Beat Steinmann

10.6k total citations · 1 hit paper
123 papers, 6.4k citations indexed

About

Beat Steinmann is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Beat Steinmann has authored 123 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Genetics, 46 papers in Molecular Biology and 30 papers in Rheumatology. Recurrent topics in Beat Steinmann's work include Connective tissue disorders research (70 papers), Dermatological and Skeletal Disorders (26 papers) and Metabolism and Genetic Disorders (16 papers). Beat Steinmann is often cited by papers focused on Connective tissue disorders research (70 papers), Dermatological and Skeletal Disorders (26 papers) and Metabolism and Genetic Disorders (16 papers). Beat Steinmann collaborates with scholars based in Switzerland, United States and Germany. Beat Steinmann's co-authors include Anne De Paepe, Richard Wenstrup, Peter Beighton, Petros Tsipouras, Peter M. Royce, Andrea Superti‐Furga, Cecilia Giunta, Michael Raghunath, R Gitzelmann and René Santer and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Beat Steinmann

121 papers receiving 6.1k citations

Hit Papers

align trajectories sort by overperformance

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.

Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997

1998 1.2k citations Beat Steinmann, Richard Wenstrup et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Beat Steinmann	3.3k	2.1k	1.1k	866	864	123	6.4k
B Steinmann	2.0k 0.6×	1.8k 0.8×	871 0.8×	493 0.6×	459 0.5×	105	4.9k
Jürgen W. Spranger	2.7k 0.8×	2.4k 1.2×	1.1k 0.9×	633 0.7×	678 0.8×	171	5.8k
Yasuteru Muragaki	1.1k 0.3×	3.4k 1.6×	677 0.6×	550 0.6×	750 0.9×	145	7.0k
Aleksander Hinek	2.4k 0.7×	2.6k 1.2×	619 0.5×	1.6k 1.8×	740 0.9×	143	6.8k
Gen Nishimura	3.7k 1.1×	3.6k 1.7×	1.2k 1.1×	631 0.7×	781 0.9×	344	7.1k
Philip C. Trackman	861 0.3×	4.3k 2.1×	688 0.6×	552 0.6×	466 0.5×	117	6.8k
Willy Lissens	1.8k 0.5×	3.3k 1.6×	265 0.2×	354 0.4×	569 0.7×	235	7.0k
Yoshiki Seino	1.4k 0.4×	1.9k 0.9×	474 0.4×	214 0.2×	773 0.9×	238	6.0k
Thorsten Schinke	1.5k 0.5×	4.4k 2.1×	1.7k 1.5×	600 0.7×	1.2k 1.4×	189	9.7k
George Bou–Gharios	714 0.2×	3.4k 1.6×	509 0.4×	449 0.5×	995 1.2×	158	6.6k

Countries citing papers authored by Beat Steinmann

Since Specialization

Citations

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

Fields of papers citing papers by Beat Steinmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beat Steinmann

This figure shows the co-authorship network connecting the top 25 collaborators of Beat Steinmann. A scholar is included among the top collaborators of Beat 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 Beat Steinmann. Beat Steinmann 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

Najafi, Arash, et al.. (2019). Variant filtering, digenic variants, and other challenges in clinical sequencing: a lesson from fibrillinopathies. Clinical Genetics. 97(2). 235–245. 18 indexed citations

Bakker, Erik N.T.P., Ed VanBavel, Urs Ziegler, et al.. (2019). Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers–Danlos syndrome. Cardiovascular Research. 116(2). 457–465. 28 indexed citations

Yeowell, Heather N. & Beat Steinmann. (2018). PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome. 13 indexed citations

Jeong, Jeeyon, Joel M. Walker, Fudi Wang, et al.. (2012). Promotion of vesicular zinc efflux by ZIP13 and its implications for spondylocheiro dysplastic Ehlers–Danlos syndrome. Proceedings of the National Academy of Sciences. 109(51). E3530–8. 91 indexed citations

