P.K. De Bree

1.4k total citations
44 papers, 1.1k citations indexed

About

P.K. De Bree is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, P.K. De Bree has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 13 papers in Biochemistry. Recurrent topics in P.K. De Bree's work include Biochemical and Molecular Research (22 papers), Metabolism and Genetic Disorders (20 papers) and Amino Acid Enzymes and Metabolism (11 papers). P.K. De Bree is often cited by papers focused on Biochemical and Molecular Research (22 papers), Metabolism and Genetic Disorders (20 papers) and Amino Acid Enzymes and Metabolism (11 papers). P.K. De Bree collaborates with scholars based in Netherlands, Belgium and Germany. P.K. De Bree's co-authors include S.K. Wadman, Colin van der Heiden, M. Durán, D. Ketting, Albert H. Gennip, J. W. Stoop, B.J.M. Zegers, F. J. van Sprang, F. A. Beemer and Matthijs L. Siegenbeek van Heukelom and has published in prestigious journals such as New England Journal of Medicine, Clinica Chimica Acta and Pediatric Research.

In The Last Decade

P.K. De Bree

44 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P.K. De Bree Netherlands 19 764 382 246 157 117 44 1.1k
S. K. Wadman Netherlands 13 388 0.5× 265 0.7× 87 0.4× 91 0.6× 70 0.6× 32 599
Matthew J. Toth United States 17 1.0k 1.4× 186 0.5× 97 0.4× 21 0.1× 86 0.7× 20 1.3k
W.F. Carey Australia 15 298 0.4× 124 0.3× 85 0.3× 58 0.4× 29 0.2× 52 709
N. Dance United Kingdom 19 617 0.8× 82 0.2× 130 0.5× 198 1.3× 26 0.2× 30 1.4k
Donald W. Horne United States 20 460 0.6× 385 1.0× 54 0.2× 102 0.6× 143 1.2× 35 1.1k
Albert H. Bootsma Netherlands 16 611 0.8× 480 1.3× 156 0.6× 175 1.1× 103 0.9× 21 1.0k
Helmut Gmünder Germany 11 448 0.6× 34 0.1× 85 0.3× 28 0.2× 359 3.1× 12 1.2k
Maria A Graziewicz United States 13 950 1.2× 308 0.8× 55 0.2× 26 0.2× 34 0.3× 15 1.1k
H Ozasa Japan 11 557 0.7× 315 0.8× 19 0.1× 43 0.3× 60 0.5× 20 725
A Slesers United States 15 445 0.6× 131 0.3× 93 0.4× 43 0.3× 69 0.6× 23 790

Countries citing papers authored by P.K. De Bree

Since Specialization
Citations

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

Fields of papers citing papers by P.K. De Bree

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P.K. De Bree. 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 P.K. De Bree. The network helps show where P.K. De Bree may publish in the future.

