J. B. de Klerk

891 total citations
5 papers, 303 citations indexed

About

J. B. de Klerk is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, J. B. de Klerk has authored 5 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Rheumatology. Recurrent topics in J. B. de Klerk's work include Folate and B Vitamins Research (3 papers), Metabolism and Genetic Disorders (3 papers) and Biochemical and Molecular Research (2 papers). J. B. de Klerk is often cited by papers focused on Folate and B Vitamins Research (3 papers), Metabolism and Genetic Disorders (3 papers) and Biochemical and Molecular Research (2 papers). J. B. de Klerk collaborates with scholars based in Netherlands, Austria and United States. J. B. de Klerk's co-authors include M. Durán, Johannes Zschocke, W. Lehnert, E. Christensen, Barbara Plecko, J. Leonard, Edith Müller, G. F. Hoffmann, Andrea Superti‐Furga and Ania C. Muntau and has published in prestigious journals such as Clinical Chemistry, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

J. B. de Klerk

5 papers receiving 293 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. B. de Klerk Netherlands	5	213	208	66	41	40	5	303
Norma Spécola Argentina	11	154 0.7×	206 1.0×	181 2.7×	32 0.8×	33 0.8×	19	376
Mike Champion United Kingdom	6	191 0.9×	198 1.0×	58 0.9×	16 0.4×	35 0.9×	6	357
Mary J. Schmidt United States	7	160 0.8×	212 1.0×	82 1.2×	28 0.7×	27 0.7×	9	349
Ljerka Cvitanović-Šojat Croatia	8	229 1.1×	273 1.3×	60 0.9×	22 0.5×	93 2.3×	16	377
Bert Dorland Netherlands	8	220 1.0×	93 0.4×	67 1.0×	46 1.1×	32 0.8×	11	347
Danijela Petković Ramadža Croatia	9	134 0.6×	118 0.6×	103 1.6×	34 0.8×	24 0.6×	26	280
Cristiana Artiola Italy	9	143 0.7×	226 1.1×	79 1.2×	43 1.0×	39 1.0×	11	315
Barbara S. Miles United States	10	357 1.7×	304 1.5×	62 0.9×	31 0.8×	28 0.7×	12	462
Peter L. Hurst United States	2	170 0.8×	212 1.0×	37 0.6×	39 1.0×	13 0.3×	6	289
Nawal Makhseed Kuwait	12	167 0.8×	104 0.5×	53 0.8×	15 0.4×	51 1.3×	18	303

Countries citing papers authored by J. B. de Klerk

Since Specialization

Citations

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

Fields of papers citing papers by J. B. de Klerk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. B. de Klerk. 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 J. B. de Klerk. The network helps show where J. B. de Klerk may publish in the future.

Co-authorship network of co-authors of J. B. de Klerk

This figure shows the co-authorship network connecting the top 25 collaborators of J. B. de Klerk. A scholar is included among the top collaborators of J. B. de Klerk 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 J. B. de Klerk. J. B. de Klerk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Houten, Sander M., Heleen te Brinke, Simone Denis, et al.. (2013). Genetic basis of hyperlysinemia. Orphanet Journal of Rare Diseases. 8(1). 57–57. 43 indexed citations

2.

Stone, Deborah L., Otto P. van Diggelen, J. B. de Klerk, et al.. (1999). Is the perinatal lethal form of Gaucher disease more common than classic type 2 Gaucher disease?. European Journal of Human Genetics. 7(4). 505–509. 35 indexed citations

3.

Hoffmann, G. F., A Burlina, M. Durán, et al.. (1996). Clinical Course, Early Diagnosis, Treatment, and Prevention of Disease in Glutaryl-CoA Dehydrogenase Deficiency. Neuropediatrics. 27(3). 115–123. 160 indexed citations

4.

Nieuwenhuizen, Onno van, et al.. (1990). Quasi-Moyamoya Disease and Heterozygosity for Homocystinuria in a Five-Year-Old Girl. Neuropediatrics. 21(2). 110–112. 15 indexed citations

5.

Durán, M., L. Bruinvis, D. Ketting, J. B. de Klerk, & S. K. Wadman. (1988). Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency.. Clinical Chemistry. 34(3). 548–551. 50 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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