Jörg Seidel

1.7k total citations
18 papers, 767 citations indexed

About

Jörg Seidel is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Jörg Seidel has authored 18 papers receiving a total of 767 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Jörg Seidel's work include Metabolism and Genetic Disorders (5 papers), Amino Acid Enzymes and Metabolism (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jörg Seidel is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Amino Acid Enzymes and Metabolism (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jörg Seidel collaborates with scholars based in Germany, United States and France. Jörg Seidel's co-authors include Markus Stümm, Heidemarie Neitzel, Patrick Concannon, Raymonda Varon, Richard A. Gatti, Andrew R. Gennery, Karen Cerosaletti, Yan Dai, Marjorie A. Oettinger and Boris Kysela and has published in prestigious journals such as Molecular Cell, Human Molecular Genetics and Human Mutation.

In The Last Decade

Jörg Seidel

16 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jörg Seidel Germany 8 505 284 118 112 93 18 767
Aaron Mammoser United States 11 462 0.9× 225 0.8× 92 0.8× 56 0.5× 58 0.6× 25 765
Jürgen Kunz Germany 15 511 1.0× 286 1.0× 189 1.6× 53 0.5× 68 0.7× 25 871
Kevin M. Pawlik United States 15 1.2k 2.3× 345 1.2× 120 1.0× 93 0.8× 104 1.1× 21 1.7k
Joanne Sutherland Canada 11 492 1.0× 264 0.9× 231 2.0× 34 0.3× 52 0.6× 16 874
Olga Ermakova Italy 16 440 0.9× 84 0.3× 66 0.6× 136 1.2× 65 0.7× 29 725
Becky Alhadeff United States 13 374 0.7× 183 0.6× 81 0.7× 62 0.6× 96 1.0× 17 538
Zeynep Coban‐Akdemir United States 18 544 1.1× 396 1.4× 51 0.4× 131 1.2× 86 0.9× 50 965
T. W. J. Hustinx Netherlands 16 451 0.9× 292 1.0× 89 0.8× 116 1.0× 178 1.9× 26 784
Bénédicte Haenig Germany 10 832 1.6× 235 0.8× 70 0.6× 67 0.6× 90 1.0× 12 1.1k
Georg Klaus Hinkel Germany 17 498 1.0× 528 1.9× 51 0.4× 167 1.5× 46 0.5× 41 933

Countries citing papers authored by Jörg Seidel

Since Specialization
Citations

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

Fields of papers citing papers by Jörg Seidel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jörg Seidel

This figure shows the co-authorship network connecting the top 25 collaborators of Jörg Seidel. A scholar is included among the top collaborators of Jörg Seidel 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 Jörg Seidel. Jörg Seidel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Karadağ, Demet, Daniel Güllmar, Ulrike Löbel, et al.. (2015). Unidentified bright objects in neurofibromatosis type 1: Results of diffusion tensor imaging in children and adolescents. Journal of Pediatric Neurology. 4(1). 27–31.
2.
Bartsch, Oliver, Hilde Van Esch, Guy Froyen, et al.. (2010). Four unrelated patients with lubs X‐linked mental retardation syndrome and different Xq28 duplications. American Journal of Medical Genetics Part A. 152A(2). 305–312. 25 indexed citations
3.
Plöger, Frank, Petra Seemann, Katarina Lehmann, et al.. (2008). Brachydactyly type A2 associated with a defect in proGDF5 processing. Human Molecular Genetics. 17(9). 1222–1233. 47 indexed citations
4.
Polityko, A., Jörg Seidel, Uwe Claussen, et al.. (2004). Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. International Journal of Molecular Medicine. 14(6). 977–9. 6 indexed citations
5.
6.
Mentzel, Hans‐Joachim, Jörg Seidel, Dieter Sauner, et al.. (2002). Radiological aspects of the Poland syndrome and implications for treatment: a case study and review. European Journal of Pediatrics. 161(8). 455–459. 14 indexed citations
7.
Starke, Heike, Jörg Seidel, Wolfram Henn, et al.. (2002). Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements. European Journal of Human Genetics. 10(12). 790–800. 91 indexed citations
8.
O’Driscoll, Mark, Karen Cerosaletti, Yan Dai, et al.. (2001). DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency. Molecular Cell. 8(6). 1175–1185. 389 indexed citations
9.
Dudešek, Aleš, Wulf Röschinger, Ania C. Muntau, et al.. (2001). Molecular analysis and long-term follow-up of patients with different forms of 6-pyruvoyl-tetrahydropterin synthase deficiency. European Journal of Pediatrics. 160(5). 267–276. 34 indexed citations
10.
Seidel, Jörg, Karel Caca, Sibylle G. Schwab, et al.. (2001). Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).. PubMed. 47 Online Pub. OL149–57. 4 indexed citations
11.
Schiller, Simone, Stephanie Spranger, Birgit Schechinger, et al.. (2000). Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome. European Journal of Human Genetics. 8(1). 54–62. 115 indexed citations
12.
Hennermann, Julia B., Barbara Vetter, P Bührdel, et al.. (2000). Phenylketonuria and hyperphenylalaninemia in eastern Germany: A characteristic molecular profile and 15 novel mutations. Human Mutation. 15(3). 254–254. 1 indexed citations
13.
Schaeffel, Frank, Stefan Weiß, & Jörg Seidel. (1999). How good is the match between the plane of the text and the plane of focus during reading? 1. Ophthalmic and Physiological Optics. 19(2). 180–192. 27 indexed citations
14.
Kauf, E, et al.. (1997). Selen bei Phenylketonuriepatienten: Effekte einer Natriumselenitsubstitution. Medizinische Klinik - Intensivmedizin und Notfallmedizin. 92(3). 31–34. 2 indexed citations
15.
Kauf, E, et al.. (1997). Selen bei Phenylketonuriepatienten. Medizinische Klinik. 92(S3). 31–34. 3 indexed citations
16.
17.
Seidel, Jörg, Peter Scheibler, & Martin J. Muller. (1986). The heterogeneity of the nucleus raphes dorsalis in albino rats. Acta Histochemica. 78(2). 131–139. 2 indexed citations
18.
Lüth, Hans‐Joachim, Jörg Seidel, & W Schöber. (1977). Morphologisch-histochemische Charakterisierung der Verbindungen des Corpus geniculatum laterale, pars dorsalis (Cgl d), mit dem Hirnstamm bei Albinoratten. Acta Histochemica. 60(1). 91–102. 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.

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