Bernard Hellkuhl
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genetic and phenotypic traits in livestock
- Hematology top 10%
- Iron Metabolism and Disorders
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetic Mapping and Diversity in Plants and Animals 2
- Genetic Associations and Epidemiology 2
-
- Lysosomal Storage Disorders Research 3
- Co-authors
- K.-H. Grzeschik (4 shared papers)R S Sparkes (1 shared paper)Thuluvancheri K. Mohandas (1 shared paper)Larry J. Shapiro (1 shared paper)Karl‐Heinz Grzeschik (5 shared papers)BRYN M. JONES (1 shared paper)Susan Roberts (1 shared paper)Mark Worwood (1 shared paper)
- Journals
- Human Genetics (6 papers)Die Naturwissenschaften (1 paper)Proceedings of the National Academy of Sciences (1 paper)Pediatric Research (1 paper)Cytogenetics and Cell Genetics (7 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Bernard Hellkuhl
9 papers receiving 279 citations
Peers
Comparison fields: 5 of 37
- Genetics 168
- Hematology 73
- Molecular Biology 59
- Developmental Biology 2
- Clinical Biochemistry 4
Countries citing papers authored by Bernard Hellkuhl
This map shows the geographic impact of Bernard Hellkuhl'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 Bernard Hellkuhl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernard Hellkuhl more than expected).
Fields of papers citing papers by Bernard Hellkuhl
This network shows the impact of papers produced by Bernard Hellkuhl. 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 Bernard Hellkuhl. The network helps show where Bernard Hellkuhl may publish in the future.
Co-authors
The 23 scholars most cited alongside Bernard Hellkuhl, 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 | 1985 | 93 | |
| 2 | 1980 | 81 | |
| 3 | 1986 | 67 | |
| 4 | 1982 | 29 | |
| 5 | 1980 | 17 | |
| 6 | 1981 | 8 | |
| 7 | 1976 | 4 | |
| 8 | 1976 | 4 | |
| 9 | 1980 | 1 | |
| 10 | 2008 | 0 | |
| 11 | 2008 | 0 | |
| 12 | 2008 | 0 | |
| 13 | 2008 | 0 | |
| 14 | 2008 | 0 | |
| 15 | 2008 | 0 | |
| 16 | 2008 | 0 |
About Bernard Hellkuhl
Bernard Hellkuhl is a scholar working on Genetics, Physiology, Rheumatology, Clinical Biochemistry and Microbiology, having authored 16 papers that have together received 304 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Lysosomal Storage Disorders Research (3 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genetic Associations and Epidemiology (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Iron Metabolism and Disorders (1 paper) and Neonatal Health and Biochemistry (1 paper). The work is most often cited by research in Genetics (168 citations), Hematology (73 citations), Molecular Biology (59 citations), Developmental Biology (2 citations) and Clinical Biochemistry (4 citations). Bernard Hellkuhl has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include K.-H. Grzeschik, R S Sparkes, Thuluvancheri K. Mohandas, Larry J. Shapiro, Karl‐Heinz Grzeschik, BRYN M. JONES, Susan Roberts, Mark Worwood, Duncan J. Shaw and John David Brook. Their work appears in journals such as Human Genetics, Die Naturwissenschaften, Proceedings of the National Academy of Sciences, Pediatric Research and Cytogenetics and Cell 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.