K. Bender
Impact in
- Genetics top 5%
- Forensic and Genetic Research
- Genetic Associations and Epidemiology
- Genetic diversity and population structure
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
- Immunology top 10%
- Complement system in diseases
Papers in
- Genetics 60
- Genetic Associations and Epidemiology 25
- Forensic and Genetic Research 25
- Genetic diversity and population structure 14
- Genetic Mapping and Diversity in Plants and Animals 11
- Genomic variations and chromosomal abnormalities 8
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- Complement system in diseases 7
- Co-authors
- Gottfried Mauff (11 shared papers)H. W. Hitzeroth (8 shared papers)Hans‐Hilger Ropers (3 shared papers)T. F. Wienker (6 shared papers)S. Bissbort (9 shared papers)Thomas F. Wienker (6 shared papers)Karl‐Heinz Grzeschik (3 shared papers)Hans J. Rahmsdorf (1 shared paper)
- Journals
- Human Genetics (30 papers)Biochemical Genetics (5 papers)Journal of Medical Genetics (3 papers)Forensic Science International (3 papers)Human Heredity (3 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
K. Bender
76 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 84
- Genetics 706
- Immunology 169
- Clinical Biochemistry 18
- Pharmacology 36
- Hematology 45
Countries citing papers authored by K. Bender
This map shows the geographic impact of K. Bender'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 K. Bender with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Bender more than expected).
Fields of papers citing papers by K. Bender
This network shows the impact of papers produced by K. Bender. 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 K. Bender. The network helps show where K. Bender may publish in the future.
Co-authors
The 25 scholars most cited alongside K. Bender, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 121 | |
| 2 | 1997 | 68 | |
| 3 | 2003 | 68 | |
| 4 | 2004 | 60 | |
| 5 | 1974 | 58 | |
| 6 | 1977 | 46 | |
| 7 | 1983 | 43 | |
| 8 | Evidence for preferential X-chromosome inactivation in a family with Fabry disease. | 1977 | 40 |
| 9 | 1978 | 38 | |
| 10 | 2003 | 35 | |
| 11 | 1984 | 34 | |
| 12 | 1991 | 34 | |
| 13 | 1975 | 33 | |
| 14 | 1983 | 28 | |
| 15 | 1984 | 28 | |
| 16 | 2004 | 27 | |
| 17 | 1982 | 22 | |
| 18 | 1976 | 20 | |
| 19 | 1976 | 20 | |
| 20 | 1969 | 18 |
About K. Bender
K. Bender is a scholar working on Genetics, Immunology, Pediatrics, Perinatology and Child Health, Transplantation and Pharmacology, having authored 79 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (25 papers), Forensic and Genetic Research (25 papers), Genetic diversity and population structure (14 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers), Genomic variations and chromosomal abnormalities (8 papers), Complement system in diseases (7 papers), Neonatal Health and Biochemistry (4 papers) and Ion channel regulation and function (3 papers). The work is most often cited by research in Genetics (706 citations), Immunology (169 citations), Clinical Biochemistry (18 citations), Pharmacology (36 citations) and Hematology (45 citations). K. Bender has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Gottfried Mauff, H. W. Hitzeroth, Hans‐Hilger Ropers, T. F. Wienker, S. Bissbort, Thomas F. Wienker, Karl‐Heinz Grzeschik, Hans J. Rahmsdorf, Christine Blattner and Axel Knebel. Their work appears in journals such as Human Genetics, Biochemical Genetics, Journal of Medical Genetics, Forensic Science International and Human Heredity.
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.