Hans Eiberg
Impact in
Papers in
-
- Mitochondrial Function and Pathology 12
- Connexins and lens biology 12
- Genetics 53
- Genetics and Neurodevelopmental Disorders 18
- Genomic variations and chromosomal abnormalities 13
- Diabetes and associated disorders 8
- Co-authors
- Jan Mohr (29 shared papers)Thomas Rosenberg (18 shared papers)Lars Hestbjerg Hansen (25 shared papers)Inge-Merete Nielsen (6 shared papers)Klaus Kjaer (15 shared papers)Torben Hansen (26 shared papers)Oluf Pedersen (24 shared papers)Birgit Kjer (4 shared papers)
In The Last Decade
Hans Eiberg
197 papers receiving 7.6k citations
Hans Eiberg's Hit Papers
Peers
Comparison fields: 5 of 143
- Urology 433
- Genetics 1.8k
- Molecular Biology 3.7k
- Clinical Biochemistry 317
- Cell Biology 773
Countries citing papers authored by Hans Eiberg
This map shows the geographic impact of Hans Eiberg'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 Hans Eiberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hans Eiberg more than expected).
Fields of papers citing papers by Hans Eiberg
This network shows the impact of papers produced by Hans Eiberg. 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 Hans Eiberg. The network helps show where Hans Eiberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Hans Eiberg, 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 202 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 403 | |
| 2 | Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker Hit paper breakdown → | 1985 | 380 |
| 3 | 2008 | 241 | |
| 4 | 2002 | 219 | |
| 5 | 1993 | 217 | |
| 6 | 1998 | 196 | |
| 7 | 2016 | 188 | |
| 8 | 1996 | 147 | |
| 9 | 1995 | 140 | |
| 10 | 1994 | 124 | |
| 11 | 2003 | 118 | |
| 12 | 2001 | 116 | |
| 13 | 1997 | 114 | |
| 14 | 2007 | 114 | |
| 15 | 2006 | 113 | |
| 16 | 1985 | 107 | |
| 17 | 1990 | 94 | |
| 18 | 2002 | 94 | |
| 19 | 1974 | 94 | |
| 20 | A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy. | 2002 | 93 |
About Hans Eiberg
Hans Eiberg is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Physiology, having authored 202 papers that have together received 8.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Pancreatic function and diabetes (13 papers), Genomic variations and chromosomal abnormalities (13 papers), Mitochondrial Function and Pathology (12 papers), Connexins and lens biology (12 papers), Urinary Bladder and Prostate Research (11 papers), Genetic Neurodegenerative Diseases (9 papers) and Diabetes and associated disorders (8 papers). The work is most often cited by research in Urology (433 citations), Genetics (1.8k citations), Molecular Biology (3.7k citations), Clinical Biochemistry (317 citations) and Cell Biology (773 citations). Hans Eiberg has collaborated with scholars based in Denmark, Hungary and Germany. Frequent co-authors include Jan Mohr, Thomas Rosenberg, Lars Hestbjerg Hansen, Inge-Merete Nielsen, Klaus Kjaer, Torben Hansen, Oluf Pedersen, Birgit Kjer, P Kjer and Niels Tommerup. Their work appears in journals such as Clinical Genetics, Human Genetics, European Journal of Human Genetics, Human Molecular Genetics and Diabetes.
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.