Jörg Seidel
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 10%
Papers in
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- Genomics and Chromatin Dynamics 2
-
- Metabolism and Genetic Disorders 5
- Co-authors
- Markus Stümm (2 shared papers)Heidemarie Neitzel (2 shared papers)Patrick Concannon (1 shared paper)Karen Cerosaletti (1 shared paper)Andrew R. Gennery (1 shared paper)Boris Kysela (1 shared paper)Richard A. Gatti (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)Human Mutation (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
Jörg Seidel
16 papers receiving 735 citations
Peers
Comparison fields: 5 of 65
- Genetics 284
- Developmental Biology 19
- Molecular Biology 505
- Cancer Research 93
- Immunology 112
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 | 389 | |
| 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, Epidemiology and Biochemistry, having authored 18 papers that have together received 767 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), Genomics and Chromatin Dynamics (2 papers), Biotin and Related Studies (2 papers), Cholinesterase and Neurodegenerative Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Advanced Neuroimaging Techniques and Applications (1 paper). The work is most often cited by research in Genetics (284 citations), Developmental Biology (19 citations), Molecular Biology (505 citations), Cancer Research (93 citations) and Immunology (112 citations). Jörg Seidel has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Markus Stümm, Heidemarie Neitzel, Patrick Concannon, Karen Cerosaletti, Andrew R. Gennery, Boris Kysela, Richard A. Gatti, Penny A. Jeggo, Raymonda Varon and Yan Dai. Their work appears in journals such as European Journal of Pediatrics, Acta Histochemica, European Journal of Human Genetics, Human Mutation and Human Molecular Genetics.
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.