Eva Rossier
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 4
- Genetic Syndromes and Imprinting 3
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- Genomics and Chromatin Dynamics 4
- Epigenetics and DNA Methylation 3
- Co-authors
- Gotthold Barbi (5 shared papers)Arif Bülent Ekici (3 shared papers)Anita M. Rauch (3 shared papers)Hildegard Kehrer‐Sawatzki (4 shared papers)Christiane Zweier (2 shared papers)Markus Zweier (2 shared papers)Eva Wohlleber (2 shared papers)André Reis (2 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)Clinical Genetics (3 papers)Journal of Inherited Metabolic Disease (2 papers)The American Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Eva Rossier
31 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 86
- Genetics 733
- Clinical Biochemistry 110
- Developmental Biology 33
- Molecular Biology 897
- Toxicology 36
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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 226 | |
| 2 | 2012 | 217 | |
| 3 | 2016 | 144 | |
| 4 | 2010 | 142 | |
| 5 | 1997 | 125 | |
| 6 | 2007 | 81 | |
| 7 | 2006 | 64 | |
| 8 | 2006 | 53 | |
| 9 | 1995 | 51 | |
| 10 | 2010 | 47 | |
| 11 | 2017 | 46 | |
| 12 | 2010 | 44 | |
| 13 | 2011 | 39 | |
| 14 | 2021 | 38 | |
| 15 | 2017 | 36 | |
| 16 | 1998 | 33 | |
| 17 | 2009 | 30 | |
| 18 | 2014 | 28 | |
| 19 | 2012 | 27 | |
| 20 | 1995 | 26 |
About Eva Rossier
Eva Rossier is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Hematology and Developmental Biology, having authored 31 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Chromatin Dynamics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (4 papers), Epigenetics and DNA Methylation (3 papers), Acute Myeloid Leukemia Research (3 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Genetics (733 citations), Clinical Biochemistry (110 citations), Developmental Biology (33 citations), Molecular Biology (897 citations) and Toxicology (36 citations). Eva Rossier has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Gotthold Barbi, Arif Bülent Ekici, Anita M. Rauch, Hildegard Kehrer‐Sawatzki, Christiane Zweier, Markus Zweier, Eva Wohlleber, André Reis, Hartmut Engels and Dagmar Wieczorek. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Journal of Inherited Metabolic Disease, The American Journal of Human Genetics and Journal of Medical 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.