Sten Jagell

910 total citations
39 papers, 686 citations indexed

About

Sten Jagell is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Sten Jagell has authored 39 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Cell Biology, 19 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in Sten Jagell's work include Skin and Cellular Biology Research (25 papers), Dermatological and Skeletal Disorders (14 papers) and Connective tissue disorders research (5 papers). Sten Jagell is often cited by papers focused on Skin and Cellular Biology Research (25 papers), Dermatological and Skeletal Disorders (14 papers) and Connective tissue disorders research (5 papers). Sten Jagell collaborates with scholars based in Sweden, United States and Türkiye. Sten Jagell's co-authors include Gösta Holmgren, J. Heijbel, S. Lidén, W. Scott Polland, O Sandgren, S. E. G. Nilsson, Anna Sillén, Claes Wadelius, Karl‐Henrik Gustavson and P.‐Å. Hofer and has published in prestigious journals such as Nature Genetics, Neurology and The Journal of Pediatrics.

In The Last Decade

Sten Jagell

38 papers receiving 644 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sten Jagell Sweden 15 383 329 181 63 51 39 686
Marvin E. Chernosky United States 18 130 0.3× 154 0.5× 434 2.4× 18 0.3× 249 4.9× 42 914
Patricia S. Walker United States 13 89 0.2× 421 1.3× 124 0.7× 58 1.1× 22 982
Jennifer J. Schoch United States 15 45 0.1× 161 0.5× 42 0.2× 15 0.2× 112 2.2× 70 685
M.L. Price United Kingdom 12 67 0.2× 36 0.1× 52 0.3× 14 0.2× 53 1.0× 29 385
Samira M. Osailan United Kingdom 11 64 0.2× 132 0.4× 18 0.1× 117 1.9× 15 0.3× 18 600
Leonie C. Jacobs Netherlands 11 189 0.5× 78 0.2× 60 0.3× 4 0.1× 25 0.5× 15 457
M Cossu Italy 13 51 0.1× 134 0.4× 13 0.1× 42 0.7× 20 0.4× 44 468
Giuseppe Hautmann Italy 12 264 0.7× 80 0.2× 19 0.1× 3 0.0× 97 1.9× 19 660
Susan H. Black United States 20 69 0.2× 275 0.8× 505 2.8× 26 0.5× 41 1.2k
Frederick A. Horner United States 10 100 0.3× 119 0.4× 63 0.3× 64 1.3× 16 379

Countries citing papers authored by Sten Jagell

Since Specialization
Citations

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

Fields of papers citing papers by Sten Jagell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sten Jagell

This figure shows the co-authorship network connecting the top 25 collaborators of Sten Jagell. A scholar is included among the top collaborators of Sten Jagell 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 Sten Jagell. Sten Jagell 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.
Heijbel, J. & Sten Jagell. (2009). Spastic paraplegia, glaucoma and mental retardation - in three sibilings. A new genetic syndrome. Hereditas. 94(2). 203–207.
2.
Annerén, Göran, Karl‐Henrik Gustavson, & Sten Jagell. (2008). Partial trisomy for the distal part of chromosome 22 (22q12→qter) in a mentally retarded girl with congenital birth defects. Hereditas. 100(1). 115–119. 1 indexed citations
3.
Eeg‐Olofsson, Orvar, Hannu Kalimo, Karin Edebol Eeg‐Olofsson, et al.. (2007). Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family. European Journal of Paediatric Neurology. 12(5). 404–407. 2 indexed citations
4.
Sillén, Anna, Anders Alderborn, Maritta Hellström Pigg, Sten Jagell, & Claes Wadelius. (2004). Detailed Genetic and Physical Mapping in the Sjögren-Larsson Syndrome Gene Region in 17p11.2. Hereditas. 128(3). 245–250. 4 indexed citations
5.
Jagell, Sten. (1998). IVIG in Landau-Kleffner syndrome.. PubMed. 19(5). 399–399. 14 indexed citations
6.
Sillén, Anna, I. Anton‐Lamprecht, Cornelia Kraus, et al.. (1998). Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome. Human Mutation. 12(6). 377–384. 38 indexed citations
7.
Jagell, Sten, et al.. (1997). A missense mutation in the FALDH gene identified in Sj�gren-Larsson syndrome patients originating from the northern part of Sweden. Human Genetics. 100(2). 201–203. 26 indexed citations
8.
Pigg, Maritta Hellström, Sten Jagell, Anna Sillén, et al.. (1994). The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association. Nature Genetics. 8(4). 361–364. 33 indexed citations
9.
Wester, Per, et al.. (1991). Monoaminergic dysfunction in Sjögren-Larsson syndrome. Molecular and Chemical Neuropathology. 15(1). 13–28. 9 indexed citations
10.
Rizzo, William B., Debra A. Craft, Susan H. Black, et al.. (1989). Sjögren-Larsson syndrome: Inherited defect in the fatty alcohol cycle. The Journal of Pediatrics. 115(2). 228–234. 53 indexed citations
11.
Iselius, Lennart & Sten Jagell. (1989). Sjögren‐Larsson syndrome in Sweden: distribution of the gene. Clinical Genetics. 35(4). 272–275. 8 indexed citations
12.
Heijbel, J., et al.. (1987). Malocclusions in physically and/or mentally handicapped children.. PubMed. 11(3). 103–19. 33 indexed citations
13.
Holmgren, Gösta, Sten Jagell, Bengt Lagerkvist, & Ingrid Nordenson. (1984). Pair of Siblings with Diastrophic Dysplasia and E Trisomy Mosaicism. Human Heredity. 34(4). 266–268. 3 indexed citations
14.
Jagell, Sten, et al.. (1983). Oral conditions in Sjögren-Larsson syndrome.. PubMed. 7(4). 141–51. 7 indexed citations
15.
Jagell, Sten & P.‐Å. Hofer. (1982). Sjögren-Larsson syndrome: microscopic and scanning electron microscopic findings in replicas of the skin. Acta Dermato Venereologica. 62(5). 397–400. 4 indexed citations
16.
Jagell, Sten & S. Lidén. (1982). Ichthyosis in the Sjögren‐Larsson syndrome. Clinical Genetics. 21(4). 243–252. 44 indexed citations
17.
Jagell, Sten. (1981). Sjögren-Larsson syndrome in Sweden : an epidemiological, genetic, clinical and biochemical study. KTH Publication Database DiVA (KTH Royal Institute of Technology). 7 indexed citations
18.
Holmgren, Gösta, et al.. (1981). Urinary amino acids and organic acids in the Sjögren‐Larsson syndrome. Clinical Genetics. 20(1). 64–66. 3 indexed citations
19.
Probst, F. P., Sten Jagell, & J. Heijbel. (1981). Cranial CT in the Sj�gren-Larsson syndrome. Neuroradiology. 21(2). 101–105. 6 indexed citations
20.
Gustavson, K. H., Sten Jagell, Hans K son Blomquist, & Ingrid Nordenson. (1981). Microcephaly, Mental Retardation and Chromosomal Aberrations in a Girl Following Radiation Therapy During Late Fetal Life. Acta Radiologica Oncology. 20(3). 209–212. 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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