennings, Paul Baron, Paul E. Sijens, F. J. van Spronsen	1
2	Maleic acid is a biomarker for maleylacetoacetate isomerase deficiency; implications for newborn screening of tyrosinemia type 1 2023 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), Marelle J. Bouva, (unknown), (unknown), (unknown), Monique G. de Sain-van der Velden, Klaas Koop, Alessandro Rossi, James A. Thomas, (unknown), Mensiena B. G. Kiewiet, Paula J. Waters, Denis Cyr, (unknown), Anita Boelen, F. J. van Spronsen, M. Rebecca Heiner‐Fokkema	7
3	High protein prescription in methylmalonic and propionic acidemia patients and its negative association with long-term outcome 2020 ·Clinical Nutrition ·Femke Molema, Hanneke A. Haijes, Mirian C. H. Janssen, Annet M. Bosch, F. J. van Spronsen, Mark Mulder, Nanda M. Verhoeven‐Duif, Judith Jans, Ans T. van der Ploeg, Margreet A. E. M. Wagenmakers, M. Estela Rubio‐Gozalbo, Martijn C.G.J. Brouwers, Maaike C. de Vries, Sabine A. Fuchs, Janneke G. Langendonk, Dimitris Rizopoulos, Peter M. van Hasselt, Monique Williams	9
4	Ataxia, dystonia and myoclonus in adult patients with Niemann-Pick type C 2016 ·Orphanet Journal of Rare Diseases ·(unknown), Anouk Kuiper, (unknown), Jan Willem J. Elting, J.J. de Vries, Marc Engelen, Johannes H.T.M. Koelman, F. J. van Spronsen, Jacoba M. Spikman, Tom J. de Koning, Marina A.J. Tijssen	24
5	Adherence Issues in Inherited Metabolic Disorders Treated by Low Natural Protein Diets 2012 ·Annals of Nutrition and Metabolism ·Anita MacDonald, M. van Rijn, François Feillet, Allan M. Lund, Laurie Bernstein, Annet M. Bosch, Maria Giżewska, F. J. van Spronsen	74
6	PGM1-DEFICIENCY WITH ABNORMAL PROTEIN GLYCOSYLATION; EASY DIAGNOSIS AND DIETARY INTERVENTION 2012 ·Data Archiving and Networked Services (DANS) ·Monique van Scherpenzeel, Sharita Timal, Kimiyo Raymond, Michael S. Adamowicz, (unknown), F. J. van Spronsen, Joris A. Veltman, Ron A. Wevers, Éva Morava, Dirk J. Lefeber	2
7	The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: Evaluation of protocol and influence of baseline phenylalanine concentration 2011 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Floris C. Hofstede, (unknown), Annet M. Bosch, (unknown), Carla E. M. Hollak, C. Jonkers, M. Estela Rubio‐Gozalbo, (unknown), Maaike C. de Vries, (unknown), Mirian C. H. Janssen, (unknown), C Boelen, (unknown), M. Rebecca Heiner‐Fokkema, Marjon van Rijn, F. J. van Spronsen	13
8	Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Miski Mohamed, Maïlys Guillard, (unknown), Sebahattin Çirak, (unknown), Helen Michelakakis, Eckhard Korsch, Michael S. Adamowicz, Berthold Koletzko, F. J. van Spronsen, Klary E. Niezen‐Koning, Gert Matthijs, Thatjana Gardeitchik, (unknown), Byung Chan Lim, Renate Zeevaert, Ron A. Wevers, Dirk J. Lefeber, Éva Morava	19
9	Biochemical Monitoring and Management During Pregnancy in Patients with Isovaleric Acidaemia is Helpful to Prevent Metabolic Decompensation 2011 ·JIMD Reports ·Daphna D.J. Habets, Nicolaas C. Schaper, (unknown), F. J. van Spronsen, M. van Rijn, Jörgen Bierau, Jaap Bakker	5
10	Final commentary: A new chapter 2009 ·Molecular Genetics and Metabolism ·Desirée A. White, Susan E. Waisbren, F. J. van Spronsen	3
11	RECURRENT THROMBO-EMBOLISM IN A CHILD WITH A CONGENITAL DISORDER OF GLYCOSYLATION (CDG) TYPE IB AND TREATMENT WITH MANNOSE 2008 ·Pediatric Hematology and Oncology ·R. Y. J. Tamminga, (unknown), W. A. Kamps, F. J. van Spronsen	10
12	Tyrosinemia type I treated by NTBC: How does AFP predict liver cancer? 2006 ·Molecular Genetics and Metabolism ·(unknown), Peter van Hasselt, A. van der Ploeg, Marry M. van den Heuvel‐Eibrink, Frits A. Wijburg, C. M. A. Bijleveld, F. J. van Spronsen	41
13	Cerebral 1H MR spectroscopy showing elevation of brain guanidinoacetate in argininosuccinate lyase deficiency 2005 ·Molecular Genetics and Metabolism ·Paul E. Sijens, Dirk‐Jan Reijngoud, R. J. Soorani‐Lunsing, Matthijs Oudkerk, F. J. van Spronsen	14
14	Normal very‐long‐chain fatty acids in peroxisomal D‐bifunctional protein deficiency: A diagnostic pitfall 2005 ·Journal of Inherited Metabolic Disease ·R. J. Soorani‐Lunsing, F. J. van Spronsen, Irene Stolte‐Dijkstra, Ronald J. A. Wanders, Sacha Ferdinandusse, Hans R. Waterham, Bwee Tien Poll‐The, J. P. Rake	12
15	Borstvoeding: ook voor het kind met fenylketonurie 2002 ·Tijdschrift voor kindergeneeskunde ·(unknown), Jolita Bekhof, (unknown), Gerrit Smit, (unknown), F. J. van Spronsen	0
16	Behaviour and school achievement in patients with early and continuously treated phenylketonuria 2000 ·Journal of Inherited Metabolic Disease ·(unknown), Alex F. Kalverboer, J.J. Van der Meere, Maurits W. van der Molen, J. Huisman, (unknown), F.M.E. Slijper, P.H. Verkerk, F. J. van Spronsen	57
17	Phenylketonuria in The Netherlands: 93&percnt; of the Mutations Are Detected by Single-Strand Conformation Analysis 1996 ·Human Heredity ·(unknown), (unknown), J. Juyn, Margreet Plaisier, Jacques C. Giltay, F. J. van Spronsen, G. P. A. Smit, R. Berger, Jan Smeıtınk, Bwee Tien Poll‐The, (unknown)	5
18	Information processing in patients with early and continuously-treated phenylketonuria 1995 ·European Journal of Pediatrics ·(unknown), J.J. Van der Meere, Maurits W. van der Molen, Alex F. Kalverboer, (unknown), J. Huisman, (unknown), F.M.E. Slijper, F. J. van Spronsen, (unknown)	25
19	Prevalence of congenital heart disease in patients with phenylketonuria 1991 ·The Journal of Pediatrics ·P.H. Verkerk, F. J. van Spronsen, G. P. A. Smit, Martina C. Cornel, Jrg Kuipers, S.P. Verloove-Vanhorick	8
20	Tyrosinaemia Type I: Orthotopic Liver Transplantation as the Only Definitive Answer to a Metabolic as well as an Oncological Problem 1989 ·Journal of Inherited Metabolic Disease ·F. J. van Spronsen, R. Berger, Gerrit Smit, J. B. C. de Klerk, M. Durán, C. M. A. Bijleveld, Henk van Faassen, M. J. H. Slooff, H. S. A. Heymans	30

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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