Hans Eiberg
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Ophthalmology top 1%
Papers in
- Genetics 79
- Genetic Associations and Epidemiology 29
- Ocular Disorders and Treatments 13
- Genomic variations and chromosomal abnormalities 11
- Co-authors
- Jan Mohr (28 shared papers)Thomas Rosenberg (18 shared papers)Lars Hestbjerg Hansen (25 shared papers)Inge-Merete Nielsen (6 shared papers)Klaus Wilbrandt Kjaer (15 shared papers)T C Bog Hansen (26 shared papers)Oluf Borbye Pedersen (25 shared papers)Birgit Kjer (4 shared papers)
- Journals
- Clinical Genetics (24 papers)Human Genetics (12 papers)European Journal of Human Genetics (11 papers)Human Molecular Genetics (6 papers)Diabetologia (6 papers)
- Partner nations
- DenmarkGermanyUnited States
In The Last Decade
Hans Eiberg
207 papers receiving 8.6k citations
Hans Eiberg's Hit Papers
Peers
Comparison fields: 5 of 140
- Genetics 2.5k
- Ophthalmology 699
- Urology 468
- Clinical Biochemistry 270
- Pediatrics, Perinatology and Child Health 641
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 210 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Localization of cystic fibrosis locus to human chromosome 7cen–q22 Hit paper breakdown → | 1985 | 405 |
| 2 | Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker Hit paper breakdown → | 1985 | 377 |
| 3 | 2008 | 265 | |
| 4 | 2002 | 224 | |
| 5 | 1993 | 220 | |
| 6 | 2016 | 200 | |
| 7 | 1998 | 194 | |
| 8 | 2006 | 184 | |
| 9 | 2015 | 159 | |
| 10 | 1996 | 153 | |
| 11 | 1995 | 136 | |
| 12 | 2015 | 126 | |
| 13 | 1994 | 125 | |
| 14 | 2001 | 118 | |
| 15 | 2003 | 118 | |
| 16 | 2006 | 117 | |
| 17 | 2007 | 116 | |
| 18 | 1997 | 114 | |
| 19 | 1990 | 108 | |
| 20 | 1985 | 106 |
About Hans Eiberg
Hans Eiberg is a scholar working on Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Urology, having authored 210 papers that have together received 9.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (29 papers), Pancreatic function and diabetes (17 papers), Ocular Disorders and Treatments (13 papers), Connexins and lens biology (11 papers), Hereditary Neurological Disorders (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Urinary Bladder and Prostate Research (11 papers) and Pediatric Urology and Nephrology Studies (9 papers). The work is most often cited by research in Genetics (2.5k citations), Ophthalmology (699 citations), Urology (468 citations), Clinical Biochemistry (270 citations) and Pediatrics, Perinatology and Child Health (641 citations). Hans Eiberg has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Jan Mohr, Thomas Rosenberg, Lars Hestbjerg Hansen, Inge-Merete Nielsen, Klaus Wilbrandt Kjaer, T C Bog Hansen, Oluf Borbye Pedersen, Birgit Kjer, Poul Kjer and Niels Tommerup. Their work appears in journals such as Clinical Genetics, Human Genetics, European Journal of Human Genetics, Human Molecular Genetics and Diabetologia.
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.