B Steinmann

6.9k total citations · 1 hit paper
105 papers, 4.9k citations indexed

About

B Steinmann is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, B Steinmann has authored 105 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 36 papers in Rheumatology and 32 papers in Molecular Biology. Recurrent topics in B Steinmann's work include Connective tissue disorders research (50 papers), Dermatological and Skeletal Disorders (15 papers) and Metabolism and Genetic Disorders (14 papers). B Steinmann is often cited by papers focused on Connective tissue disorders research (50 papers), Dermatological and Skeletal Disorders (15 papers) and Metabolism and Genetic Disorders (14 papers). B Steinmann collaborates with scholars based in Switzerland, United States and Germany. B Steinmann's co-authors include R Gitzelmann, Andrea Superti‐Furga, Peter Brückner, Margret Schlumpf, W. Lichtensteiger, Peter H. Byers, René Santer, J. Schaub, Francesco Ramirez and David W. Hollister and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

B Steinmann

103 papers receiving 4.7k citations

Hit Papers

In vitro and in vivo estrogenicity of UV screens. 2001 2026 2009 2017 2001 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. In vitro and in vivo estrogenicity of UV screens.
    2001 685 citations B Steinmann et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B Steinmann Switzerland 38 2.0k 1.8k 871 493 466 105 4.9k
Beverly Peterkofsky United States 32 717 0.4× 1.9k 1.1× 735 0.8× 908 1.8× 155 0.3× 76 5.2k
Beat Steinmann Switzerland 45 3.3k 1.6× 2.1k 1.2× 1.1k 1.3× 866 1.8× 503 1.1× 123 6.4k
Philip C. Trackman United States 47 861 0.4× 4.3k 2.5× 688 0.8× 552 1.1× 504 1.1× 117 6.8k
Raili Myllylä Finland 48 1.4k 0.7× 4.0k 2.3× 963 1.1× 2.0k 4.1× 340 0.7× 123 6.9k
Herbert M. Kagan United States 49 1.3k 0.7× 5.3k 3.0× 725 0.8× 817 1.7× 177 0.4× 126 8.0k
Johan M. TeKoppele Netherlands 28 399 0.2× 1.0k 0.6× 1.8k 2.1× 389 0.8× 1.0k 2.2× 30 4.4k
Barbara E. Kream United States 41 1.3k 0.6× 3.1k 1.8× 784 0.9× 445 0.9× 53 0.1× 102 6.0k
R L Jilka United States 27 1.8k 0.9× 4.5k 2.5× 545 0.6× 231 0.5× 94 0.2× 37 7.7k
Nicole Verzijl Netherlands 26 274 0.1× 987 0.6× 1.5k 1.8× 379 0.8× 965 2.1× 29 4.0k
Shunji Tomatsu United States 55 867 0.4× 2.1k 1.2× 2.0k 2.3× 1.2k 2.5× 256 0.5× 311 10.2k

Countries citing papers authored by B Steinmann

Since Specialization
Citations

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

Fields of papers citing papers by B Steinmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Steinmann

This figure shows the co-authorship network connecting the top 25 collaborators of B Steinmann. A scholar is included among the top collaborators of B Steinmann 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 B Steinmann. B Steinmann 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.
Meienberg, Janine, Irene Keller, Michał Okoniewski, et al.. (2015). New insights into the performance of human whole-exome capture platforms. Nucleic Acids Research. 43(11). e76–e76. 76 indexed citations
2.
Bonafé, Luisa, Cecilia Giunta, Markus Gassner, B Steinmann, & A Superti‐Furga. (2003). A cluster of autosomal recessive spondylocostal dysostosis caused by three newly identified DLL3 mutations segregating in a small village. Clinical Genetics. 64(1). 28–35. 29 indexed citations
3.
Giunta, Cecilia, Lieve Nuytinck, Michael Raghunath, et al.. (2002). Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers‐Danlos syndrome. American Journal of Medical Genetics. 109(4). 284–290. 29 indexed citations
4.
5.
6.
Santer, René, Reinhard Schneppenheim, Diane E. Suter, J. Schaub, & B Steinmann. (1998). Fanconi-Bickel syndrome - the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature. European Journal of Pediatrics. 157(10). 783–797. 116 indexed citations
7.
Heim, Peter, Michael Raghunath, L. Meiss, et al.. (1998). Ehlers-Danlos Syndrome Type VI (EDS VI): problems of diagnosis and management. Acta Paediatrica. 87(6). 708–710. 17 indexed citations
8.
9.
Eich, Georg, B Steinmann, J Hodler, G. Ulrich Exner, & A Giedion. (1996). Metaphyseal peg in geroderma osteodysplasticum: A new genetic bone marker and a specific finding?. American Journal of Medical Genetics. 63(1). 62–67. 5 indexed citations
10.
Pollak, Martin R., Yah-Huei Chou, Stephen J. Marx, et al.. (1994). Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.. Journal of Clinical Investigation. 93(3). 1108–1112. 197 indexed citations
11.
Boesiger, Peter, R. Buchli, Daniel M. Meier, B Steinmann, & R Gitzelmann. (1994). Changes of Liver Metabolite Concentrations in Adults with Disorders of Fructose Metabolism after Intravenous Fructose by 31P Magnetic Resonance Spectroscopy. Pediatric Research. 36(4). 436–440. 41 indexed citations
12.
Beighton, Peter, A. De Paepe, Judith G. Hall, et al.. (1992). Molecular nosology of heritable disorders of connective tissue. American Journal of Medical Genetics. 42(4). 431–448. 46 indexed citations
13.
Cross, Nicholas C.P., Timothy M. Cox, R. de Franchis, et al.. (1990). Molecular analysis of aldolase B genes in hereditary fructose intolerance. The Lancet. 335(8685). 306–309. 82 indexed citations
14.
15.
Steinlin, Maja, Eugen Boltshauser, B Steinmann, W. Wichmann, & Günter Niemeyer. (1989). Hyperprolinaemia type I and white matter disease: Coincidence or causal relationship. European Journal of Pediatrics. 149(1). 40–42. 16 indexed citations
16.
Rudin, Christoph, et al.. (1988). The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). European Journal of Pediatrics. 147(4). 433–438. 22 indexed citations
17.
Superti‐Furga, Andrea, et al.. (1988). Delayed Triple‐Helix Formation of Abnormal Type I Collagen Is Corrected by Reduced Temperature. Annals of the New York Academy of Sciences. 543(1). 85–92. 4 indexed citations
18.
Royce, Peter M., et al.. (1988). Lethal osteogenesis imperfecta: abnormal collagen metabolism and biochemical characteristics of hypophosphatasia. European Journal of Pediatrics. 147(6). 626–631. 16 indexed citations
19.
Steinmann, B, Shu Abe, George R. Martin, & V.A. McKusick. (1977). Collagen Disorders. Upsala Journal of Medical Sciences. 82(2). 80–80. 1 indexed citations
20.
Dubs, R, B Steinmann, & R Gitzelmann. (1973). Demonstration of an inactive enzyme antigen in sucrase-isomaltase deficiency.. PubMed. 28(3). 187–98. 18 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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