G. P. A. Smit

905 total citations
23 papers, 655 citations indexed

About

G. P. A. Smit is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, G. P. A. Smit has authored 23 papers receiving a total of 655 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 12 papers in Molecular Biology and 6 papers in Rheumatology. Recurrent topics in G. P. A. Smit's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (5 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). G. P. A. Smit is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (5 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). G. P. A. Smit collaborates with scholars based in Netherlands, United States and France. G. P. A. Smit's co-authors include Klary E. Niezen‐Koning, F. J. van Spronsen, E. B. Haagsma, P.H. Verkerk, Ronald J. A. Wanders, Rolf M.F. Berger, M. Durán, J. S. Bynon, J. A. Barnard and Alain Lachaux and has published in prestigious journals such as Hepatology, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

G. P. A. Smit

23 papers receiving 632 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. P. A. Smit Netherlands 14 313 270 220 150 103 23 655
Udo Wendel Germany 12 245 0.8× 229 0.8× 233 1.1× 68 0.5× 48 0.5× 18 525
Lorne E. Seargeant Canada 11 377 1.2× 251 0.9× 200 0.9× 75 0.5× 75 0.7× 14 679
Albina Tummolo Italy 14 199 0.6× 197 0.7× 96 0.4× 264 1.8× 74 0.7× 39 603
A Grenier Canada 13 231 0.7× 402 1.5× 92 0.4× 121 0.8× 104 1.0× 24 616
Isabelle Redonnet‐Vernhet France 13 179 0.6× 85 0.3× 86 0.4× 147 1.0× 51 0.5× 26 398
Monique Mathieu France 10 264 0.8× 291 1.1× 69 0.3× 115 0.8× 27 0.3× 13 450
Aleix Navarro‐Sastre Spain 17 331 1.1× 230 0.9× 55 0.3× 48 0.3× 36 0.3× 21 624
Roshni Vara United Kingdom 13 157 0.5× 221 0.8× 85 0.4× 115 0.8× 66 0.6× 34 462
N Hobolth Denmark 14 369 1.2× 212 0.8× 30 0.1× 114 0.8× 308 3.0× 37 848
Tomozumi Takatani Japan 13 238 0.8× 89 0.3× 47 0.2× 68 0.5× 115 1.1× 48 525

Countries citing papers authored by G. P. A. Smit

Since Specialization
Citations

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

Fields of papers citing papers by G. P. A. Smit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. P. A. Smit. 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 G. P. A. Smit. The network helps show where G. P. A. Smit may publish in the future.

Co-authorship network of co-authors of G. P. A. Smit

This figure shows the co-authorship network connecting the top 25 collaborators of G. P. A. Smit. A scholar is included among the top collaborators of G. P. A. Smit 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 G. P. A. Smit. G. P. A. Smit 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.
Joosse, Pieter, et al.. (2009). Outcome and prognostic factors of traumatic brain injury: a prospective evaluation in a Jakarta University hospital. Journal of Clinical Neuroscience. 16(7). 925–928. 23 indexed citations
2.
Derks, Terry G. J., Theo Boer, Trijnie Bos, et al.. (2008). Neonatal screening for medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency. Journal of Inherited Metabolic Disease. 31(1). 88–96. 48 indexed citations
3.
Meer, K. de, Mark J. Roef, J. B. C. de Klerk, et al.. (2005). Increasing fat in the diet does not improve muscle performance in patients with mitochondrial myopathy due to complex I deficiency. Journal of Inherited Metabolic Disease. 28(1). 95–98. 12 indexed citations
4.
Melis, Daniela, Adrie C. Havelaar, Elly Verbeek, et al.. (2004). NPT4, a new microsomal phosphate transporter: Mutation analysis in glycogen storage disease type Ic. Journal of Inherited Metabolic Disease. 27(6). 725–733. 21 indexed citations
5.
Rake, Jan Peter, Gepke Visser, Edwin Verlind, et al.. (2000). Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes. Human Mutation. 15(4). 381–381. 10 indexed citations
6.
Matern, Dietrich, TE Starzl, Walid S. Arnaout, et al.. (1999). Liver transplantation for glycogen storage disease types I, III, and IV. European Journal of Pediatrics. 158(S2). S043–S048. 118 indexed citations
7.
Houten, Sander M., G. J. Romeijn, Janet Koster, et al.. (1999). Identification and Characterization of Three Novel Missense Mutations in Mevalonate Kinase cDNA Causing Mevalonic Aciduria, a Disorder of Isoprene Biosynthesis. Human Molecular Genetics. 8(8). 1523–1528. 54 indexed citations
8.
Haagsma, E. B., et al.. (1997). Type Iiib Glycogen Storage Disease Associated With End–Stage Cirrhosis and Hepatocellular Carcinoma. Hepatology. 25(3). 537–540. 46 indexed citations
9.
Houten, Mark van, et al.. (1997). Does impaired growth of PKU patients correlate with the strictness of dietary treatment?. Acta Paediatrica. 86(8). 816–818. 24 indexed citations
10.
Juyn, J., Margreet Plaisier, Jacques C. Giltay, et al.. (1996). Phenylketonuria in The Netherlands: 93% of the Mutations Are Detected by Single-Strand Conformation Analysis. Human Heredity. 46(4). 185–190. 5 indexed citations
11.
12.
Spronsen, Francjan J. van, G. P. A. Smit, Margreet van Rijn, et al.. (1996). Phenylketonuria: Plasma Phenylalanine Responses to Different Distributions of the Daily Phenylalanine Allowance Over the Day. PEDIATRICS. 97(6). 839–844. 17 indexed citations
13.
Smit, G. P. A., et al.. (1994). Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Acta Paediatrica. 83(s407). 70–72. 5 indexed citations
14.
Verkerk, P.H., et al.. (1994). Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee.. Archives of Disease in Childhood. 71(2). 114–118. 57 indexed citations
15.
Verkerk, P.H., F. J. van Spronsen, G. P. A. Smit, et al.. (1991). Prevalence of congenital heart disease in patients with phenylketonuria. The Journal of Pediatrics. 119(2). 282–283. 8 indexed citations
16.
Ruiters, Marcel H.J., E. A. van Spronsen, Ola H. Skjeldal, et al.. (1990). Confocal scanning laser microscopy of mitochondria: a possible tool in the diagnosis of mitochondrial disorders. Journal of Inherited Metabolic Disease. 14(1). 45–48. 8 indexed citations
17.
Willems, Patrick J., et al.. (1988). Activation of fatty acid oxidation in the Silver–Russell syndrome and the Brachmann–de Lange syndrome. American Journal of Medical Genetics. 30(4). 865–873. 8 indexed citations
18.
Wanders, Ronald J. A., Watske Smit, H. S. A. Heymans, et al.. (1987). Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome. Clinica Chimica Acta. 166(1). 45–56. 32 indexed citations
19.
Berger, Rolf M.F., et al.. (1985). Mevalonic aciduria: an inborn error of cholesterol biosynthesis?. Clinica Chimica Acta. 152(1-2). 219–222. 60 indexed citations
20.
Wadman, S.K., M. Durán, F. A. Beemer, et al.. (1983). Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase. Journal of Inherited Metabolic Disease. 6(S1). 78–83. 46 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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