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, Petros Tsipouras, Peter Beighton, 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

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 Peter Beighton, Anne De Paepe et al. American Journal of Medical Genetics profile →

Peers

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

#	Work	Indexed citations
1	Variant filtering, digenic variants, and other challenges in clinical sequencing: a lesson from fibrillinopathies 2019 ·Clinical Genetics ·Arash Najafi, (unknown), Janine Meienberg, Marianne Rohrbach, Beat Steinmann, Gábor Mátyás	18
2	Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers–Danlos syndrome 2019 ·Cardiovascular Research ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Erik N.T.P. Bakker, Ed VanBavel, Urs Ziegler, Thierry Carrel, Beat Steinmann, Steffen M. Zeisberger, Janine Meienberg, Gábor Mátyás	28
3	PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome 2018 ·Heather N. Yeowell, Beat Steinmann	13
4	Promotion of vesicular zinc efflux by ZIP13 and its implications for spondylocheiro dysplastic Ehlers–Danlos syndrome 2012 ·Proceedings of the National Academy of Sciences ·Jeeyon Jeong, Joel M. Walker, Fudi Wang, J. Genevieve Park, Amy E. Palmer, Cecilia Giunta, Marianne Rohrbach, Beat Steinmann, David Eide	91
5	Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency 2010 ·European Journal of Human Genetics ·Janine Meienberg, Marianne Rohrbach, Stefan Neuenschwander, Katharina Spanaus, Cecilia Giunta, (unknown), (unknown), (unknown), Stephan Regenass, Andrea Patrignani, Silvia Azzarello‐Burri, Bernhard Steiner, Anders O.H. Nygren, Thierry Carrel, Beat Steinmann, Gábor Mátyás	28
6	Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome 2009 ·The American Journal of Human Genetics ·Munis Dündar, Thomas Müller, Qi Zhang, Jing Pan, Beat Steinmann, Julia Vodopiutz, Robert Gruber, Tohru Sonoda, Birgit Krabichler, Gerd Utermann, Jacques Baenziger, Lijuan Zhang, Andreas Janecke	110
7	Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13 2008 ·The American Journal of Human Genetics ·Cecilia Giunta, Nursel Elçioğlu, Beate Albrecht, Georg Eich, Céline Chambaz, Andreas Janecke, Heather N. Yeowell, MaryAnn Weis, David R. Eyre, Marius Kraenzlin, Beat Steinmann	149
8	Diagnostic power of aortic elastic properties in young patients with Marfan syndrome 2005 ·Journal of Thoracic and Cardiovascular Surgery ·Daniela Baumgartner, Christian Baumgärtner, Gábor Mátyás, Beat Steinmann, Judith Löffler‐Ragg, (unknown), Ulrich Schweigmann, I. Baldissera, B. Frischhut, John Hess, I Hammerer	50
9	The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe 2005 ·Human Mutation ·René Santer, Johannes Rischewski, (unknown), (unknown), Sonja Schneppenheim, K Baerlocher, Alfried Kohlschütter, Ania C. Muntau, Hans‐Georg Posselt, Beat Steinmann, Reinhard Schneppenheim	46
10	A bioinformatics framework for genotype–phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations 2005 ·Journal of Biomedical Informatics ·Christian Baumgärtner, Gábor Mátyás, Beat Steinmann, Martin Eberle, Jörg Stein, Daniela Baumgartner	9
11	Intestinal glucose transport: Evidence for a membrane traffic–based pathway in humans 2003 ·Gastroenterology ·René Santer, Georg Hillebrand, Beat Steinmann, Jürgen Schaub	48
12	Missense mutations in SGLT1 cause glucose–galactose malabsorption by trafficking defects 1999 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jason T. Lam, Martı́n G. Martı́n, Eric Turk, Bruce A. Hirayama, N. U. Bosshard, Beat Steinmann, Ernest M. Wright	52
13	Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 breakdown → 1998 ·American Journal of Medical Genetics ·Peter Beighton, Anne De Paepe, Beat Steinmann, Petros Tsipouras, Richard Wenstrup	1192
14	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 1998 ·Matrix Biology ·Antonio Rossi, Ilkka Kaitila, William R. Wilcox, David L. Rimoin, Beat Steinmann, Giuseppe Cetta, Andrea Superti‐Furga	52
15	Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene 1996 ·Nature Genetics ·Andrea Superti‐Furga, Johanna Hästbacka, William R. Wilcox, Daniel H. Cohn, Hans J. van der Harten, Antonio Rossi, Nenad Blau, David L. Rimoin, Beat Steinmann, Eric S. Lander, R Gitzelmann	167
16	Genetic counselling on brittle grounds: Recurring osteogenesis imperfecta due to parental mosaicism for a dominant mutation 1995 ·European Journal of Pediatrics ·Michael Raghunath, Katrina Mackay, Raymond Dalgleish, Beat Steinmann	26
17	Connective tissue and its heritable disorders : molecular, genetic, and medical aspects 1993 ·Peter M. Royce, Beat Steinmann	380
18	Long‐term follow‐up of two sibs with Larsen syndrome possibly due to parental germ‐line mosaicism 1993 ·American Journal of Medical Genetics ·(unknown), Jack G. Rabinowitz, Beat Steinmann, Kurt Hirschhorn	15
19	Normal Production, Nature, and Extent of Intracellular Degradation of Newly Synthesized Collagen in Fibroblasts from a Patient with Prolidase Deficiency 1993 ·Connective Tissue Research ·Velidi H. Rao, Peter M. Royce, Beat Steinmann	8
20	Lysyl Oxidase in Osteogenesis Imperfecta and Marfan's Syndrome 1988 ·Collagen and Related Research ·Peter M. Royce, Beat Steinmann	3

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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