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
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 2
- Congenital Ear and Nasal Anomalies 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 3
- Co-authors
- Jörg Schmidtke (5 shared papers)Julianne Behnke (2 shared papers)Barbara Zoll (1 shared paper)Mine Arslan‐Kirchner (6 shared papers)Martin Hermann (1 shared paper)U. Braun (1 shared paper)Konstantin Miller (3 shared papers)I. Hansmann (3 shared papers)
- Journals
- European Journal of Human Genetics (2 papers)Journal of Neurology (2 papers)Journal of Molecular and Cellular Cardiology (1 paper)British Journal of Haematology (1 paper)International Journal of Oral and Maxillofacial Surgery (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Brigitte Pabst
30 papers receiving 382 citations
Peers
Comparison fields: 5 of 68
- Genetics 46
- Genetics 112
- Pediatrics, Perinatology and Child Health 65
- Hematology 31
- Transplantation 5
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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 70 | |
| 2 | 2011 | 35 | |
| 3 | 2003 | 27 | |
| 4 | 2012 | 27 | |
| 5 | 2011 | 26 | |
| 6 | 1989 | 23 | |
| 7 | 2019 | 23 | |
| 8 | 2007 | 19 | |
| 9 | 2005 | 17 | |
| 10 | 2005 | 14 | |
| 11 | 2010 | 14 | |
| 12 | 1992 | 13 | |
| 13 | 2013 | 12 | |
| 14 | 2018 | 11 | |
| 15 | 2002 | 10 | |
| 16 | 2019 | 9 | |
| 17 | 2016 | 8 | |
| 18 | Analysis of K-ras mutations in pancreatic tissue after fine needle aspirates. | 1999 | 8 |
| 19 | 2014 | 7 | |
| 20 | 2003 | 7 |
About Brigitte Pabst
Brigitte Pabst is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 30 papers that have together received 407 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers), Chromosomal and Genetic Variations (3 papers), Prenatal Screening and Diagnostics (3 papers), BRCA gene mutations in cancer (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Cytomegalovirus and herpesvirus research (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (46 citations), Genetics (112 citations), Pediatrics, Perinatology and Child Health (65 citations), Hematology (31 citations) and Transplantation (5 citations). Brigitte Pabst has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Jörg Schmidtke, Julianne Behnke, Barbara Zoll, Mine Arslan‐Kirchner, Martin Hermann, U. Braun, Konstantin Miller, I. Hansmann, Irmgard Nippert and Doris Steinemann. Their work appears in journals such as European Journal of Human Genetics, Journal of Neurology, Journal of Molecular and Cellular Cardiology, British Journal of Haematology and International Journal of Oral and Maxillofacial Surgery.
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.