Ewa Obersztyn
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 22
- Genetics and Neurodevelopmental Disorders 22
- Genomics and Rare Diseases 5
- Sensory Systems top 5%
- Molecular Biology top 10%
- Congenital heart defects research 7
- Mitochondrial Function and Pathology 4
- Ubiquitin and proteasome pathways 4
- Developmental Biology top 10%
- Cell Biology top 10%
-
- Chromosomal and Genetic Variations 10
-
- Prenatal Screening and Diagnostics 6
- Co-authors
- Paweł StankiewiczEwa BocianTadeusz MazurczakMonika GośSau Wai CheungBeata NowakowskaAnna Kutkowska‐KaźmierczakMagdalena Nawara
- Partner nations
- PolandUnited StatesUnited Kingdom
In The Last Decade
Ewa Obersztyn
72 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 75
- Genetics 711
- Sensory Systems 61
- Molecular Biology 692
- Developmental Biology 17
- Cell Biology 124
Countries citing papers authored by Ewa Obersztyn
This map shows the geographic impact of Ewa Obersztyn'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 Ewa Obersztyn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ewa Obersztyn more than expected).
Fields of papers citing papers by Ewa Obersztyn
This network shows the impact of papers produced by Ewa Obersztyn. 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 Ewa Obersztyn. The network helps show where Ewa Obersztyn may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Ewa Obersztyn, 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 | 2023 | 2 | |
| 2 | 2023 | 0 | |
| 3 | 2023 | 3 | |
| 4 | 2022 | 12 | |
| 5 | 2022 | 7 | |
| 6 | 2021 | 4 | |
| 7 | 2021 | 4 | |
| 8 | 2019 | 3 | |
| 9 | 2014 | 10 | |
| 10 | 2014 | 18 | |
| 11 | 2013 | 26 | |
| 12 | 2011 | 38 | |
| 13 | 2009 | 18 | |
| 14 | 2009 | 146 | |
| 15 | 2007 | 47 | |
| 16 | 2007 | 25 | |
| 17 | 2001 | 21 | |
| 18 | Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH) | 1996 | 1 |
| 19 | 1996 | 10 | |
| 20 | 1995 | 172 |
About Ewa Obersztyn
Ewa Obersztyn is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 78 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (22 papers), Chromosomal and Genetic Variations (10 papers), Congenital heart defects research (7 papers), Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Ubiquitin and proteasome pathways (4 papers). The work is most often cited by research in Genetics (711 citations), Sensory Systems (61 citations) and Molecular Biology (692 citations). Ewa Obersztyn has collaborated with scholars based in Poland, United States and United Kingdom. Frequent co-authors include Paweł Stankiewicz, Ewa Bocian, Tadeusz Mazurczak, Monika Goś, Sau Wai Cheung, Beata Nowakowska, Anna Kutkowska‐Kaźmierczak, Magdalena Nawara, Krzysztof Szczałuba and Hanna Mierzewska.
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.