J Spranger

1.5k citations

22 papers · 936 indexed · 1 hit paper · h-index 12

Impact in

Genetics top 5%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
Immunology and Allergy top 5%
- Cell Adhesion Molecules Research

Papers in

Anatomy 1
Rheumatology 7
- Glycogen Storage Diseases and Myoclonus 2

Co-authors: Bernhard Zabel Andrea Superti‐Furga Sheila Unger Gen Nishimura Ravi Savarirayan Geert Mortier Christine M Hall Valérie Cormier‐Daire
Journals: Human Mutation (1 paper)European Journal of Pediatrics (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren (1 paper)The Lancet (1 paper)
Partner nations: Switzerland Germany United Kingdom

In The Last Decade

J Spranger

22 papers receiving 905 citations

Hit Papers

align trajectories log scale

Nosology and classification of genetic skeletal disorders: 2010 revision 2011 · 450 citations

Peers

Countries citing papers authored by J Spranger

Since Specialization

Citations

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

Fields of papers citing papers by J Spranger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside J Spranger, 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 J Spranger Line = papers co-authored together J Spranger links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Hyperostosis in siblings South African Medical Journal ·J Spranger, I. A. Englezos	2016	2
2	TRPV4‐associated skeletal dysplasias American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Gen Nishimura, Ekkehart Lausch, Ravi Savarirayan, Masahiro Shiba, J Spranger, Bernhard Zabel, Shiro Ikegawa, Andrea Superti‐Furga, Sheila Unger	2012	64
3	Nosology and classification of genetic skeletal disorders: 2010 revision American Journal of Medical Genetics Part A ·Matthew L. Warman, Valérie Cormier‐Daire, Christine M Hall, Deborah Krakow, Ralph Lachman, Martine LeMerrer, Geert Mortier, Stefan Mundlos, Gen Nishimura, David L. Rimoin, Stephen P. Robertson, Ravi Savarirayan, David Sillence, J Spranger, Sheila Unger, Bernhard Zabel, Andrea Superti‐Furga Hit paper breakdown →	2011	450
4	Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7‐year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution Human Mutation ·Gail C. Jackson, García Cabrera, Jacqueline Taylor, Geert Mortier, J Spranger, Bernhard Zabel, Martine Le Merrer, Valérie Cormier‐Daire, Christine M Hall, Amaka C Offiah, Michael Wright, Ravi Savarirayan, Gen Nishimura, Simon Ramsden, Rob Elles, Luisa Bonafé, Andrea Superti‐Furga, Sheila Unger, Andreas Zankl, Michael D. Briggs	2011	81
5	Patterns of postural asymmetry in infants: a standardized video-based analysis European Journal of Pediatrics ·Heike Philippi, Andreas Faldum, Ana María Núñez-Gaytán, Holger Bergmann, Katharina Bauer, Jehad Hassan Alkhalaf, J Spranger	2005	20
6	Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies American Journal of Medical Genetics Part A ·Andreas Zankl, Luitgard M. Neumann, T Athay, Peter G. J. Nikkels, Connie Schrander‐Stumpel, Geert Mortier, Heymut Omran, Michael Wright, Katja Hilbert, Luisa Bonafé, J Spranger, Bernhard Zabel, Andrea Superti‐Furga	2005	39
7	A disorder resembling pseudoachondroplasia but without COMP mutation American Journal of Medical Genetics Part A ·J Spranger, Bernhard Zabel, Jason Kennedy, Gail C. Jackson, Michael D. Briggs	2004	3
8	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
9	Pattern recognition in bone dysplasias. PubMed ·J Spranger	1985	37
10	Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family. PubMed ·J. Gehler, Shengao Yi, D. U. Mmadu, J. Hartmann, J Spranger	1981	13
11	[Does dietary phosphate change the neurophysiologic functions and behavioral signs of hyperkinetic and impulsive children?]. PubMed ·A. Faiz, M. H. Staatz, J Spranger	1980	1
12	Quantitation of muscle cells of the ureter. PubMed ·J Spranger	1977	6
13	[Ring chromosome 18]. PubMed ·J. Kunze, J Spranger, M Tolksdorf	1976	1
14	Difficulties in the classification of the epiphyseal dysplasias. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Sarbeswar Haldar, Rimoin Dl, Judith G. Hall, K. Kozlowski, 裕彦斎野, 祝平, J Spranger	1975	5
15	[Diagnosis and differential diagnosis of Morquio's disease]. PubMed ·J Spranger, Lilis Nur Hayati	1969	2
16	[Dysosteosclerosis--a special form of generalized osteosclerosis]. PubMed ·J Spranger, 靳鑫, Luke P. Sturtevant, H. ‐R. Wiedemann	1968	21
17	Die Dysosteosklerose — eine Sonderform der generalisierten Osteosklerose RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren ·J Spranger, P. Harris, L.G. Gorenkova, H. ‐R. Wiedemann	1968	27
18	Dysplasia spondyloepiphysaria congenital J Spranger	1966	29
19	[Studies on mucopolysaccharide excretion in healthy children and in those with dysostosis]. PubMed ·J Spranger, Wiedemann Hr, (unknown), (unknown), (unknown), (unknown)	1966	2
20	DYSPLASIA SPONDYLOEPIPHYSARIA CONGENITA The Lancet ·J Spranger, H. ‐R. Wiedemann	1966	31

About J Spranger

J Spranger is a scholar working on Anatomy, Rheumatology, Developmental Biology, Genetics and Toxicology, having authored 22 papers that have together received 936 indexed citations. Recurring topics across this work include Bone health and treatments (6 papers), Connective tissue disorders research (6 papers), Dermatological and Skeletal Disorders (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Pleural and Pulmonary Diseases (2 papers), Lysosomal Storage Disorders Research (2 papers), Ubiquitin and proteasome pathways (2 papers) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (589 citations), Immunology and Allergy (93 citations), Rheumatology (189 citations), Developmental Biology (20 citations) and Sensory Systems (41 citations). J Spranger has collaborated with scholars based in Switzerland, Germany and United Kingdom. Frequent co-authors include Bernhard Zabel, Andrea Superti‐Furga, Sheila Unger, Gen Nishimura, Ravi Savarirayan, Geert Mortier, Christine M Hall, Valérie Cormier‐Daire, H. ‐R. Wiedemann and Stephen P. Robertson. Their work appears in journals such as Human Mutation, European Journal of Pediatrics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren and The Lancet.

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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