Jörg Seidel
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
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- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
Papers in
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- Genomics and Chromatin Dynamics 2
- DNA Repair Mechanisms 1
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- Metabolism and Genetic Disorders 5
- Co-authors
- Markus Stümm (2 shared papers)Heidemarie Neitzel (2 shared papers)Raymonda Varon (1 shared paper)Andrew R. Gennery (1 shared paper)S.E. Palmer (1 shared paper)Richard A. Gatti (1 shared paper)Mark O’Driscoll (1 shared paper)Penny A. Jeggo (1 shared paper)
- Journals
- European Journal of Pediatrics (3 papers)Acta Histochemica (3 papers)European Journal of Human Genetics (2 papers)Molecular Cell (1 paper)International Journal of Molecular Medicine (1 paper)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Jörg Seidel
16 papers receiving 737 citations
Peers
Comparison fields: 5 of 61
- Genetics 251
- Molecular Biology 460
- Developmental Biology 13
- Cancer Research 79
- Clinical Biochemistry 34
Countries citing papers authored by Jörg Seidel
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
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-authors
The 25 scholars most cited alongside Jörg Seidel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 391 | |
| 2 | 2000 | 115 | |
| 3 | 2002 | 91 | |
| 4 | 2008 | 47 | |
| 5 | 2001 | 34 | |
| 6 | 1999 | 27 | |
| 7 | 2010 | 25 | |
| 8 | 2002 | 14 | |
| 9 | 2004 | 6 | |
| 10 | 1977 | 4 | |
| 11 | Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD). | 2001 | 4 |
| 12 | 1997 | 3 | |
| 13 | 2003 | 3 | |
| 14 | Selen bei Phenylketonuriepatienten: Effekte einer Natriumselenitsubstitution | 1997 | 2 |
| 15 | 1986 | 2 | |
| 16 | 2000 | 1 | |
| 17 | 1989 | 0 | |
| 18 | 2015 | 0 |
About Jörg Seidel
Jörg Seidel is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Biochemistry and Surgery, having authored 18 papers that have together received 769 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (5 papers), Amino Acid Enzymes and Metabolism (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Cholinesterase and Neurodegenerative Diseases (2 papers), Biotin and Related Studies (2 papers), Genomics and Chromatin Dynamics (2 papers), Ophthalmology and Visual Impairment Studies (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Genetics (251 citations), Molecular Biology (460 citations), Developmental Biology (13 citations), Cancer Research (79 citations) and Clinical Biochemistry (34 citations). Jörg Seidel has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Markus Stümm, Heidemarie Neitzel, Raymonda Varon, Andrew R. Gennery, S.E. Palmer, Richard A. Gatti, Mark O’Driscoll, Penny A. Jeggo, Patrick Concannon and Yan Dai. Their work appears in journals such as European Journal of Pediatrics, Acta Histochemica, European Journal of Human Genetics, Molecular Cell and International Journal of Molecular Medicine.
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.