B Steinmann

6.9k citations

105 papers · 4.9k indexed · 1 hit paper · h-index 38

Impact in

Genetics top 0.5%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders

Papers in ⓘ

Rheumatology 36
- Dupuytren's Contracture and Treatments 11
- Bone and Dental Protein Studies 10
Genetics 59
- Connective tissue disorders research 50
- Dermatological and Skeletal Disorders 15

Co-authors: R Gitzelmann (29 shared papers)Andrea Superti‐Furga (20 shared papers)Peter Brückner (3 shared papers)Margret Schlumpf (1 shared paper)W. Lichtensteiger (1 shared paper)Peter H. Byers (4 shared papers)René Santer (4 shared papers)J. Schaub (3 shared papers)
Journals: Journal of Biological Chemistry (15 papers)European Journal of Pediatrics (11 papers)Journal of Inherited Metabolic Disease (7 papers)Pediatric Research (5 papers)Journal of Clinical Investigation (3 papers)
Partner nations: Switzerland United States Germany

In The Last Decade

B Steinmann

103 papers receiving 4.7k citations

Hit Papers

align trajectories log scale

In vitro and in vivo estrogenicity of UV screens. 2001 · 685 citations

Peers

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-authors

The 25 scholars most cited alongside B Steinmann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with B Steinmann Line = papers co-authored together B Steinmann links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 105 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	In vitro and in vivo estrogenicity of UV screens. Environmental Health Perspectives ·Margret Schlumpf, Beata Cotton, M Conscience, Vreni Haller, B Steinmann, W. Lichtensteiger Hit paper breakdown →	2001	685
2	Cyclosporin A slows collagen triple-helix formation in vivo: indirect evidence for a physiologic role of peptidyl-prolyl cis-trans-isomerase. Journal of Biological Chemistry ·B Steinmann, Peter Brückner, Andrea Superti‐Furga	1991	254
3	Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5 New England Journal of Medicine ·Petros Tsipouras, R. Del Mastro, M. Sarfarazi, B Lee, Emilia Vitale, A. H. Child, Maurice Godfrey, Richard B. Devereux, D. Hewett, B Steinmann, (unknown), (unknown), (unknown), (unknown)	1992	205
4	Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype. Journal of Clinical Investigation ·Martin R. Pollak, Yah-Huei Chou, Stephen J. Marx, B Steinmann, David E.C. Cole, Maria Luisa Brandi, Socrates E. Papapoulos, Fred H. Menko, Geoffrey N. Hendy, Edward M. Brown	1994	197
5	Cysteine in the triple-helical domain of one allelic product of the alpha 1(I) gene of type I collagen produces a lethal form of osteogenesis imperfecta. Journal of Biological Chemistry ·B Steinmann, V H Rao, A. Vogel, Peter Brückner, R Gitzelmann, Peter H. Byers	1984	172
6	Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen. Journal of Biological Chemistry ·Andrea Superti‐Furga, E Gugler, R Gitzelmann, B Steinmann	1988	151
7	In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia. Journal of Clinical Investigation ·Ming Bai, Simon H. S. Pearce, Olga Kifor, Sweety Trivedi, U. Stauffer, Rajesh V. Thakker, Edward M. Brown, B Steinmann	1997	144
8	Abnormal collagen fibril structure in the gravis form (type I) of Ehlers-Danlos syndrome. PubMed ·A. Vogel, K A Holbrook, B Steinmann, R Gitzelmann, Peter H. Byers	1979	136
9	Identification of a mutation that causes exon skipping during collagen pre-mRNA splicing in an Ehlers-Danlos syndrome variant. Journal of Biological Chemistry ·Dominique Weil, Michael P. Bernard, Nicholas J. Combates, Markus Wirtz, David W. Hollister, B Steinmann, Francesco Ramirez	1988	122
10	Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VII. Journal of Biological Chemistry ·B Steinmann, Leena Tuderman, Leena Peltonen, George R. Martin, V.A. McKusick, Darwin J. Prockop	1980	122
