Barbara Zoll
Impact in
-
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
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- Cancer-related gene regulation 7
- Genetics 32
- Genomic variations and chromosomal abnormalities 21
- Genomics and Rare Diseases 7
- Co-authors
- Michaël Otto (4 shared papers)K. Ricker (4 shared papers)Manuela C. Koch (5 shared papers)Thomas J. Jentsch (2 shared papers)Klaus Steinmeyer (2 shared papers)Frank Lehmann‐Horn (2 shared papers)C Lorenz (2 shared papers)Karl‐Heinz Grzeschik (1 shared paper)
- Journals
- Human Genetics (11 papers)Clinical Genetics (6 papers)Cytogenetic and Genome Research (5 papers)Journal of Medical Genetics (4 papers)Molecular Cytogenetics (3 papers)
- Partner nations
- GermanyUnited KingdomPoland
In The Last Decade
Barbara Zoll
74 papers receiving 1.7k citations
Barbara Zoll's Hit Papers
Peers
Comparison fields: 5 of 96
- Cellular and Molecular Neuroscience 460
- Genetics 528
- Molecular Biology 1.1k
- Cardiology and Cardiovascular Medicine 365
- Genetics 164
Countries citing papers authored by Barbara Zoll
This map shows the geographic impact of Barbara Zoll'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 Barbara Zoll with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Zoll more than expected).
Fields of papers citing papers by Barbara Zoll
This network shows the impact of papers produced by Barbara Zoll. 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 Barbara Zoll. The network helps show where Barbara Zoll may publish in the future.
Co-authors
The 25 scholars most cited alongside Barbara Zoll, 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia Hit paper breakdown → | 1992 | 556 |
| 2 | 1995 | 65 | |
| 3 | 2001 | 61 | |
| 4 | 2012 | 55 | |
| 5 | 2003 | 52 | |
| 6 | 2014 | 50 | |
| 7 | 1991 | 47 | |
| 8 | 2006 | 42 | |
| 9 | 2002 | 37 | |
| 10 | 1997 | 37 | |
| 11 | 1993 | 37 | |
| 12 | Segregation of all four major fibrillar collagen genes in the Marfan syndrome. | 1987 | 34 |
| 13 | 1990 | 34 | |
| 14 | 1991 | 34 | |
| 15 | 1993 | 32 | |
| 16 | 2003 | 32 | |
| 17 | 1993 | 31 | |
| 18 | 2014 | 28 | |
| 19 | 2005 | 28 | |
| 20 | 1993 | 27 |
About Barbara Zoll
Barbara Zoll is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 76 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (14 papers), Chromosomal and Genetic Variations (10 papers), Cancer-related gene regulation (7 papers), Hemophilia Treatment and Research (7 papers), Genetic Neurodegenerative Diseases (7 papers), Genomics and Rare Diseases (7 papers) and Blood Coagulation and Thrombosis Mechanisms (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (460 citations), Genetics (528 citations), Molecular Biology (1.1k citations), Cardiology and Cardiovascular Medicine (365 citations) and Genetics (164 citations). Barbara Zoll has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Michaël Otto, K. Ricker, Manuela C. Koch, Thomas J. Jentsch, Klaus Steinmeyer, Frank Lehmann‐Horn, C Lorenz, Karl‐Heinz Grzeschik, Friedrich Wolf and Iris Bartels. Their work appears in journals such as Human Genetics, Clinical Genetics, Cytogenetic and Genome Research, Journal of Medical Genetics and Molecular Cytogenetics.
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.