Co-authorship network of co-authors of P.K. De Bree

This figure shows the co-authorship network connecting the top 25 collaborators of P.K. De Bree. A scholar is included among the top collaborators of P.K. De Bree 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 P.K. De Bree. P.K. De Bree 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.
Durán, M., et al.. (1991). Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism. Journal of Inherited Metabolic Disease. 14(3). 367–370. 35 indexed citations
2.
Dorland, L., et al.. (1990). O-Phosphohydroxylysinuria: a new inborn error of metabolism?. Clinica Chimica Acta. 188(3). 221–226. 4 indexed citations
3.
Kulik, Willem, W. Heerma, L. Dorland, P.K. De Bree, & M. Durán. (1989). Fast‐atom bombardment tandem mass spectrometry of phosphohydroxylysine and related phosphohydroxy amino acids. Rapid Communications in Mass Spectrometry. 3(3). 76–78. 4 indexed citations
4.
Kleijer, Wim J., et al.. (1989). Prenatal diagnosis of purine nucleoside phosphorylase deficiency in the first and second trimesters of pregnancy. Prenatal Diagnosis. 9(6). 401–407. 4 indexed citations
5.
Wadman, S.K., Rolf M.F. Berger, M. Durán, et al.. (1985). Dihydropyrimidine dehydrogenase deficiency leading to thymine‐uraciluria. An inborn error of pyrimidine metabolism. Journal of Inherited Metabolic Disease. 8(S2). 113–114. 18 indexed citations
6.
Wadman, S.K., et al.. (1985). DETECTION OF INHERITED ADENYLOSUCCINASE DEFICIENCY BY 2-DIM. THIN LAYER CHROMATOGRAPHY OF URINARY IMIDAZOLES: 224. Pediatric Research. 19(7). 781–781. 1 indexed citations
7.
Wadman, S.K., F. A. Beemer, P.K. De Bree, et al.. (1984). New Defects of Pyrimidine Metabolism. Advances in experimental medicine and biology. 165 Pt A. 109–114. 22 indexed citations
8.
Berger, Rolf M.F., S.K. Wadman, M. Durán, et al.. (1984). Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism. Clinica Chimica Acta. 141(2-3). 227–234. 76 indexed citations
9.
Wadman, S.K., B. P. Cats, & P.K. De Bree. (1983). Sulfite oxidase deficiency and the detection of urinary sulfite. European Journal of Pediatrics. 141(1). 62–63. 13 indexed citations
10.
Durán, M., D. Ketting, P.K. De Bree, et al.. (1981). A case of formiminoglutamic aciduria. European Journal of Pediatrics. 136(3). 319–323. 2 indexed citations
11.
Wadman, S.K., P.K. De Bree, Albert H. Gennip, et al.. (1977). Urinary Purines in a Patient with a Severely Defective T Cell Immunity and a Purine Nucleoside Phosphorylase Deficiency. PubMed. 76A. 471–476. 12 indexed citations
12.
Heukelom, Matthijs L. Siegenbeek van, J W N Akkerman, G.E.J. Staal, et al.. (1977). A patient with purine nucleoside phosphorylase deficiency: Enzymological and metabolic aspects. Clinica Chimica Acta. 74(3). 271–279. 25 indexed citations
13.
Wadman, S.K., P.K. De Bree, F. J. van Sprang, et al.. (1975). Nϵ-(carboxymethyd)lysine, a constituent of human urine. Clinica Chimica Acta. 59(3). 313–320. 44 indexed citations
14.
Wadman, S.K., et al.. (1975). Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental development. Clinica Chimica Acta. 65(2). 197–204. 5 indexed citations
15.
Bakker, H. D., P.K. De Bree, D. Ketting, F. J. van Sprang, & S.K. Wadman. (1974). Fructose-1,6-diphosphatase deficiency: Another enzyme defect which can present itself with the clinical features of “tyrosinosis”. Clinica Chimica Acta. 55(1). 41–47. 6 indexed citations
16.
Durán, M., D. Ketting, P.K. De Bree, Colin van der Heiden, & S.K. Wadman. (1973). Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals. Clinica Chimica Acta. 45(4). 341–347. 25 indexed citations
17.
Heiden, Colin van der, S.K. Wadman, D. Ketting, & P.K. De Bree. (1971). Urinary and faecal excretion of metabolizes of tyrosine and phenylalanine in a patient with cystic fibrosis and severely impaired amino acid absorption. Clinica Chimica Acta. 31(1). 133–141. 37 indexed citations
18.
Bree, P.K. De, et al.. (1971). A sensitive automatic determination of protein in urine serum and cerebrospinal fluid. Clinica Chimica Acta. 32(3). 321–325. 5 indexed citations
19.
Wadman, S.K., P.K. De Bree, Colin van der Heiden, & F. J. van Sprang. (1971). Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals. Clinica Chimica Acta. 31(1). 215–224. 19 indexed citations
20.
Bree, P.K. De, et al.. (1970). A micromodification of the flow diagram for the determination of protein-bound lodine with the technicon autoanalyzer system. Biochemical Medicine. 3(5). 431–436. 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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