Dündar, Munis, Thomas Müller, Qi Zhang, et al.. (2009). Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome. The American Journal of Human Genetics. 85(6). 873–882. 110 indexed citations

Giunta, Cecilia, Nursel Elçioğlu, Beate Albrecht, et al.. (2008). Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13. The American Journal of Human Genetics. 82(6). 1290–1305. 149 indexed citations

Giunta, Cecilia, Céline Chambaz, Marina Pedemonte, Sara Scapolan, & Beat Steinmann. (2008). The arthrochalasia type of Ehlers–Danlos syndrome (EDS VIIA and VIIB): The diagnostic value of collagen fibril ultrastructure. American Journal of Medical Genetics Part A. 146A(10). 1341–1346. 24 indexed citations

Yam, Gary Hin‐Fai, N. U. Bosshard, Christian Zuber, Beat Steinmann, & Jürgen Roth. (2006). Pharmacological chaperone corrects lysosomal storage in Fabry disease caused by trafficking-incompetent variants. American Journal of Physiology-Cell Physiology. 290(4). C1076–C1082. 107 indexed citations

Mátyás, Gábor, Thierry Carrel, Daniela Baumgartner, et al.. (2006). Identification and in silico analyses of novelTGFBR1 andTGFBR2 mutations in Marfan syndrome-related disorders. Human Mutation. 27(8). 760–769. 82 indexed citations

10.

Baumgärtner, Christian, Gábor Mátyás, Beat Steinmann, et al.. (2005). A bioinformatics framework for genotype–phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations. Journal of Biomedical Informatics. 39(2). 171–183. 9 indexed citations

11.

Santer, René, Georg Hillebrand, Beat Steinmann, & Jürgen Schaub. (2003). Intestinal glucose transport: Evidence for a membrane traffic–based pathway in humans. Gastroenterology. 124(1). 34–39. 48 indexed citations

12.

Wenstrup, Richard, Jane B. Florer, Marcia Willing, et al.. (2000). COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS. The American Journal of Human Genetics. 66(6). 1766–1776. 91 indexed citations

13.

Lam, Jason T., Martı́n G. Martı́n, Eric Turk, et al.. (1999). Missense mutations in SGLT1 cause glucose–galactose malabsorption by trafficking defects. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1453(2). 297–303. 52 indexed citations

14.

Rossi, Antonio, Ilkka Kaitila, William R. Wilcox, et al.. (1998). Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: Relationship to clinical severity and indications on the role of intracellular sulfate production. Matrix Biology. 17(5). 361–369. 52 indexed citations

15.

Superti‐Furga, Andrea, Johanna Hästbacka, William R. Wilcox, et al.. (1996). Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene. Nature Genetics. 12(1). 100–102. 167 indexed citations

16.

Royce, Peter M. & Beat Steinmann. (1993). Connective tissue and its heritable disorders : molecular, genetic, and medical aspects. 380 indexed citations

17.

Rao, Velidi H., Peter M. Royce, & Beat Steinmann. (1993). Normal Production, Nature, and Extent of Intracellular Degradation of Newly Synthesized Collagen in Fibroblasts from a Patient with Prolidase Deficiency. Connective Tissue Research. 29(1). 23–30. 8 indexed citations

18.

Gitzelmann, R, Beat Steinmann, & P. Tuchschmid. (1989). Patients with hereditary fructose intolerance have normal erythrocyte aldolase activity. Clinica Chimica Acta. 181(2). 163–166. 2 indexed citations

19.

Royce, Peter M. & Beat Steinmann. (1988). Lysyl Oxidase in Osteogenesis Imperfecta and Marfan's Syndrome. Collagen and Related Research. 8(2). 183–184. 3 indexed citations

20.

Steinmann, Beat, Andrea Superti‐Furga, & Peter M. Royce. (1988). Imperfect Collagenesis in Osteogenesis Imperfecta The Consequences of Cysteine‐Glycine Substitutions upon Collagen Structure and Metabolism^a. Annals of the New York Academy of Sciences. 543(1). 47–61. 11 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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