Brigitte Pabst
Impact in
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- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
- Connective tissue disorders research
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- Prenatal Screening and Diagnostics
- Neonatal Health and Biochemistry
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 4
- Glioma Diagnosis and Treatment 2
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Jörg Schmidtke (5 shared papers)Barbara Zoll (1 shared paper)Julianne Behnke (2 shared papers)Mine Arslan‐Kirchner (6 shared papers)U. Braun (1 shared paper)Konstantin R. Miller (3 shared papers)Martin Hermann (1 shared paper)Ingo Hansmann (3 shared papers)
- Journals
- European Journal of Human Genetics (2 papers)Journal of Neurology (2 papers)PLoS ONE (1 paper)Human Genetics (1 paper)Breast Cancer Research and Treatment (1 paper)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Brigitte Pabst
29 papers receiving 395 citations
Peers
Comparison fields: 5 of 70
- Genetics 48
- Genetics 117
- Pediatrics, Perinatology and Child Health 70
- Hematology 34
- 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-authors
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
Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 69 | |
| 2 | 2011 | 40 | |
| 3 | 2012 | 29 | |
| 4 | 2011 | 28 | |
| 5 | 2003 | 27 | |
| 6 | 2019 | 26 | |
| 7 | 1989 | 23 | |
| 8 | 2007 | 19 | |
| 9 | 2005 | 17 | |
| 10 | 2005 | 15 | |
| 11 | 2010 | 14 | |
| 12 | 1992 | 13 | |
| 13 | 2013 | 13 | |
| 14 | 2018 | 12 | |
| 15 | 2002 | 10 | |
| 16 | 2019 | 10 | |
| 17 | Analysis of K-ras mutations in pancreatic tissue after fine needle aspirates. | 1999 | 8 |
| 18 | 2014 | 8 | |
| 19 | 2016 | 8 | |
| 20 | 2003 | 7 |
About Brigitte Pabst
Brigitte Pabst is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Epidemiology, having authored 29 papers that have together received 422 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers), Chromosomal and Genetic Variations (3 papers), Congenital heart defects research (3 papers), Tracheal and airway disorders (2 papers), Glioma Diagnosis and Treatment (2 papers), Congenital Heart Disease Studies (2 papers) and Reproductive Biology and Fertility (2 papers). The work is most often cited by research in Genetics (48 citations), Genetics (117 citations), Pediatrics, Perinatology and Child Health (70 citations), Hematology (34 citations) and Transplantation (6 citations). Brigitte Pabst has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Jörg Schmidtke, Barbara Zoll, Julianne Behnke, Mine Arslan‐Kirchner, U. Braun, Konstantin R. Miller, Martin Hermann, Ingo Hansmann, Doris Steinemann and Irmgard Nippert. Their work appears in journals such as European Journal of Human Genetics, Journal of Neurology, PLoS ONE, Human Genetics and Breast Cancer Research and Treatment.
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.