Hans Eiberg
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 21
- Genomic variations and chromosomal abnormalities 13
- Diabetes and associated disorders 9
- Urology top 1%
- Urinary Bladder and Prostate Research 9
- Molecular Biology top 2%
- Connexins and lens biology 16
- Mitochondrial Function and Pathology 14
- Cell Biology top 1%
- Ophthalmology top 1%
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- Pancreatic function and diabetes 17
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- Genetic Neurodegenerative Diseases 10
Hans Eiberg
192 papers receiving 7.0k citations
Hit Papers
Peers
Comparison fields: 5 of 144
- Genetics 2.0k
- Urology 455
- Molecular Biology 3.9k
- Cell Biology 787
- Ophthalmology 401
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 7 | |
| 2 | 2011 | 3 | |
| 3 | 2009 | 33 | |
| 4 | 2008 | 37 | |
| 5 | 2008 | 1 | |
| 6 | Branchio-Oto-Renal Syndrome: Detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, sequencing and MLPA analyses | 2007 | 1 |
| 7 | 2007 | 3 | |
| 8 | 2007 | 4 | |
| 9 | 2005 | 5 | |
| 10 | 2002 | 77 | |
| 11 | 2002 | 4 | |
| 12 | 2002 | 207 | |
| 13 | 2001 | 50 | |
| 14 | 1999 | 46 | |
| 15 | 1996 | 28 | |
| 16 | 1995 | 79 | |
| 17 | 1994 | 115 | |
| 18 | 1989 | 50 | |
| 19 | 1989 | 3 | |
| 20 | 1976 | 3 |
About Hans Eiberg
Hans Eiberg is a scholar working on Developmental Biology, Genetics and Urology, having authored 196 papers that have together received 7.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (21 papers), Pancreatic function and diabetes (17 papers), Connexins and lens biology (16 papers), Mitochondrial Function and Pathology (14 papers), Genomic variations and chromosomal abnormalities (13 papers), Genetic Neurodegenerative Diseases (10 papers), Diabetes and associated disorders (9 papers) and Urinary Bladder and Prostate Research (9 papers). The work is most often cited by research in Genetics (2.0k citations), Urology (455 citations) and Molecular Biology (3.9k citations). Hans Eiberg has collaborated with scholars based in Denmark, Germany and Hungary. Frequent co-authors include Jan Mohr, Thomas Rosenberg, Lars Hestbjerg Hansen, Inge-Merete Nielsen, Klaus Kjaer, Torben Hansen, Oluf Pedersen, P Kjer, Birgit 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.