Walter Pretsch
Impact in
- Molecular Biology top 10%
- Connexins and lens biology
- Developmental Biology and Gene Regulation
- Renal and related cancers
- Retinal Development and Disorders
- CRISPR and Genetic Engineering
- Congenital heart defects research
- Epigenetics and DNA Methylation
- Cancer Research top 10%
Papers in
-
- Connexins and lens biology 9
- DNA Repair Mechanisms 5
- Molecular Biology Techniques and Applications 4
- Retinal Development and Disorders 4
- Genetics 16
- Animal Genetics and Reproduction 6
- Co-authors
- Jack Favor (24 shared papers)Daniel J. Charles (15 shared papers)A. Neuhäuser-Klaus (13 shared papers)Rodica Sandulache (5 shared papers)Jochen Graw (11 shared papers)Patricia A. Grimes (3 shared papers)Bimal Chatterjee (3 shared papers)Wolfgang Wurst (1 shared paper)
- Journals
- Mammalian Genome (10 papers)Genetics Research (7 papers)Genetics (6 papers)Biochemical Genetics (5 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (3 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Walter Pretsch
58 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 87
- Molecular Biology 995
- Cancer Research 155
- Aging 19
- Genetics 288
- Developmental Neuroscience 40
Countries citing papers authored by Walter Pretsch
This map shows the geographic impact of Walter Pretsch'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 Walter Pretsch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Walter Pretsch more than expected).
Fields of papers citing papers by Walter Pretsch
This network shows the impact of papers produced by Walter Pretsch. 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 Walter Pretsch. The network helps show where Walter Pretsch may publish in the future.
Co-authors
The 25 scholars most cited alongside Walter Pretsch, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 314 | |
| 2 | 2006 | 100 | |
| 3 | 2012 | 76 | |
| 4 | 1985 | 73 | |
| 5 | 1998 | 57 | |
| 6 | 1989 | 46 | |
| 7 | 2004 | 44 | |
| 8 | An ENU-induced mutation in Rs1h causes disruption of retinal structure and function. | 2005 | 43 |
| 9 | 1987 | 42 | |
| 10 | 1996 | 40 | |
| 11 | 2008 | 39 | |
| 12 | 2005 | 36 | |
| 13 | 2001 | 32 | |
| 14 | 1986 | 26 | |
| 15 | 1981 | 24 | |
| 16 | 1997 | 24 | |
| 17 | 1992 | 23 | |
| 18 | 1999 | 20 | |
| 19 | 2002 | 19 | |
| 20 | 1990 | 18 |
About Walter Pretsch
Walter Pretsch is a scholar working on Molecular Biology, Genetics, Surgery, Cell Biology and Physiology, having authored 60 papers that have together received 1.4k indexed citations. Recurring topics across this work include Connexins and lens biology (9 papers), Erythrocyte Function and Pathophysiology (6 papers), Pancreatic function and diabetes (6 papers), Animal Genetics and Reproduction (6 papers), DNA Repair Mechanisms (5 papers), Amino Acid Enzymes and Metabolism (4 papers), Molecular Biology Techniques and Applications (4 papers) and Retinal Development and Disorders (4 papers). The work is most often cited by research in Molecular Biology (995 citations), Cancer Research (155 citations), Aging (19 citations), Genetics (288 citations) and Developmental Neuroscience (40 citations). Walter Pretsch has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Jack Favor, Daniel J. Charles, A. Neuhäuser-Klaus, Rodica Sandulache, Jochen Graw, Patricia A. Grimes, Bimal Chatterjee, Wolfgang Wurst, Klaus Schughart and Ralf Spörle. Their work appears in journals such as Mammalian Genome, Genetics Research, Genetics, Biochemical Genetics and Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis.
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.