Birgit Krabichler
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 3
- Connective tissue disorders research 2
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- Nuclear Structure and Function 2
- Co-authors
- Johannes Zschocke (9 shared papers)Stephan Pabinger (1 shared paper)René Snajder (1 shared paper)Zlatko Trajanoski (1 shared paper)Mirjana Efremova (1 shared paper)Andreas Dander (1 shared paper)Michael R. Speicher (1 shared paper)Andreas Janecke (5 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Annals of Human Genetics (1 paper)Briefings in Bioinformatics (1 paper)
- Partner nations
- AustriaGermanyUnited States
In The Last Decade
Birgit Krabichler
17 papers receiving 791 citations
Birgit Krabichler's Hit Papers
Peers
Comparison fields: 5 of 102
- Genetics 390
- Cancer Research 119
- Cell Biology 132
- Molecular Biology 462
- Information Systems and Management 24
Countries citing papers authored by Birgit Krabichler
This map shows the geographic impact of Birgit Krabichler'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 Birgit Krabichler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Krabichler more than expected).
Fields of papers citing papers by Birgit Krabichler
This network shows the impact of papers produced by Birgit Krabichler. 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 Birgit Krabichler. The network helps show where Birgit Krabichler may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Krabichler, 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 | A survey of tools for variant analysis of next-generation genome sequencing data Hit paper breakdown → | 2013 | 433 |
| 2 | 2009 | 118 | |
| 3 | 2015 | 52 | |
| 4 | 2016 | 40 | |
| 5 | 2012 | 36 | |
| 6 | 2016 | 31 | |
| 7 | 2012 | 26 | |
| 8 | 2011 | 21 | |
| 9 | 2013 | 19 | |
| 10 | 2018 | 19 | |
| 11 | 2018 | 16 | |
| 12 | 2015 | 15 | |
| 13 | 2019 | 7 | |
| 14 | 2017 | 7 | |
| 15 | 2018 | 3 | |
| 16 | 2011 | 1 | |
| 17 | 2012 | 1 |
About Birgit Krabichler
Birgit Krabichler is a scholar working on Genetics, Molecular Biology, Cell Biology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 845 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (3 papers), Hereditary Neurological Disorders (2 papers), Skin and Cellular Biology Research (2 papers), Connective tissue disorders research (2 papers), Chromosomal and Genetic Variations (2 papers), Proteoglycans and glycosaminoglycans research (2 papers) and Nuclear Structure and Function (2 papers). The work is most often cited by research in Genetics (390 citations), Cancer Research (119 citations), Cell Biology (132 citations), Molecular Biology (462 citations) and Information Systems and Management (24 citations). Birgit Krabichler has collaborated with scholars based in Austria, Germany and United States. Frequent co-authors include Johannes Zschocke, Stephan Pabinger, René Snajder, Zlatko Trajanoski, Mirjana Efremova, Andreas Dander, Michael R. Speicher, Andreas Janecke, Thomas Müller and Beat Steinmann. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, European Journal of Medical Genetics, Annals of Human Genetics and Briefings in Bioinformatics.
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.