Eva Rossier
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Developmental Biology top 10%
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 3
- Genetic and rare skin diseases. 2
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- Chromatin Remodeling and Cancer 3
- Epigenetics and DNA Methylation 2
- Co-authors
- Gotthold Barbi (5 shared papers)Arif B. Ekici (3 shared papers)Hildegard Kehrer‐Sawatzki (4 shared papers)Anita Rauch (3 shared papers)André Reis (2 shared papers)Markus Zweier (2 shared papers)Christiane Zweier (2 shared papers)Dagmar Wieczorek (4 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)Journal of Inherited Metabolic Disease (2 papers)Journal of Neurochemistry (1 paper)The American Journal of Human Genetics (1 paper)Human Mutation (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Eva Rossier
21 papers receiving 636 citations
Peers
Comparison fields: 5 of 67
- Genetics 366
- Developmental Biology 21
- Clinical Biochemistry 40
- Molecular Biology 367
- Toxicology 16
Countries citing papers authored by Eva Rossier
This map shows the geographic impact of Eva Rossier'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 Rossier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Rossier more than expected).
Fields of papers citing papers by Eva Rossier
This network shows the impact of papers produced by Eva Rossier. 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 Rossier. The network helps show where Eva Rossier may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva Rossier, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 174 | |
| 2 | 2010 | 115 | |
| 3 | 2006 | 51 | |
| 4 | 1995 | 45 | |
| 5 | 2011 | 34 | |
| 6 | 2017 | 31 | |
| 7 | 2010 | 30 | |
| 8 | 2009 | 28 | |
| 9 | 1995 | 24 | |
| 10 | 2014 | 23 | |
| 11 | 2009 | 19 | |
| 12 | 1998 | 17 | |
| 13 | 1994 | 16 | |
| 14 | 2002 | 12 | |
| 15 | 2005 | 12 | |
| 16 | 2018 | 7 | |
| 17 | 2015 | 3 | |
| 18 | 2005 | 3 | |
| 19 | A 10-year evaluation study of the productivity of free-running light mares. Growth of foals from birth to 6 months. | 1990 | 1 |
| 20 | 2014 | 1 |
About Eva Rossier
Eva Rossier is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 21 papers that have together received 647 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Chromatin Remodeling and Cancer (3 papers), Metabolism and Genetic Disorders (2 papers), Epigenetics and DNA Methylation (2 papers) and Genetic and rare skin diseases. (2 papers). The work is most often cited by research in Genetics (366 citations), Developmental Biology (21 citations), Clinical Biochemistry (40 citations), Molecular Biology (367 citations) and Toxicology (16 citations). Eva Rossier has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Gotthold Barbi, Arif B. Ekici, Hildegard Kehrer‐Sawatzki, Anita Rauch, André Reis, Markus Zweier, Christiane Zweier, Dagmar Wieczorek, Hartmut Engels and Eva Wohlleber. Their work appears in journals such as European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Journal of Neurochemistry, The American Journal of Human Genetics and Human Mutation.
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.