11	Mass fragmentography of dopamine and 6-hydroxydopamine Journal of Chromatography A ·H.‐Ch. Curtius, M. Wolfensberger, B Steinmann, U. Redweik, J. Siegfried	1974	117
12	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 ·René Santer, Reinhard Schneppenheim, Diane E. Suter, J. Schaub, B Steinmann	1998	116
13	Lethal osteogenesis imperfecta resulting from a single nucleotide change in one human pro alpha 1(I) collagen allele. Proceedings of the National Academy of Sciences ·Daniel H. Cohn, Peter H. Byers, B Steinmann, Richard Gelinas	1986	100
14	Fanconi-Bickel Syndrome - A Congenital Defect of Facilitative Glucose Transport Current Molecular Medicine ·René Santer, B Steinmann, J. Schaub	2002	91
15	Recessively inherited multiple epiphyseal dysplasia with normal stature, club foot, and double layered patella caused by a DTDST mutation. PubMed ·A Superti‐Furga, Luitgard M. Neumann, T Riebel, Georg Eich, B Steinmann, J Spranger, J Kunze	1999	89
16	Pyridoxal 5′‐phosphate may be curative in early‐onset epileptic encephalopathy Journal of Inherited Metabolic Disease ·Georg F. Hoffmann, Bernhard Schmitt, Marisa Windfuhr, Nicola Wagner, H. Strehl, Soyhan Bağcı, Axel R. Franz, Philippa B. Mills, Peter T. Clayton, Matthias R. Baumgartner, B Steinmann, Thomas Bast, Nicole I. Wolf, Johannes Zschocke	2006	87
17	Cross-linking of the dermo-epidermal junction of skin regenerating from keratinocyte autografts. Anchoring fibrils are a target for tissue transglutaminase. Journal of Clinical Investigation ·Michael Raghunath, Bianca Höpfner, Daniel Aeschlimann, Urs Lüthi, Martin Meuli, Stefan Altermatt, Rita Gobet, Leena Bruckner‐Tuderman, B Steinmann	1996	86
18	Temperature-dependent expression of a collagen splicing defect in the fibroblasts of a patient with Ehlers-Danlos syndrome type VII Journal of Biological Chemistry ·Dominique Weil, Marina D’Alessio, Francesco Ramirez, B Steinmann, Markus Wirtz, R W Glanville, David W. Hollister	1989	84
19	Molecular analysis of aldolase B genes in hereditary fructose intolerance The Lancet ·Nicholas C.P. Cross, Timothy M. Cox, R. de Franchis, Gianfranco Sebastio, C. Dazzo, Dean R. Tolan, C. Grégori, M Odièvre, M. Vidailhet, Valentino Romano, Giovanna Mascali, Corrado Romano, S Musumeci, B Steinmann, R Gitzelmann	1990	82
20	New insights into the performance of human whole-exome capture platforms Nucleic Acids Research ·Janine Meienberg, K. Žerjavic, Irene Keller, Michał Okoniewski, Andrea Patrignani, Katja Ludin, Zhenyu Xu, B Steinmann, Thierry Carrel, Benno Röthlisberger, Ralph Schlapbach, Rémy Bruggmann, Gábor Mátyás	2015	76

About B Steinmann

B Steinmann is a scholar working on Rheumatology, Genetics, Clinical Biochemistry, Immunology and Allergy and Developmental Biology, having authored 105 papers that have together received 4.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (50 papers), Dermatological and Skeletal Disorders (15 papers), Metabolism and Genetic Disorders (14 papers), Dupuytren's Contracture and Treatments (11 papers), Bone and Dental Protein Studies (10 papers), Bone health and treatments (8 papers), Cell Adhesion Molecules Research (6 papers) and Amino Acid Enzymes and Metabolism (6 papers). The work is most often cited by research in Genetics (2.0k citations), Clinical Biochemistry (466 citations), Rheumatology (871 citations), Dermatology (399 citations) and Nephrology (306 citations). B Steinmann has collaborated with scholars based in Switzerland, United States and Germany. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, European Journal of Pediatrics, Journal of Inherited Metabolic Disease, Pediatric Research and Journal of Clinical Investigation.

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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