Ingrid Bader
Impact in
- Ophthalmology top 10%
- Retinal Diseases and Treatments
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- Retinal Development and Disorders
- Advanced biosensing and bioanalysis techniques
- RNA regulation and disease
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
Papers in
-
- Genomics and Chromatin Dynamics 2
- Genetics 6
- Genetic and Kidney Cyst Diseases 3
- Genomics and Rare Diseases 2
- Genetic Syndromes and Imprinting 1
- Co-authors
- Thomas Meitinger (2 shared papers)Martin Hergersberg (1 shared paper)Helene Achatz (1 shared paper)Alfons Meindl (1 shared paper)Bernd Wissinger (1 shared paper)Eckart Apfelstedt-Sylla (1 shared paper)Birgit Lorenz (1 shared paper)Oliver Brandau (1 shared paper)
- Journals
- Human Molecular Genetics (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Genome Research (1 paper)Investigative Ophthalmology & Visual Science (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- GermanyAustriaSwitzerland
In The Last Decade
Ingrid Bader
11 papers receiving 213 citations
Peers
Comparison fields: 5 of 32
- Ophthalmology 32
- Molecular Biology 185
- Genetics 59
- Cell Biology 25
- Cancer Research 10
Countries citing papers authored by Ingrid Bader
This map shows the geographic impact of Ingrid Bader'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 Ingrid Bader with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid Bader more than expected).
Fields of papers citing papers by Ingrid Bader
This network shows the impact of papers produced by Ingrid Bader. 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 Ingrid Bader. The network helps show where Ingrid Bader may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingrid Bader, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 108 | |
| 2 | 1996 | 24 | |
| 3 | 2014 | 20 | |
| 4 | Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation | 2022 | 16 |
| 5 | 2020 | 15 | |
| 6 | 2016 | 13 | |
| 7 | 2020 | 12 | |
| 8 | 2022 | 5 | |
| 9 | 2022 | 2 | |
| 10 | 2023 | 2 | |
| 11 | 2017 | 1 | |
| 12 | 2018 | 0 |
About Ingrid Bader
Ingrid Bader is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cell Biology and Plant Science, having authored 12 papers that have together received 218 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (3 papers), Genomics and Rare Diseases (2 papers), Genomics and Chromatin Dynamics (2 papers), Metabolism and Genetic Disorders (2 papers), Genetic Syndromes and Imprinting (1 paper), Amino Acid Enzymes and Metabolism (1 paper), Microtubule and mitosis dynamics (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Ophthalmology (32 citations), Molecular Biology (185 citations), Genetics (59 citations), Cell Biology (25 citations) and Cancer Research (10 citations). Ingrid Bader has collaborated with scholars based in Germany, Austria and Switzerland. Frequent co-authors include Thomas Meitinger, Martin Hergersberg, Helene Achatz, Alfons Meindl, Bernd Wissinger, Eckart Apfelstedt-Sylla, Birgit Lorenz, Oliver Brandau, Johannes A. Mayr and Eugen Boltshauser. Their work appears in journals such as Human Molecular Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Genome Research, Investigative Ophthalmology & Visual Science and European Journal of Medical 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.