Vera Beyer
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 4
-
- DNA Repair Mechanisms 2
- Congenital heart defects research 2
- Ubiquitin and proteasome pathways 1
- Cell death mechanisms and regulation 1
- Co-authors
- Thomas Haaf (9 shared papers)Martin Poot (4 shared papers)Ruben van’t Slot (3 shared papers)Oliver Bartsch (9 shared papers)Ulrich Zechner (8 shared papers)Sue Holder (1 shared paper)Ira Schwaab (1 shared paper)Nicolai Kohlschmidt (3 shared papers)
- Journals
- Cytogenetic and Genome Research (2 papers)European Journal of Medical Genetics (2 papers)Human Molecular Genetics (1 paper)Cell Death and Differentiation (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- GermanyNetherlandsUnited States
In The Last Decade
Vera Beyer
16 papers receiving 330 citations
Peers
Comparison fields: 5 of 60
- Sensory Systems 36
- Genetics 176
- Cognitive Neuroscience 68
- Molecular Biology 177
- Pediatrics, Perinatology and Child Health 33
Countries citing papers authored by Vera Beyer
This map shows the geographic impact of Vera Beyer'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 Vera Beyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vera Beyer more than expected).
Fields of papers citing papers by Vera Beyer
This network shows the impact of papers produced by Vera Beyer. 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 Vera Beyer. The network helps show where Vera Beyer may publish in the future.
Co-authors
The 25 scholars most cited alongside Vera Beyer, 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 | 2009 | 105 | |
| 2 | 2008 | 46 | |
| 3 | 2012 | 39 | |
| 4 | 2007 | 39 | |
| 5 | 2009 | 34 | |
| 6 | 2003 | 24 | |
| 7 | 2008 | 14 | |
| 8 | 2010 | 10 | |
| 9 | 2000 | 9 | |
| 10 | 2011 | 7 | |
| 11 | 2007 | 7 | |
| 12 | 2020 | 7 | |
| 13 | 2013 | 5 | |
| 14 | 2012 | 5 | |
| 15 | 2009 | 3 | |
| 16 | 2012 | 3 |
About Vera Beyer
Vera Beyer is a scholar working on Genetics, Molecular Biology, Plant Science, Oncology and Surgery, having authored 16 papers that have together received 357 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (3 papers), DNA Repair Mechanisms (2 papers), Congenital heart defects research (2 papers), Ubiquitin and proteasome pathways (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper) and Cell death mechanisms and regulation (1 paper). The work is most often cited by research in Sensory Systems (36 citations), Genetics (176 citations), Cognitive Neuroscience (68 citations), Molecular Biology (177 citations) and Pediatrics, Perinatology and Child Health (33 citations). Vera Beyer has collaborated with scholars based in Germany, Netherlands and United States. Frequent co-authors include Thomas Haaf, Martin Poot, Ruben van’t Slot, Oliver Bartsch, Ulrich Zechner, Sue Holder, Ira Schwaab, Nicolai Kohlschmidt, E. Schneider and Martin Schüler. Their work appears in journals such as Cytogenetic and Genome Research, European Journal of Medical Genetics, Human Molecular Genetics, Cell Death and Differentiation and Molecular Genetics and Metabolism.
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.