Eva Wohlleber
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
-
- Chromatin Remodeling and Cancer
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Congenital Ear and Nasal Anomalies 1
- Co-authors
- Hartmut Engels (8 shared papers)Anita M. Rauch (3 shared papers)Alexander M. Zink (7 shared papers)Dagmar Wieczorek (3 shared papers)Markus Zweier (2 shared papers)Eva Rossier (2 shared papers)Christiane Zweier (2 shared papers)Arif B. Ekici (2 shared papers)
- Journals
- European Journal of Medical Genetics (1 paper)The American Journal of Human Genetics (1 paper)Cytogenetic and Genome Research (1 paper)Human Mutation (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- GermanyUnited KingdomSwitzerland
In The Last Decade
Eva Wohlleber
11 papers receiving 459 citations
Peers
Comparison fields: 5 of 53
- Genetics 297
- Molecular Biology 280
- Developmental Neuroscience 15
- Genetics 31
- Pathology and Forensic Medicine 51
Countries citing papers authored by Eva Wohlleber
This map shows the geographic impact of Eva Wohlleber'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 Eva Wohlleber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Wohlleber more than expected).
Fields of papers citing papers by Eva Wohlleber
This network shows the impact of papers produced by Eva Wohlleber. 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 Eva Wohlleber. The network helps show where Eva Wohlleber may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva Wohlleber, 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 | 2012 | 183 | |
| 2 | 2010 | 125 | |
| 3 | 2009 | 78 | |
| 4 | 2012 | 25 | |
| 5 | 2012 | 22 | |
| 6 | 2016 | 18 | |
| 7 | 2012 | 14 | |
| 8 | 2015 | 11 | |
| 9 | 2010 | 10 | |
| 10 | 2014 | 6 | |
| 11 | 2023 | 3 | |
| 12 | 2025 | 0 |
About Eva Wohlleber
Eva Wohlleber is a scholar working on Genetics, Neurology, Molecular Biology, Genetics and Cancer Research, having authored 12 papers that have together received 495 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers), Chromatin Remodeling and Cancer (2 papers), Congenital heart defects research (2 papers), Cancer Genomics and Diagnostics (1 paper), Congenital Ear and Nasal Anomalies (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (297 citations), Molecular Biology (280 citations), Developmental Neuroscience (15 citations), Genetics (31 citations) and Pathology and Forensic Medicine (51 citations). Eva Wohlleber has collaborated with scholars based in Germany, United Kingdom and Switzerland. Frequent co-authors include Hartmut Engels, Anita M. Rauch, Alexander M. Zink, Dagmar Wieczorek, Markus Zweier, Eva Rossier, Christiane Zweier, Arif B. Ekici, André Reis and Juliane Hoyer. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, Cytogenetic and Genome Research, Human Mutation and European Journal of Human Genetics.
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.