S. K. Wadman

767 total citations
32 papers, 599 citations indexed

About

S. K. Wadman is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, S. K. Wadman has authored 32 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 6 papers in Epidemiology. Recurrent topics in S. K. Wadman's work include Metabolism and Genetic Disorders (13 papers), Biochemical and Molecular Research (9 papers) and Cytomegalovirus and herpesvirus research (5 papers). S. K. Wadman is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Biochemical and Molecular Research (9 papers) and Cytomegalovirus and herpesvirus research (5 papers). S. K. Wadman collaborates with scholars based in Netherlands, United States and France. S. K. Wadman's co-authors include M. Durán, D. Ketting, Colin van der Heiden, P.K. De Bree, L. Bruinvis, Marcel R.M. van den Brink, F. A. Beemer, I. Lombeck, J. B. de Klerk and Greet Van den Berghe and has published in prestigious journals such as Nature, The Lancet and The Journal of Immunology.

In The Last Decade

S. K. Wadman

30 papers receiving 559 citations

Peers

S. K. Wadman

RHEUM

PPCH

EPIDE

Ching‐Wan Lam Hong Kong

Joy Yaplito‐Lee Australia

Aleix Navarro‐Sastre Spain

Keizo Tsushima Japan

Mary G. Ampola United States

W.F. Carey Australia

J. M. Noronha India

H Ozasa Japan

F. J. van Sprang Netherlands

P Walter Switzerland

Ching‐Wan Lam Hong Kong

S. K. Wadman

237 ×0.6

77 ×0.3

89 ×0.8

RHEUM

26 ×0.3

PPCH

66 ×0.8

EPIDE

Citations per year, relative to S. K. Wadman S. K. Wadman (= 1×) peers Ching‐Wan Lam

Countries citing papers authored by S. K. Wadman

Since Specialization

Citations

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

Fields of papers citing papers by S. K. Wadman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. K. Wadman. 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 S. K. Wadman. The network helps show where S. K. Wadman may publish in the future.

Co-authorship network of co-authors of S. K. Wadman

This figure shows the co-authorship network connecting the top 25 collaborators of S. K. Wadman. A scholar is included among the top collaborators of S. K. Wadman 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 S. K. Wadman. S. K. Wadman 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

Staal, G.E.J., et al.. (2015). Red Cell Metabolism in Purine Nucleoside Phosphorylase Deficiency after Enzyme Replacement Therapy. PubMed. 10. 104–107.

Picat, C., Marie Hélène Delfau, B.G. Wolthers, et al.. (1989). Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria. Journal of Inherited Metabolic Disease. 13(5). 684–686. 15 indexed citations

Wolthers, B.G., et al.. (1989). A retrospective study of a patient with homozygous form of acute intermittent porphyria. Journal of Inherited Metabolic Disease. 13(5). 673–683. 29 indexed citations

Gibson, K. Michael, William L. Nyhan, L. Sweetman, et al.. (1988). 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal. European Journal of Pediatrics. 148(1). 76–82. 21 indexed citations

Jaeken, Jaak, S. K. Wadman, M. Durán, et al.. (1988). Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis. European Journal of Pediatrics. 148(2). 126–131. 103 indexed citations

Spaapen, L. J. M., et al.. (1986). Intracellular Purine and Pyrimidine Nucleotide Pools of Human T and B Lymphocytes. Advances in experimental medicine and biology. 195 Pt A. 567–573. 10 indexed citations

Spaapen, L. J. M., G T Rijkers, G.E.J. Staal, et al.. (1984). The effect of deoxyguanosine on human lymphocyte function. I. Analysis of the interference with lymphocyte proliferation in vitro.. The Journal of Immunology. 132(5). 2311–2317. 29 indexed citations

Stoop, J. W., B.J.M. Zegers, L. J. M. Spaapen, et al.. (1984). The Effect of Deoxycytidine and Tetrahydrouridine in Purine Nucleoside Phosphorylase Deficiency. Advances in experimental medicine and biology. 165 Pt A. 61–66. 4 indexed citations

Durán, M., et al.. (1979). Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase. Journal of Inherited Metabolic Disease. 2(1). 15–18. 6 indexed citations

10.

Heiden, Colin van der, Marcel R.M. van den Brink, P.K. De Bree, et al.. (1978). Familial hyperlysinaemia due to L‐lysineα‐ketoglutarate reductase deficiency: Results of attempted treatment. Journal of Inherited Metabolic Disease. 1(3). 89–94. 10 indexed citations

11.

Durán, M., F. A. Beemer, Colin van der Heiden, et al.. (1978). Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?. Journal of Inherited Metabolic Disease. 1(4). 175–178. 93 indexed citations

12.

Biervliet, J.P. Van, et al.. (1976). HAZARDS OF PARENTERAL GLUCOSE IN NEONATAL LACTIC ACIDÆMIA. The Lancet. 307(7959). 594–594. 2 indexed citations

13.

Biervliet, J.P. Van, et al.. (1974). BASE EXCESS AND ORGANIC ACIDÆMIA. The Lancet. 304(7895). 1518–1519. 8 indexed citations

14.

Heiden, Colin van der, et al.. (1974). Time course of gamma glutamyl transpeptidase in the serum of low birth weight infants. Clinica Chimica Acta. 50(2). 281–288. 7 indexed citations

15.

Wadman, S. K., et al.. (1964). [CALIBRATION OF HEMOGLOBIN DETERMINATION ON THE BASIS OF IRON].. PubMed. 108. 265–8. 3 indexed citations

16.

Meester, Geert T., et al.. (1963). Reversible Hypogammaglobulinaemia in Cyanocobalamin (B₁₂) Deficiency. Acta Medica Scandinavica. 174(2). 193–200. 21 indexed citations

17.

Wadman, S. K., et al.. (1960). The estimation of phenylalanine in serum by paper chromatography at elevated temperatures. Clinica Chimica Acta. 5(6). 824–827. 3 indexed citations

18.

Brandt, Kathleen R., et al.. (1959). Abnormally Low α₂‐ and β‐Globulin Levels in Serious Hepatic Insufficiency. Acta Medica Scandinavica. 165(3). 211–216. 2 indexed citations

19.

Jonxis, J. H. P. & S. K. Wadman. (1952). A Fœtal Form of Myoglobin. Nature. 169(4308). 884–886. 15 indexed citations

20.

Jonxis, J. H. P. & S. K. Wadman. (1951). [A case of hypoproteinemia due to protein deficiency in an infant].. PubMed. 95(44). 3253–6.

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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