U Friedrich
Impact in
- Ophthalmology top 2%
- Retinal Diseases and Treatments
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 27
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetic Syndromes and Imprinting 4
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- Retinal Development and Disorders 13
- Sexual Differentiation and Disorders 5
- Co-authors
- Bernhard H. F. Weber (14 shared papers)Philip Coffino (1 shared paper)Jørgen Nielsen (3 shared papers)H. B�nisch (1 shared paper)Peter Gerner‐Smidt (1 shared paper)Takayuki Tsuboi (3 shared papers)Ulrich S Zimmermann (2 shared papers)Thorsten Walles (1 shared paper)
In The Last Decade
U Friedrich
65 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 123
- Ophthalmology 154
- Genetics 483
- Sensory Systems 67
- Biotechnology 104
- Molecular Biology 709
Countries citing papers authored by U Friedrich
This map shows the geographic impact of U Friedrich'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 U Friedrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites U Friedrich more than expected).
Fields of papers citing papers by U Friedrich
This network shows the impact of papers produced by U Friedrich. 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 U Friedrich. The network helps show where U Friedrich may publish in the future.
Co-authors
The 25 scholars most cited alongside U Friedrich, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 160 | |
| 2 | 1994 | 150 | |
| 3 | 2000 | 103 | |
| 4 | 1996 | 88 | |
| 5 | 2016 | 84 | |
| 6 | 1977 | 83 | |
| 7 | 1986 | 65 | |
| 8 | 2011 | 62 | |
| 9 | 1978 | 58 | |
| 10 | 2015 | 52 | |
| 11 | 1969 | 48 | |
| 12 | 1998 | 47 | |
| 13 | 2015 | 41 | |
| 14 | 2010 | 39 | |
| 15 | 1970 | 35 | |
| 16 | 2017 | 30 | |
| 17 | 1984 | 26 | |
| 18 | Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1. | 1982 | 26 |
| 19 | 2016 | 24 | |
| 20 | 1996 | 24 |
About U Friedrich
U Friedrich is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Ophthalmology and Cell Biology, having authored 67 papers that have together received 1.7k indexed citations. Recurring topics across this work include Retinal Development and Disorders (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (11 papers), Chromosomal and Genetic Variations (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sexual Differentiation and Disorders (5 papers), Retinal Diseases and Treatments (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Ophthalmology (154 citations), Genetics (483 citations), Sensory Systems (67 citations), Biotechnology (104 citations) and Molecular Biology (709 citations). U Friedrich has collaborated with scholars based in Germany, Denmark and Poland. Frequent co-authors include Bernhard H. F. Weber, Philip Coffino, Jørgen Nielsen, H. B�nisch, Peter Gerner‐Smidt, Takayuki Tsuboi, Ulrich S Zimmermann, Thorsten Walles, Rainer Ehmann and Godehard Friedel. Their work appears in journals such as Clinical Genetics, Human Genetics, Prenatal Diagnosis, Investigative Ophthalmology & Visual Science and Human Molecular 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.