Birgit Zirn
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Renal and related cancers
- Ion Transport and Channel Regulation
Papers in
-
- Renal and related cancers 8
- Congenital heart defects research 4
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Manfred Gessler (7 shared papers)Norbert Graf (6 shared papers)Stefanie Wittmann (6 shared papers)Knut Brockmann (8 shared papers)Jutta Gärtner (5 shared papers)Birgit Samans (3 shared papers)Martin Eilers (2 shared papers)Peter Frommolt (1 shared paper)
- Journals
- Genes Chromosomes and Cancer (3 papers)Clinical Genetics (3 papers)Neuropediatrics (3 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)Neurogenetics (2 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Birgit Zirn
33 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 77
- Genetics 368
- Molecular Biology 589
- Neurology 110
- Clinical Biochemistry 51
- Pediatrics, Perinatology and Child Health 123
Countries citing papers authored by Birgit Zirn
This map shows the geographic impact of Birgit Zirn'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 Zirn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Zirn more than expected).
Fields of papers citing papers by Birgit Zirn
This network shows the impact of papers produced by Birgit Zirn. 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 Zirn. The network helps show where Birgit Zirn may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Zirn, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 175 | |
| 2 | 2015 | 148 | |
| 3 | 2005 | 79 | |
| 4 | 2006 | 71 | |
| 5 | 2008 | 55 | |
| 6 | 2012 | 55 | |
| 7 | 2015 | 49 | |
| 8 | 2008 | 47 | |
| 9 | 2005 | 44 | |
| 10 | 2006 | 43 | |
| 11 | 2013 | 38 | |
| 12 | 2008 | 33 | |
| 13 | 2013 | 32 | |
| 14 | 2010 | 31 | |
| 15 | 2007 | 27 | |
| 16 | 2006 | 21 | |
| 17 | 2011 | 20 | |
| 18 | 2020 | 19 | |
| 19 | 2005 | 18 | |
| 20 | 2017 | 17 |
About Birgit Zirn
Birgit Zirn is a scholar working on Molecular Biology, Genetics, Neurology, Cellular and Molecular Neuroscience and Surgery, having authored 33 papers that have together received 1.1k indexed citations. Recurring topics across this work include Renal and related cancers (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (4 papers), Genomics and Rare Diseases (4 papers), Neurological disorders and treatments (4 papers), Genetic Neurodegenerative Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). The work is most often cited by research in Genetics (368 citations), Molecular Biology (589 citations), Neurology (110 citations), Clinical Biochemistry (51 citations) and Pediatrics, Perinatology and Child Health (123 citations). Birgit Zirn has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Manfred Gessler, Norbert Graf, Stefanie Wittmann, Knut Brockmann, Jutta Gärtner, Birgit Samans, Martin Eilers, Peter Frommolt, Friedrich Ebinger and Elisa Wirthgen. Their work appears in journals such as Genes Chromosomes and Cancer, Clinical Genetics, Neuropediatrics, Journal of Neurology Neurosurgery & Psychiatry and Neurogenetics.
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.