R. Baumgartner

959 total citations
38 papers, 646 citations indexed

About

R. Baumgartner is a scholar working on Clinical Biochemistry, Cell Biology and Molecular Biology. According to data from OpenAlex, R. Baumgartner has authored 38 papers receiving a total of 646 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 16 papers in Cell Biology and 13 papers in Molecular Biology. Recurrent topics in R. Baumgartner's work include Metabolism and Genetic Disorders (20 papers), Biotin and Related Studies (14 papers) and Folate and B Vitamins Research (12 papers). R. Baumgartner is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Biotin and Related Studies (14 papers) and Folate and B Vitamins Research (12 papers). R. Baumgartner collaborates with scholars based in Switzerland, Germany and United States. R. Baumgartner's co-authors include Terttu Suormala, Thomas Kühne, H. Wick, William L. Nyhan, Toshiyuki Ando, C. Bachmann, U. Wendel, Katrin Schweizer, Ulrich Wiesmann and Brian Fowler and has published in prestigious journals such as Journal of Clinical Investigation, Diabetologia and The Journal of Pediatrics.

In The Last Decade

R. Baumgartner

37 papers receiving 597 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Baumgartner Switzerland 17 310 293 201 168 102 38 646
T. Baykal Türkiye 14 237 0.8× 228 0.8× 135 0.7× 88 0.5× 115 1.1× 18 449
Parvin Justice United States 14 140 0.5× 219 0.7× 49 0.2× 132 0.8× 57 0.6× 36 639
F. J. van Sprang Netherlands 15 357 1.2× 350 1.2× 61 0.3× 54 0.3× 46 0.5× 30 619
Sara Boenzi Italy 20 524 1.7× 539 1.8× 57 0.3× 247 1.5× 42 0.4× 43 1.0k
Maria Luı́s Cardoso Portugal 15 294 0.9× 257 0.9× 121 0.6× 89 0.5× 9 0.1× 29 542
Stephen Cederbaum United States 17 682 2.2× 508 1.7× 60 0.3× 158 0.9× 19 0.2× 24 919
D. Leupold Germany 11 283 0.9× 234 0.8× 25 0.1× 99 0.6× 20 0.2× 32 479
F. Van Hoof Belgium 11 41 0.1× 156 0.5× 69 0.3× 122 0.7× 43 0.4× 14 483
H. D. Bakker Netherlands 14 354 1.1× 267 0.9× 29 0.1× 83 0.5× 9 0.1× 28 556
F. Šmíd Czechia 13 27 0.1× 272 0.9× 155 0.8× 91 0.5× 122 1.2× 29 629

Countries citing papers authored by R. Baumgartner

Since Specialization
Citations

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

Fields of papers citing papers by R. Baumgartner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Baumgartner

