Ulpu Seppänen

1.0k total citations
20 papers, 700 citations indexed

About

Ulpu Seppänen is a scholar working on Urology, Genetics and Surgery. According to data from OpenAlex, Ulpu Seppänen has authored 20 papers receiving a total of 700 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Urology, 7 papers in Genetics and 6 papers in Surgery. Recurrent topics in Ulpu Seppänen's work include Urological Disorders and Treatments (8 papers), Pediatric Urology and Nephrology Studies (5 papers) and Connective tissue disorders research (4 papers). Ulpu Seppänen is often cited by papers focused on Urological Disorders and Treatments (8 papers), Pediatric Urology and Nephrology Studies (5 papers) and Connective tissue disorders research (4 papers). Ulpu Seppänen collaborates with scholars based in Finland, Germany and Australia. Ulpu Seppänen's co-authors include Tytti Tamminen-Möbius, H Olbing, Kl.-D. Ebel, Riitta Herva, I. Wikstad, J. M. Smellie, Rune Sixt, Ingemar Claësson, Robert L. Lebowitz and John M. Opitz and has published in prestigious journals such as Radiology, The American Journal of Human Genetics and The Journal of Urology.

In The Last Decade

Ulpu Seppänen

20 papers receiving 662 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ulpu Seppänen Finland 11 357 326 178 131 115 20 700
V Latin Croatia 12 263 0.7× 74 0.2× 63 0.4× 73 0.6× 93 0.8× 27 705
B. Gasser France 14 223 0.6× 93 0.3× 39 0.2× 91 0.7× 133 1.2× 48 690
Maximilian Stehr Germany 18 207 0.6× 315 1.0× 48 0.3× 46 0.4× 122 1.1× 66 843
Iêda M. Orioli Brazil 12 164 0.5× 141 0.4× 51 0.3× 694 5.3× 121 1.1× 17 1.1k
Dieter Bettelheim Austria 17 569 1.6× 54 0.2× 68 0.4× 150 1.1× 20 0.2× 66 900
M L Martínez-Frías Spain 10 103 0.3× 44 0.1× 40 0.2× 152 1.2× 48 0.4× 20 459
Sei Kwang Kim South Korea 19 61 0.2× 180 0.6× 91 0.5× 50 0.4× 473 4.1× 67 929
Solveig Nordén‐Lindeberg Sweden 7 310 0.9× 24 0.1× 88 0.5× 64 0.5× 43 0.4× 11 692
Philippe Loget France 16 281 0.8× 58 0.2× 34 0.2× 291 2.2× 24 0.2× 40 749
Claudette Hajaj Gonzalez Brazil 15 207 0.6× 22 0.1× 32 0.2× 196 1.5× 63 0.5× 33 712

Countries citing papers authored by Ulpu Seppänen

Since Specialization
Citations

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

Fields of papers citing papers by Ulpu Seppänen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulpu Seppänen

