Brigitte Pabst
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- Genomic variations and chromosomal abnormalities 5
- BRCA gene mutations in cancer 2
- Glioma Diagnosis and Treatment 2
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- Genomic variations and chromosomal abnormalities 5
- BRCA gene mutations in cancer 2
- Glioma Diagnosis and Treatment 2
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- Congenital heart defects research 3
- Protein Tyrosine Phosphatases 2
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- Chromosomal and Genetic Variations 3
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- Tracheal and airway disorders 2
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- Congenital Heart Disease Studies 2
- Co-authors
- Jörg SchmidtkeJulianne BehnkeBarbara ZollI. HansmannMine Arslan‐KirchnerU. BraunMartin HermannDoris Steinemann
- Journals
- European Journal of Human Genetics (2 papers)Journal of Neurology (2 papers)British Journal of Haematology (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Brigitte Pabst
29 papers receiving 363 citations
Peers
Comparison fields: 5 of 69
- Genetics 56
- Genetics 109
- Pediatrics, Perinatology and Child Health 65
- Hematology 32
- Transplantation 6
Countries citing papers authored by Brigitte Pabst
This map shows the geographic impact of Brigitte Pabst'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 Brigitte Pabst with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brigitte Pabst more than expected).
Fields of papers citing papers by Brigitte Pabst
This network shows the impact of papers produced by Brigitte Pabst. 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 Brigitte Pabst. The network helps show where Brigitte Pabst may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Brigitte Pabst, 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 | 2023 | 2 | |
| 2 | 2019 | 20 | |
| 3 | 2019 | 9 | |
| 4 | 2018 | 11 | |
| 5 | 2016 | 7 | |
| 6 | 2012 | 1 | |
| 7 | 2012 | 27 | |
| 8 | 2011 | 25 | |
| 9 | 2011 | 34 | |
| 10 | 2010 | 14 | |
| 11 | 2009 | 6 | |
| 12 | 2006 | 2 | |
| 13 | 2005 | 16 | |
| 14 | 2005 | 13 | |
| 15 | 2003 | 4 | |
| 16 | 2003 | 8 | |
| 17 | 2003 | 12 | |
| 18 | 2002 | 8 | |
| 19 | 1995 | 65 | |
| 20 | 1992 | 13 |
About Brigitte Pabst
Brigitte Pabst is a scholar working on Genetics, Transplantation, Genetics, Pediatrics, Perinatology and Child Health and Developmental Neuroscience, having authored 29 papers that have together received 374 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers), Chromosomal and Genetic Variations (3 papers), BRCA gene mutations in cancer (2 papers), Glioma Diagnosis and Treatment (2 papers), Tracheal and airway disorders (2 papers), Congenital Heart Disease Studies (2 papers) and Protein Tyrosine Phosphatases (2 papers). The work is most often cited by research in Genetics (56 citations), Genetics (109 citations), Pediatrics, Perinatology and Child Health (65 citations), Hematology (32 citations) and Transplantation (6 citations). Brigitte Pabst has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Jörg Schmidtke, Julianne Behnke, Barbara Zoll, I. Hansmann, Mine Arslan‐Kirchner, U. Braun, Martin Hermann, Doris Steinemann, Irmgard Nippert and Konstantin Miller. Their work appears in journals such as European Journal of Human Genetics, Journal of Neurology, British Journal of Haematology, Journal of Molecular and Cellular Cardiology and International Journal of Cardiology.
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.