Eberhard Passarge
Impact in
- Ophthalmology top 1%
- Ocular Oncology and Treatments
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Genetics 73
- Genomic variations and chromosomal abnormalities 24
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 17
- Genetics and Neurodevelopmental Disorders 14
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- DNA Repair Mechanisms 18
- Sexual Differentiation and Disorders 13
- Co-authors
- Bernhard Horsthemke (17 shared papers)James German (9 shared papers)Valerie Greger (9 shared papers)Elmar P. Messmer (3 shared papers)A. James McAdams (3 shared papers)Dietmar Lohmann (5 shared papers)David C. Bloom (4 shared papers)W. Lenz (1 shared paper)
- Journals
- Human Genetics (26 papers)Journal of Medical Genetics (7 papers)Clinical Genetics (7 papers)The Journal of Pediatrics (6 papers)The Lancet (5 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Eberhard Passarge
153 papers receiving 4.1k citations
Peers
Comparison fields: 5 of 129
- Ophthalmology 523
- Genetics 1.4k
- Cancer Research 517
- Molecular Biology 2.3k
- Pediatrics, Perinatology and Child Health 566
Countries citing papers authored by Eberhard Passarge
This map shows the geographic impact of Eberhard Passarge'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 Eberhard Passarge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eberhard Passarge more than expected).
Fields of papers citing papers by Eberhard Passarge
This network shows the impact of papers produced by Eberhard Passarge. 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 Eberhard Passarge. The network helps show where Eberhard Passarge may publish in the future.
Co-authors
The 25 scholars most cited alongside Eberhard Passarge, 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 168 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 427 | |
| 2 | 1997 | 211 | |
| 3 | 1967 | 187 | |
| 4 | 1966 | 152 | |
| 5 | 1994 | 139 | |
| 6 | The spectrum of RB1 germ-line mutations in hereditary retinoblastoma. | 1996 | 133 |
| 7 | 1967 | 122 | |
| 8 | 1997 | 113 | |
| 9 | 1994 | 110 | |
| 10 | 1989 | 99 | |
| 11 | 1995 | 94 | |
| 12 | 1985 | 94 | |
| 13 | 1977 | 90 | |
| 14 | 1995 | 77 | |
| 15 | 1989 | 76 | |
| 16 | 1974 | 75 | |
| 17 | 1976 | 73 | |
| 18 | Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome. | 1971 | 71 |
| 19 | 1979 | 68 | |
| 20 | Emil Heitz and the concept of heterochromatin: longitudinal chromosome differentiation was recognized fifty years ago. | 1979 | 66 |
About Eberhard Passarge
Eberhard Passarge is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Ophthalmology, having authored 168 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), DNA Repair Mechanisms (18 papers), Prenatal Screening and Diagnostics (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers), Ocular Oncology and Treatments (16 papers), Cancer-related Molecular Pathways (14 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Sexual Differentiation and Disorders (13 papers). The work is most often cited by research in Ophthalmology (523 citations), Genetics (1.4k citations), Cancer Research (517 citations), Molecular Biology (2.3k citations) and Pediatrics, Perinatology and Child Health (566 citations). Eberhard Passarge has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Bernhard Horsthemke, James German, Valerie Greger, Elmar P. Messmer, A. James McAdams, Dietmar Lohmann, David C. Bloom, W. Lenz, Claus R. Bartram and Hugo W. Rüdiger. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, The Journal of Pediatrics and The Lancet.
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.