Tanja Obermeier
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
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- Epilepsy research and treatment
Papers in
- Genetics 3
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 1
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- Glycosylation and Glycoproteins Research 1
- Co-authors
- Heather C. Mefford (3 shared papers)Evan E. Eichler (2 shared papers)André Franke (2 shared papers)T. Sander (1 shared paper)Katherine L. Helbig (1 shared paper)Zühal Yapıcı (1 shared paper)Costin Leu (1 shared paper)Ingrid E. Scheffer (1 shared paper)
- Journals
- Epilepsia (1 paper)Human Molecular Genetics (1 paper)Epilepsy Research (1 paper)Zeitschrift für Orthopädie und Unfallchirurgie (1 paper)
- Partner nations
- GermanyUnited StatesTürkiye
In The Last Decade
Tanja Obermeier
3 papers receiving 203 citations
Peers
Comparison fields: 5 of 20
- Genetics 156
- Psychiatry and Mental health 44
- Cellular and Molecular Neuroscience 21
- Molecular Biology 67
- Clinical Biochemistry 6
Countries citing papers authored by Tanja Obermeier
This map shows the geographic impact of Tanja Obermeier'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 Tanja Obermeier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tanja Obermeier more than expected).
Fields of papers citing papers by Tanja Obermeier
This network shows the impact of papers produced by Tanja Obermeier. 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 Tanja Obermeier. The network helps show where Tanja Obermeier may publish in the future.
Co-authors
The 23 scholars most cited alongside Tanja Obermeier, 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 | 167 | |
| 2 | 2011 | 22 | |
| 3 | 2013 | 18 | |
| 4 | 2016 | 1 |
About Tanja Obermeier
Tanja Obermeier is a scholar working on Genetics, Molecular Biology, Rehabilitation, Psychiatry and Mental health and Infectious Diseases, having authored 4 papers that have together received 208 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (1 paper), Glycosylation and Glycoproteins Research (1 paper), Epilepsy research and treatment (1 paper) and Musculoskeletal Disorders and Rehabilitation (1 paper). The work is most often cited by research in Genetics (156 citations), Psychiatry and Mental health (44 citations), Cellular and Molecular Neuroscience (21 citations), Molecular Biology (67 citations) and Clinical Biochemistry (6 citations). Tanja Obermeier has collaborated with scholars based in Germany, United States and Türkiye. Frequent co-authors include Heather C. Mefford, Evan E. Eichler, André Franke, T. Sander, Katherine L. Helbig, Zühal Yapıcı, Costin Leu, Ingrid E. Scheffer, Hande Çağlayan and Marta A. Bayly. Their work appears in journals such as Epilepsia, Human Molecular Genetics, Epilepsy Research and Zeitschrift für Orthopädie und Unfallchirurgie.
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.