This figure shows the co-authorship network connecting the top 25 collaborators of R. Baumgartner. A scholar is included among the top collaborators of R. Baumgartner 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. Baumgartner. R. Baumgartner 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.
Suormala, Terttu, Ulrich Wiesmann, Fátima Cruz, et al.. (2002). Biotin-Dependent Carboxylase Activities in Different CNS and Skin-Derived Cells, and their Sensitivity to Biotin-Depletion. International Journal for Vitamin and Nutrition Research. 72(4). 278–286. 12 indexed citations
2.
Sperl, Wolfgang, C. Murr, Daniela Skladal, et al.. (2000). Odd-numbered long-chain fatty acids in propionic acidaemia. European Journal of Pediatrics. 159(1-2). 54–58. 20 indexed citations
3.
Suormala, Terttu, Brian Fowler, Marinus Durán, et al.. (1997). Five Patients with a Biotin-Responsive Defect in Holocarboxylase Formation: Evaluation of Responsiveness to Biotin Therapy in Vivo and Comparative Biochemical Studies in Vi1. Pediatric Research. 41(5). 666–673. 32 indexed citations
4.
Pomponio, Robert J., Jeanne Hymes, Thomas Reynolds, et al.. (1997). Arg538 to Cys mutation in a CpG dinucleotide of the human biotinidase gene is the second most common cause of profound biotinidase deficiency in symptomatic children. Human Genetics. 99(4). 506–512. 34 indexed citations
5.
Mayatepek, Ertan, Georg F. Hoffmann, R. Baumgartner, et al.. (1996). Atypical vitamin B12-unresponsive methylmalonic aciduria in a sibship with severe progressive encephalomyelopathy: A new genetic disease?. European Journal of Pediatrics. 155(5). 398–403. 6 indexed citations
6.
Limat, Alain, et al.. (1996). Proliferation and differentiation of cultured human follicular keratinocytes are not influenced by biotin. Archives of Dermatological Research. 288(1). 31–38. 14 indexed citations
7.
Seitz, Rainer, et al.. (1995). Thrombomodulin and ristocetincofactor in homocystinuria: A study in two siblings. Thrombosis Research. 77(1). 79–86. 5 indexed citations
8.
Seitz, Rainer, et al.. (1994). Coagulation factors and markers of activation of coagulation in homocystinuria (HOCY): a study in two siblings. Blood Coagulation & Fibrinolysis. 5(6). 873–878. 9 indexed citations
9.
Blum, Denise, Harry Dorchy, Eszter P. Vamos, et al.. (1993). Congenital absence of insulin cells in a neonate with diabetes mellitus and mutase-deficient methylmalonic acidaemia. Diabetologia. 36(4). 352–357. 11 indexed citations
10.
Bannwart, C., Bendicht Wermuth, R. Baumgartner, Terttu Suormala, & Ulrich Wiesmann. (1992). Isolated biotin‐resistant deficiency of 3‐methylcrotonyl‐CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome. Journal of Inherited Metabolic Disease. 15(6). 863–868. 31 indexed citations
11.
Kühne, Thomas, et al.. (1991). Maternal vegan diet causing a serious infantile neurological disorder due to vitamin B12 deficiency. European Journal of Pediatrics. 150(3). 205–208. 66 indexed citations
12.
Wendel, U., R. Baumgartner, S. B. van der Meer, & L. J. M. Spaapen. (1991). Accumulation of Odd-Numbered Long-Chain Fatty Acids in Fetuses and Neonates with Inherited Disorders of Propionate Metabolism. Pediatric Research. 29(4). 403–405. 18 indexed citations
13.
Ribes, Antònia, P. Briones, Marta Vilaseca, et al.. (1990). Methylmalonic aciduria with homocystinuria: Biochemical studies, treatment, and clinical course of a Cbl-C patient. European Journal of Pediatrics. 149(6). 412–415. 18 indexed citations
14.
Hayasaka, Kiyoshi, et al.. (1987). Feasibility of prenatal diagnosis of nonketotic hyperglycinemia: Existence of the glycine cleavage system in placenta. The Journal of Pediatrics. 110(1). 124–126. 18 indexed citations
15.
Rocco, Maja Di, Andrea Superti‐Furga, P. Durand, et al.. (1984). Different Organic Acid Patterns in Urine and in Cerebrospinal Fluid in a Patient with Biotinidase Deficiency. PubMed. 7 Suppl 2. 119–120. 17 indexed citations
16.
Maldague, Pierre, et al.. (1983). S-86451, a New Derivative of Gentamicin With Reduced Nephrotoxicity - Biochemical, Morphological and Functional-studies. Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)). 9(6). 467–477. 11 indexed citations
17.
Trefz, Friedrich K., H. Schmidt, B. Tauscher, et al.. (1981). Improved prenatal diagnosis of methylmalonic acidemia: Mass fragmentography of methylmalonic acid in amniotic fluid and maternal urine. European Journal of Pediatrics. 137(3). 261–266. 9 indexed citations
18.
Baumgartner, R., et al.. (1980). Vascular lesions in two patients with congenital homocystinuria due to different defects of remethylation. Journal of Inherited Metabolic Disease. 3(1). 101–103. 14 indexed citations
19.
Cohen, Sanford N., R. Baumgartner, Michael S. Steinberg, & Wendell W. Weber. (1973). Changes in the physicochemical characteristics of rabbit liver N-acetyltransferase during post-natal development. Biochimica et Biophysica Acta (BBA) - General Subjects. 304(2). 473–481. 18 indexed citations
20.
Baumgartner, R., Toshiyuki Ando, & William L. Nyhan. (1969). Nonketotic hyperglycinemia. The Journal of Pediatrics. 75(6). 1022–1030. 56 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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