E Rupprecht

500 total citations
53 papers, 296 citations indexed

About

E Rupprecht is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Surgery. According to data from OpenAlex, E Rupprecht has authored 53 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Pulmonary and Respiratory Medicine and 12 papers in Surgery. Recurrent topics in E Rupprecht's work include Congenital Diaphragmatic Hernia Studies (6 papers), Connective tissue disorders research (6 papers) and Bone health and treatments (6 papers). E Rupprecht is often cited by papers focused on Congenital Diaphragmatic Hernia Studies (6 papers), Connective tissue disorders research (6 papers) and Bone health and treatments (6 papers). E Rupprecht collaborates with scholars based in Germany, Netherlands and France. E Rupprecht's co-authors include Peter Lorenz, Ralf Knöfler, Jürgen Dinger, R Schwarze, Dirk Müller, S. Gehrisch, Gabriele Siegert, P Wunderlich, G Weissbach and Georg Klaus Hinkel and has published in prestigious journals such as Journal of Molecular Medicine, Acta Paediatrica and The Pediatric Infectious Disease Journal.

In The Last Decade

E Rupprecht

47 papers receiving 274 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E Rupprecht Germany 10 85 76 75 73 57 53 296
M. D. Yohannan Saudi Arabia 7 85 1.0× 10 0.1× 64 0.9× 10 0.1× 74 1.3× 14 279
Julie Wohrley United States 7 249 2.9× 20 0.3× 270 3.6× 74 1.0× 91 1.6× 9 484
Shivanshu Singh India 12 78 0.9× 21 0.3× 101 1.3× 23 0.3× 12 0.2× 32 292
Sushma Vashisht India 10 93 1.1× 18 0.2× 253 3.4× 27 0.4× 7 0.1× 44 347
Henry B. So United States 11 73 0.9× 56 0.7× 324 4.3× 6 0.1× 12 0.2× 20 467
Alla Godelman United States 10 233 2.7× 13 0.2× 99 1.3× 31 0.4× 9 0.2× 19 381
J Conard France 8 45 0.5× 72 0.9× 99 1.3× 117 1.6× 281 4.9× 29 458
P Chaumont France 10 87 1.0× 23 0.3× 194 2.6× 9 0.1× 5 0.1× 40 306
M. Baldt Austria 8 85 1.0× 11 0.1× 178 2.4× 131 1.8× 8 0.1× 19 360
Iman Ragab Egypt 9 58 0.7× 26 0.3× 53 0.7× 7 0.1× 114 2.0× 37 269

Countries citing papers authored by E Rupprecht

Since Specialization
Citations

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

Fields of papers citing papers by E Rupprecht

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Rupprecht

This figure shows the co-authorship network connecting the top 25 collaborators of E Rupprecht. A scholar is included among the top collaborators of E Rupprecht 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 E Rupprecht. E Rupprecht 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.
Laaß, Martin W., Anna Jauch, Gabriele Hahn, et al.. (2004). Tuberous sclerosis and polycystic kidney disease in a 3-month-old infant. Pediatric Nephrology. 19(6). 602–608. 21 indexed citations
2.
Rupprecht, E, et al.. (2003). Osteonecrosis after meningococcemia and disseminated intravascular coagulation. The Pediatric Infectious Disease Journal. 22(11). 1021–1022. 5 indexed citations
3.
Sobottka, Stephan B., Angela Huebner, Markus Haase, et al.. (2001). Albright’s Hereditary Osteodystrophy Associated with Cerebellar Pilocytic Astrocytoma: Coincidence or Genetic Relationship?. Hormone Research in Paediatrics. 55(4). 196–200. 4 indexed citations
4.
Knöfler, Ralf, et al.. (1999). Clinical importance of prothrombotic risk factors in pediatric patients with malignancy – impact of central venous lines. European Journal of Pediatrics. 158(S3). S147–S150. 54 indexed citations
5.
Uhlmann, D., et al.. (1998). Spondyloenchondrodysplasia: several phenotypes - the same syndrome. Pediatric Radiology. 28(8). 617–621. 12 indexed citations
6.
Dinger, Jürgen, R Schwarze, & E Rupprecht. (1997). Radiological changes after therapeutic use of surfactant in infants with respiratory distress syndrome. Pediatric Radiology. 27(1). 26–31. 16 indexed citations
7.
Schrander‐Stumpel, C. T. R. M., Peter Meinecke, E Rupprecht, et al.. (1996). Cerebro-costo-mandibular syndrome: a follow-up study with 6 patients.. PubMed. 7(1). 71–2. 3 indexed citations
8.
Paditz, Ekkehart, Marianne E. Schläfke, Thorsten Schäfer, et al.. (1995). Nocturnal ventilation by nasal mask in an 8‐year‐old girl with thoracic scoliosis, hypercapnic respiratory failure, and cor pulmonale. Pediatric Pulmonology. 19(1). 60–65. 2 indexed citations
9.
Lorenz, Peter, et al.. (1990). The craniodigital syndrome of Scott: Report of a second family. American Journal of Medical Genetics. 37(2). 224–226. 6 indexed citations
10.
Lorenz, Peter, et al.. (1990). An unusual type of acrocephalosyndactyly with bilateral parietooccipital “encephalocele”, micropenis, and severe mental retardation. American Journal of Medical Genetics. 36(3). 265–268. 18 indexed citations
11.
Lorenz, Peter & E Rupprecht. (1990). Spondylocostal dysostosis: Dominant type. American Journal of Medical Genetics. 35(2). 219–221. 20 indexed citations
12.
Hinkel, Georg Klaus & E Rupprecht. (1989). Hemihypertrophie als Leitsymptom einer Dysplasia epiphysealis hemimelica. Klinische Pädiatrie. 201(1). 58–62. 3 indexed citations
13.
Rupprecht, E, et al.. (1989). [Proteus syndrome. A contribution to the further differential diagnosis of congenital local gigantism].. PubMed. 43(5-6). 473–82. 1 indexed citations
14.
Wunderlich, P, et al.. (1985). Chest radiographs of near-drowned children. Pediatric Radiology. 15(5). 297–299. 10 indexed citations
15.
Rupprecht, E, et al.. (1978). [Contribution to the treatment of idiopathic pulmonary hemosiderosis by means of immunosuppressive agents].. PubMed. 17(4). 213–20. 2 indexed citations
16.
Rupprecht, E, et al.. (1977). [Unilateral aplasia and hypoplasia of pulmonary artery in childhood (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 147(1). 57–72. 1 indexed citations
17.
Rupprecht, E, et al.. (1974). [Morphological and clinical contribution to lethal congenital hypophosphatasia].. PubMed. 42(4). 148–55. 2 indexed citations
18.
Rupprecht, E. (1973). [Pneumothorax and pneumomediastinum in the newborn infant].. PubMed. 41(9). 383–98. 2 indexed citations
19.
Wunderlich, P, et al.. (1967). �ber eine t�dliche Lungenkomplikation der infekti�sen Mononucleose. European Journal of Pediatrics. 98(1). 95–106. 1 indexed citations
20.
Rupprecht, E, et al.. (1963). Untersuchungen der Atemmechanik bei Silikose unter besonderer Berücksichtigung des obstruktiven Syndroms. Respiration. 20(1). 19–43. 4 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026