This figure shows the co-authorship network connecting the top 25 collaborators of Ulpu Seppänen. A scholar is included among the top collaborators of Ulpu Seppänen 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 Ulpu Seppänen. Ulpu Seppänen 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.
Löppönen, Tuija, Jarmo Körkkö, Tuija Lundán, et al.. (2004). Childhood‐onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75‐Cys mutation in procollagen type II gene (COL2A1). Arthritis Care & Research. 51(6). 925–932. 32 indexed citations
2.
Czarny‐Ratajczak, Malwina, Jaana Lohiniva, Piotr Rogala, et al.. (2001). A Mutation in COL9A1 Causes Multiple Epiphyseal Dysplasia: Further Evidence for Locus Heterogeneity. The American Journal of Human Genetics. 69(5). 969–980. 134 indexed citations
3.
Olbing, H, H. Hirche, Olli Koskimies, et al.. (2000). Renal Growth in Children with Severe Vesicoureteral Reflux: 10-year Prospective Study of Medical and Surgical Treatment. Radiology. 216(3). 731–737. 38 indexed citations
4.
Lohiniva, Jaana, Petteri Paassilta, Ulpu Seppänen, et al.. (2000). Splicing mutations in the COL3 domain of collagen IX cause multiple epiphyseal dysplasia. American Journal of Medical Genetics. 90(3). 216–216. 3 indexed citations
5.
Heikkinen, Erkki, et al.. (1999). Congenital pseudarthrosis of the tibia: Treatment and outcome at skeletal maturity in 10 children. Acta Orthopaedica Scandinavica. 70(3). 275–282. 27 indexed citations
6.
Tamminen-Möbius, Tytti, H Olbing, Ingemar Claësson, et al.. (1993). [Radiologic findings in the kidney of children with severe reflux. Five-year comparative study of conservative and surgical treatment].. PubMed. 32(1). 22–9. 8 indexed citations
7.
Tamminen-Möbius, Tytti, Kl.-D. Ebel, Robert L. Lebowitz, et al.. (1992). Cessation of Vesicoureteral Reflux For 5 Years in Infants and Children Allocated to Medical Treatment. The Journal of Urology. 148(5 Part 2). 1662–1666. 134 indexed citations
8.
Olbing, H, Ingemar Claësson, Kl.-D. Ebel, et al.. (1992). Renal Scars and Parenchymal Thinning in Children with Vesicoureteral Reflux: A 5-Year Report of the International Reflux Study in Children (European Branch). The Journal of Urology. 148(5 Part 2). 1653–1656. 123 indexed citations
9.
Järvelin, Marjo‐Riitta, et al.. (1990). Screening of Urinary Tract Abnormalities Among Day and Nightwetting Children. Scandinavian Journal of Urology and Nephrology. 24(3). 181–189. 43 indexed citations
10.
Seppänen, Ulpu, Willy Serlo, & A. -L. Saukkonen. (1987). Valvography in the assessment of hydrocephalus shunt function in children. Neuroradiology. 29(1). 53–57. 11 indexed citations
11.
Pãivänsalo, M., et al.. (1987). Problematic diagnosis of bronchial foreign bodies in children.. PubMed. 40(2). 46–9. 1 indexed citations
12.
Pãivänsalo, M., T Siniluoto, & Ulpu Seppänen. (1986). Cavernous hemangioma of the adrenal gland.. PubMed. 55(3). 168–71. 4 indexed citations
13.
Seppänen, Ulpu. (1986). Perinatal Postmortem Radiography. Acta Radiologica Diagnosis. 27(5). 481–494. 9 indexed citations
14.
Seppänen, Ulpu. (1985). The value of perinatal post-mortem radiography. Experience of 514 cases.. PubMed. 17 Suppl 44. 1–59. 21 indexed citations
15.
Herva, Riitta, Jaakko Leisti, Pertti Kirkinen, et al.. (1985). A lethal autosomal recessive syndrome of multiple congenital contractures. American Journal of Medical Genetics. 20(3). 431–439. 74 indexed citations
16.
Herva, Riitta & Ulpu Seppänen. (1985). Multisynostotic osteodysgenesis. Pediatric Radiology. 15(1). 63–64. 4 indexed citations
17.
Herva, Riitta & Ulpu Seppänen. (1984). Roentgenologic findings of the hydrolethalus syndrome. Pediatric Radiology. 14(1). 41–43. 16 indexed citations
18.
Similä, S, et al.. (1983). Radio-digito-facial dysplasia associated with dwarfism.. PubMed. 38(1). 81–6. 2 indexed citations
19.
Seppänen, Ulpu & Riitta Herva. (1983). Roentgenologic features of the Meckel syndrome. Pediatric Radiology. 13(6). 329–331. 6 indexed citations
20.
Lanning, P, Ulpu Seppänen, Niilo‐Pekka Huttunen, & Matti Uhari. (1979). Prediction of vesico-ureteral reflux in children from intravenous urography films. Clinical Radiology. 30(1). 67–70. 10 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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