R. D. Scholem

730 total citations
12 papers, 589 citations indexed

About

R. D. Scholem is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R. D. Scholem has authored 12 papers receiving a total of 589 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Clinical Biochemistry, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R. D. Scholem's work include Metabolism and Genetic Disorders (10 papers), Biochemical and Molecular Research (3 papers) and Muscle metabolism and nutrition (3 papers). R. D. Scholem is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Biochemical and Molecular Research (3 papers) and Muscle metabolism and nutrition (3 papers). R. D. Scholem collaborates with scholars based in Australia and Austria. R. D. Scholem's co-authors include Garry K. Brown, David M. Danks, G. K. Brown, Eric Haan, Denise M. Kirby, Carol Wicking, Richard G.H. Cotton, Alan T. Bankier, Susan M. Hunt and John C. Rogers and has published in prestigious journals such as Neurology, PEDIATRICS and Biochemical Journal.

In The Last Decade

R. D. Scholem

12 papers receiving 576 citations

Peers

R. D. Scholem
K Takki Finland
N. Chamoles Argentina
A. E. M. Stroomer Netherlands
Andrew A.M. Morris United Kingdom
Darius J. Adams United States
K Takki Finland
R. D. Scholem
Citations per year, relative to R. D. Scholem R. D. Scholem (= 1×) peers K Takki

Countries citing papers authored by R. D. Scholem

Since Specialization
Citations

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

Fields of papers citing papers by R. D. Scholem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. D. Scholem. 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 R. D. Scholem. The network helps show where R. D. Scholem may publish in the future.

Co-authorship network of co-authors of R. D. Scholem

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

All Works

12 of 12 papers shown
1.
Scholem, R. D., et al.. (1989). Sulfite oxidase deficiency. Neurology. 39(2). 252–252. 42 indexed citations
2.
Brown, Garry K., et al.. (1989). The Clinical and Biochemical Spectrum of Human Pyruvate Dehydrogenase Complex Deficiency. Annals of the New York Academy of Sciences. 573(1). 360–368. 59 indexed citations
3.
Brown, Garry K., Eric Haan, Denise M. Kirby, et al.. (1988). ?Cerebral? lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis. European Journal of Pediatrics. 147(1). 10–14. 73 indexed citations
4.
Haan, Eric, R. D. Scholem, James Pitt, J. E. Wraith, & Garry K. Brown. (1987). Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria. European Journal of Pediatrics. 146(5). 484–488. 10 indexed citations
5.
Brown, Garry K., et al.. (1987). Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 10(4). 359–366. 36 indexed citations
6.
Haan, Eric, et al.. (1986). Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect. European Journal of Pediatrics. 144(6). 567–570. 40 indexed citations
7.
Wicking, Carol, et al.. (1986). Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenase. Biochemical Journal. 239(1). 89–96. 80 indexed citations
8.
Brown, Garry K., R. D. Scholem, Alan T. Bankier, & David M. Danks. (1983). Malonyl coenzyme a decarboxylase deficiency. Journal of Inherited Metabolic Disease. 7(1). 21–26. 64 indexed citations
9.
Scholem, R. D., et al.. (1983). Deoxyribose‐5‐phosphate aldolase deficiency — A harmless inborn error of metabolism. Journal of Inherited Metabolic Disease. 6(3). 105–107. 2 indexed citations
10.
Scholem, R. D. & G. K. Brown. (1983). Metabolism of malonic semialdehyde in man. Biochemical Journal. 216(1). 81–85. 20 indexed citations
11.
Brown, Garry K., Susan M. Hunt, R. D. Scholem, et al.. (1982). beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations.. PubMed. 70(4). 532–8. 83 indexed citations
12.
Brown, Garry K., Susan M. Hunt, R. D. Scholem, et al.. (1982). β-Hydroxyisobutyryl Coenzyme A Deacylase Deficiency: A Defect in Valine Metabolism Associated with Physical Malformations. PEDIATRICS. 70(4). 532–538. 80 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026