Ursula Friedrich
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 50
- Genomic variations and chromosomal abnormalities 30
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 15
- Genetics and Neurodevelopmental Disorders 8
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- Sexual Differentiation and Disorders 7
- DNA Repair Mechanisms 4
- Co-authors
- Johannes Nielsen (18 shared papers)Claus Højbjerg Gravholt (4 shared papers)Philip Coffino (5 shared papers)Robert A. Steinberg (2 shared papers)Patrick H. O’Farrell (1 shared paper)Mette Warburg (4 shared papers)Johannes Nielsen (6 shared papers)Hans‐Hilger Ropers (4 shared papers)
- Journals
- Human Genetics (24 papers)Clinical Genetics (8 papers)Hereditas (7 papers)European Journal of Human Genetics (3 papers)The Lancet (3 papers)
- Partner nations
- DenmarkGermanyUnited States
In The Last Decade
Ursula Friedrich
78 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 112
- Genetics 1.0k
- Pediatrics, Perinatology and Child Health 319
- Developmental Biology 38
- Molecular Biology 878
- Plant Science 431
Countries citing papers authored by Ursula Friedrich
This map shows the geographic impact of Ursula 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 Ursula Friedrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ursula Friedrich more than expected).
Fields of papers citing papers by Ursula Friedrich
This network shows the impact of papers produced by Ursula 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 Ursula Friedrich. The network helps show where Ursula Friedrich may publish in the future.
Co-authors
The 25 scholars most cited alongside Ursula 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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1977 | 200 | |
| 2 | 1973 | 139 | |
| 3 | 1995 | 108 | |
| 4 | 1974 | 96 | |
| 5 | 1992 | 60 | |
| 6 | 2001 | 55 | |
| 7 | 1974 | 49 | |
| 8 | 1985 | 46 | |
| 9 | 1976 | 45 | |
| 10 | 1986 | 44 | |
| 11 | 1972 | 43 | |
| 12 | 1985 | 43 | |
| 13 | 1985 | 42 | |
| 14 | 1974 | 37 | |
| 15 | 1975 | 37 | |
| 16 | 1995 | 33 | |
| 17 | 1987 | 31 | |
| 18 | 1987 | 31 | |
| 19 | 1974 | 30 | |
| 20 | 1973 | 29 |
About Ursula Friedrich
Ursula Friedrich is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 85 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Chromosomal and Genetic Variations (18 papers), Prenatal Screening and Diagnostics (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (8 papers), Sexual Differentiation and Disorders (7 papers), Carcinogens and Genotoxicity Assessment (7 papers) and DNA Repair Mechanisms (4 papers). The work is most often cited by research in Genetics (1.0k citations), Pediatrics, Perinatology and Child Health (319 citations), Developmental Biology (38 citations), Molecular Biology (878 citations) and Plant Science (431 citations). Ursula Friedrich has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Johannes Nielsen, Claus Højbjerg Gravholt, Philip Coffino, Robert A. Steinberg, Patrick H. O’Farrell, Mette Warburg, Johannes Nielsen, Hans‐Hilger Ropers, Helga Rehder and Steffen E. Petersen. Their work appears in journals such as Human Genetics, Clinical Genetics, Hereditas, European Journal of Human Genetics 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.