Ingrid Bader
Impact in
- Ophthalmology top 5%
- Retinal Diseases and Treatments
-
- Retinal Development and Disorders
- RNA regulation and disease
- Advanced biosensing and bioanalysis techniques
Papers in
-
- Genomics and Chromatin Dynamics 2
- Signaling Pathways in Disease 1
- Hedgehog Signaling Pathway Studies 1
- Genetics 7
- Genetic and Kidney Cyst Diseases 3
- Genomics and Rare Diseases 2
- Craniofacial Disorders and Treatments 1
- Co-authors
- Thomas Meitinger (2 shared papers)Eckart Apfelstedt-Sylla (1 shared paper)Alfons Meindl (1 shared paper)Martin Hergersberg (1 shared paper)Birgit Lorenz (1 shared paper)Oliver Brandau (1 shared paper)Bernd Wissinger (1 shared paper)Helene Achatz (1 shared paper)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Orphanet Journal of Rare Diseases (1 paper)Human Molecular Genetics (1 paper)European Journal of Medical Genetics (1 paper)Genome Research (1 paper)
- Partner nations
- GermanyAustriaSwitzerland
In The Last Decade
Ingrid Bader
11 papers receiving 202 citations
Peers
Comparison fields: 5 of 36
- Ophthalmology 61
- Molecular Biology 186
- Genetics 69
- Cell Biology 27
- Cellular and Molecular Neuroscience 18
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 | 101 | |
| 2 | 1996 | 24 | |
| 3 | 2014 | 20 | |
| 4 | Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation | 2022 | 15 |
| 5 | 2020 | 14 | |
| 6 | 2016 | 13 | |
| 7 | 2020 | 10 | |
| 8 | 2022 | 5 | |
| 9 | 2022 | 2 | |
| 10 | 2023 | 1 | |
| 11 | 2017 | 1 | |
| 12 | 2018 | 0 |
About Ingrid Bader
Ingrid Bader is a scholar working on Molecular Biology, Genetics, Cell Biology, Clinical Biochemistry and Plant Science, having authored 12 papers that have together received 206 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (3 papers), Metabolism and Genetic Disorders (2 papers), Genomics and Chromatin Dynamics (2 papers), Genomics and Rare Diseases (2 papers), Signaling Pathways in Disease (1 paper), Hedgehog Signaling Pathway Studies (1 paper), Craniofacial Disorders and Treatments (1 paper) and Neuropeptides and Animal Physiology (1 paper). The work is most often cited by research in Ophthalmology (61 citations), Molecular Biology (186 citations), Genetics (69 citations), Cell Biology (27 citations) and Cellular and Molecular Neuroscience (18 citations). Ingrid Bader has collaborated with scholars based in Germany, Austria and Switzerland. Frequent co-authors include Thomas Meitinger, Eckart Apfelstedt-Sylla, Alfons Meindl, Martin Hergersberg, Birgit Lorenz, Oliver Brandau, Bernd Wissinger, Helene Achatz, Johannes A. Mayr and Heide Hellebrand. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Orphanet Journal of Rare Diseases, Human Molecular Genetics, European Journal of Medical Genetics and Genome Research.
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.